Affiliations
Department of Medicine, Division of Hospital Medicine, University of California San Francisco, San Francisco, California
Given name(s)
Lawrence A.
Family name
Haber
Degrees
MD

Electronic Cigarettes

Article Type
Changed
Mon, 01/02/2017 - 19:34
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Clearing the air: Inpatient providers' knowledge, perspectives, and experience with electronic cigarettes

Electronic cigarettes are increasingly prevalent battery‐operated devices that heat a solution to generate an inhalable nicotine‐containing aerosol.[1, 2] Despite a diverse array of devices on the market, the US Food and Drug Administration (FDA) has only recently proposed expanding its regulatory ability to include electronic cigarettes.[3] States, municipalities, and institutions have enacted variable regulations on electronic nicotine delivery systems.[4, 5] Advocates of electronic cigarettes propose that they are a less‐toxic alternative to tobacco cigarettes, with potential for use as a nicotine replacement therapy (NRT).[6, 7, 8] Opponents argue that electronic cigarettes may undermine tobacco cessation goals and potentially expose nonusers to secondhand nicotine vapor.[9, 10]

Hospital providers frequently care for nicotine‐dependent patients.[11] We investigated inpatient healthcare providers' knowledge, perceptions, and experience with electronic cigarettes, with the goals of informing educational efforts and guiding policy decisions around hospital‐based use of electronic nicotine delivery systems.

METHODS

The study was conducted at a 183‐bed urban safety‐net medical center affiliated with a residency training program using a cross‐sectional survey to query a diverse array of inpatient providers (Table 1). Respondents who had not cared for an inpatient in the past 5 years were excluded. Surveys were designed based on prior literature, personal experience, and expert suggestions.[12] Surveys were disseminated in March 2014 via e‐mail, with embedded informed consent and a link that connected anonymously to the online survey (Qualtrics, Provo, UT). We did not collect unique identifiers and offered no incentive for participation. Data were downloaded to a secure database and analyzed using Microsoft Excel 2010 (Microsoft Corp., Redmond, WA) and GraphPad Prism version 6.04 (GraphPad Software, Inc., La Jolla, CA). The study was approved by the institutional review board.

Provider Perspectives on Electronic Cigarettes
Group (No.) Do you know what an electronic cigarette is?* Has a hospitalized patient ever asked you if he or she could use an electronic cigarette on hospital grounds?* Do you see electronic cigarettes as a nicotine replacement option for hospitalized patients? If you were caring for a patient, would you be okay with the patient using an electronic cigarette while hospitalized? If you were hospitalized in a shared hospital room, would you be okay with your roommate using an electronic cigarette? Should electronic cigarettes be banned from healthcare settings? Should electronic cigarettes be banned in the same locations as traditional cigarettes? Should electronic cigarettes be regulated by the US Food and Drug Administration?
  • NOTE: Percentages indicate percent of respondents within each group responding yes to the stated question. Further breakdown of answer responses are presented in the text. Abbreviations: MD, medical doctor. *Denotes a question with yes/no answer choices. Denotes a question with yes/no/unsure answer choices. P<0.005 using a 2 test for faculty and resident physicians compared to all other respondents. P<0.001 using a 2 test for nurses compared to all other respondents.

Faculty MD (32) 96.9% 12.5% 28.1% 34.4% 12.5% 37.5% 53.1% 100%
Resident MD (33) 97.0% 9.1% 27.3% 45.5% 24.2% 45.5% 36.4% 93.9%
Registered nurse (35) 94.3% 42.9% 25.7% 28.6% 25.7% 40.0% 54.3% 68.6%
Rehabilitation staff (18) 88.9% 11.1% 11.1% 5.6% 5.6% 66.7% 55.6% 88.9%
Social worker (6) 100% 33.3% 16.7% 16.7% 0.0% 50.0% 50.0% 83.3%
Pharmacist (18) 100% 5.6% 11.1% 27.8% 22.2% 61.1% 50.0% 83.3%
All respondents (142) 95.8% 19.0% 22.5% 30.3% 18.3% 47.2% 49.3% 86.6%

RESULTS

Study Participants

There were 242 survey respondents (response rate of 41%), of whom 100 were excluded based on study criteria. The median age of the 142 included participants was 34.0 years. There were significantly more female respondents (69%, P=0.001, 2 test), equally over‐represented across all inpatient provider groups. Only 1.4% of all respondents reported personal active tobacco use, whereas 24.6% of study participants reported prior tobacco use. Tobacco use history was similar across inpatient provider groups and gender. Respondents over 50 years of age demonstrated a higher rate of current or prior tobacco use compared with participants from other age groups combined (53% vs 23%, P=0.01, 2 test).

Electronic Cigarette Familiarity and Patient Requests

Of the participants, 95.8% reported familiarity with electronic cigarettes, without differences across age or gender. Of all of the providers, 19.0% reported being asked by a hospitalized patient for permission to use an electronic cigarette in the hospital. Registered nurses were significantly more likely to have been asked by patients compared to all other study participants (43% vs 11%, P<0.001, 2 test).

Electronic Cigarettes as NRT

Whereas 22.5% of study participants felt that electronic cigarettes could serve as a viable in‐hospital NRT, 48.6% felt that electronic cigarettes should not be used, and 28.9% were unsure (Table 1), irrespective of demographics or personal tobacco use history. One‐third of respondents would allow an inpatient under their care to use an electronic cigarette. Groups most likely to permit use were faculty (34.4%) and resident physicians (45.5%), though this difference was not statistically significant.

Perspectives on Exposure

Only 18.3% of study participants would agree to share a hospital room with a patient using an electronic cigarette. Of all participants, 47.2% and 49.3% felt that electronic cigarettes should be banned from healthcare settings and from the same locations as traditional cigarettes, respectively. There were no significant differences in perspectives when stratified by age or gender. Current or prior tobacco users were more likely to be accepting of the use of electronic cigarettes in healthcare settings compared to nonusers (50% vs 29%, P=0.02, Fisher exact test).

FDA Regulation

Of all study participants, 86.6% responded that electronic cigarettes should be regulated by the FDA. Physicians most strongly agreed with this statement compared with all other provider groups (97% vs 78%, P=0.004, 2 test). Conversely, registered nurses were least likely to feel that electronic cigarettes should be FDA‐regulated compared to all other provider groups (69% vs 93%, P<0.005, 2 test).

DISCUSSION

Our study is the first to provide hospital‐based providers' experience and perspectives surrounding electronic cigarette use. The vast majority of participants reported familiarity with electronic cigarettes, consistent with prior findings.[13] Though electronic cigarettes have yet to achieve a use in the hospital setting, 19% of our respondents reported receiving requests from hospitalized patients to use these devices. With increasing patient demand for electronic cigarettes, hospitals will need to update their tobacco policies to include these novel devices as well as target educational efforts toward front‐line providers, such as nurses, who receive the majority of requests.

Participants perceived traditional cigarettes to be significantly more harmful than electronic cigarettes, while established forms of NRT were felt to be less harmful than electronic cigarettes (data not shown). Concern about the health effects of electronic cigarettes is further reflected in providers' hesitancy to view these devices as an NRT option in the hospital, reluctance to consider sharing a room with an electronic cigarette user, and near majority opinion that electronic cigarettes should be banned from healthcare settings altogether. Current regulation by the US Department of Transportation bans electronic cigarette use on airplanes, whereas a host of states currently ban electronic cigarette use in similarly enclosed spaces such as correctional facilities and commuter trains.[14] More knowledge is needed on the health effects of electronic cigarettes on the primary user, secondhand exposure range, and their potential to aid in short‐ and long‐term nicotine cessation before providers and hospitals can make an informed risk‐benefit analysis for appropriate inpatient use. As current or past tobacco users were more accepting of the use of electronic cigarettes in hospital settings, these providers' opinions should be sought for a unique understanding of the interplay between electronic cigarettes and the healthcare environment.

Concern over the unknown safety effects can also be seen in the overwhelming provider support for FDA regulation. Healthcare advocacy groups, such as the American Heart Association, the American Lung Association, and the Legacy Foundation already support federal regulation.[15, 16, 17] FDA regulation may lead to the ability to standardize device content, regulate purchasing and marketing requirements, and ensure that claims to health effects are supported by scientific evidence, though agency involvement may also slow the process of integration into hospital use. Perhaps reflective of the immediacy of the problem, nurses who receive the majority of requests for electronic cigarettes from patients are least likely to want FDA regulation. Until more is known, patients and staff may benefit from pairing vaporizing patients in shared rooms or providing users with designated inhaling spaces.

Nicotine addiction is a strong driving force and, due to a strict no‐smoking policy at our institution, we have witnessed patients making unsafe decisions to leave the hospital (in some cases against medical advice) in an effort to continue smoking. Patients may be starting to look toward electronic cigarettes as an NRT option that more closely satisfies nicotine cravings as well as the ritualistic and tactile components of cigarette use. Electronic cigarettes could have the potential to act as a harm reduction method for nicotine‐dependent inpatients by decreasing the nicotine‐withdrawal related impetus for unsafe hospital discharges. Institutions should take this into account when formulating new policy.

Our study has several limitations. First, it was a single‐center study that may not be representative of provider perspectives at other institutions. Second, the survey was a cross‐sectional sample, missing providers who did not receive the e‐mail during the enrollment period. Third, responses may not accurately reflect perspectives of smaller responding groups such as social workers. Fourth, the survey did not include all types of physicians who deal with smoking cessation, though internal and family medicine physicians provide the majority of care for hospitalized patients at our institution. Fifth, we recorded self‐reported familiarity with electronic cigarettes and did not formally test providers' knowledge of the subject.

Our study provides new perspectives and data on electronic cigarettes to inform future research as well as hospital and healthcare policy. Hospitals should educate patients and front‐line providers around the paucity of health information on these novel devices, while formulating policy that acknowledges patient demand for electronic cigarettes and their potential for cessation therapy and harm reduction. Further research should focus on the effects of nicotine vapor inhalation on patients, the consequences of secondhand nicotine vapor, and the potential for electronic nicotine delivery systems to act as a novel NRT for hospital use.

Disclosure

Nothing to report.

Files
References
  1. Grana R, Benowitz NL, Glantz SA. E‐cigarettes: a scientific review. Circulation. 2014;129:19721986.
  2. Pearson JL, Richardson A, Niaura RS, Vallone DM, Abrams DB. E‐Cigarette awareness, use, and harm perceptions in US adults. Am J Public Health. 2012;102(9):17581766.
  3. U.S. Food and Drug Administration. FDA proposes to extend its tobacco authority to additional tobacco products, including e‐cigarettes. Available at: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm394667.htm. Accessed May 5, 2014.
  4. Paradise J. Electronic cigarettes: smoke‐free laws, sale restrictions, and the public health. Am J Public Health. 2014;104(6):e17e18.
  5. American Nonsmokers' Rights Foundation. US state and local laws regulating use of electronic cigarettes. Available at: http://www.no‐smoke.org/pdf/ecigslaws.pdf. Accessed September 2, 2014.
  6. Etter JF, Bullen C. Electronic cigarette: users profile, utilization, satisfaction and perceived efficacy. Addiction. 2011;106(11):20172028.
  7. Polosa R, Caponnetto P, Morjaria JB, Papale G, Campagna D, Russo C. Effect of an electronic nicotine delivery device (e‐cigarette) on smoking reduction and cessation: a prospective 6‐month pilot study. BMC Public Health. 2011;11:786.
  8. Brown S, Bears E, Kotz D, Michie S, West R. Real‐world effectiveness of e‐cigarettes when used to aid smoking cessation: a cross‐sectional population study. Addiction. 2014;109(9):15311540.
  9. Benowitz NL, Goniewicz ML. The regulatory challenge of electronic cigarettes. JAMA. 2013;310(7):685686.
  10. Abrams DB. Promise and peril of e‐Cigarettes: can disruptive technology make cigarettes obsolete? JAMA. 2014;311(2):135136.
  11. Harrington KF, Hull NC, Akindoju O, et al. Electronic cigarette awareness, use history, and expected future use among hospitalized cigarette smokers. Nicotine Tob Res. 2014;16(11):15121517.
  12. Global Adult Tobacco Survey Collaborative Group. Tobacco Questions for Surveys: A Subset of Key Questions From the Global Adult Tobacco Survey (GATS). 2nd ed. Atlanta, GA: Centers for Disease Control and Prevention; 2011. Available at: http://www.who.int/tobacco/surveillance/en_tfi_tqs.pdf. Accessed April 23, 2014.
  13. Pepper JK, McRee AL, Gilkey MB. Healthcare providers' beliefs and attitudes about electronic cigarettes and preventive counseling for adolescent patients. J Adolesc Health. 2014;54(6):678683.
  14. U.S. Department of Transportation. DOT policy on e‐cigarettes. Available at: http://www.dot.gov/sites/dot.gov/files/docs/PolicyOnECigarettes.pdf. Accessed September 2, 2014.
  15. American Heart Association. AHA: E‐cigarettes threaten to addict next generation of smokers; regulation, further study needed. Available at: http://blog.heart.org/aha‐e‐cigarettes‐threaten‐to‐addict‐next‐generation‐of‐smokers‐regulation‐further‐study‐needed/. Accessed August 25, 2014.
  16. American Lung Association. American Lung Association statement on e‐cigarettes. Available at: http://www.lung.org/stop‐smoking/tobacco‐control‐advocacy/federal/e‐cigarettes.html. Accesses August 25, 2014.
  17. Legacy for Health. E‐cigarette policy: the FDA should promptly exercise regulatory authority and over e‐cigarettes. Available at: http://www.legacyforhealth.org/content/download/3962/56088/version/1/file/LEG‐Policy_Statement‐ECigarette‐JAN2014.pdf. Accessed August 25, 2014.
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Electronic cigarettes are increasingly prevalent battery‐operated devices that heat a solution to generate an inhalable nicotine‐containing aerosol.[1, 2] Despite a diverse array of devices on the market, the US Food and Drug Administration (FDA) has only recently proposed expanding its regulatory ability to include electronic cigarettes.[3] States, municipalities, and institutions have enacted variable regulations on electronic nicotine delivery systems.[4, 5] Advocates of electronic cigarettes propose that they are a less‐toxic alternative to tobacco cigarettes, with potential for use as a nicotine replacement therapy (NRT).[6, 7, 8] Opponents argue that electronic cigarettes may undermine tobacco cessation goals and potentially expose nonusers to secondhand nicotine vapor.[9, 10]

