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PET scans could prevent unnecessary RT in HL
Image by Jens Langner
Performing PET scans immediately after chemotherapy may reveal which Hodgkin lymphoma (HL) patients need radiotherapy (RT).
A study published in NEJM showed similar rates of progression-free survival in HL patients who werePET-negative after chemotherapy, whether they received subsequent RT or not.
However, the investigators said longer follow-up is needed to determine if eliminating RT in PET-negative patients will lead to fewer late effects and improved overall survival.
The 602 patients who agreed to take part in this trial, known as RAPID, had a PET scan performed after chemotherapy. Patients who tested positive received RT.
Those who tested negative were divided into 2 groups. One group of 211 patients received no further treatment, and the other group of 209 patients had the standard RT.
At a median of 60 months of follow-up, the proportion of patients who were alive and disease-free was 94.6% in the RT group and 90.8% in the group that hadn’t received further treatment.
Eight patients in the RT group progressed, and 8 died (3 with disease progression, 1 of whom died from HL). Five of the deaths occurred in patients who did not ultimately receive RT.
In the untreated group, 20 patients progressed, and 4 patients died (2 with disease progression and none from HL).
“This research is an important step forward,” said study author John Radford, of The University of Manchester and The Christie NHS Foundation Trust in the UK.
“The results of RAPID show that, in early stage Hodgkin lymphoma, radiotherapy after initial chemotherapy marginally reduces the recurrence rate, but this is bought at the expense of exposing to radiation all patients with negative PET findings, most of whom are already cured.” 
Image by Jens Langner
Performing PET scans immediately after chemotherapy may reveal which Hodgkin lymphoma (HL) patients need radiotherapy (RT).
A study published in NEJM showed similar rates of progression-free survival in HL patients who werePET-negative after chemotherapy, whether they received subsequent RT or not.
However, the investigators said longer follow-up is needed to determine if eliminating RT in PET-negative patients will lead to fewer late effects and improved overall survival.
The 602 patients who agreed to take part in this trial, known as RAPID, had a PET scan performed after chemotherapy. Patients who tested positive received RT.
Those who tested negative were divided into 2 groups. One group of 211 patients received no further treatment, and the other group of 209 patients had the standard RT.
At a median of 60 months of follow-up, the proportion of patients who were alive and disease-free was 94.6% in the RT group and 90.8% in the group that hadn’t received further treatment.
Eight patients in the RT group progressed, and 8 died (3 with disease progression, 1 of whom died from HL). Five of the deaths occurred in patients who did not ultimately receive RT.
In the untreated group, 20 patients progressed, and 4 patients died (2 with disease progression and none from HL).
“This research is an important step forward,” said study author John Radford, of The University of Manchester and The Christie NHS Foundation Trust in the UK.
“The results of RAPID show that, in early stage Hodgkin lymphoma, radiotherapy after initial chemotherapy marginally reduces the recurrence rate, but this is bought at the expense of exposing to radiation all patients with negative PET findings, most of whom are already cured.”
Image by Jens Langner
Performing PET scans immediately after chemotherapy may reveal which Hodgkin lymphoma (HL) patients need radiotherapy (RT).
A study published in NEJM showed similar rates of progression-free survival in HL patients who werePET-negative after chemotherapy, whether they received subsequent RT or not.
However, the investigators said longer follow-up is needed to determine if eliminating RT in PET-negative patients will lead to fewer late effects and improved overall survival.
The 602 patients who agreed to take part in this trial, known as RAPID, had a PET scan performed after chemotherapy. Patients who tested positive received RT.
Those who tested negative were divided into 2 groups. One group of 211 patients received no further treatment, and the other group of 209 patients had the standard RT.
At a median of 60 months of follow-up, the proportion of patients who were alive and disease-free was 94.6% in the RT group and 90.8% in the group that hadn’t received further treatment.
Eight patients in the RT group progressed, and 8 died (3 with disease progression, 1 of whom died from HL). Five of the deaths occurred in patients who did not ultimately receive RT.
In the untreated group, 20 patients progressed, and 4 patients died (2 with disease progression and none from HL).
“This research is an important step forward,” said study author John Radford, of The University of Manchester and The Christie NHS Foundation Trust in the UK.
“The results of RAPID show that, in early stage Hodgkin lymphoma, radiotherapy after initial chemotherapy marginally reduces the recurrence rate, but this is bought at the expense of exposing to radiation all patients with negative PET findings, most of whom are already cured.”
Concerns Regarding Long‐term Opioid Use
Overall rates of opioid use and chronic use for noncancer pain have increased markedly in the last 1 to 2 decades.[1, 2] Recognition of such rapidly increasing use has prompted a flurry of investigations examining the impact of what has been referred to as the opioid epidemic.[1, 3, 4] Patients receiving chronic opioid analgesics have previously been demonstrated to consume disproportionate shares of healthcare resources, including significantly more emergency room visits and days in the hospital.[5] In this issue of the Journal of Hospital Medicine, Liang and Turner[6] further demonstrate the impressive scope of healthcare resources consumed by this patient population, and extend these findings by examining the relationship between opioid dose and subsequent hospitalization in a large national cohort of middle‐aged health maintenance organization enrollees with noncancer pain. This is the first study to investigate the relationship in a general cohort of patients.
Perhaps the most striking finding of the study was an all‐cause hospitalization rate of 1120 per 10,000 person‐years among their cohort of opioid users. Considering that 5 to 8 million Americans use long‐term opioids,[7] this translates to about 500,000 to 900,000 admissions per year. The degree to which opioids themselves contribute to such hospitalizations (attributable risk) is uncertain, and it is likely that some of this risk can be explained by the idea that opioids are a marker for comorbidity, and that the conditions prompting opioid use independently increase risk of hospitalization. Studies examining more homogeneous patient populations could serve to shed light on this question. The issue of attributable risk notwithstanding, it is clear that this is a patient population that should have the attention of physicians, hospital administrators, and policy makers.
The main finding of their study is that the total opioid dose in any given 6‐month interval was more strongly associated with subsequent all‐cause hospitalization than the daily dose. This suggests that cumulative exposure is important, and possibly more important than the strength of any given prescription, at least when it comes to the outcome of hospitalization. That is not to say that the daily dose is unimportant, and the authors appropriately caution against such an interpretation. Daily dose matters, and to conclude otherwise would be incorrect for several reasons. First, among patients receiving high total doses of opioids, higher daily doses did seem to confer additional risk. Second, hospitalization is only 1 measure of risk, and multiple prior studies and a recent systematic review have concluded that higher opioid doses are strongly associated with adverse events, including overdose, abuse, addiction, motor vehicle accidents, and myocardial infarction.[8] Last, their finding that total dose more strongly predicts hospitalization than daily dose may reflect confounding by indication and underlying patient characteristics not captured in their analysis. Patients receiving a daily dose of 100 mg or more, but with a total dose of <1830 mg over 6 months, would necessarily have received opioids for a relatively brief period of time (<20 days). The indications forand patients receivingsuch short‐course, high‐dose therapy are likely to be vastly different from those for longer‐course, high‐dose therapy, in ways that could be meaningfully associated with hospitalization risk. Nonetheless, their results suggest that cumulative exposure is important as an additional metric by which to predict possible adverse consequences of opioid use.
That cumulative exposure and percent of time on opioids are associated with increased risk of subsequent hospitalization casts further doubt on the already questionable risk‐to‐benefit ratio of long‐term use of opioids for noncancer pain. A recent systematic review of the effectiveness and risks of long‐term opioid therapy for chronic pain found existing evidence insufficient to determine effectiveness for chronic pain and function, owing to lack of a single study evaluating long‐term outcomes in patients on opioid therapy versus no opioid therapy, and found evidence for a dose‐dependent risk for serious harms.[8] The authors conclude that the lack of scientific evidence on effectiveness of long‐term opioid therapy for chronic pain is in striking contrast to its widespread use in this setting. Studies examining the effect of long‐term opioid therapy on pain and function, and defining patient subgroups that may benefit from such therapy, are imperative and long overdue.
