For the week ending June 15, 2012 |
Last week 716 articles were evaluated via DynaMed's Systematic Literature Surveillance and 335 were added to DynaMed content.
Based on the editors' criteria of selecting "articles most likely to change clinical practice," one article of significant interest was selected for the DynaMed Weekly Update. |
Feature Article |
Zidovudine plus Nevirapine May Reduce HIV Transmission to Infants Born to Mothers with HIV Infection and No Previous Antiretroviral Therapy
Zidovudine monotherapy has been commonly used for postexposure HIV prophylaxis in formula-fed infants whose mothers did not receive antenatal antiretroviral therapy, but the use of combination antiretroviral therapy has increased in recent years (AIDS Patient Care STDS 2011 Jan;25(1):1, HIV Med 2011 Aug;12(7):422). The optimal approach in this population remains unknown. A new unblinded randomized trial compared 3 antiretroviral regimens in infants born to mothers with HIV infection who had not received previous antiretroviral therapy.
A total of 1,745 formula-fed infants (gestational age ≥ 32 weeks, birth weight ≥ 1.5 kg) were randomized within 48 hours of birth to single vs. double. vs. triple oral antiretroviral regimens. The single antiretroviral group received zidovudine twice daily for 6 weeks. The double therapy group received the same zidovudine regimen plus 3 doses of nevirapine, the first within 48 of birth, the second 48 hours later, and the third 96 hours after the second. The triple therapy group received zidovudine for 6 weeks plus 2 weeks of lamivudine and nelfinavir twice daily. Maternal HIV was diagnosed during labor and delivery in 73%, and none of the mothers had received previous antiretroviral therapy. Women who had any antiretroviral drug other than zidovudine during labor were excluded.
The efficacy analysis included 1,684 infants (61 infants who did not receive study drug or whose mothers were HIV-negative on confirmatory testing were excluded). At 3 months the overall HIV infection rates in infants were 11.1% for zidovudine alone, 7.1% for double therapy (p = 0.03 vs. zidovudine alone, NNT 25), and 7.4% for triple therapy (p = 0.03 vs. zidovudine alone, NNT 27) (level 2 [mid-level] evidence). The intrapartum transmission rates were 4.8%for zidovudine alone, 2.2% for double therapy (p = 0.046, NNT 37), and 2.4% for triple therapy (p = 0.046, NNT 42). There were no significant differences in in utero infection rates. Triple therapy was associated with significantly higher incidence of neutropenia compared to double therapy (27.5% vs. 14.9%, p < 0.001, NNH 7) (N Engl J Med 2012 Jun 21;366(25):2368). These data are the basis for recent updates to perinatal guidelines which now recommend double therapy with zidovudine plus nevirapine over triple therapy for at risk infants (AIDSinfo.nih.gov/guidelines).
For more information, see the Prevention of maternal-child HIV transmission topic in DynaMed. |
Earn Credit for Reading this e-Newsletter
For more information on this educational activity, see the CME sidebar. | DynaMed Extra |
DynaMed Extra: Lorcaserin (Belviq) FDA Approved for Chronic Weight Management in Adults
Lorcaserin (Belviq) was FDA approved today to be used in addition to diet and exercise for chronic weight management in adults who are obese (body mass index [BMI] ≥ 30 kg/m2), or overweight (BMI ≥ 27 kg/m2) with a weight-related condition (such as hypertension, diabetes, or dyslipidemia) (FDA Press Release 2012 Jun 27). Randomized trial evidence (limited by losses to follow-up of about 50%) suggests that lorcaserin 10 mg twice daily for 52 weeks increases the likelihood of losing at least 5% body weight from 20%-25% with placebo to 47.5% (NNT 4-5) (level 2 [mid-level] evidence). Lorcaserin was not associated with a significant increase in heart valve problems on echocardiography (a reason other weight loss medications were withdrawn from the market), but was associated with a potential risk for serotonin syndrome, especially if combined with other serotonergic drugs.
For more information, see the Weight loss medications for obesity in adults topic in DynaMed. |
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CME Information
CREDITS
Physicians: 0.25 AMA PRA Category I Credit(s)™ Family Physicians: 0.25 Prescribed credits Nurse Practitioners: 0.25 Contact hours Release Date: June 27, 2012
Expiration Date: June 27, 2013 Estimated Completion Time:
15 minutes
There is no fee for this activity.
In order to receive your certificate of participation, you should read the information about this activity, including the disclosure statements, review the entire activity, take the post-test, and complete the evaluation form. You may then follow the directions to print your certificate of participation. To begin, click the CME icon at the end of the article.
Upon successful completion of this educational program, the reader should be able to:
1. Discuss the significance of this article as it relates to your clinical practice. 2. Be able to apply this knowledge to your patient's diagnosis, treatment and management.
Alan Ehrlich, MD- Assistant Clinical Professor in Family Medicine, University of Massachusetts Medical School, Worcester, Massachusetts, USA; Deputy Editor, DynaMed, Ipswich, Massachusetts, USA
Michael Fleming, MD, FAAFP - Assistant Clinical Professor of Family Medicine and Comprehensive Care, LSU Health Science Center School of Medicine, Shreveport, Louisiana, USA; Assistant Clinical Professor of Family Medicine, Department of Family and Community Medicine, Tulane University Medical School, New Orleans, Louisiana, USA; Chief Medical Officer, Amedisys, Inc. & Antidote Education Company
Dr. Ehrlich, Dr. Fleming, DynaMed Editorial Team members, and the staff of Antidote Education Company have disclosed that they have no relevant financial relationships or conflicts of interest with commercial interests related directly or indirectly to this educational activity.
No commercial support has been received for this activity.
ACCME: This activity has been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education through the joint sponsorship of Antidote Education Company and EBSCO Publishing. Antidote is accredited by the ACCME to provide continuing medical education for physicians. Antidote Education Company designates this enduring activity for a maximum of 0.25 AMA PRA Category 1 Credits™. Physicians should only claim credit commensurate with the extent of their participation in the activity.
AAFP: Enduring Material activity, DynaMed Weekly Update, has been reviewed and is acceptable for up to 13 Prescribed credits by the American Academy of Family Physicians. AAFP certification begins March 7, 2012. Term of approval is for one year from this date with the option of yearly renewal. Each Weekly Update is worth .25 Prescribed credits. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
AANP: This program is approved for 0.25 contact hour of continuing education by the American Academy of Nurse Practitioners.
Program ID 1102072Q.
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