Hospital providers frequently care for nicotine‐dependent patients.[11] We investigated inpatient healthcare providers' knowledge, perceptions, and experience with electronic cigarettes, with the goals of informing educational efforts and guiding policy decisions around hospital‐based use of electronic nicotine delivery systems.

METHODS

The study was conducted at a 183‐bed urban safety‐net medical center affiliated with a residency training program using a cross‐sectional survey to query a diverse array of inpatient providers (Table 1). Respondents who had not cared for an inpatient in the past 5 years were excluded. Surveys were designed based on prior literature, personal experience, and expert suggestions.[12] Surveys were disseminated in March 2014 via e‐mail, with embedded informed consent and a link that connected anonymously to the online survey (Qualtrics, Provo, UT). We did not collect unique identifiers and offered no incentive for participation. Data were downloaded to a secure database and analyzed using Microsoft Excel 2010 (Microsoft Corp., Redmond, WA) and GraphPad Prism version 6.04 (GraphPad Software, Inc., La Jolla, CA). The study was approved by the institutional review board.

Provider Perspectives on Electronic Cigarettes
Group (No.) Do you know what an electronic cigarette is?* Has a hospitalized patient ever asked you if he or she could use an electronic cigarette on hospital grounds?* Do you see electronic cigarettes as a nicotine replacement option for hospitalized patients? If you were caring for a patient, would you be okay with the patient using an electronic cigarette while hospitalized? If you were hospitalized in a shared hospital room, would you be okay with your roommate using an electronic cigarette? Should electronic cigarettes be banned from healthcare settings? Should electronic cigarettes be banned in the same locations as traditional cigarettes? Should electronic cigarettes be regulated by the US Food and Drug Administration?
  • NOTE: Percentages indicate percent of respondents within each group responding yes to the stated question. Further breakdown of answer responses are presented in the text. Abbreviations: MD, medical doctor. *Denotes a question with yes/no answer choices. Denotes a question with yes/no/unsure answer choices. P<0.005 using a 2 test for faculty and resident physicians compared to all other respondents. P<0.001 using a 2 test for nurses compared to all other respondents.

Faculty MD (32) 96.9% 12.5% 28.1% 34.4% 12.5% 37.5% 53.1% 100%
Resident MD (33) 97.0% 9.1% 27.3% 45.5% 24.2% 45.5% 36.4% 93.9%
Registered nurse (35) 94.3% 42.9% 25.7% 28.6% 25.7% 40.0% 54.3% 68.6%
Rehabilitation staff (18) 88.9% 11.1% 11.1% 5.6% 5.6% 66.7% 55.6% 88.9%
Social worker (6) 100% 33.3% 16.7% 16.7% 0.0% 50.0% 50.0% 83.3%
Pharmacist (18) 100% 5.6% 11.1% 27.8% 22.2% 61.1% 50.0% 83.3%
All respondents (142) 95.8% 19.0% 22.5% 30.3% 18.3% 47.2% 49.3% 86.6%

RESULTS

Study Participants

There were 242 survey respondents (response rate of 41%), of whom 100 were excluded based on study criteria. The median age of the 142 included participants was 34.0 years. There were significantly more female respondents (69%, P=0.001, 2 test), equally over‐represented across all inpatient provider groups. Only 1.4% of all respondents reported personal active tobacco use, whereas 24.6% of study participants reported prior tobacco use. Tobacco use history was similar across inpatient provider groups and gender. Respondents over 50 years of age demonstrated a higher rate of current or prior tobacco use compared with participants from other age groups combined (53% vs 23%, P=0.01, 2 test).

Electronic Cigarette Familiarity and Patient Requests

Of the participants, 95.8% reported familiarity with electronic cigarettes, without differences across age or gender. Of all of the providers, 19.0% reported being asked by a hospitalized patient for permission to use an electronic cigarette in the hospital. Registered nurses were significantly more likely to have been asked by patients compared to all other study participants (43% vs 11%, P<0.001, 2 test).

Electronic Cigarettes as NRT

Whereas 22.5% of study participants felt that electronic cigarettes could serve as a viable in‐hospital NRT, 48.6% felt that electronic cigarettes should not be used, and 28.9% were unsure (Table 1), irrespective of demographics or personal tobacco use history. One‐third of respondents would allow an inpatient under their care to use an electronic cigarette. Groups most likely to permit use were faculty (34.4%) and resident physicians (45.5%), though this difference was not statistically significant.

Perspectives on Exposure

Only 18.3% of study participants would agree to share a hospital room with a patient using an electronic cigarette. Of all participants, 47.2% and 49.3% felt that electronic cigarettes should be banned from healthcare settings and from the same locations as traditional cigarettes, respectively. There were no significant differences in perspectives when stratified by age or gender. Current or prior tobacco users were more likely to be accepting of the use of electronic cigarettes in healthcare settings compared to nonusers (50% vs 29%, P=0.02, Fisher exact test).

FDA Regulation

Of all study participants, 86.6% responded that electronic cigarettes should be regulated by the FDA. Physicians most strongly agreed with this statement compared with all other provider groups (97% vs 78%, P=0.004, 2 test). Conversely, registered nurses were least likely to feel that electronic cigarettes should be FDA‐regulated compared to all other provider groups (69% vs 93%, P<0.005, 2 test).

DISCUSSION

Our study is the first to provide hospital‐based providers' experience and perspectives surrounding electronic cigarette use. The vast majority of participants reported familiarity with electronic cigarettes, consistent with prior findings.[13] Though electronic cigarettes have yet to achieve a use in the hospital setting, 19% of our respondents reported receiving requests from hospitalized patients to use these devices. With increasing patient demand for electronic cigarettes, hospitals will need to update their tobacco policies to include these novel devices as well as target educational efforts toward front‐line providers, such as nurses, who receive the majority of requests.

Participants perceived traditional cigarettes to be significantly more harmful than electronic cigarettes, while established forms of NRT were felt to be less harmful than electronic cigarettes (data not shown). Concern about the health effects of electronic cigarettes is further reflected in providers' hesitancy to view these devices as an NRT option in the hospital, reluctance to consider sharing a room with an electronic cigarette user, and near majority opinion that electronic cigarettes should be banned from healthcare settings altogether. Current regulation by the US Department of Transportation bans electronic cigarette use on airplanes, whereas a host of states currently ban electronic cigarette use in similarly enclosed spaces such as correctional facilities and commuter trains.[14] More knowledge is needed on the health effects of electronic cigarettes on the primary user, secondhand exposure range, and their potential to aid in short‐ and long‐term nicotine cessation before providers and hospitals can make an informed risk‐benefit analysis for appropriate inpatient use. As current or past tobacco users were more accepting of the use of electronic cigarettes in hospital settings, these providers' opinions should be sought for a unique understanding of the interplay between electronic cigarettes and the healthcare environment.

Concern over the unknown safety effects can also be seen in the overwhelming provider support for FDA regulation. Healthcare advocacy groups, such as the American Heart Association, the American Lung Association, and the Legacy Foundation already support federal regulation.[15, 16, 17] FDA regulation may lead to the ability to standardize device content, regulate purchasing and marketing requirements, and ensure that claims to health effects are supported by scientific evidence, though agency involvement may also slow the process of integration into hospital use. Perhaps reflective of the immediacy of the problem, nurses who receive the majority of requests for electronic cigarettes from patients are least likely to want FDA regulation. Until more is known, patients and staff may benefit from pairing vaporizing patients in shared rooms or providing users with designated inhaling spaces.

Nicotine addiction is a strong driving force and, due to a strict no‐smoking policy at our institution, we have witnessed patients making unsafe decisions to leave the hospital (in some cases against medical advice) in an effort to continue smoking. Patients may be starting to look toward electronic cigarettes as an NRT option that more closely satisfies nicotine cravings as well as the ritualistic and tactile components of cigarette use. Electronic cigarettes could have the potential to act as a harm reduction method for nicotine‐dependent inpatients by decreasing the nicotine‐withdrawal related impetus for unsafe hospital discharges. Institutions should take this into account when formulating new policy.

Our study has several limitations. First, it was a single‐center study that may not be representative of provider perspectives at other institutions. Second, the survey was a cross‐sectional sample, missing providers who did not receive the e‐mail during the enrollment period. Third, responses may not accurately reflect perspectives of smaller responding groups such as social workers. Fourth, the survey did not include all types of physicians who deal with smoking cessation, though internal and family medicine physicians provide the majority of care for hospitalized patients at our institution. Fifth, we recorded self‐reported familiarity with electronic cigarettes and did not formally test providers' knowledge of the subject.

Our study provides new perspectives and data on electronic cigarettes to inform future research as well as hospital and healthcare policy. Hospitals should educate patients and front‐line providers around the paucity of health information on these novel devices, while formulating policy that acknowledges patient demand for electronic cigarettes and their potential for cessation therapy and harm reduction. Further research should focus on the effects of nicotine vapor inhalation on patients, the consequences of secondhand nicotine vapor, and the potential for electronic nicotine delivery systems to act as a novel NRT for hospital use.

Disclosure

Nothing to report.

Electronic cigarettes are increasingly prevalent battery‐operated devices that heat a solution to generate an inhalable nicotine‐containing aerosol.[1, 2] Despite a diverse array of devices on the market, the US Food and Drug Administration (FDA) has only recently proposed expanding its regulatory ability to include electronic cigarettes.[3] States, municipalities, and institutions have enacted variable regulations on electronic nicotine delivery systems.[4, 5] Advocates of electronic cigarettes propose that they are a less‐toxic alternative to tobacco cigarettes, with potential for use as a nicotine replacement therapy (NRT).[6, 7, 8] Opponents argue that electronic cigarettes may undermine tobacco cessation goals and potentially expose nonusers to secondhand nicotine vapor.[9, 10]

Hospital providers frequently care for nicotine‐dependent patients.[11] We investigated inpatient healthcare providers' knowledge, perceptions, and experience with electronic cigarettes, with the goals of informing educational efforts and guiding policy decisions around hospital‐based use of electronic nicotine delivery systems.