In the absence of data showing benefit, and in the face of a growing body of evidence demonstrating harm, we are obligated to reevaluate opioid prescribing for chronic noncancer pain. Until studies have evaluated the impact of opioid use on long‐term outcomes, physicians are missing a key piece of the risk‐benefit calculation, and prescribing must be done judiciously. Curbing the opioid epidemic will require initiatives of epidemic proportions, involving the entire spectrum of healthcare, from the primary care setting to the emergency department (where up to 25% of patients with chronic pain receive their opioids[7]), from researchers to policy makers, and ultimately from patient expectations to physician decision making.
Disclosures
Dr. Herzig was funded by grant number K23AG042459 from the National Institute on Aging. The funding organization had no involvement in any aspect of the study, including design, conduct, and reporting of the study. The author reports no conflicts of interest.
- Vital signs: overdoses of prescription opioid pain relievers—United States, 1999—2008. MMWR Morb Mortal Wkly Rep. 2011;60:1487–1492.
- , , , et al. Trends in long‐term opioid therapy for chronic non‐cancer pain. Pharmacoepidemiol Drug Saf. 2009;18:1166–1175.
- CDC grand rounds: prescription drug overdoses—a U.S. epidemic. MMWR Morb Mortal Wkly Rep. 2012;61:10–13.
- . A flood of opioids, a rising tide of deaths. N Engl J Med. 2010;363:1981–1985.
- , , , , , . Co‐morbidity and utilization of medical services by pain patients receiving opioid medications: data from an insurance claims database. Pain. 2009;144:20–27.
- , . National cohort study of opioid analgesic dose and risk of future hospitalization. J Hosp Med. 2015;10:000–000.
- , , , et al. National institutes of health pathways to prevention workshop: the role of opioids in the treatment of chronic pain. Ann Intern Med. 2015;162:295–300.
- , , , et al. The effectiveness and risks of long‐term opioid therapy for chronic pain: a systematic review for a national institutes of health pathways to prevention workshop. Ann Intern Med. 2015;162:276–286.
Overall rates of opioid use and chronic use for noncancer pain have increased markedly in the last 1 to 2 decades.[1, 2] Recognition of such rapidly increasing use has prompted a flurry of investigations examining the impact of what has been referred to as the opioid epidemic.[1, 3, 4] Patients receiving chronic opioid analgesics have previously been demonstrated to consume disproportionate shares of healthcare resources, including significantly more emergency room visits and days in the hospital.[5] In this issue of the Journal of Hospital Medicine, Liang and Turner[6] further demonstrate the impressive scope of healthcare resources consumed by this patient population, and extend these findings by examining the relationship between opioid dose and subsequent hospitalization in a large national cohort of middle‐aged health maintenance organization enrollees with noncancer pain. This is the first study to investigate the relationship in a general cohort of patients.
Perhaps the most striking finding of the study was an all‐cause hospitalization rate of 1120 per 10,000 person‐years among their cohort of opioid users. Considering that 5 to 8 million Americans use long‐term opioids,[7] this translates to about 500,000 to 900,000 admissions per year. The degree to which opioids themselves contribute to such hospitalizations (attributable risk) is uncertain, and it is likely that some of this risk can be explained by the idea that opioids are a marker for comorbidity, and that the conditions prompting opioid use independently increase risk of hospitalization. Studies examining more homogeneous patient populations could serve to shed light on this question. The issue of attributable risk notwithstanding, it is clear that this is a patient population that should have the attention of physicians, hospital administrators, and policy makers.
The main finding of their study is that the total opioid dose in any given 6‐month interval was more strongly associated with subsequent all‐cause hospitalization than the daily dose. This suggests that cumulative exposure is important, and possibly more important than the strength of any given prescription, at least when it comes to the outcome of hospitalization. That is not to say that the daily dose is unimportant, and the authors appropriately caution against such an interpretation. Daily dose matters, and to conclude otherwise would be incorrect for several reasons. First, among patients receiving high total doses of opioids, higher daily doses did seem to confer additional risk. Second, hospitalization is only 1 measure of risk, and multiple prior studies and a recent systematic review have concluded that higher opioid doses are strongly associated with adverse events, including overdose, abuse, addiction, motor vehicle accidents, and myocardial infarction.[8] Last, their finding that total dose more strongly predicts hospitalization than daily dose may reflect confounding by indication and underlying patient characteristics not captured in their analysis. Patients receiving a daily dose of 100 mg or more, but with a total dose of <1830 mg over 6 months, would necessarily have received opioids for a relatively brief period of time (<20 days). The indications forand patients receivingsuch short‐course, high‐dose therapy are likely to be vastly different from those for longer‐course, high‐dose therapy, in ways that could be meaningfully associated with hospitalization risk. Nonetheless, their results suggest that cumulative exposure is important as an additional metric by which to predict possible adverse consequences of opioid use.
That cumulative exposure and percent of time on opioids are associated with increased risk of subsequent hospitalization casts further doubt on the already questionable risk‐to‐benefit ratio of long‐term use of opioids for noncancer pain. A recent systematic review of the effectiveness and risks of long‐term opioid therapy for chronic pain found existing evidence insufficient to determine effectiveness for chronic pain and function, owing to lack of a single study evaluating long‐term outcomes in patients on opioid therapy versus no opioid therapy, and found evidence for a dose‐dependent risk for serious harms.[8] The authors conclude that the lack of scientific evidence on effectiveness of long‐term opioid therapy for chronic pain is in striking contrast to its widespread use in this setting. Studies examining the effect of long‐term opioid therapy on pain and function, and defining patient subgroups that may benefit from such therapy, are imperative and long overdue.
In the absence of data showing benefit, and in the face of a growing body of evidence demonstrating harm, we are obligated to reevaluate opioid prescribing for chronic noncancer pain. Until studies have evaluated the impact of opioid use on long‐term outcomes, physicians are missing a key piece of the risk‐benefit calculation, and prescribing must be done judiciously. Curbing the opioid epidemic will require initiatives of epidemic proportions, involving the entire spectrum of healthcare, from the primary care setting to the emergency department (where up to 25% of patients with chronic pain receive their opioids[7]), from researchers to policy makers, and ultimately from patient expectations to physician decision making.
Disclosures
Dr. Herzig was funded by grant number K23AG042459 from the National Institute on Aging. The funding organization had no involvement in any aspect of the study, including design, conduct, and reporting of the study. The author reports no conflicts of interest.
Overall rates of opioid use and chronic use for noncancer pain have increased markedly in the last 1 to 2 decades.[1, 2] Recognition of such rapidly increasing use has prompted a flurry of investigations examining the impact of what has been referred to as the opioid epidemic.[1, 3, 4] Patients receiving chronic opioid analgesics have previously been demonstrated to consume disproportionate shares of healthcare resources, including significantly more emergency room visits and days in the hospital.[5] In this issue of the Journal of Hospital Medicine, Liang and Turner[6] further demonstrate the impressive scope of healthcare resources consumed by this patient population, and extend these findings by examining the relationship between opioid dose and subsequent hospitalization in a large national cohort of middle‐aged health maintenance organization enrollees with noncancer pain. This is the first study to investigate the relationship in a general cohort of patients.
Perhaps the most striking finding of the study was an all‐cause hospitalization rate of 1120 per 10,000 person‐years among their cohort of opioid users. Considering that 5 to 8 million Americans use long‐term opioids,[7] this translates to about 500,000 to 900,000 admissions per year. The degree to which opioids themselves contribute to such hospitalizations (attributable risk) is uncertain, and it is likely that some of this risk can be explained by the idea that opioids are a marker for comorbidity, and that the conditions prompting opioid use independently increase risk of hospitalization. Studies examining more homogeneous patient populations could serve to shed light on this question. The issue of attributable risk notwithstanding, it is clear that this is a patient population that should have the attention of physicians, hospital administrators, and policy makers.
