Culture Transformation in Action: The Experience of One VA Community Living Center

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You-Ying W. Whipple, MSS, Mick Magill, MSW, Cathy Decker, MSN, DeeAnn Koegel, BS, Danielle Keen, BS-HSA, and Marc Wooten, MD

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Ms. Whipple is a program specialist for extended care and rehabilitation services, Mr. Magill is a presidential management fellow, Ms. Decker is an associate chief nurse at the veterans' community living center, Ms. Koegel is a recreation therapist, Ms. Keen is an administrative intern, and Dr. Wooten is the chief of compensation and pension, all at VA Northern Indiana Health Care System in Marion. Dr. Wooten is also a member of the Federal Practitioner Editorial Advisory Association.

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Culture Transformation in Action: The Experience of One VA Community Living Center
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Reflections of a VA Clerk

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Jacob Scott, MD

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The Current State of Affairs of VA Emergency Medicine

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Eliminating Ethnic and Racial Disparities in Health Care

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Debra Shipman, RN, MSN, MBA and Jack Hooten, RN, MSN, MHA

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Posttraumatic Stress Disorder: Learning the Lessons of the Past

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Oral or IV steroids for inpatient COPD?

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Although the oral bioavailability of corticosteroids is excellent, many physicians persist in using IV steroids for patients with exacerbations of COPD.

In this study, 210 hospitalized adults older than 40 years with COPD and at least 24 hours of exacerbation were randomized to receive 5 days of oral or IV prednisolone (60 mg daily) followed by a tapering oral dose. Patients with a severe exacerbation (pH <7.26 or PaCO2 >9.3 kPa) were excluded. Allocation was concealed and patients were randomized using a “minimization protocol” that balances groups for key variables such as age, sex, smoking history, and supplemental oxygen use.

The primary outcome was treatment failure, defined as death, admission to the intensive care unit, readmission, or the need to intensify treatment. Groups were balanced at the start of the study, and analysis was by intent to treat; withdrawals and exclusions were uncommon and similar between groups.

No difference was noted between groups in the primary outcome either early (ie, within 2 weeks), late (ie, after 2 weeks), or overall. The treatment failure rate was relatively high in both groups, usually because of the need to intensify treatment.

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de Jong YP, Uil SM, Grotjohan HP, Postma DS, Kerstjens HA, van den Berg JW. Oral or IV prednisolone in the treatment of COPD exacerbations: a randomized, controlled, double-blind study. Chest. 2007;132:1741-1747.

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de Jong YP, Uil SM, Grotjohan HP, Postma DS, Kerstjens HA, van den Berg JW. Oral or IV prednisolone in the treatment of COPD exacerbations: a randomized, controlled, double-blind study. Chest. 2007;132:1741-1747.

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Although the oral bioavailability of corticosteroids is excellent, many physicians persist in using IV steroids for patients with exacerbations of COPD.

In this study, 210 hospitalized adults older than 40 years with COPD and at least 24 hours of exacerbation were randomized to receive 5 days of oral or IV prednisolone (60 mg daily) followed by a tapering oral dose. Patients with a severe exacerbation (pH <7.26 or PaCO2 >9.3 kPa) were excluded. Allocation was concealed and patients were randomized using a “minimization protocol” that balances groups for key variables such as age, sex, smoking history, and supplemental oxygen use.

The primary outcome was treatment failure, defined as death, admission to the intensive care unit, readmission, or the need to intensify treatment. Groups were balanced at the start of the study, and analysis was by intent to treat; withdrawals and exclusions were uncommon and similar between groups.

No difference was noted between groups in the primary outcome either early (ie, within 2 weeks), late (ie, after 2 weeks), or overall. The treatment failure rate was relatively high in both groups, usually because of the need to intensify treatment.

Although the oral bioavailability of corticosteroids is excellent, many physicians persist in using IV steroids for patients with exacerbations of COPD.

In this study, 210 hospitalized adults older than 40 years with COPD and at least 24 hours of exacerbation were randomized to receive 5 days of oral or IV prednisolone (60 mg daily) followed by a tapering oral dose. Patients with a severe exacerbation (pH <7.26 or PaCO2 >9.3 kPa) were excluded. Allocation was concealed and patients were randomized using a “minimization protocol” that balances groups for key variables such as age, sex, smoking history, and supplemental oxygen use.

The primary outcome was treatment failure, defined as death, admission to the intensive care unit, readmission, or the need to intensify treatment. Groups were balanced at the start of the study, and analysis was by intent to treat; withdrawals and exclusions were uncommon and similar between groups.

No difference was noted between groups in the primary outcome either early (ie, within 2 weeks), late (ie, after 2 weeks), or overall. The treatment failure rate was relatively high in both groups, usually because of the need to intensify treatment.

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Integration of Preventive Health Screening into Mental Health Clinics

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Discharging the Undischargeable Patient

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I Feel Safe Here

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I Feel Safe Here
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Combat Trauma: A Personal Perspective

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Combat Trauma: A Personal Perspective

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Early intrathecal analgesia does not increase cesarean sections

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Intrathecal fentanyl followed by epidural bupivacaine plus fentanyl, if needed for pain relief, in early labor is not associated with a higher cesarean delivery than systemic hydromorphone for early labor. The neuraxial approach also provides more effective analgesia and a shorter mean duration of first-stage labor. (LOE=1b)

 
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Wong CA, Scavone BM, Peaceman AM, et al. The risk of cesarean delivery with neuraxial analgesia given early versus late in labor. N Eng J Med 1005; 352:655–665.

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Wong CA, Scavone BM, Peaceman AM, et al. The risk of cesarean delivery with neuraxial analgesia given early versus late in labor. N Eng J Med 1005; 352:655–665.

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Wong CA, Scavone BM, Peaceman AM, et al. The risk of cesarean delivery with neuraxial analgesia given early versus late in labor. N Eng J Med 1005; 352:655–665.

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Bottom Line

Intrathecal fentanyl followed by epidural bupivacaine plus fentanyl, if needed for pain relief, in early labor is not associated with a higher cesarean delivery than systemic hydromorphone for early labor. The neuraxial approach also provides more effective analgesia and a shorter mean duration of first-stage labor. (LOE=1b)

 
Bottom Line

Intrathecal fentanyl followed by epidural bupivacaine plus fentanyl, if needed for pain relief, in early labor is not associated with a higher cesarean delivery than systemic hydromorphone for early labor. The neuraxial approach also provides more effective analgesia and a shorter mean duration of first-stage labor. (LOE=1b)

 
Issue
The Journal of Family Practice - 54(6)
Issue
The Journal of Family Practice - 54(6)
Page Number
493-500
Page Number
493-500
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Early intrathecal analgesia does not increase cesarean sections
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Early intrathecal analgesia does not increase cesarean sections
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