METHODS

The study was conducted at a 183‐bed urban safety‐net medical center affiliated with a residency training program using a cross‐sectional survey to query a diverse array of inpatient providers (Table 1). Respondents who had not cared for an inpatient in the past 5 years were excluded. Surveys were designed based on prior literature, personal experience, and expert suggestions.[12] Surveys were disseminated in March 2014 via e‐mail, with embedded informed consent and a link that connected anonymously to the online survey (Qualtrics, Provo, UT). We did not collect unique identifiers and offered no incentive for participation. Data were downloaded to a secure database and analyzed using Microsoft Excel 2010 (Microsoft Corp., Redmond, WA) and GraphPad Prism version 6.04 (GraphPad Software, Inc., La Jolla, CA). The study was approved by the institutional review board.

Provider Perspectives on Electronic Cigarettes
Group (No.) Do you know what an electronic cigarette is?* Has a hospitalized patient ever asked you if he or she could use an electronic cigarette on hospital grounds?* Do you see electronic cigarettes as a nicotine replacement option for hospitalized patients? If you were caring for a patient, would you be okay with the patient using an electronic cigarette while hospitalized? If you were hospitalized in a shared hospital room, would you be okay with your roommate using an electronic cigarette? Should electronic cigarettes be banned from healthcare settings? Should electronic cigarettes be banned in the same locations as traditional cigarettes? Should electronic cigarettes be regulated by the US Food and Drug Administration?
  • NOTE: Percentages indicate percent of respondents within each group responding yes to the stated question. Further breakdown of answer responses are presented in the text. Abbreviations: MD, medical doctor. *Denotes a question with yes/no answer choices. Denotes a question with yes/no/unsure answer choices. P<0.005 using a 2 test for faculty and resident physicians compared to all other respondents. P<0.001 using a 2 test for nurses compared to all other respondents.

Faculty MD (32) 96.9% 12.5% 28.1% 34.4% 12.5% 37.5% 53.1% 100%
Resident MD (33) 97.0% 9.1% 27.3% 45.5% 24.2% 45.5% 36.4% 93.9%
Registered nurse (35) 94.3% 42.9% 25.7% 28.6% 25.7% 40.0% 54.3% 68.6%
Rehabilitation staff (18) 88.9% 11.1% 11.1% 5.6% 5.6% 66.7% 55.6% 88.9%
Social worker (6) 100% 33.3% 16.7% 16.7% 0.0% 50.0% 50.0% 83.3%
Pharmacist (18) 100% 5.6% 11.1% 27.8% 22.2% 61.1% 50.0% 83.3%
All respondents (142) 95.8% 19.0% 22.5% 30.3% 18.3% 47.2% 49.3% 86.6%

RESULTS

Study Participants

There were 242 survey respondents (response rate of 41%), of whom 100 were excluded based on study criteria. The median age of the 142 included participants was 34.0 years. There were significantly more female respondents (69%, P=0.001, 2 test), equally over‐represented across all inpatient provider groups. Only 1.4% of all respondents reported personal active tobacco use, whereas 24.6% of study participants reported prior tobacco use. Tobacco use history was similar across inpatient provider groups and gender. Respondents over 50 years of age demonstrated a higher rate of current or prior tobacco use compared with participants from other age groups combined (53% vs 23%, P=0.01, 2 test).

Electronic Cigarette Familiarity and Patient Requests

Of the participants, 95.8% reported familiarity with electronic cigarettes, without differences across age or gender. Of all of the providers, 19.0% reported being asked by a hospitalized patient for permission to use an electronic cigarette in the hospital. Registered nurses were significantly more likely to have been asked by patients compared to all other study participants (43% vs 11%, P<0.001, 2 test).

Electronic Cigarettes as NRT

Whereas 22.5% of study participants felt that electronic cigarettes could serve as a viable in‐hospital NRT, 48.6% felt that electronic cigarettes should not be used, and 28.9% were unsure (Table 1), irrespective of demographics or personal tobacco use history. One‐third of respondents would allow an inpatient under their care to use an electronic cigarette. Groups most likely to permit use were faculty (34.4%) and resident physicians (45.5%), though this difference was not statistically significant.

Perspectives on Exposure

Only 18.3% of study participants would agree to share a hospital room with a patient using an electronic cigarette. Of all participants, 47.2% and 49.3% felt that electronic cigarettes should be banned from healthcare settings and from the same locations as traditional cigarettes, respectively. There were no significant differences in perspectives when stratified by age or gender. Current or prior tobacco users were more likely to be accepting of the use of electronic cigarettes in healthcare settings compared to nonusers (50% vs 29%, P=0.02, Fisher exact test).

FDA Regulation

Of all study participants, 86.6% responded that electronic cigarettes should be regulated by the FDA. Physicians most strongly agreed with this statement compared with all other provider groups (97% vs 78%, P=0.004, 2 test). Conversely, registered nurses were least likely to feel that electronic cigarettes should be FDA‐regulated compared to all other provider groups (69% vs 93%, P<0.005, 2 test).

DISCUSSION

Our study is the first to provide hospital‐based providers' experience and perspectives surrounding electronic cigarette use. The vast majority of participants reported familiarity with electronic cigarettes, consistent with prior findings.[13] Though electronic cigarettes have yet to achieve a use in the hospital setting, 19% of our respondents reported receiving requests from hospitalized patients to use these devices. With increasing patient demand for electronic cigarettes, hospitals will need to update their tobacco policies to include these novel devices as well as target educational efforts toward front‐line providers, such as nurses, who receive the majority of requests.

Participants perceived traditional cigarettes to be significantly more harmful than electronic cigarettes, while established forms of NRT were felt to be less harmful than electronic cigarettes (data not shown). Concern about the health effects of electronic cigarettes is further reflected in providers' hesitancy to view these devices as an NRT option in the hospital, reluctance to consider sharing a room with an electronic cigarette user, and near majority opinion that electronic cigarettes should be banned from healthcare settings altogether. Current regulation by the US Department of Transportation bans electronic cigarette use on airplanes, whereas a host of states currently ban electronic cigarette use in similarly enclosed spaces such as correctional facilities and commuter trains.[14] More knowledge is needed on the health effects of electronic cigarettes on the primary user, secondhand exposure range, and their potential to aid in short‐ and long‐term nicotine cessation before providers and hospitals can make an informed risk‐benefit analysis for appropriate inpatient use. As current or past tobacco users were more accepting of the use of electronic cigarettes in hospital settings, these providers' opinions should be sought for a unique understanding of the interplay between electronic cigarettes and the healthcare environment.

Concern over the unknown safety effects can also be seen in the overwhelming provider support for FDA regulation. Healthcare advocacy groups, such as the American Heart Association, the American Lung Association, and the Legacy Foundation already support federal regulation.[15, 16, 17] FDA regulation may lead to the ability to standardize device content, regulate purchasing and marketing requirements, and ensure that claims to health effects are supported by scientific evidence, though agency involvement may also slow the process of integration into hospital use. Perhaps reflective of the immediacy of the problem, nurses who receive the majority of requests for electronic cigarettes from patients are least likely to want FDA regulation. Until more is known, patients and staff may benefit from pairing vaporizing patients in shared rooms or providing users with designated inhaling spaces.

Nicotine addiction is a strong driving force and, due to a strict no‐smoking policy at our institution, we have witnessed patients making unsafe decisions to leave the hospital (in some cases against medical advice) in an effort to continue smoking. Patients may be starting to look toward electronic cigarettes as an NRT option that more closely satisfies nicotine cravings as well as the ritualistic and tactile components of cigarette use. Electronic cigarettes could have the potential to act as a harm reduction method for nicotine‐dependent inpatients by decreasing the nicotine‐withdrawal related impetus for unsafe hospital discharges. Institutions should take this into account when formulating new policy.

Our study has several limitations. First, it was a single‐center study that may not be representative of provider perspectives at other institutions. Second, the survey was a cross‐sectional sample, missing providers who did not receive the e‐mail during the enrollment period. Third, responses may not accurately reflect perspectives of smaller responding groups such as social workers. Fourth, the survey did not include all types of physicians who deal with smoking cessation, though internal and family medicine physicians provide the majority of care for hospitalized patients at our institution. Fifth, we recorded self‐reported familiarity with electronic cigarettes and did not formally test providers' knowledge of the subject.

Our study provides new perspectives and data on electronic cigarettes to inform future research as well as hospital and healthcare policy. Hospitals should educate patients and front‐line providers around the paucity of health information on these novel devices, while formulating policy that acknowledges patient demand for electronic cigarettes and their potential for cessation therapy and harm reduction. Further research should focus on the effects of nicotine vapor inhalation on patients, the consequences of secondhand nicotine vapor, and the potential for electronic nicotine delivery systems to act as a novel NRT for hospital use.

Disclosure

Nothing to report.

References
  1. Grana R, Benowitz NL, Glantz SA. E‐cigarettes: a scientific review. Circulation. 2014;129:19721986.
  2. Pearson JL, Richardson A, Niaura RS, Vallone DM, Abrams DB. E‐Cigarette awareness, use, and harm perceptions in US adults. Am J Public Health. 2012;102(9):17581766.
  3. U.S. Food and Drug Administration. FDA proposes to extend its tobacco authority to additional tobacco products, including e‐cigarettes. Available at: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm394667.htm. Accessed May 5, 2014.
  4. Paradise J. Electronic cigarettes: smoke‐free laws, sale restrictions, and the public health. Am J Public Health. 2014;104(6):e17e18.
  5. American Nonsmokers' Rights Foundation. US state and local laws regulating use of electronic cigarettes. Available at: http://www.no‐smoke.org/pdf/ecigslaws.pdf. Accessed September 2, 2014.
  6. Etter JF, Bullen C. Electronic cigarette: users profile, utilization, satisfaction and perceived efficacy. Addiction. 2011;106(11):20172028.
  7. Polosa R, Caponnetto P, Morjaria JB, Papale G, Campagna D, Russo C. Effect of an electronic nicotine delivery device (e‐cigarette) on smoking reduction and cessation: a prospective 6‐month pilot study. BMC Public Health. 2011;11:786.
  8. Brown S, Bears E, Kotz D, Michie S, West R. Real‐world effectiveness of e‐cigarettes when used to aid smoking cessation: a cross‐sectional population study. Addiction. 2014;109(9):15311540.
  9. Benowitz NL, Goniewicz ML. The regulatory challenge of electronic cigarettes. JAMA. 2013;310(7):685686.
  10. Abrams DB. Promise and peril of e‐Cigarettes: can disruptive technology make cigarettes obsolete? JAMA. 2014;311(2):135136.
  11. Harrington KF, Hull NC, Akindoju O, et al. Electronic cigarette awareness, use history, and expected future use among hospitalized cigarette smokers. Nicotine Tob Res. 2014;16(11):15121517.
  12. Global Adult Tobacco Survey Collaborative Group. Tobacco Questions for Surveys: A Subset of Key Questions From the Global Adult Tobacco Survey (GATS). 2nd ed. Atlanta, GA: Centers for Disease Control and Prevention; 2011. Available at: http://www.who.int/tobacco/surveillance/en_tfi_tqs.pdf. Accessed April 23, 2014.
  13. Pepper JK, McRee AL, Gilkey MB. Healthcare providers' beliefs and attitudes about electronic cigarettes and preventive counseling for adolescent patients. J Adolesc Health. 2014;54(6):678683.
  14. U.S. Department of Transportation. DOT policy on e‐cigarettes. Available at: http://www.dot.gov/sites/dot.gov/files/docs/PolicyOnECigarettes.pdf. Accessed September 2, 2014.
  15. American Heart Association. AHA: E‐cigarettes threaten to addict next generation of smokers; regulation, further study needed. Available at: http://blog.heart.org/aha‐e‐cigarettes‐threaten‐to‐addict‐next‐generation‐of‐smokers‐regulation‐further‐study‐needed/. Accessed August 25, 2014.
  16. American Lung Association. American Lung Association statement on e‐cigarettes. Available at: http://www.lung.org/stop‐smoking/tobacco‐control‐advocacy/federal/e‐cigarettes.html. Accesses August 25, 2014.
  17. Legacy for Health. E‐cigarette policy: the FDA should promptly exercise regulatory authority and over e‐cigarettes. Available at: http://www.legacyforhealth.org/content/download/3962/56088/version/1/file/LEG‐Policy_Statement‐ECigarette‐JAN2014.pdf. Accessed August 25, 2014.
References
  1. Grana R, Benowitz NL, Glantz SA. E‐cigarettes: a scientific review. Circulation. 2014;129:19721986.
  2. Pearson JL, Richardson A, Niaura RS, Vallone DM, Abrams DB. E‐Cigarette awareness, use, and harm perceptions in US adults. Am J Public Health. 2012;102(9):17581766.
  3. U.S. Food and Drug Administration. FDA proposes to extend its tobacco authority to additional tobacco products, including e‐cigarettes. Available at: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm394667.htm. Accessed May 5, 2014.
  4. Paradise J. Electronic cigarettes: smoke‐free laws, sale restrictions, and the public health. Am J Public Health. 2014;104(6):e17e18.
  5. American Nonsmokers' Rights Foundation. US state and local laws regulating use of electronic cigarettes. Available at: http://www.no‐smoke.org/pdf/ecigslaws.pdf. Accessed September 2, 2014.
  6. Etter JF, Bullen C. Electronic cigarette: users profile, utilization, satisfaction and perceived efficacy. Addiction. 2011;106(11):20172028.
  7. Polosa R, Caponnetto P, Morjaria JB, Papale G, Campagna D, Russo C. Effect of an electronic nicotine delivery device (e‐cigarette) on smoking reduction and cessation: a prospective 6‐month pilot study. BMC Public Health. 2011;11:786.
  8. Brown S, Bears E, Kotz D, Michie S, West R. Real‐world effectiveness of e‐cigarettes when used to aid smoking cessation: a cross‐sectional population study. Addiction. 2014;109(9):15311540.
  9. Benowitz NL, Goniewicz ML. The regulatory challenge of electronic cigarettes. JAMA. 2013;310(7):685686.
  10. Abrams DB. Promise and peril of e‐Cigarettes: can disruptive technology make cigarettes obsolete? JAMA. 2014;311(2):135136.
  11. Harrington KF, Hull NC, Akindoju O, et al. Electronic cigarette awareness, use history, and expected future use among hospitalized cigarette smokers. Nicotine Tob Res. 2014;16(11):15121517.
  12. Global Adult Tobacco Survey Collaborative Group. Tobacco Questions for Surveys: A Subset of Key Questions From the Global Adult Tobacco Survey (GATS). 2nd ed. Atlanta, GA: Centers for Disease Control and Prevention; 2011. Available at: http://www.who.int/tobacco/surveillance/en_tfi_tqs.pdf. Accessed April 23, 2014.
  13. Pepper JK, McRee AL, Gilkey MB. Healthcare providers' beliefs and attitudes about electronic cigarettes and preventive counseling for adolescent patients. J Adolesc Health. 2014;54(6):678683.
  14. U.S. Department of Transportation. DOT policy on e‐cigarettes. Available at: http://www.dot.gov/sites/dot.gov/files/docs/PolicyOnECigarettes.pdf. Accessed September 2, 2014.
  15. American Heart Association. AHA: E‐cigarettes threaten to addict next generation of smokers; regulation, further study needed. Available at: http://blog.heart.org/aha‐e‐cigarettes‐threaten‐to‐addict‐next‐generation‐of‐smokers‐regulation‐further‐study‐needed/. Accessed August 25, 2014.
  16. American Lung Association. American Lung Association statement on e‐cigarettes. Available at: http://www.lung.org/stop‐smoking/tobacco‐control‐advocacy/federal/e‐cigarettes.html. Accesses August 25, 2014.
  17. Legacy for Health. E‐cigarette policy: the FDA should promptly exercise regulatory authority and over e‐cigarettes. Available at: http://www.legacyforhealth.org/content/download/3962/56088/version/1/file/LEG‐Policy_Statement‐ECigarette‐JAN2014.pdf. Accessed August 25, 2014.
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Effects of increased overnight supervision on resident education, decision‐making, and autonomy