The main finding of their study is that the total opioid dose in any given 6‐month interval was more strongly associated with subsequent all‐cause hospitalization than the daily dose. This suggests that cumulative exposure is important, and possibly more important than the strength of any given prescription, at least when it comes to the outcome of hospitalization. That is not to say that the daily dose is unimportant, and the authors appropriately caution against such an interpretation. Daily dose matters, and to conclude otherwise would be incorrect for several reasons. First, among patients receiving high total doses of opioids, higher daily doses did seem to confer additional risk. Second, hospitalization is only 1 measure of risk, and multiple prior studies and a recent systematic review have concluded that higher opioid doses are strongly associated with adverse events, including overdose, abuse, addiction, motor vehicle accidents, and myocardial infarction.[8] Last, their finding that total dose more strongly predicts hospitalization than daily dose may reflect confounding by indication and underlying patient characteristics not captured in their analysis. Patients receiving a daily dose of 100 mg or more, but with a total dose of <1830 mg over 6 months, would necessarily have received opioids for a relatively brief period of time (<20 days). The indications forand patients receivingsuch short‐course, high‐dose therapy are likely to be vastly different from those for longer‐course, high‐dose therapy, in ways that could be meaningfully associated with hospitalization risk. Nonetheless, their results suggest that cumulative exposure is important as an additional metric by which to predict possible adverse consequences of opioid use.
That cumulative exposure and percent of time on opioids are associated with increased risk of subsequent hospitalization casts further doubt on the already questionable risk‐to‐benefit ratio of long‐term use of opioids for noncancer pain. A recent systematic review of the effectiveness and risks of long‐term opioid therapy for chronic pain found existing evidence insufficient to determine effectiveness for chronic pain and function, owing to lack of a single study evaluating long‐term outcomes in patients on opioid therapy versus no opioid therapy, and found evidence for a dose‐dependent risk for serious harms.[8] The authors conclude that the lack of scientific evidence on effectiveness of long‐term opioid therapy for chronic pain is in striking contrast to its widespread use in this setting. Studies examining the effect of long‐term opioid therapy on pain and function, and defining patient subgroups that may benefit from such therapy, are imperative and long overdue.
In the absence of data showing benefit, and in the face of a growing body of evidence demonstrating harm, we are obligated to reevaluate opioid prescribing for chronic noncancer pain. Until studies have evaluated the impact of opioid use on long‐term outcomes, physicians are missing a key piece of the risk‐benefit calculation, and prescribing must be done judiciously. Curbing the opioid epidemic will require initiatives of epidemic proportions, involving the entire spectrum of healthcare, from the primary care setting to the emergency department (where up to 25% of patients with chronic pain receive their opioids[7]), from researchers to policy makers, and ultimately from patient expectations to physician decision making.
Disclosures
Dr. Herzig was funded by grant number K23AG042459 from the National Institute on Aging. The funding organization had no involvement in any aspect of the study, including design, conduct, and reporting of the study. The author reports no conflicts of interest.
- Vital signs: overdoses of prescription opioid pain relievers—United States, 1999—2008. MMWR Morb Mortal Wkly Rep. 2011;60:1487–1492.
- , , , et al. Trends in long‐term opioid therapy for chronic non‐cancer pain. Pharmacoepidemiol Drug Saf. 2009;18:1166–1175.
- CDC grand rounds: prescription drug overdoses—a U.S. epidemic. MMWR Morb Mortal Wkly Rep. 2012;61:10–13.
- . A flood of opioids, a rising tide of deaths. N Engl J Med. 2010;363:1981–1985.
- , , , , , . Co‐morbidity and utilization of medical services by pain patients receiving opioid medications: data from an insurance claims database. Pain. 2009;144:20–27.
- , . National cohort study of opioid analgesic dose and risk of future hospitalization. J Hosp Med. 2015;10:000–000.
- , , , et al. National institutes of health pathways to prevention workshop: the role of opioids in the treatment of chronic pain. Ann Intern Med. 2015;162:295–300.
- , , , et al. The effectiveness and risks of long‐term opioid therapy for chronic pain: a systematic review for a national institutes of health pathways to prevention workshop. Ann Intern Med. 2015;162:276–286.
- Vital signs: overdoses of prescription opioid pain relievers—United States, 1999—2008. MMWR Morb Mortal Wkly Rep. 2011;60:1487–1492.
- , , , et al. Trends in long‐term opioid therapy for chronic non‐cancer pain. Pharmacoepidemiol Drug Saf. 2009;18:1166–1175.
- CDC grand rounds: prescription drug overdoses—a U.S. epidemic. MMWR Morb Mortal Wkly Rep. 2012;61:10–13.
- . A flood of opioids, a rising tide of deaths. N Engl J Med. 2010;363:1981–1985.
- , , , , , . Co‐morbidity and utilization of medical services by pain patients receiving opioid medications: data from an insurance claims database. Pain. 2009;144:20–27.
- , . National cohort study of opioid analgesic dose and risk of future hospitalization. J Hosp Med. 2015;10:000–000.
- , , , et al. National institutes of health pathways to prevention workshop: the role of opioids in the treatment of chronic pain. Ann Intern Med. 2015;162:295–300.
- , , , et al. The effectiveness and risks of long‐term opioid therapy for chronic pain: a systematic review for a national institutes of health pathways to prevention workshop. Ann Intern Med. 2015;162:276–286.
Teens who tan indoors do it often
More than one-third of teens who undergo indoor tanning do so frequently, according to data from a survey of 1,850 public high school students from 27 schools in New Jersey.
The data were part of the 2012 New Jersey Youth Tobacco Survey, taken before New Jersey banned indoor tanning for individuals younger than 17 years of age in 2013. A total of 146 respondents reported indoor tanning within the past year, and approximately 38% reported 10 or more tanning sessions, wrote Elliot J. Coups, Ph.D., of Rutgers Cancer Institute of New Jersey, New Brunswick, and colleagues.
Overall, “frequent indoor tanning was significantly more common among indoor tanners who were current smokers, tanned to improve their mood, had used social media related to tanning salons, or indicated it would be very hard to stop indoor tanning,” the researchers noted, adding that social media might be an opportunity for interventions to reduce indoor tanning in this population.
Find the study in the Journal of the American Academy of Dermatology (doi:10.1016/j.jaad.2015.01.035).
More than one-third of teens who undergo indoor tanning do so frequently, according to data from a survey of 1,850 public high school students from 27 schools in New Jersey.
The data were part of the 2012 New Jersey Youth Tobacco Survey, taken before New Jersey banned indoor tanning for individuals younger than 17 years of age in 2013. A total of 146 respondents reported indoor tanning within the past year, and approximately 38% reported 10 or more tanning sessions, wrote Elliot J. Coups, Ph.D., of Rutgers Cancer Institute of New Jersey, New Brunswick, and colleagues.
Overall, “frequent indoor tanning was significantly more common among indoor tanners who were current smokers, tanned to improve their mood, had used social media related to tanning salons, or indicated it would be very hard to stop indoor tanning,” the researchers noted, adding that social media might be an opportunity for interventions to reduce indoor tanning in this population.
Find the study in the Journal of the American Academy of Dermatology (doi:10.1016/j.jaad.2015.01.035).
More than one-third of teens who undergo indoor tanning do so frequently, according to data from a survey of 1,850 public high school students from 27 schools in New Jersey.
The data were part of the 2012 New Jersey Youth Tobacco Survey, taken before New Jersey banned indoor tanning for individuals younger than 17 years of age in 2013. A total of 146 respondents reported indoor tanning within the past year, and approximately 38% reported 10 or more tanning sessions, wrote Elliot J. Coups, Ph.D., of Rutgers Cancer Institute of New Jersey, New Brunswick, and colleagues.
Overall, “frequent indoor tanning was significantly more common among indoor tanners who were current smokers, tanned to improve their mood, had used social media related to tanning salons, or indicated it would be very hard to stop indoor tanning,” the researchers noted, adding that social media might be an opportunity for interventions to reduce indoor tanning in this population.
Find the study in the Journal of the American Academy of Dermatology (doi:10.1016/j.jaad.2015.01.035).
Short but simple theme guides AK treatment recommendations
An expert panel of seven dermatologists has generated recommendations to aid clinicians in prescribing topical treatments for actinic keratoses. Dr. Eggert Stockfleth and his colleagues acknowledged that patient compliance with topical AK therapy remains a challenge.
Their recommendations included the need to develop topical treatments with shorter duration but equal effectiveness, to keep regimens as simple as possible, and to manage patient expectations.“Our experts believe that real-world efficacy could be vastly improved by shorter treatments coupled with effective patient management,” they noted.Read the full article in the International Journal of Dermatology (doi:10.1111/ijd.12840).
An expert panel of seven dermatologists has generated recommendations to aid clinicians in prescribing topical treatments for actinic keratoses. Dr. Eggert Stockfleth and his colleagues acknowledged that patient compliance with topical AK therapy remains a challenge.
Their recommendations included the need to develop topical treatments with shorter duration but equal effectiveness, to keep regimens as simple as possible, and to manage patient expectations.“Our experts believe that real-world efficacy could be vastly improved by shorter treatments coupled with effective patient management,” they noted.Read the full article in the International Journal of Dermatology (doi:10.1111/ijd.12840).
An expert panel of seven dermatologists has generated recommendations to aid clinicians in prescribing topical treatments for actinic keratoses. Dr. Eggert Stockfleth and his colleagues acknowledged that patient compliance with topical AK therapy remains a challenge.
Their recommendations included the need to develop topical treatments with shorter duration but equal effectiveness, to keep regimens as simple as possible, and to manage patient expectations.“Our experts believe that real-world efficacy could be vastly improved by shorter treatments coupled with effective patient management,” they noted.Read the full article in the International Journal of Dermatology (doi:10.1111/ijd.12840).
Finally, an end to the SGR game of chicken
Well, in a remarkable moment in what is likely the most dysfunctional American government on record, all sides agreed to repeal the sustainable growth rate formula and change the way Medicare payments are done.
For the foreseeable future, this eliminates the annual game of chicken that political parties play at our expense.
For more than 10 years now, the cuts have come up, the medical journals decry them, doctors threaten to stop seeing Medicare patients, and eventually the politicians reach an agreement to stop the cuts that had grown to a high of 27.4% in 2012 ... until the next year. The classic game of political kick the can.
The dysfunctional waltz had been going on for so long that only the medical press and doctors seemed to care.
So, after years of wrapping duct tape around a leaking pipe, they called a plumber and replaced the pipe. The cost is far higher than it would have been if they’d actually addressed the problem when it started in 2003.
I’m sure the new law will have its own issues, but it stops – for now – the nightmare scenario where the cuts are allowed to go through. That would have left many of us in the difficult situation of turning away new Medicare patients. None of us wants to do that.
It’s nice to have seen the government function in the way it’s supposed to – with negotiations and compromise – rather than more threats, vitriolic posturing, and finger-pointing that have been the recent norm. Members of Congress, regrettably, don’t have their health care affected by their decisions. Regardless of age, the majority aren’t on Medicare. They’re all covered through the Federal Employees Health Benefits Program, which uses private plans. So it doesn’t directly affect them if a doctor’s office is shuttered or sick constituents can’t find someone to help them. They figure by the next election cycle they’ll be able to distract voters with some other topic.
I’m glad that reason and concern for the health care of ordinary citizens prevailed. It’s easy to play chicken when someone else’s life and livelihood are involved, and not yours. I hope this leads to greater cooperation and willingness to work together between the two sides in the future.
But I’m not optimistic.
Dr. Block has a solo neurology practice in Scottsdale, Ariz.
Well, in a remarkable moment in what is likely the most dysfunctional American government on record, all sides agreed to repeal the sustainable growth rate formula and change the way Medicare payments are done.
For the foreseeable future, this eliminates the annual game of chicken that political parties play at our expense.
For more than 10 years now, the cuts have come up, the medical journals decry them, doctors threaten to stop seeing Medicare patients, and eventually the politicians reach an agreement to stop the cuts that had grown to a high of 27.4% in 2012 ... until the next year. The classic game of political kick the can.
The dysfunctional waltz had been going on for so long that only the medical press and doctors seemed to care.
So, after years of wrapping duct tape around a leaking pipe, they called a plumber and replaced the pipe. The cost is far higher than it would have been if they’d actually addressed the problem when it started in 2003.
I’m sure the new law will have its own issues, but it stops – for now – the nightmare scenario where the cuts are allowed to go through. That would have left many of us in the difficult situation of turning away new Medicare patients. None of us wants to do that.
It’s nice to have seen the government function in the way it’s supposed to – with negotiations and compromise – rather than more threats, vitriolic posturing, and finger-pointing that have been the recent norm. Members of Congress, regrettably, don’t have their health care affected by their decisions. Regardless of age, the majority aren’t on Medicare. They’re all covered through the Federal Employees Health Benefits Program, which uses private plans. So it doesn’t directly affect them if a doctor’s office is shuttered or sick constituents can’t find someone to help them. They figure by the next election cycle they’ll be able to distract voters with some other topic.
I’m glad that reason and concern for the health care of ordinary citizens prevailed. It’s easy to play chicken when someone else’s life and livelihood are involved, and not yours. I hope this leads to greater cooperation and willingness to work together between the two sides in the future.
But I’m not optimistic.
Dr. Block has a solo neurology practice in Scottsdale, Ariz.
Well, in a remarkable moment in what is likely the most dysfunctional American government on record, all sides agreed to repeal the sustainable growth rate formula and change the way Medicare payments are done.
For the foreseeable future, this eliminates the annual game of chicken that political parties play at our expense.
For more than 10 years now, the cuts have come up, the medical journals decry them, doctors threaten to stop seeing Medicare patients, and eventually the politicians reach an agreement to stop the cuts that had grown to a high of 27.4% in 2012 ... until the next year. The classic game of political kick the can.
The dysfunctional waltz had been going on for so long that only the medical press and doctors seemed to care.
So, after years of wrapping duct tape around a leaking pipe, they called a plumber and replaced the pipe. The cost is far higher than it would have been if they’d actually addressed the problem when it started in 2003.
I’m sure the new law will have its own issues, but it stops – for now – the nightmare scenario where the cuts are allowed to go through. That would have left many of us in the difficult situation of turning away new Medicare patients. None of us wants to do that.
It’s nice to have seen the government function in the way it’s supposed to – with negotiations and compromise – rather than more threats, vitriolic posturing, and finger-pointing that have been the recent norm. Members of Congress, regrettably, don’t have their health care affected by their decisions. Regardless of age, the majority aren’t on Medicare. They’re all covered through the Federal Employees Health Benefits Program, which uses private plans. So it doesn’t directly affect them if a doctor’s office is shuttered or sick constituents can’t find someone to help them. They figure by the next election cycle they’ll be able to distract voters with some other topic.
I’m glad that reason and concern for the health care of ordinary citizens prevailed. It’s easy to play chicken when someone else’s life and livelihood are involved, and not yours. I hope this leads to greater cooperation and willingness to work together between the two sides in the future.
But I’m not optimistic.
Dr. Block has a solo neurology practice in Scottsdale, Ariz.
Bath salts – the new designer high
“Bath salts” is a dangerous illicit drug that teens may be using. It hit the U.S. scene in 2010 after being a big hit in Europe. It’s called “bath salts” because it resembled Epsom salt, but shares no chemical properties with it.
Because it was called bath salts, it initially evaded the Food and Drug Administration, and was sold at gas stations and clubs marked “not for human consumption,” which earned it its name as the “legal high.” Bath salts are creatively packaged in containers that are colorful and attractive, and have aliases such as “plant food,” “Ivory Wave,” “Purple Wave,” “Bloom,” “Cloud Nine,” or “Vanilla Sky,” according to the National Institute on Drug Abuse.
Shortly after the drug’s debut, emergency departments were seeing several hundreds of people with amphetamine-like intoxication and “naked rages.” In 2012, when it became known that these substances were being use as illicit drugs, they were made illegal, but the problem now is there are many derivatives of this drug and their use is becoming more widespread.
Mephedrone is one of the possible active ingredients, and it is derived from the synthetic cathinone, similar to cathinone found naturally in the khat plant (Catha edulis). It stimulates the adrenergic receptors to release dopamine and norepinephrine, and block their reuptake, which makes them act like a stimulant on the nervous system. The result is agitation, hyperalertness, hypertension, tachycardia, diaphoresis, and elevated temperatures to 106<scaps>˚ </scaps>F. The term “naked rage” came into use because users would become overheated and angry, and would rip off their clothes as they raged.
Other synthetic canthinones being used as drugs of abuse include butylone, dimethylcathinone, ethcathinone, ethylone, 3- and 4-fluoromethcathinone, mephedrone, methedrone, methylenedioxypyrovalerone (MDPV), methylone, and pyrovalerone (J. Med. Toxicol. 2012;8:33-42).