Postgraduate medical education has traditionally relied on a training model of progressive independence, where housestaff learn patient care through increasing autonomy and decreasing levels of supervision.1 While this framework has little empirical backing, it is grounded in sound educational theory from similar disciplines and endorsed by medical associations.1, 2 The Accreditation Council for Graduate Medical Education (ACGME) recently implemented regulations requiring that first‐year residents have a qualified supervisor physically present or immediately available at all times.3 Previously, oversight by an offsite supervisor (for example, an attending physician at home) was considered adequate. These new regulations, although motivated by patient safety imperatives,4 have elicited concerns that increased supervision may lead to decreased housestaff autonomy and an increased reliance on supervisors for clinical guidance.5 Such changes could ultimately produce less qualified practitioners by the completion of training.

Critics of the current training model point to a patient safety mechanism where housestaff must take responsibility for requesting attending‐level help when situations arise that surpass their skill level.5 For resident physicians, however, the decision to request support is often complex and dependent not only on the clinical question, but also on unique and variable trainee and supervisor factors.6 Survey data from 1999, prior to the current training regulations, showed that increased faculty presence improved resident reports of educational value, quality of patient care, and autonomy.7 A recent survey, performed after the initiation of overnight attending supervision at an academic medical center, demonstrated perceived improvements in educational value and patient‐level outcomes by both faculty and housestaff.8 Whether increased supervision and resident autonomy can coexist remains undetermined.

Overnight rotations for residents (commonly referred to as night float) are often times of little direct or indirect supervision. A recent systematic review of clinical supervision practices for housestaff in all fields found scarce literature on overnight supervision practices.9 There remains limited and conflicting data regarding the quality of patient care provided by the resident night float,10 as well as evidence revealing a low perceived educational value of night rotations when compared with non‐night float rotations.11 Yet in 2006, more than three‐quarters of all internal medicine programs employed night float rotations.12 In response to ACGME guidelines mandating decreased shift lengths with continued restrictions on overall duty hours, it appears likely even more training programs will implement night float systems.

The presence of overnight hospitalists (also known as nocturnists) is growing within the academic setting, yet their role in relation to trainees is either poorly defined13 or independent of housestaff.14 To better understand the impact of increasing levels of supervision on residency training, we investigated housestaff perceptions of education, autonomy, and clinical decision‐making before and after implementation of an in‐hospital, overnight attending physician (nocturnist).

METHODS

The study was conducted at a 570‐bed academic, tertiary care medical center affiliated with an internal medicine residency program of 170 housestaff. At our institution, all first year residents perform a week of intern night float consisting of overnight cross‐coverage of general medicine patients on the floor, step‐down, and intensive care units (ICUs). Second and third year residents each complete 4 to 6 days of resident night float each year at this hospital. They are responsible for assisting the intern night float with cross‐coverage, in addition to admitting general medicine patients to the floor, step‐down unit, and intensive care units. Every night at our medical center, 1 intern night float and 1 resident night float are on duty in the hospital; this is in addition to a resident from the on‐call medicine team and a resident working in the ICU. Prior to July 2010, no internal medicine attending physicians were physically present in the hospital at night. Oversight for the intern and resident night float was provided by the attending physician for the on‐call resident ward team, who was at home and available by pager. The night float housestaff were instructed to contact the responsible attending physician only when a major change in clinical status occurred for hospitalized or newly admitted patients, though this expectation was neither standardized nor monitored.

We established a nocturnist program at the start of the 2010 academic year. The position was staffed by hospitalists from within the Division of Hospital Medicine without the use of moonlighters. Two‐thirds of shifts were filled by 3 dedicated nocturnists with remaining staffing provided by junior hospitalist faculty. The dedicated nocturnists had recently completed their internal medicine residency at our institution. Shift length was 12 hours and dedicated nocturnists worked, on average, 10 shifts per month. The nocturnist filled a critical overnight safety role through mandatory bedside staffing of newly admitted ICU patients within 2 hours of admission, discussion in person or via telephone of newly admitted step‐down unit patients within 6 hours of admission, and direct or indirect supervision of the care of any patients undergoing a major change in clinical status. The overnight hospitalist was also available for clinical questions and to assist housestaff with triaging of overnight admissions. After nocturnist implementation, overnight housestaff received direct supervision or had immediate access to direct supervision, while prior to the nocturnist, residents had access only to indirect supervision.

In addition, the nocturnist admitted medicine patients after 1 AM in a 1:1 ratio with the admitting night float resident, performed medical consults, and provided coverage of non‐teaching medicine services. While actual volume numbers were not obtained, the estimated average of resident admissions per night was 2 to 3, and the number of nocturnist admissions was 1 to 2. The nocturnist also met nightly with night float housestaff for half‐hour didactics focusing on the management of common overnight clinical scenarios. The role of the new nocturnist was described to all housestaff in orientation materials given prior to their night float rotation and their general medicine ward rotation.

We administered pre‐rolling surveys and post‐rolling surveys of internal medicine intern and resident physicians who underwent the night float rotation at our hospital during the 2010 to 2011 academic year. Surveys examined housestaff perceptions of the night float rotation with regard to supervisory roles, educational and clinical value, and clinical decision‐making prior to and after implementation of the nocturnist. Surveys were designed by the study investigators based on prior literature,1, 510 personal experience, and housestaff suggestion, and were refined during works‐in‐progress meetings. Surveys were composed of Likert‐style questions asking housestaff to rate their level of agreement (15, strongly disagree to strongly agree) with statements regarding the supervisory and educational experience of the night float rotation, and to judge their frequency of contact (15, never to always/nightly) with an attending physician for specific clinical scenarios. The clinical scenarios described situations dealing with attendingresident communication around transfers of care, diagnostic evaluation, therapeutic interventions, and adverse events. Scenarios were taken from previous literature describing supervision preferences of faculty and residents during times of critical clinical decision‐making.15

One week prior to the beginning their night float rotation for the 20102011 academic year, housestaff were sent an e‐mail request to complete an online survey asking about their night float rotation during the prior academic year, when no nocturnist was present. One week after completion of their night float rotation for the 20102011 academic year, housestaff received an e‐mail with a link to a post‐survey asking about their recently completed, nocturnist‐supervised, night float rotation. First year residents received only a post‐survey at the completion of their night float rotation, as they would be unable to reflect on prior experience.

Informed consent was imbedded within the e‐mail survey request. Survey requests were sent by a fellow within the Division of Hospital Medicine with a brief message cosigned by an associate program director of the residency program. We did not collect unique identifiers from respondents in order to offer additional assurances to the participants that the survey was anonymous. There was no incentive offered for completion of the survey. Survey data were anonymous and downloaded to a database by a third party. Data were analyzed using Microsoft Excel, and pre‐responses and post‐responses compared using a Student t test. The study was approved by the medical center's Institutional Review Board.

RESULTS

Rates of response for pre‐surveys and post‐surveys were 57% (43 respondents) and 51% (53 respondents), respectively. Due to response rates and in order to convey accurately the perceptions of the training program as a whole, we collapsed responses of the pre‐surveys and post‐surveys based on level of training. After implementation of the overnight attending, we observed a significant increase in the perceived clinical value of the night float rotation (3.95 vs 4.27, P = 0.01) as well as in the adequacy of overnight supervision (3.65 vs 4.30, P < 0.0001; Table 1). There was no reported change in housestaff decision‐making autonomy (4.35 vs 4.45, P = 0.44). In addition, we noted a nonsignificant trend towards an increased perception of the night float rotation as a valuable educational experience (3.83 vs 4.04, P = 0.24). After implementation of the nocturnist, more resident physicians agreed that overnight supervision by an attending positively impacted patient outcomes (3.79 vs 4.30, P = 0.002).

General Perceptions of the Night Float Rotation
StatementPre‐Nocturnist (n = 43) Mean (SD)Post‐Nocturnist (n = 53) Mean (SD)P Value
  • NOTE: Responses are strongly disagree (1) to strongly agree (5). Response rate (n) fluctuates due to item non‐response. Abbreviations: SD, standard deviation.

Night float is a valuable educational rotation3.83 (0.81)4.04 (0.83)0.24
Night float is a valuable clinical rotation3.95 (0.65)4.27 (0.59)0.01
I have adequate overnight supervision3.65 (0.76)4.30 (0.72)<0.0001
I have sufficient autonomy to make clinical decisions4.35 (0.57)4.45 (0.60)0.44
Overnight supervision by an attending positively impacts patient outcomes3.79 (0.88)4.30 (0.74)0.002

After implementation of the nocturnist, night float providers demonstrated increased rates of contacting an attending physician overnight (Table 2). There were significantly greater rates of attending contact for transfers from outside facilities (2.00 vs 3.20, P = 0.006) and during times of adverse events (2.51 vs 3.25, P = 0.04). We observed a reported increase in attending contact prior to ordering invasive diagnostic procedures (1.75 vs 2.76, P = 0.004) and noninvasive diagnostic procedures (1.09 vs 1.31, P = 0.03), as well as prior to initiation of intravenous antibiotics (1.11 vs 1.47, P = 0.007) and vasopressors (1.52 vs 2.40, P = 0.004).

Self‐Reported Incidence of Overnight Attending Contact During Critical Decision‐Making
ScenarioPre‐Nocturnist (n = 42) Mean (SD)Post‐Nocturnist (n = 51) Mean (SD)P Value
  • NOTE: Responses are never contact (1) to always contact (5). Response rate (n) fluctuates due to item non‐response. Abbreviations: SD, standard deviation.

Receive transfer from outside facility2.00 (1.27)3.20 (1.58)0.006
Prior to ordering noninvasive diagnostic procedure1.09 (0.29)1.31 (0.58)0.03
Prior to ordering an invasive procedure1.75 (0.84)2.76 (1.45)0.004
Prior to initiation of intravenous antibiotics1.11 (0.32)1.47 (0.76)0.007
Prior to initiation of vasopressors1.52 (0.82)2.40 (1.49)0.004
Patient experiencing adverse event, regardless of cause2.51 (1.31)3.25 (1.34)0.04

After initiating the program, the nocturnist became the most commonly contacted overnight provider by the night float housestaff (Table 3). We observed a decrease in peer to peer contact between the night float housestaff and the on‐call overnight resident after implementation of the nocturnist (2.67 vs 2.04, P = 0.006).

Self‐Reported Incidence of Night Float Contact With Overnight Providers for Patient Care
ProviderPre‐Nocturnist (n = 43) Mean (SD)Post‐Nocturnist (n = 53) Mean (SD)P Value
  • NOTE: Responses are never (1) to nightly (5). Response rate (n) fluctuates due to item non‐response. Abbreviations: ICU, intensive care unit; PMD, primary medical doctor; SD, standard deviation.

ICU Fellow1.86 (0.70)1.86 (0.83)0.96
On‐call resident2.67 (0.89)2.04 (0.92)0.006
ICU resident2.14 (0.74)2.04 (0.91)0.56
On‐call medicine attending1.41 (0.79)1.26 (0.52)0.26
Patient's PMD1.27 (0.31)1.15 (0.41)0.31
Referring MD1.32 (0.60)1.15 (0.45)0.11
Nocturnist 3.59 (1.22) 

Attending presence led to increased agreement that there was a defined overnight attending to contact (2.97 vs 1.96, P < 0.0001) and a decreased fear of waking an attending overnight for assistance (3.26 vs 2.72, P = 0.03). Increased attending availability, however, did not change resident physician's fear of revealing knowledge gaps, their desire to make decisions independently, or their belief that contacting an attending would not change a patient's outcome (Table 4).

Reasons Night Float Housestaff Do Not Contact an Attending Physician
StatementPre‐Nocturnist (n = 42) Mean (SD)Post‐Nocturnist (n = 52) Mean (SD)P Value
  • NOTE: Responses are strongly disagree (1) to strongly agree (5). Response rate (n) fluctuates due to item non‐response. Abbreviations: SD, standard deviation.

No defined attending to contact2.97 (1.35)1.96 (0.92)<0.0001
Fear of waking an attending3.26 (1.25)2.72 (1.09)0.03
Fear of revealing knowledge gaps2.26 (1.14)2.25 (0.96)0.95
Would rather make decision on own3.40 (0.93)3.03 (1.06)0.08
Will not change patient outcome3.26 (1.06)3.21 (1.03)0.81

DISCUSSION

The ACGME's new duty hour regulations require that supervision for first‐year residents be provided by a qualified physician (advanced resident, fellow, or attending physician) who is physically present at the hospital. Our study demonstrates that increased direct overnight supervision provided by an in‐house nocturnist enhanced the clinical value of the night float rotation and the perceived quality of patient care. In our study, increased attending supervision did not reduce perceived decision‐making autonomy, and in fact led to increased rates of attending contact during times of critical clinical decision‐making. Such results may help assuage fears that recent regulations mandating enhanced attending supervision will produce less capable practitioners, and offers reassurance that such changes are positively impacting patient care.

Many academic institutions are implementing nocturnists, although their precise roles and responsibilities are still being defined. Our nocturnist program was explicitly designed with housestaff supervision as a core responsibility, with the goal of improving patient safety and housestaff education overnight. We found that availability barriers to attending contact were logically decreased with in‐house faculty presence. Potentially harmful attitudes, however, around requesting support (such as fear of revealing knowledge gaps or the desire to make decisions independently) remained. Furthermore, despite statistically significant increases in contact between faculty and residents at times of critical decision‐making, overall rates of attending contact for diagnostic and therapeutic interventions remained low. It is unknown from our study or previous research, however, what level of contact is appropriate or ideal for many clinical scenarios.

Additionally, we described a novel role of an academic nocturnist at a tertiary care teaching hospital and offered a potential template for the development of academic nocturnists at similar institutions seeking to increase direct overnight supervision. Such roles have not been previously well defined in the literature. Based on our experience, the nocturnist's role was manageable and well utilized by housestaff, particularly for assistance with critically ill patients and overnight triaging. We believe there are a number of factors associated with the success of this role. First, clear guidelines were presented to housestaff and nocturnists regarding expectations for supervision (for example, staffing ICU admissions within 2 hours). These guidelines likely contributed to the increased attending contact observed during critical clinical decision‐making, as well as the perceived improved patient outcomes by our housestaff. Second, the nocturnists were expected to be an integral part of the overnight care team. In many systems, the nocturnists act completely independently of the housestaff teams, creating an additional barrier to contact and communication. In our system, because of clear guidelines and their integral role in staffing overnight admissions, the nocturnists were an essential partner in care for the housestaff. Third, most of the nocturnists had recently completed their residency training at this institution. Although our survey does not directly address this, we believe their knowledge of the hospital, appreciation of the role of the intern and the resident within our system, and understanding of the need to preserve housestaff autonomy were essential to building a successful nocturnist role. Lastly, the nocturnists were not only expected to supervise and staff new admissions, but were also given a teaching expectation. We believe they were viewed by housestaff as qualified teaching attendings, similar to the daytime hospitalist. These findings may provide guidelines for other institutions seeking to balance overnight hospitalist supervision with preserving resident's ability to make autonomous decisions.

There are several limitations to our study. The findings represent the experience of internal medicine housestaff at a single academic, tertiary care medical center and may not be reflective of other institutions or specialties. We asked housestaff to recall night float experiences from the prior year, which may have introduced recall bias, though responses were obtained before participants underwent the new curriculum. Maturation of housestaff over time could have led to changes in perceived autonomy, value of the night float rotation, and rates of attending contact independent of nocturnist implementation. In addition, there may have been unaccounted changes to other elements of the residency program, hospital, or patient volume between rotations. The implementation of the nocturnist, however, was the only major change to our training program that academic year, and there were no significant changes in patient volume, structure of the teaching or non‐resident services, or other policies around resident supervision.

It is possible that the nocturnist may have contributed to reports of increased clinical value and perceived quality of patient care simply by decreasing overnight workload for housestaff, and enhanced supervision and teaching may have played a lesser role. Even if this were true, optimizing resident workload is in itself an important goal for teaching hospitals and residency programs alike in order to maximize patient safety. Inclusion of intern post‐rotation surveys may have influenced data; though, we had no reason to suspect the surveyed interns would respond in a different manner than prior resident groups. The responses of both junior and senior housestaff were pooled; while this potentially weighted the results in favor of higher responding groups, we felt that it conveyed the residents' accurate sentiments on the program. Finally, while we compared two models of overnight supervision, we reported only housestaff perceptions of education, autonomy, patient outcomes, and supervisory contact, and not direct measures of knowledge or patient care. Further research will be required to define the relationship between supervision practices and patient‐level clinical outcomes.

The new ACGME regulations around resident supervision, as well as the broader movement to improve the safety and quality of care, require residency programs to negotiate a delicate balance between providing high‐quality patient care while preserving graduated independence in clinical training. Our study demonstrates that increased overnight supervision by nocturnists with well‐defined supervisory and teaching roles can preserve housestaff autonomy, improve the clinical experience for trainees, increase access to support during times of critical decision‐making, and potentially lead to improved patient outcomes.

Acknowledgements

Disclosures: No authors received commercial support for the submitted work. Dr Arora reports being an editorial board member for Agency for Healthcare Research and Quality (AHRQ) Web M&M, receiving grants from the ACGME for previous work, and receiving payment for speaking on graduate medical education supervision.

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References
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  2. Joint Committee of the Group on Resident Affairs and Organization of Resident Representatives.Patient Safety and Graduate Medical Education.Washington, DC:Association of American Medical Colleges; February2003:6.
  3. Accreditation Council on Graduate Medical Education.Common Program Requirements. Available at: http://www.acgme.org/acWebsite/home/Common_Program_Requirements_07012011.pdf. Accessed October 16,2011.
  4. The IOM medical errors report: 5 years later, the journey continues.Qual Lett Health Lead.2005;17(1):210.
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Postgraduate medical education has traditionally relied on a training model of progressive independence, where housestaff learn patient care through increasing autonomy and decreasing levels of supervision.1 While this framework has little empirical backing, it is grounded in sound educational theory from similar disciplines and endorsed by medical associations.1, 2 The Accreditation Council for Graduate Medical Education (ACGME) recently implemented regulations requiring that first‐year residents have a qualified supervisor physically present or immediately available at all times.3 Previously, oversight by an offsite supervisor (for example, an attending physician at home) was considered adequate. These new regulations, although motivated by patient safety imperatives,4 have elicited concerns that increased supervision may lead to decreased housestaff autonomy and an increased reliance on supervisors for clinical guidance.5 Such changes could ultimately produce less qualified practitioners by the completion of training.

Critics of the current training model point to a patient safety mechanism where housestaff must take responsibility for requesting attending‐level help when situations arise that surpass their skill level.5 For resident physicians, however, the decision to request support is often complex and dependent not only on the clinical question, but also on unique and variable trainee and supervisor factors.6 Survey data from 1999, prior to the current training regulations, showed that increased faculty presence improved resident reports of educational value, quality of patient care, and autonomy.7 A recent survey, performed after the initiation of overnight attending supervision at an academic medical center, demonstrated perceived improvements in educational value and patient‐level outcomes by both faculty and housestaff.8 Whether increased supervision and resident autonomy can coexist remains undetermined.

Overnight rotations for residents (commonly referred to as night float) are often times of little direct or indirect supervision. A recent systematic review of clinical supervision practices for housestaff in all fields found scarce literature on overnight supervision practices.9 There remains limited and conflicting data regarding the quality of patient care provided by the resident night float,10 as well as evidence revealing a low perceived educational value of night rotations when compared with non‐night float rotations.11 Yet in 2006, more than three‐quarters of all internal medicine programs employed night float rotations.12 In response to ACGME guidelines mandating decreased shift lengths with continued restrictions on overall duty hours, it appears likely even more training programs will implement night float systems.

The presence of overnight hospitalists (also known as nocturnists) is growing within the academic setting, yet their role in relation to trainees is either poorly defined13 or independent of housestaff.14 To better understand the impact of increasing levels of supervision on residency training, we investigated housestaff perceptions of education, autonomy, and clinical decision‐making before and after implementation of an in‐hospital, overnight attending physician (nocturnist).

METHODS

The study was conducted at a 570‐bed academic, tertiary care medical center affiliated with an internal medicine residency program of 170 housestaff. At our institution, all first year residents perform a week of intern night float consisting of overnight cross‐coverage of general medicine patients on the floor, step‐down, and intensive care units (ICUs). Second and third year residents each complete 4 to 6 days of resident night float each year at this hospital. They are responsible for assisting the intern night float with cross‐coverage, in addition to admitting general medicine patients to the floor, step‐down unit, and intensive care units. Every night at our medical center, 1 intern night float and 1 resident night float are on duty in the hospital; this is in addition to a resident from the on‐call medicine team and a resident working in the ICU. Prior to July 2010, no internal medicine attending physicians were physically present in the hospital at night. Oversight for the intern and resident night float was provided by the attending physician for the on‐call resident ward team, who was at home and available by pager. The night float housestaff were instructed to contact the responsible attending physician only when a major change in clinical status occurred for hospitalized or newly admitted patients, though this expectation was neither standardized nor monitored.