MDPV raises dopamine levels in the brain as does cocaine, but is at least 10 times as potent, according to the National Institute on Drug Abuse.
Bath salts can be administered by snorting, ingesting, smoking, or injecting. Necrotizing fasciitis has been associated with its use. Most patients present with elevated temperatures, hypertension, palpitations, and delirium. Hydration and sedation are usually required, and patients usually need to be restrained to prevent them from hurting themselves further. Psychiatric symptoms may include paranoia, hallucinations, and panic attacks. Several deaths have been reported in association with its use.
In the time since this drug was made illegal, several other designer drugs have presented, which are just modifications of the mephedrone. “Flakka” and “jewelry cleaner” are examples of the modified synthetic cathinone. They all cause amphetamine-like reactions and the risk of overdose is great.
The cost to manufacture the drug is about $8 per unit, but its retail price is $20-$40. Though it takes only 3-5 mg to be effective, packages are sold with 500 mg, making the risk for overdose even greater. It usually takes about 1.5 hours to reach peak rush and the entire experience can last 6-8 hours. There is little difference between the euphoric level and intoxication level, which is what makes the drug so dangerous.
Synthetic drugs are a great danger to all age groups, including toddlers, because of the misleading packaging. But they are especially dangerous because the ingredients vary, and overdose occurs quickly.
It is imperative that parents and teens are made aware of the dangers associated with these drugs and their street names; www.streetdrugs.org is a website designed to educate teachers, parents and students about these drugs and their dangers.
Dr. Pearce is a pediatrician in Frankfort, Ill. E-mail her at [email protected].
“Bath salts” is a dangerous illicit drug that teens may be using. It hit the U.S. scene in 2010 after being a big hit in Europe. It’s called “bath salts” because it resembled Epsom salt, but shares no chemical properties with it.
Because it was called bath salts, it initially evaded the Food and Drug Administration, and was sold at gas stations and clubs marked “not for human consumption,” which earned it its name as the “legal high.” Bath salts are creatively packaged in containers that are colorful and attractive, and have aliases such as “plant food,” “Ivory Wave,” “Purple Wave,” “Bloom,” “Cloud Nine,” or “Vanilla Sky,” according to the National Institute on Drug Abuse.
Shortly after the drug’s debut, emergency departments were seeing several hundreds of people with amphetamine-like intoxication and “naked rages.” In 2012, when it became known that these substances were being use as illicit drugs, they were made illegal, but the problem now is there are many derivatives of this drug and their use is becoming more widespread.
Mephedrone is one of the possible active ingredients, and it is derived from the synthetic cathinone, similar to cathinone found naturally in the khat plant (Catha edulis). It stimulates the adrenergic receptors to release dopamine and norepinephrine, and block their reuptake, which makes them act like a stimulant on the nervous system. The result is agitation, hyperalertness, hypertension, tachycardia, diaphoresis, and elevated temperatures to 106<scaps>˚ </scaps>F. The term “naked rage” came into use because users would become overheated and angry, and would rip off their clothes as they raged.
Other synthetic canthinones being used as drugs of abuse include butylone, dimethylcathinone, ethcathinone, ethylone, 3- and 4-fluoromethcathinone, mephedrone, methedrone, methylenedioxypyrovalerone (MDPV), methylone, and pyrovalerone (J. Med. Toxicol. 2012;8:33-42).
MDPV raises dopamine levels in the brain as does cocaine, but is at least 10 times as potent, according to the National Institute on Drug Abuse.
Bath salts can be administered by snorting, ingesting, smoking, or injecting. Necrotizing fasciitis has been associated with its use. Most patients present with elevated temperatures, hypertension, palpitations, and delirium. Hydration and sedation are usually required, and patients usually need to be restrained to prevent them from hurting themselves further. Psychiatric symptoms may include paranoia, hallucinations, and panic attacks. Several deaths have been reported in association with its use.
In the time since this drug was made illegal, several other designer drugs have presented, which are just modifications of the mephedrone. “Flakka” and “jewelry cleaner” are examples of the modified synthetic cathinone. They all cause amphetamine-like reactions and the risk of overdose is great.
The cost to manufacture the drug is about $8 per unit, but its retail price is $20-$40. Though it takes only 3-5 mg to be effective, packages are sold with 500 mg, making the risk for overdose even greater. It usually takes about 1.5 hours to reach peak rush and the entire experience can last 6-8 hours. There is little difference between the euphoric level and intoxication level, which is what makes the drug so dangerous.
Synthetic drugs are a great danger to all age groups, including toddlers, because of the misleading packaging. But they are especially dangerous because the ingredients vary, and overdose occurs quickly.
It is imperative that parents and teens are made aware of the dangers associated with these drugs and their street names; www.streetdrugs.org is a website designed to educate teachers, parents and students about these drugs and their dangers.
Dr. Pearce is a pediatrician in Frankfort, Ill. E-mail her at [email protected].
“Bath salts” is a dangerous illicit drug that teens may be using. It hit the U.S. scene in 2010 after being a big hit in Europe. It’s called “bath salts” because it resembled Epsom salt, but shares no chemical properties with it.
Because it was called bath salts, it initially evaded the Food and Drug Administration, and was sold at gas stations and clubs marked “not for human consumption,” which earned it its name as the “legal high.” Bath salts are creatively packaged in containers that are colorful and attractive, and have aliases such as “plant food,” “Ivory Wave,” “Purple Wave,” “Bloom,” “Cloud Nine,” or “Vanilla Sky,” according to the National Institute on Drug Abuse.
Shortly after the drug’s debut, emergency departments were seeing several hundreds of people with amphetamine-like intoxication and “naked rages.” In 2012, when it became known that these substances were being use as illicit drugs, they were made illegal, but the problem now is there are many derivatives of this drug and their use is becoming more widespread.
Mephedrone is one of the possible active ingredients, and it is derived from the synthetic cathinone, similar to cathinone found naturally in the khat plant (Catha edulis). It stimulates the adrenergic receptors to release dopamine and norepinephrine, and block their reuptake, which makes them act like a stimulant on the nervous system. The result is agitation, hyperalertness, hypertension, tachycardia, diaphoresis, and elevated temperatures to 106<scaps>˚ </scaps>F. The term “naked rage” came into use because users would become overheated and angry, and would rip off their clothes as they raged.
Other synthetic canthinones being used as drugs of abuse include butylone, dimethylcathinone, ethcathinone, ethylone, 3- and 4-fluoromethcathinone, mephedrone, methedrone, methylenedioxypyrovalerone (MDPV), methylone, and pyrovalerone (J. Med. Toxicol. 2012;8:33-42).
MDPV raises dopamine levels in the brain as does cocaine, but is at least 10 times as potent, according to the National Institute on Drug Abuse.
Bath salts can be administered by snorting, ingesting, smoking, or injecting. Necrotizing fasciitis has been associated with its use. Most patients present with elevated temperatures, hypertension, palpitations, and delirium. Hydration and sedation are usually required, and patients usually need to be restrained to prevent them from hurting themselves further. Psychiatric symptoms may include paranoia, hallucinations, and panic attacks. Several deaths have been reported in association with its use.
In the time since this drug was made illegal, several other designer drugs have presented, which are just modifications of the mephedrone. “Flakka” and “jewelry cleaner” are examples of the modified synthetic cathinone. They all cause amphetamine-like reactions and the risk of overdose is great.
The cost to manufacture the drug is about $8 per unit, but its retail price is $20-$40. Though it takes only 3-5 mg to be effective, packages are sold with 500 mg, making the risk for overdose even greater. It usually takes about 1.5 hours to reach peak rush and the entire experience can last 6-8 hours. There is little difference between the euphoric level and intoxication level, which is what makes the drug so dangerous.
Synthetic drugs are a great danger to all age groups, including toddlers, because of the misleading packaging. But they are especially dangerous because the ingredients vary, and overdose occurs quickly.
It is imperative that parents and teens are made aware of the dangers associated with these drugs and their street names; www.streetdrugs.org is a website designed to educate teachers, parents and students about these drugs and their dangers.
Dr. Pearce is a pediatrician in Frankfort, Ill. E-mail her at [email protected].
May 2015 Quiz 2
ANSWER: C
Critique
Sulfasalazine can cause reversible azoospermia and infertility. About 80% of patients taking sulfasalazine have semen abnormalities and 72% have oligospermia. Only one case of azoospermia has been reported in patients taking pure mesalamines. The sperm abnormalities are thought to be caused by the sulfapyridine moiety in the sulfasalazine molecule. Therefore, a switch from sulfasalazine to Asacol® or any other pure mesalamine is indicated.
Sulfasalazine inhibits dihydrofolate reductase and can cause folate deficiency. As a result, it should always be given along with oral folic acid supplementation. There is no clear evidence that 6-mercaptopurine affects male fertility. Holding both medications in a patient with UC would put him at increased risk of recurrence and should not be recommended. Withdrawal of an immunomodulatory agent such as 6-mercaptopurine or azathioprine in patients who are in remission can lead to rapid relapse in up to one-third of patients in 1 year and two-thirds within 5 years. Since 6-mercaptopurine is maintaining remission, there is no need for a switch to infliximab. An in vitro fertilization specialist might be required if there is no conception despite sulfasalazine withdrawal.
References
1. Nielsen O.H., Munck L.K. Drug insight: aminosalicylates for the treatment of IBD. Nat. Clin. Pract. Gastroenterol. Hepatol. 2007;4:160-70.
2. Cassinotti A., Actis G.C., Duca P., et al. Maintenance treatment with azathioprine in ulcerative colitis: outcome and predictive factors after drug withdrawal. Am. J. Gastroenterol. 2009;104:2760-7.
ANSWER: C
Critique
Sulfasalazine can cause reversible azoospermia and infertility. About 80% of patients taking sulfasalazine have semen abnormalities and 72% have oligospermia. Only one case of azoospermia has been reported in patients taking pure mesalamines. The sperm abnormalities are thought to be caused by the sulfapyridine moiety in the sulfasalazine molecule. Therefore, a switch from sulfasalazine to Asacol® or any other pure mesalamine is indicated.
Sulfasalazine inhibits dihydrofolate reductase and can cause folate deficiency. As a result, it should always be given along with oral folic acid supplementation. There is no clear evidence that 6-mercaptopurine affects male fertility. Holding both medications in a patient with UC would put him at increased risk of recurrence and should not be recommended. Withdrawal of an immunomodulatory agent such as 6-mercaptopurine or azathioprine in patients who are in remission can lead to rapid relapse in up to one-third of patients in 1 year and two-thirds within 5 years. Since 6-mercaptopurine is maintaining remission, there is no need for a switch to infliximab. An in vitro fertilization specialist might be required if there is no conception despite sulfasalazine withdrawal.
References
1. Nielsen O.H., Munck L.K. Drug insight: aminosalicylates for the treatment of IBD. Nat. Clin. Pract. Gastroenterol. Hepatol. 2007;4:160-70.
2. Cassinotti A., Actis G.C., Duca P., et al. Maintenance treatment with azathioprine in ulcerative colitis: outcome and predictive factors after drug withdrawal. Am. J. Gastroenterol. 2009;104:2760-7.
ANSWER: C
Critique
Sulfasalazine can cause reversible azoospermia and infertility. About 80% of patients taking sulfasalazine have semen abnormalities and 72% have oligospermia. Only one case of azoospermia has been reported in patients taking pure mesalamines. The sperm abnormalities are thought to be caused by the sulfapyridine moiety in the sulfasalazine molecule. Therefore, a switch from sulfasalazine to Asacol® or any other pure mesalamine is indicated.
Sulfasalazine inhibits dihydrofolate reductase and can cause folate deficiency. As a result, it should always be given along with oral folic acid supplementation. There is no clear evidence that 6-mercaptopurine affects male fertility. Holding both medications in a patient with UC would put him at increased risk of recurrence and should not be recommended. Withdrawal of an immunomodulatory agent such as 6-mercaptopurine or azathioprine in patients who are in remission can lead to rapid relapse in up to one-third of patients in 1 year and two-thirds within 5 years. Since 6-mercaptopurine is maintaining remission, there is no need for a switch to infliximab. An in vitro fertilization specialist might be required if there is no conception despite sulfasalazine withdrawal.
References
1. Nielsen O.H., Munck L.K. Drug insight: aminosalicylates for the treatment of IBD. Nat. Clin. Pract. Gastroenterol. Hepatol. 2007;4:160-70.
2. Cassinotti A., Actis G.C., Duca P., et al. Maintenance treatment with azathioprine in ulcerative colitis: outcome and predictive factors after drug withdrawal. Am. J. Gastroenterol. 2009;104:2760-7.
May 2015 Quiz 1
ANSWER: C
Critique
A recent Olmstead County, Minn., study was undertaken to understand the epidemiology of community-acquired C. difficile infections. In the cohort of 385 proven C. difficile infections, 41% were community acquired. Compared to cases acquired in the hospital, community C. difficile infections were observed in younger (B) females (A) who had lower comorbidity scores and fewer chronic illnesses (D). Also, these outpatient cases were less likely to have recent antibiotic exposure (E) and fortunately had less severe clinical courses. A large population-based study and several others have confirmed that the use of gastric acid-suppressive agents such as PPIs (C) increases the risk of C. difficile-associated disease (adjusted risk ratio 2.9, 95% CI: 2.4-3.4).
References
1. Khanna S., Pardi D.S., Aronson S.L., et al. The epidemiology of community-acquired Clostridium difficile infection: a population-based study. Am. J. Gastroenterol. 2012;107:89-95.
2. Dial S., Delaney J.A., Barkun A.N., Suissa S. Use of gastric acid-suppressive agents and the risk of community-acquired Clostridium difficile-associated disease. JAMA 2005;294:2989.
ANSWER: C
Critique
A recent Olmstead County, Minn., study was undertaken to understand the epidemiology of community-acquired C. difficile infections. In the cohort of 385 proven C. difficile infections, 41% were community acquired. Compared to cases acquired in the hospital, community C. difficile infections were observed in younger (B) females (A) who had lower comorbidity scores and fewer chronic illnesses (D). Also, these outpatient cases were less likely to have recent antibiotic exposure (E) and fortunately had less severe clinical courses. A large population-based study and several others have confirmed that the use of gastric acid-suppressive agents such as PPIs (C) increases the risk of C. difficile-associated disease (adjusted risk ratio 2.9, 95% CI: 2.4-3.4).
References
1. Khanna S., Pardi D.S., Aronson S.L., et al. The epidemiology of community-acquired Clostridium difficile infection: a population-based study. Am. J. Gastroenterol. 2012;107:89-95.
2. Dial S., Delaney J.A., Barkun A.N., Suissa S. Use of gastric acid-suppressive agents and the risk of community-acquired Clostridium difficile-associated disease. JAMA 2005;294:2989.
ANSWER: C
Critique
A recent Olmstead County, Minn., study was undertaken to understand the epidemiology of community-acquired C. difficile infections. In the cohort of 385 proven C. difficile infections, 41% were community acquired. Compared to cases acquired in the hospital, community C. difficile infections were observed in younger (B) females (A) who had lower comorbidity scores and fewer chronic illnesses (D). Also, these outpatient cases were less likely to have recent antibiotic exposure (E) and fortunately had less severe clinical courses. A large population-based study and several others have confirmed that the use of gastric acid-suppressive agents such as PPIs (C) increases the risk of C. difficile-associated disease (adjusted risk ratio 2.9, 95% CI: 2.4-3.4).
References
1. Khanna S., Pardi D.S., Aronson S.L., et al. The epidemiology of community-acquired Clostridium difficile infection: a population-based study. Am. J. Gastroenterol. 2012;107:89-95.
2. Dial S., Delaney J.A., Barkun A.N., Suissa S. Use of gastric acid-suppressive agents and the risk of community-acquired Clostridium difficile-associated disease. JAMA 2005;294:2989.