We established a nocturnist program at the start of the 2010 academic year. The position was staffed by hospitalists from within the Division of Hospital Medicine without the use of moonlighters. Two‐thirds of shifts were filled by 3 dedicated nocturnists with remaining staffing provided by junior hospitalist faculty. The dedicated nocturnists had recently completed their internal medicine residency at our institution. Shift length was 12 hours and dedicated nocturnists worked, on average, 10 shifts per month. The nocturnist filled a critical overnight safety role through mandatory bedside staffing of newly admitted ICU patients within 2 hours of admission, discussion in person or via telephone of newly admitted step‐down unit patients within 6 hours of admission, and direct or indirect supervision of the care of any patients undergoing a major change in clinical status. The overnight hospitalist was also available for clinical questions and to assist housestaff with triaging of overnight admissions. After nocturnist implementation, overnight housestaff received direct supervision or had immediate access to direct supervision, while prior to the nocturnist, residents had access only to indirect supervision.

In addition, the nocturnist admitted medicine patients after 1 AM in a 1:1 ratio with the admitting night float resident, performed medical consults, and provided coverage of non‐teaching medicine services. While actual volume numbers were not obtained, the estimated average of resident admissions per night was 2 to 3, and the number of nocturnist admissions was 1 to 2. The nocturnist also met nightly with night float housestaff for half‐hour didactics focusing on the management of common overnight clinical scenarios. The role of the new nocturnist was described to all housestaff in orientation materials given prior to their night float rotation and their general medicine ward rotation.

We administered pre‐rolling surveys and post‐rolling surveys of internal medicine intern and resident physicians who underwent the night float rotation at our hospital during the 2010 to 2011 academic year. Surveys examined housestaff perceptions of the night float rotation with regard to supervisory roles, educational and clinical value, and clinical decision‐making prior to and after implementation of the nocturnist. Surveys were designed by the study investigators based on prior literature,1, 510 personal experience, and housestaff suggestion, and were refined during works‐in‐progress meetings. Surveys were composed of Likert‐style questions asking housestaff to rate their level of agreement (15, strongly disagree to strongly agree) with statements regarding the supervisory and educational experience of the night float rotation, and to judge their frequency of contact (15, never to always/nightly) with an attending physician for specific clinical scenarios. The clinical scenarios described situations dealing with attendingresident communication around transfers of care, diagnostic evaluation, therapeutic interventions, and adverse events. Scenarios were taken from previous literature describing supervision preferences of faculty and residents during times of critical clinical decision‐making.15

One week prior to the beginning their night float rotation for the 20102011 academic year, housestaff were sent an e‐mail request to complete an online survey asking about their night float rotation during the prior academic year, when no nocturnist was present. One week after completion of their night float rotation for the 20102011 academic year, housestaff received an e‐mail with a link to a post‐survey asking about their recently completed, nocturnist‐supervised, night float rotation. First year residents received only a post‐survey at the completion of their night float rotation, as they would be unable to reflect on prior experience.

Informed consent was imbedded within the e‐mail survey request. Survey requests were sent by a fellow within the Division of Hospital Medicine with a brief message cosigned by an associate program director of the residency program. We did not collect unique identifiers from respondents in order to offer additional assurances to the participants that the survey was anonymous. There was no incentive offered for completion of the survey. Survey data were anonymous and downloaded to a database by a third party. Data were analyzed using Microsoft Excel, and pre‐responses and post‐responses compared using a Student t test. The study was approved by the medical center's Institutional Review Board.

RESULTS

Rates of response for pre‐surveys and post‐surveys were 57% (43 respondents) and 51% (53 respondents), respectively. Due to response rates and in order to convey accurately the perceptions of the training program as a whole, we collapsed responses of the pre‐surveys and post‐surveys based on level of training. After implementation of the overnight attending, we observed a significant increase in the perceived clinical value of the night float rotation (3.95 vs 4.27, P = 0.01) as well as in the adequacy of overnight supervision (3.65 vs 4.30, P < 0.0001; Table 1). There was no reported change in housestaff decision‐making autonomy (4.35 vs 4.45, P = 0.44). In addition, we noted a nonsignificant trend towards an increased perception of the night float rotation as a valuable educational experience (3.83 vs 4.04, P = 0.24). After implementation of the nocturnist, more resident physicians agreed that overnight supervision by an attending positively impacted patient outcomes (3.79 vs 4.30, P = 0.002).

General Perceptions of the Night Float Rotation
StatementPre‐Nocturnist (n = 43) Mean (SD)Post‐Nocturnist (n = 53) Mean (SD)P Value
  • NOTE: Responses are strongly disagree (1) to strongly agree (5). Response rate (n) fluctuates due to item non‐response. Abbreviations: SD, standard deviation.

Night float is a valuable educational rotation3.83 (0.81)4.04 (0.83)0.24
Night float is a valuable clinical rotation3.95 (0.65)4.27 (0.59)0.01
I have adequate overnight supervision3.65 (0.76)4.30 (0.72)<0.0001
I have sufficient autonomy to make clinical decisions4.35 (0.57)4.45 (0.60)0.44
Overnight supervision by an attending positively impacts patient outcomes3.79 (0.88)4.30 (0.74)0.002

After implementation of the nocturnist, night float providers demonstrated increased rates of contacting an attending physician overnight (Table 2). There were significantly greater rates of attending contact for transfers from outside facilities (2.00 vs 3.20, P = 0.006) and during times of adverse events (2.51 vs 3.25, P = 0.04). We observed a reported increase in attending contact prior to ordering invasive diagnostic procedures (1.75 vs 2.76, P = 0.004) and noninvasive diagnostic procedures (1.09 vs 1.31, P = 0.03), as well as prior to initiation of intravenous antibiotics (1.11 vs 1.47, P = 0.007) and vasopressors (1.52 vs 2.40, P = 0.004).

Self‐Reported Incidence of Overnight Attending Contact During Critical Decision‐Making
ScenarioPre‐Nocturnist (n = 42) Mean (SD)Post‐Nocturnist (n = 51) Mean (SD)P Value
  • NOTE: Responses are never contact (1) to always contact (5). Response rate (n) fluctuates due to item non‐response. Abbreviations: SD, standard deviation.

Receive transfer from outside facility2.00 (1.27)3.20 (1.58)0.006
Prior to ordering noninvasive diagnostic procedure1.09 (0.29)1.31 (0.58)0.03
Prior to ordering an invasive procedure1.75 (0.84)2.76 (1.45)0.004
Prior to initiation of intravenous antibiotics1.11 (0.32)1.47 (0.76)0.007
Prior to initiation of vasopressors1.52 (0.82)2.40 (1.49)0.004
Patient experiencing adverse event, regardless of cause2.51 (1.31)3.25 (1.34)0.04

After initiating the program, the nocturnist became the most commonly contacted overnight provider by the night float housestaff (Table 3). We observed a decrease in peer to peer contact between the night float housestaff and the on‐call overnight resident after implementation of the nocturnist (2.67 vs 2.04, P = 0.006).

Self‐Reported Incidence of Night Float Contact With Overnight Providers for Patient Care
ProviderPre‐Nocturnist (n = 43) Mean (SD)Post‐Nocturnist (n = 53) Mean (SD)P Value
  • NOTE: Responses are never (1) to nightly (5). Response rate (n) fluctuates due to item non‐response. Abbreviations: ICU, intensive care unit; PMD, primary medical doctor; SD, standard deviation.

ICU Fellow1.86 (0.70)1.86 (0.83)0.96
On‐call resident2.67 (0.89)2.04 (0.92)0.006
ICU resident2.14 (0.74)2.04 (0.91)0.56
On‐call medicine attending1.41 (0.79)1.26 (0.52)0.26
Patient's PMD1.27 (0.31)1.15 (0.41)0.31
Referring MD1.32 (0.60)1.15 (0.45)0.11
Nocturnist 3.59 (1.22) 

Attending presence led to increased agreement that there was a defined overnight attending to contact (2.97 vs 1.96, P < 0.0001) and a decreased fear of waking an attending overnight for assistance (3.26 vs 2.72, P = 0.03). Increased attending availability, however, did not change resident physician's fear of revealing knowledge gaps, their desire to make decisions independently, or their belief that contacting an attending would not change a patient's outcome (Table 4).

Reasons Night Float Housestaff Do Not Contact an Attending Physician
StatementPre‐Nocturnist (n = 42) Mean (SD)Post‐Nocturnist (n = 52) Mean (SD)P Value
  • NOTE: Responses are strongly disagree (1) to strongly agree (5). Response rate (n) fluctuates due to item non‐response. Abbreviations: SD, standard deviation.

No defined attending to contact2.97 (1.35)1.96 (0.92)<0.0001
Fear of waking an attending3.26 (1.25)2.72 (1.09)0.03
Fear of revealing knowledge gaps2.26 (1.14)2.25 (0.96)0.95
Would rather make decision on own3.40 (0.93)3.03 (1.06)0.08
Will not change patient outcome3.26 (1.06)3.21 (1.03)0.81

DISCUSSION

The ACGME's new duty hour regulations require that supervision for first‐year residents be provided by a qualified physician (advanced resident, fellow, or attending physician) who is physically present at the hospital. Our study demonstrates that increased direct overnight supervision provided by an in‐house nocturnist enhanced the clinical value of the night float rotation and the perceived quality of patient care. In our study, increased attending supervision did not reduce perceived decision‐making autonomy, and in fact led to increased rates of attending contact during times of critical clinical decision‐making. Such results may help assuage fears that recent regulations mandating enhanced attending supervision will produce less capable practitioners, and offers reassurance that such changes are positively impacting patient care.

Many academic institutions are implementing nocturnists, although their precise roles and responsibilities are still being defined. Our nocturnist program was explicitly designed with housestaff supervision as a core responsibility, with the goal of improving patient safety and housestaff education overnight. We found that availability barriers to attending contact were logically decreased with in‐house faculty presence. Potentially harmful attitudes, however, around requesting support (such as fear of revealing knowledge gaps or the desire to make decisions independently) remained. Furthermore, despite statistically significant increases in contact between faculty and residents at times of critical decision‐making, overall rates of attending contact for diagnostic and therapeutic interventions remained low. It is unknown from our study or previous research, however, what level of contact is appropriate or ideal for many clinical scenarios.

Additionally, we described a novel role of an academic nocturnist at a tertiary care teaching hospital and offered a potential template for the development of academic nocturnists at similar institutions seeking to increase direct overnight supervision. Such roles have not been previously well defined in the literature. Based on our experience, the nocturnist's role was manageable and well utilized by housestaff, particularly for assistance with critically ill patients and overnight triaging. We believe there are a number of factors associated with the success of this role. First, clear guidelines were presented to housestaff and nocturnists regarding expectations for supervision (for example, staffing ICU admissions within 2 hours). These guidelines likely contributed to the increased attending contact observed during critical clinical decision‐making, as well as the perceived improved patient outcomes by our housestaff. Second, the nocturnists were expected to be an integral part of the overnight care team. In many systems, the nocturnists act completely independently of the housestaff teams, creating an additional barrier to contact and communication. In our system, because of clear guidelines and their integral role in staffing overnight admissions, the nocturnists were an essential partner in care for the housestaff. Third, most of the nocturnists had recently completed their residency training at this institution. Although our survey does not directly address this, we believe their knowledge of the hospital, appreciation of the role of the intern and the resident within our system, and understanding of the need to preserve housestaff autonomy were essential to building a successful nocturnist role. Lastly, the nocturnists were not only expected to supervise and staff new admissions, but were also given a teaching expectation. We believe they were viewed by housestaff as qualified teaching attendings, similar to the daytime hospitalist. These findings may provide guidelines for other institutions seeking to balance overnight hospitalist supervision with preserving resident's ability to make autonomous decisions.

There are several limitations to our study. The findings represent the experience of internal medicine housestaff at a single academic, tertiary care medical center and may not be reflective of other institutions or specialties. We asked housestaff to recall night float experiences from the prior year, which may have introduced recall bias, though responses were obtained before participants underwent the new curriculum. Maturation of housestaff over time could have led to changes in perceived autonomy, value of the night float rotation, and rates of attending contact independent of nocturnist implementation. In addition, there may have been unaccounted changes to other elements of the residency program, hospital, or patient volume between rotations. The implementation of the nocturnist, however, was the only major change to our training program that academic year, and there were no significant changes in patient volume, structure of the teaching or non‐resident services, or other policies around resident supervision.