What the SGR Repeal Means for Hospitalists
The long awaited permanent repeal of the poorly designed Sustainable Growth Rate (SGR) came just in time to avert the 21.2% Medicare physician payment cut that would have taken effect on April 1st, 2015. The SGR formula was first enacted in the Balanced Budget Act of 1997 with the intent to control Medicare spending on physician services. The federal budget sequester in the Budget Control Act of 2011 led to heightened speculation of doom and gloom about the U.S. debt and, ultimately, the necessity of a massive reduction in Medicare payments. Over the past decade, lawmakers have managed to pass 17 various delays and adjustments to keep spending in line with the target SGR. In its place, Congress finally passed H.R. 2, the Medicare Access and CHIP Reauthorization Act (MACRA), which was signed into law by President Obama on April 16, 2015.
What physicians should expect:
(1) The bill includes a 0.5% physician pay increase per year for the next five years beginning July 1, 2015.
(2) It incentivizes physicians to use alternate payment models that focus on care coordination and preventive care.
(3) It consolidates the three existing Medicare quality reporting programs known as the Physician Quality Reporting System (PQRS), Meaningful Use of Electronic Health Records, and the Physician Value-Based Payment Modifier, as well as their associated penalties into a single value-based performance program called the Merit-based Incentive Payment System (MIPS) which starts in 2019.
Is this good for hospitalists? While hospitalists are now protected from the 21% pay cut, we are still faced with increasing burden of legislative mandates on quality metrics. This has created unique challenges for acute inpatient care. The current individual incentive programs will remain in effect until MIPS in 2019, mandating the reporting of PQRS and VBPMs in order to avoid penalties. As such, we will need to continue to focus our efforts on meeting these challenges by aligning our performance measures with that of our institutions. This includes helping to develop alternative payment mechanisms (APMs), such as accountable care organizations (ACOs), patient-centered medical homes, bundled-payment arrangements, and other models. Of note, physicians involved in APMs will not be subject to MIPS assessment and will receive an annual 5% increase from 2019-2024.
The legislation creates other concerns such as the planned enforcement of Medicare's “2-midnight” rule, the requirement of EHR to be interoperable by the end of 2018, and the uncertainty of fairness of CMS in assessing quality and incentive payments. And the question remains, will Congress shift its attention to lowering payments for hospitals and non-physician providers to offset the once expected Medicare cuts? Hospitalists are distinctively qualified to potentially make headway given our already very active involvement in hospital process improvements. It will be in our best interest to stay vocal at the hospital, local, and national level.
The long awaited permanent repeal of the poorly designed Sustainable Growth Rate (SGR) came just in time to avert the 21.2% Medicare physician payment cut that would have taken effect on April 1st, 2015. The SGR formula was first enacted in the Balanced Budget Act of 1997 with the intent to control Medicare spending on physician services. The federal budget sequester in the Budget Control Act of 2011 led to heightened speculation of doom and gloom about the U.S. debt and, ultimately, the necessity of a massive reduction in Medicare payments. Over the past decade, lawmakers have managed to pass 17 various delays and adjustments to keep spending in line with the target SGR. In its place, Congress finally passed H.R. 2, the Medicare Access and CHIP Reauthorization Act (MACRA), which was signed into law by President Obama on April 16, 2015.
What physicians should expect:
(1) The bill includes a 0.5% physician pay increase per year for the next five years beginning July 1, 2015.
(2) It incentivizes physicians to use alternate payment models that focus on care coordination and preventive care.
(3) It consolidates the three existing Medicare quality reporting programs known as the Physician Quality Reporting System (PQRS), Meaningful Use of Electronic Health Records, and the Physician Value-Based Payment Modifier, as well as their associated penalties into a single value-based performance program called the Merit-based Incentive Payment System (MIPS) which starts in 2019.
Is this good for hospitalists? While hospitalists are now protected from the 21% pay cut, we are still faced with increasing burden of legislative mandates on quality metrics. This has created unique challenges for acute inpatient care. The current individual incentive programs will remain in effect until MIPS in 2019, mandating the reporting of PQRS and VBPMs in order to avoid penalties. As such, we will need to continue to focus our efforts on meeting these challenges by aligning our performance measures with that of our institutions. This includes helping to develop alternative payment mechanisms (APMs), such as accountable care organizations (ACOs), patient-centered medical homes, bundled-payment arrangements, and other models. Of note, physicians involved in APMs will not be subject to MIPS assessment and will receive an annual 5% increase from 2019-2024.
The legislation creates other concerns such as the planned enforcement of Medicare's “2-midnight” rule, the requirement of EHR to be interoperable by the end of 2018, and the uncertainty of fairness of CMS in assessing quality and incentive payments. And the question remains, will Congress shift its attention to lowering payments for hospitals and non-physician providers to offset the once expected Medicare cuts? Hospitalists are distinctively qualified to potentially make headway given our already very active involvement in hospital process improvements. It will be in our best interest to stay vocal at the hospital, local, and national level.
The long awaited permanent repeal of the poorly designed Sustainable Growth Rate (SGR) came just in time to avert the 21.2% Medicare physician payment cut that would have taken effect on April 1st, 2015. The SGR formula was first enacted in the Balanced Budget Act of 1997 with the intent to control Medicare spending on physician services. The federal budget sequester in the Budget Control Act of 2011 led to heightened speculation of doom and gloom about the U.S. debt and, ultimately, the necessity of a massive reduction in Medicare payments. Over the past decade, lawmakers have managed to pass 17 various delays and adjustments to keep spending in line with the target SGR. In its place, Congress finally passed H.R. 2, the Medicare Access and CHIP Reauthorization Act (MACRA), which was signed into law by President Obama on April 16, 2015.
What physicians should expect:
(1) The bill includes a 0.5% physician pay increase per year for the next five years beginning July 1, 2015.
(2) It incentivizes physicians to use alternate payment models that focus on care coordination and preventive care.
(3) It consolidates the three existing Medicare quality reporting programs known as the Physician Quality Reporting System (PQRS), Meaningful Use of Electronic Health Records, and the Physician Value-Based Payment Modifier, as well as their associated penalties into a single value-based performance program called the Merit-based Incentive Payment System (MIPS) which starts in 2019.
Is this good for hospitalists? While hospitalists are now protected from the 21% pay cut, we are still faced with increasing burden of legislative mandates on quality metrics. This has created unique challenges for acute inpatient care. The current individual incentive programs will remain in effect until MIPS in 2019, mandating the reporting of PQRS and VBPMs in order to avoid penalties. As such, we will need to continue to focus our efforts on meeting these challenges by aligning our performance measures with that of our institutions. This includes helping to develop alternative payment mechanisms (APMs), such as accountable care organizations (ACOs), patient-centered medical homes, bundled-payment arrangements, and other models. Of note, physicians involved in APMs will not be subject to MIPS assessment and will receive an annual 5% increase from 2019-2024.
The legislation creates other concerns such as the planned enforcement of Medicare's “2-midnight” rule, the requirement of EHR to be interoperable by the end of 2018, and the uncertainty of fairness of CMS in assessing quality and incentive payments. And the question remains, will Congress shift its attention to lowering payments for hospitals and non-physician providers to offset the once expected Medicare cuts? Hospitalists are distinctively qualified to potentially make headway given our already very active involvement in hospital process improvements. It will be in our best interest to stay vocal at the hospital, local, and national level.
Decreased RBC clearance predicts ill health
New research suggests that increased red blood cell distribution width (RDW) is caused by reduced clearance of aging red blood cells (RBCs) from the bloodstream.
And previous studies showed that elevations in RDW predict the development, progression, and risk of death from many conditions.
“It appears that the human body slightly slows down the production and destruction of red blood cells in just about every major disease,” said John Higgins, MD, of Massachusetts General Hospital in Boston.
“If we can accurately measure the production or destruction rates, we might be able to identify many of these diseases in their earlier stages when they are most treatable. Existing measures of the production rate are far too imprecise to detect these subtle changes, but this paper shows how the destruction rate can be estimated using existing blood count data and a mathematical model.”
The paper has been published in the American Journal of Hematology.
Healthy adults generate RBCs at a rate of more than 2 million per second, and the cells circulate in the bloodstream for 100 to 120 days, during which their size decreases by around 30%. Aged RBCs are then cleared at about the same rate of 2 million per second.
Prior to the reports linking elevated RDW with an increased risk for many diseases, that measure had only been used to help distinguish between different forms of anemia.
To understand the correlation between RDW and disease prognosis, Dr Higgins and his colleagues analyzed raw data from more than 60,000 randomly selected blood samples. They used a mathematical model to replicate how RBC populations behave differently in health and in disease.
The researchers measured the extent to which RBCs in different phases of their life cycle contribute to increased RDW and found that the variance in size was strongly determined by mild increases in the numbers of the smallest and oldest cells.
Since the most important mechanism controlling the number of the oldest cells is the rate at which they are cleared from the bloodstream, the team made several predictions, which were validated by applying their model to clinical data from the blood samples and to data from several published studies.
The researchers found that increased RDW was associated with delayed RBC clearance, and increased RDW was associated with increased average age of RBCs.
Delayed RBC clearance was as strongly associated with overall risk of death, as was increased RDW, and delayed RBC clearance was associated with the presence of early signs of hidden diseases associated with increased RDW.
Patients with delayed RBC clearance had a greater risk of developing signs of those diseases in the future than patients with a typical clearance rate. In healthy patients, the rate of RBC clearance varied less than any other traditional blood-count characteristic.
Dr Higgins said there are many potential clinical applications of these findings, which need to be validated by future studies.
“Finding a reduced clearance rate in an apparently healthy person would likely mean that an underlying disease process was developing—such as the early stages of iron deficiency, kidney disease, colon cancer, or congestive heart failure—and would warrant further diagnostic evaluation,” Dr Higgins said.
“Based on this analysis of routine blood tests, a primary care physician could immediately consider appropriate follow-up diagnostic testing, instead of waiting for other signs and symptoms to appear as the condition progresses. In a patient with established disease, a reduced clearance rate could mean progression of disease or treatment failure, and imminent complications could be avoided or reduced by adjusting treatment right away or at least by more frequent monitoring.”
“In addition to confirming our findings in prospective studies that would follow a group of patients over time, we hope to identify the diseases for which an early warning provided by delayed clearance would lead to the most significant improvements in patient outcomes. We’d also like to understand more about the processes controlling red blood cell clearance and are actively developing similar models for populations of white blood cells and platelets.”
New research suggests that increased red blood cell distribution width (RDW) is caused by reduced clearance of aging red blood cells (RBCs) from the bloodstream.
And previous studies showed that elevations in RDW predict the development, progression, and risk of death from many conditions.
“It appears that the human body slightly slows down the production and destruction of red blood cells in just about every major disease,” said John Higgins, MD, of Massachusetts General Hospital in Boston.
“If we can accurately measure the production or destruction rates, we might be able to identify many of these diseases in their earlier stages when they are most treatable. Existing measures of the production rate are far too imprecise to detect these subtle changes, but this paper shows how the destruction rate can be estimated using existing blood count data and a mathematical model.”
The paper has been published in the American Journal of Hematology.
Healthy adults generate RBCs at a rate of more than 2 million per second, and the cells circulate in the bloodstream for 100 to 120 days, during which their size decreases by around 30%. Aged RBCs are then cleared at about the same rate of 2 million per second.
Prior to the reports linking elevated RDW with an increased risk for many diseases, that measure had only been used to help distinguish between different forms of anemia.
To understand the correlation between RDW and disease prognosis, Dr Higgins and his colleagues analyzed raw data from more than 60,000 randomly selected blood samples. They used a mathematical model to replicate how RBC populations behave differently in health and in disease.
The researchers measured the extent to which RBCs in different phases of their life cycle contribute to increased RDW and found that the variance in size was strongly determined by mild increases in the numbers of the smallest and oldest cells.
Since the most important mechanism controlling the number of the oldest cells is the rate at which they are cleared from the bloodstream, the team made several predictions, which were validated by applying their model to clinical data from the blood samples and to data from several published studies.
The researchers found that increased RDW was associated with delayed RBC clearance, and increased RDW was associated with increased average age of RBCs.
Delayed RBC clearance was as strongly associated with overall risk of death, as was increased RDW, and delayed RBC clearance was associated with the presence of early signs of hidden diseases associated with increased RDW.
Patients with delayed RBC clearance had a greater risk of developing signs of those diseases in the future than patients with a typical clearance rate. In healthy patients, the rate of RBC clearance varied less than any other traditional blood-count characteristic.
Dr Higgins said there are many potential clinical applications of these findings, which need to be validated by future studies.
“Finding a reduced clearance rate in an apparently healthy person would likely mean that an underlying disease process was developing—such as the early stages of iron deficiency, kidney disease, colon cancer, or congestive heart failure—and would warrant further diagnostic evaluation,” Dr Higgins said.
“Based on this analysis of routine blood tests, a primary care physician could immediately consider appropriate follow-up diagnostic testing, instead of waiting for other signs and symptoms to appear as the condition progresses. In a patient with established disease, a reduced clearance rate could mean progression of disease or treatment failure, and imminent complications could be avoided or reduced by adjusting treatment right away or at least by more frequent monitoring.”
“In addition to confirming our findings in prospective studies that would follow a group of patients over time, we hope to identify the diseases for which an early warning provided by delayed clearance would lead to the most significant improvements in patient outcomes. We’d also like to understand more about the processes controlling red blood cell clearance and are actively developing similar models for populations of white blood cells and platelets.”
New research suggests that increased red blood cell distribution width (RDW) is caused by reduced clearance of aging red blood cells (RBCs) from the bloodstream.
And previous studies showed that elevations in RDW predict the development, progression, and risk of death from many conditions.
“It appears that the human body slightly slows down the production and destruction of red blood cells in just about every major disease,” said John Higgins, MD, of Massachusetts General Hospital in Boston.
“If we can accurately measure the production or destruction rates, we might be able to identify many of these diseases in their earlier stages when they are most treatable. Existing measures of the production rate are far too imprecise to detect these subtle changes, but this paper shows how the destruction rate can be estimated using existing blood count data and a mathematical model.”
The paper has been published in the American Journal of Hematology.
Healthy adults generate RBCs at a rate of more than 2 million per second, and the cells circulate in the bloodstream for 100 to 120 days, during which their size decreases by around 30%. Aged RBCs are then cleared at about the same rate of 2 million per second.
Prior to the reports linking elevated RDW with an increased risk for many diseases, that measure had only been used to help distinguish between different forms of anemia.
To understand the correlation between RDW and disease prognosis, Dr Higgins and his colleagues analyzed raw data from more than 60,000 randomly selected blood samples. They used a mathematical model to replicate how RBC populations behave differently in health and in disease.
The researchers measured the extent to which RBCs in different phases of their life cycle contribute to increased RDW and found that the variance in size was strongly determined by mild increases in the numbers of the smallest and oldest cells.
Since the most important mechanism controlling the number of the oldest cells is the rate at which they are cleared from the bloodstream, the team made several predictions, which were validated by applying their model to clinical data from the blood samples and to data from several published studies.
The researchers found that increased RDW was associated with delayed RBC clearance, and increased RDW was associated with increased average age of RBCs.
Delayed RBC clearance was as strongly associated with overall risk of death, as was increased RDW, and delayed RBC clearance was associated with the presence of early signs of hidden diseases associated with increased RDW.
Patients with delayed RBC clearance had a greater risk of developing signs of those diseases in the future than patients with a typical clearance rate. In healthy patients, the rate of RBC clearance varied less than any other traditional blood-count characteristic.
Dr Higgins said there are many potential clinical applications of these findings, which need to be validated by future studies.
“Finding a reduced clearance rate in an apparently healthy person would likely mean that an underlying disease process was developing—such as the early stages of iron deficiency, kidney disease, colon cancer, or congestive heart failure—and would warrant further diagnostic evaluation,” Dr Higgins said.
“Based on this analysis of routine blood tests, a primary care physician could immediately consider appropriate follow-up diagnostic testing, instead of waiting for other signs and symptoms to appear as the condition progresses. In a patient with established disease, a reduced clearance rate could mean progression of disease or treatment failure, and imminent complications could be avoided or reduced by adjusting treatment right away or at least by more frequent monitoring.”
“In addition to confirming our findings in prospective studies that would follow a group of patients over time, we hope to identify the diseases for which an early warning provided by delayed clearance would lead to the most significant improvements in patient outcomes. We’d also like to understand more about the processes controlling red blood cell clearance and are actively developing similar models for populations of white blood cells and platelets.”