It is possible that the nocturnist may have contributed to reports of increased clinical value and perceived quality of patient care simply by decreasing overnight workload for housestaff, and enhanced supervision and teaching may have played a lesser role. Even if this were true, optimizing resident workload is in itself an important goal for teaching hospitals and residency programs alike in order to maximize patient safety. Inclusion of intern post‐rotation surveys may have influenced data; though, we had no reason to suspect the surveyed interns would respond in a different manner than prior resident groups. The responses of both junior and senior housestaff were pooled; while this potentially weighted the results in favor of higher responding groups, we felt that it conveyed the residents' accurate sentiments on the program. Finally, while we compared two models of overnight supervision, we reported only housestaff perceptions of education, autonomy, patient outcomes, and supervisory contact, and not direct measures of knowledge or patient care. Further research will be required to define the relationship between supervision practices and patient‐level clinical outcomes.

The new ACGME regulations around resident supervision, as well as the broader movement to improve the safety and quality of care, require residency programs to negotiate a delicate balance between providing high‐quality patient care while preserving graduated independence in clinical training. Our study demonstrates that increased overnight supervision by nocturnists with well‐defined supervisory and teaching roles can preserve housestaff autonomy, improve the clinical experience for trainees, increase access to support during times of critical decision‐making, and potentially lead to improved patient outcomes.

Acknowledgements

Disclosures: No authors received commercial support for the submitted work. Dr Arora reports being an editorial board member for Agency for Healthcare Research and Quality (AHRQ) Web M&M, receiving grants from the ACGME for previous work, and receiving payment for speaking on graduate medical education supervision.

Postgraduate medical education has traditionally relied on a training model of progressive independence, where housestaff learn patient care through increasing autonomy and decreasing levels of supervision.1 While this framework has little empirical backing, it is grounded in sound educational theory from similar disciplines and endorsed by medical associations.1, 2 The Accreditation Council for Graduate Medical Education (ACGME) recently implemented regulations requiring that first‐year residents have a qualified supervisor physically present or immediately available at all times.3 Previously, oversight by an offsite supervisor (for example, an attending physician at home) was considered adequate. These new regulations, although motivated by patient safety imperatives,4 have elicited concerns that increased supervision may lead to decreased housestaff autonomy and an increased reliance on supervisors for clinical guidance.5 Such changes could ultimately produce less qualified practitioners by the completion of training.

Critics of the current training model point to a patient safety mechanism where housestaff must take responsibility for requesting attending‐level help when situations arise that surpass their skill level.5 For resident physicians, however, the decision to request support is often complex and dependent not only on the clinical question, but also on unique and variable trainee and supervisor factors.6 Survey data from 1999, prior to the current training regulations, showed that increased faculty presence improved resident reports of educational value, quality of patient care, and autonomy.7 A recent survey, performed after the initiation of overnight attending supervision at an academic medical center, demonstrated perceived improvements in educational value and patient‐level outcomes by both faculty and housestaff.8 Whether increased supervision and resident autonomy can coexist remains undetermined.

Overnight rotations for residents (commonly referred to as night float) are often times of little direct or indirect supervision. A recent systematic review of clinical supervision practices for housestaff in all fields found scarce literature on overnight supervision practices.9 There remains limited and conflicting data regarding the quality of patient care provided by the resident night float,10 as well as evidence revealing a low perceived educational value of night rotations when compared with non‐night float rotations.11 Yet in 2006, more than three‐quarters of all internal medicine programs employed night float rotations.12 In response to ACGME guidelines mandating decreased shift lengths with continued restrictions on overall duty hours, it appears likely even more training programs will implement night float systems.

The presence of overnight hospitalists (also known as nocturnists) is growing within the academic setting, yet their role in relation to trainees is either poorly defined13 or independent of housestaff.14 To better understand the impact of increasing levels of supervision on residency training, we investigated housestaff perceptions of education, autonomy, and clinical decision‐making before and after implementation of an in‐hospital, overnight attending physician (nocturnist).

METHODS

The study was conducted at a 570‐bed academic, tertiary care medical center affiliated with an internal medicine residency program of 170 housestaff. At our institution, all first year residents perform a week of intern night float consisting of overnight cross‐coverage of general medicine patients on the floor, step‐down, and intensive care units (ICUs). Second and third year residents each complete 4 to 6 days of resident night float each year at this hospital. They are responsible for assisting the intern night float with cross‐coverage, in addition to admitting general medicine patients to the floor, step‐down unit, and intensive care units. Every night at our medical center, 1 intern night float and 1 resident night float are on duty in the hospital; this is in addition to a resident from the on‐call medicine team and a resident working in the ICU. Prior to July 2010, no internal medicine attending physicians were physically present in the hospital at night. Oversight for the intern and resident night float was provided by the attending physician for the on‐call resident ward team, who was at home and available by pager. The night float housestaff were instructed to contact the responsible attending physician only when a major change in clinical status occurred for hospitalized or newly admitted patients, though this expectation was neither standardized nor monitored.

We established a nocturnist program at the start of the 2010 academic year. The position was staffed by hospitalists from within the Division of Hospital Medicine without the use of moonlighters. Two‐thirds of shifts were filled by 3 dedicated nocturnists with remaining staffing provided by junior hospitalist faculty. The dedicated nocturnists had recently completed their internal medicine residency at our institution. Shift length was 12 hours and dedicated nocturnists worked, on average, 10 shifts per month. The nocturnist filled a critical overnight safety role through mandatory bedside staffing of newly admitted ICU patients within 2 hours of admission, discussion in person or via telephone of newly admitted step‐down unit patients within 6 hours of admission, and direct or indirect supervision of the care of any patients undergoing a major change in clinical status. The overnight hospitalist was also available for clinical questions and to assist housestaff with triaging of overnight admissions. After nocturnist implementation, overnight housestaff received direct supervision or had immediate access to direct supervision, while prior to the nocturnist, residents had access only to indirect supervision.

In addition, the nocturnist admitted medicine patients after 1 AM in a 1:1 ratio with the admitting night float resident, performed medical consults, and provided coverage of non‐teaching medicine services. While actual volume numbers were not obtained, the estimated average of resident admissions per night was 2 to 3, and the number of nocturnist admissions was 1 to 2. The nocturnist also met nightly with night float housestaff for half‐hour didactics focusing on the management of common overnight clinical scenarios. The role of the new nocturnist was described to all housestaff in orientation materials given prior to their night float rotation and their general medicine ward rotation.

We administered pre‐rolling surveys and post‐rolling surveys of internal medicine intern and resident physicians who underwent the night float rotation at our hospital during the 2010 to 2011 academic year. Surveys examined housestaff perceptions of the night float rotation with regard to supervisory roles, educational and clinical value, and clinical decision‐making prior to and after implementation of the nocturnist. Surveys were designed by the study investigators based on prior literature,1, 510 personal experience, and housestaff suggestion, and were refined during works‐in‐progress meetings. Surveys were composed of Likert‐style questions asking housestaff to rate their level of agreement (15, strongly disagree to strongly agree) with statements regarding the supervisory and educational experience of the night float rotation, and to judge their frequency of contact (15, never to always/nightly) with an attending physician for specific clinical scenarios. The clinical scenarios described situations dealing with attendingresident communication around transfers of care, diagnostic evaluation, therapeutic interventions, and adverse events. Scenarios were taken from previous literature describing supervision preferences of faculty and residents during times of critical clinical decision‐making.15

One week prior to the beginning their night float rotation for the 20102011 academic year, housestaff were sent an e‐mail request to complete an online survey asking about their night float rotation during the prior academic year, when no nocturnist was present. One week after completion of their night float rotation for the 20102011 academic year, housestaff received an e‐mail with a link to a post‐survey asking about their recently completed, nocturnist‐supervised, night float rotation. First year residents received only a post‐survey at the completion of their night float rotation, as they would be unable to reflect on prior experience.

Informed consent was imbedded within the e‐mail survey request. Survey requests were sent by a fellow within the Division of Hospital Medicine with a brief message cosigned by an associate program director of the residency program. We did not collect unique identifiers from respondents in order to offer additional assurances to the participants that the survey was anonymous. There was no incentive offered for completion of the survey. Survey data were anonymous and downloaded to a database by a third party. Data were analyzed using Microsoft Excel, and pre‐responses and post‐responses compared using a Student t test. The study was approved by the medical center's Institutional Review Board.

RESULTS

Rates of response for pre‐surveys and post‐surveys were 57% (43 respondents) and 51% (53 respondents), respectively. Due to response rates and in order to convey accurately the perceptions of the training program as a whole, we collapsed responses of the pre‐surveys and post‐surveys based on level of training. After implementation of the overnight attending, we observed a significant increase in the perceived clinical value of the night float rotation (3.95 vs 4.27, P = 0.01) as well as in the adequacy of overnight supervision (3.65 vs 4.30, P < 0.0001; Table 1). There was no reported change in housestaff decision‐making autonomy (4.35 vs 4.45, P = 0.44). In addition, we noted a nonsignificant trend towards an increased perception of the night float rotation as a valuable educational experience (3.83 vs 4.04, P = 0.24). After implementation of the nocturnist, more resident physicians agreed that overnight supervision by an attending positively impacted patient outcomes (3.79 vs 4.30, P = 0.002).

General Perceptions of the Night Float Rotation
StatementPre‐Nocturnist (n = 43) Mean (SD)Post‐Nocturnist (n = 53) Mean (SD)P Value
  • NOTE: Responses are strongly disagree (1) to strongly agree (5). Response rate (n) fluctuates due to item non‐response. Abbreviations: SD, standard deviation.

Night float is a valuable educational rotation3.83 (0.81)4.04 (0.83)0.24
Night float is a valuable clinical rotation3.95 (0.65)4.27 (0.59)0.01
I have adequate overnight supervision3.65 (0.76)4.30 (0.72)<0.0001
I have sufficient autonomy to make clinical decisions4.35 (0.57)4.45 (0.60)0.44
Overnight supervision by an attending positively impacts patient outcomes3.79 (0.88)4.30 (0.74)0.002

After implementation of the nocturnist, night float providers demonstrated increased rates of contacting an attending physician overnight (Table 2). There were significantly greater rates of attending contact for transfers from outside facilities (2.00 vs 3.20, P = 0.006) and during times of adverse events (2.51 vs 3.25, P = 0.04). We observed a reported increase in attending contact prior to ordering invasive diagnostic procedures (1.75 vs 2.76, P = 0.004) and noninvasive diagnostic procedures (1.09 vs 1.31, P = 0.03), as well as prior to initiation of intravenous antibiotics (1.11 vs 1.47, P = 0.007) and vasopressors (1.52 vs 2.40, P = 0.004).

Self‐Reported Incidence of Overnight Attending Contact During Critical Decision‐Making
ScenarioPre‐Nocturnist (n = 42) Mean (SD)Post‐Nocturnist (n = 51) Mean (SD)P Value
  • NOTE: Responses are never contact (1) to always contact (5). Response rate (n) fluctuates due to item non‐response. Abbreviations: SD, standard deviation.

Receive transfer from outside facility2.00 (1.27)3.20 (1.58)0.006
Prior to ordering noninvasive diagnostic procedure1.09 (0.29)1.31 (0.58)0.03
Prior to ordering an invasive procedure1.75 (0.84)2.76 (1.45)0.004
Prior to initiation of intravenous antibiotics1.11 (0.32)1.47 (0.76)0.007
Prior to initiation of vasopressors1.52 (0.82)2.40 (1.49)0.004
Patient experiencing adverse event, regardless of cause2.51 (1.31)3.25 (1.34)0.04

After initiating the program, the nocturnist became the most commonly contacted overnight provider by the night float housestaff (Table 3). We observed a decrease in peer to peer contact between the night float housestaff and the on‐call overnight resident after implementation of the nocturnist (2.67 vs 2.04, P = 0.006).

Self‐Reported Incidence of Night Float Contact With Overnight Providers for Patient Care
ProviderPre‐Nocturnist (n = 43) Mean (SD)Post‐Nocturnist (n = 53) Mean (SD)P Value
  • NOTE: Responses are never (1) to nightly (5). Response rate (n) fluctuates due to item non‐response. Abbreviations: ICU, intensive care unit; PMD, primary medical doctor; SD, standard deviation.

ICU Fellow1.86 (0.70)1.86 (0.83)0.96
On‐call resident2.67 (0.89)2.04 (0.92)0.006
ICU resident2.14 (0.74)2.04 (0.91)0.56
On‐call medicine attending1.41 (0.79)1.26 (0.52)0.26
Patient's PMD1.27 (0.31)1.15 (0.41)0.31
Referring MD1.32 (0.60)1.15 (0.45)0.11
Nocturnist 3.59 (1.22) 

Attending presence led to increased agreement that there was a defined overnight attending to contact (2.97 vs 1.96, P < 0.0001) and a decreased fear of waking an attending overnight for assistance (3.26 vs 2.72, P = 0.03). Increased attending availability, however, did not change resident physician's fear of revealing knowledge gaps, their desire to make decisions independently, or their belief that contacting an attending would not change a patient's outcome (Table 4).

Reasons Night Float Housestaff Do Not Contact an Attending Physician
StatementPre‐Nocturnist (n = 42) Mean (SD)Post‐Nocturnist (n = 52) Mean (SD)P Value
  • NOTE: Responses are strongly disagree (1) to strongly agree (5). Response rate (n) fluctuates due to item non‐response. Abbreviations: SD, standard deviation.

No defined attending to contact2.97 (1.35)1.96 (0.92)<0.0001
Fear of waking an attending3.26 (1.25)2.72 (1.09)0.03
Fear of revealing knowledge gaps2.26 (1.14)2.25 (0.96)0.95
Would rather make decision on own3.40 (0.93)3.03 (1.06)0.08
Will not change patient outcome3.26 (1.06)3.21 (1.03)0.81

DISCUSSION

The ACGME's new duty hour regulations require that supervision for first‐year residents be provided by a qualified physician (advanced resident, fellow, or attending physician) who is physically present at the hospital. Our study demonstrates that increased direct overnight supervision provided by an in‐house nocturnist enhanced the clinical value of the night float rotation and the perceived quality of patient care. In our study, increased attending supervision did not reduce perceived decision‐making autonomy, and in fact led to increased rates of attending contact during times of critical clinical decision‐making. Such results may help assuage fears that recent regulations mandating enhanced attending supervision will produce less capable practitioners, and offers reassurance that such changes are positively impacting patient care.

Many academic institutions are implementing nocturnists, although their precise roles and responsibilities are still being defined. Our nocturnist program was explicitly designed with housestaff supervision as a core responsibility, with the goal of improving patient safety and housestaff education overnight. We found that availability barriers to attending contact were logically decreased with in‐house faculty presence. Potentially harmful attitudes, however, around requesting support (such as fear of revealing knowledge gaps or the desire to make decisions independently) remained. Furthermore, despite statistically significant increases in contact between faculty and residents at times of critical decision‐making, overall rates of attending contact for diagnostic and therapeutic interventions remained low. It is unknown from our study or previous research, however, what level of contact is appropriate or ideal for many clinical scenarios.

Additionally, we described a novel role of an academic nocturnist at a tertiary care teaching hospital and offered a potential template for the development of academic nocturnists at similar institutions seeking to increase direct overnight supervision. Such roles have not been previously well defined in the literature. Based on our experience, the nocturnist's role was manageable and well utilized by housestaff, particularly for assistance with critically ill patients and overnight triaging. We believe there are a number of factors associated with the success of this role. First, clear guidelines were presented to housestaff and nocturnists regarding expectations for supervision (for example, staffing ICU admissions within 2 hours). These guidelines likely contributed to the increased attending contact observed during critical clinical decision‐making, as well as the perceived improved patient outcomes by our housestaff. Second, the nocturnists were expected to be an integral part of the overnight care team. In many systems, the nocturnists act completely independently of the housestaff teams, creating an additional barrier to contact and communication. In our system, because of clear guidelines and their integral role in staffing overnight admissions, the nocturnists were an essential partner in care for the housestaff. Third, most of the nocturnists had recently completed their residency training at this institution. Although our survey does not directly address this, we believe their knowledge of the hospital, appreciation of the role of the intern and the resident within our system, and understanding of the need to preserve housestaff autonomy were essential to building a successful nocturnist role. Lastly, the nocturnists were not only expected to supervise and staff new admissions, but were also given a teaching expectation. We believe they were viewed by housestaff as qualified teaching attendings, similar to the daytime hospitalist. These findings may provide guidelines for other institutions seeking to balance overnight hospitalist supervision with preserving resident's ability to make autonomous decisions.

There are several limitations to our study. The findings represent the experience of internal medicine housestaff at a single academic, tertiary care medical center and may not be reflective of other institutions or specialties. We asked housestaff to recall night float experiences from the prior year, which may have introduced recall bias, though responses were obtained before participants underwent the new curriculum. Maturation of housestaff over time could have led to changes in perceived autonomy, value of the night float rotation, and rates of attending contact independent of nocturnist implementation. In addition, there may have been unaccounted changes to other elements of the residency program, hospital, or patient volume between rotations. The implementation of the nocturnist, however, was the only major change to our training program that academic year, and there were no significant changes in patient volume, structure of the teaching or non‐resident services, or other policies around resident supervision.

It is possible that the nocturnist may have contributed to reports of increased clinical value and perceived quality of patient care simply by decreasing overnight workload for housestaff, and enhanced supervision and teaching may have played a lesser role. Even if this were true, optimizing resident workload is in itself an important goal for teaching hospitals and residency programs alike in order to maximize patient safety. Inclusion of intern post‐rotation surveys may have influenced data; though, we had no reason to suspect the surveyed interns would respond in a different manner than prior resident groups. The responses of both junior and senior housestaff were pooled; while this potentially weighted the results in favor of higher responding groups, we felt that it conveyed the residents' accurate sentiments on the program. Finally, while we compared two models of overnight supervision, we reported only housestaff perceptions of education, autonomy, patient outcomes, and supervisory contact, and not direct measures of knowledge or patient care. Further research will be required to define the relationship between supervision practices and patient‐level clinical outcomes.

The new ACGME regulations around resident supervision, as well as the broader movement to improve the safety and quality of care, require residency programs to negotiate a delicate balance between providing high‐quality patient care while preserving graduated independence in clinical training. Our study demonstrates that increased overnight supervision by nocturnists with well‐defined supervisory and teaching roles can preserve housestaff autonomy, improve the clinical experience for trainees, increase access to support during times of critical decision‐making, and potentially lead to improved patient outcomes.

Acknowledgements

Disclosures: No authors received commercial support for the submitted work. Dr Arora reports being an editorial board member for Agency for Healthcare Research and Quality (AHRQ) Web M&M, receiving grants from the ACGME for previous work, and receiving payment for speaking on graduate medical education supervision.

References
  1. Kennedy TJ,Regehr G,Baker GR,Lingard LA.Progressive independence in clinical training: a tradition worth defending?Acad Med.2005;80(10 suppl):S106S111.
  2. Joint Committee of the Group on Resident Affairs and Organization of Resident Representatives.Patient Safety and Graduate Medical Education.Washington, DC:Association of American Medical Colleges; February2003:6.
  3. Accreditation Council on Graduate Medical Education.Common Program Requirements. Available at: http://www.acgme.org/acWebsite/home/Common_Program_Requirements_07012011.pdf. Accessed October 16,2011.
  4. The IOM medical errors report: 5 years later, the journey continues.Qual Lett Health Lead.2005;17(1):210.
  5. Bush RW.Supervision in medical education: logical fallacies and clear choices.J Grad Med Educ.2010;2(1):141143.
  6. Kennedy TJ,Regehr G,Baker GR,Lingard L.Preserving professional credibility: grounded theory study of medical trainees' requests for clinical support.BMJ.2009;338:b128.
  7. Phy MP,Offord KP,Manning DM,Bundrick JB,Huddleston JM.Increased faculty presence on inpatient teaching services.Mayo Clin Proc.2004;79(3):332336.
  8. Trowbridge RL,Almeder L,Jacquet M,Fairfield KM.The effect of overnight in‐house attending coverage on perceptions of care and education on a general medical service.J Grad Med Educ.2010;2(1):5356.
  9. Farnan JM,Petty LA,Georgitis E, et al.A systematic review: the effect of clinical supervision on patient and residency education outcomes.Acad Med.2012;87(4):428442.
  10. Jasti H,Hanusa BH,Switzer GE,Granieri R,Elnicki M.Residents' perceptions of a night float system.BMC Med Educ.2009;9:52.
  11. Luks AM,Smith CS,Robins L,Wipf JE.Resident perceptions of the educational value of night float rotations.Teach Learn Med.2010;22(3):196201.
  12. Wallach SL,Alam K,Diaz N,Shine D.How do internal medicine residency programs evaluate their resident float experiences?South Med J.2006;99(9):919923.
  13. Beasley BW,McBride J,McDonald FS.Hospitalist involvement in internal medicine residencies.J Hosp Med.2009;4(8):471475.
  14. Ogden PE,Sibbitt S,Howell M, et al.Complying with ACGME resident duty hour restrictions: restructuring the 80 hour workweek to enhance education and patient safety at Texas A81(12):10261031.
  15. Farnan JM,Johnson JK,Meltzer DO,Humphrey HJ,Arora VM.On‐call supervision and resident autonomy: from micromanager to absentee attending.Am J Med.2009;122(8):784788.
References
  1. Kennedy TJ,Regehr G,Baker GR,Lingard LA.Progressive independence in clinical training: a tradition worth defending?Acad Med.2005;80(10 suppl):S106S111.
  2. Joint Committee of the Group on Resident Affairs and Organization of Resident Representatives.Patient Safety and Graduate Medical Education.Washington, DC:Association of American Medical Colleges; February2003:6.
  3. Accreditation Council on Graduate Medical Education.Common Program Requirements. Available at: http://www.acgme.org/acWebsite/home/Common_Program_Requirements_07012011.pdf. Accessed October 16,2011.
  4. The IOM medical errors report: 5 years later, the journey continues.Qual Lett Health Lead.2005;17(1):210.
  5. Bush RW.Supervision in medical education: logical fallacies and clear choices.J Grad Med Educ.2010;2(1):141143.
  6. Kennedy TJ,Regehr G,Baker GR,Lingard L.Preserving professional credibility: grounded theory study of medical trainees' requests for clinical support.BMJ.2009;338:b128.
  7. Phy MP,Offord KP,Manning DM,Bundrick JB,Huddleston JM.Increased faculty presence on inpatient teaching services.Mayo Clin Proc.2004;79(3):332336.
  8. Trowbridge RL,Almeder L,Jacquet M,Fairfield KM.The effect of overnight in‐house attending coverage on perceptions of care and education on a general medical service.J Grad Med Educ.2010;2(1):5356.
  9. Farnan JM,Petty LA,Georgitis E, et al.A systematic review: the effect of clinical supervision on patient and residency education outcomes.Acad Med.2012;87(4):428442.
  10. Jasti H,Hanusa BH,Switzer GE,Granieri R,Elnicki M.Residents' perceptions of a night float system.BMC Med Educ.2009;9:52.
  11. Luks AM,Smith CS,Robins L,Wipf JE.Resident perceptions of the educational value of night float rotations.Teach Learn Med.2010;22(3):196201.
  12. Wallach SL,Alam K,Diaz N,Shine D.How do internal medicine residency programs evaluate their resident float experiences?South Med J.2006;99(9):919923.
  13. Beasley BW,McBride J,McDonald FS.Hospitalist involvement in internal medicine residencies.J Hosp Med.2009;4(8):471475.
  14. Ogden PE,Sibbitt S,Howell M, et al.Complying with ACGME resident duty hour restrictions: restructuring the 80 hour workweek to enhance education and patient safety at Texas A81(12):10261031.
  15. Farnan JM,Johnson JK,Meltzer DO,Humphrey HJ,Arora VM.On‐call supervision and resident autonomy: from micromanager to absentee attending.Am J Med.2009;122(8):784788.
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Journal of Hospital Medicine - 7(8)
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Journal of Hospital Medicine - 7(8)
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Effects of increased overnight supervision on resident education, decision‐making, and autonomy
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