Skip to Main Content

Browse issues

Volume 62, Issue 7, 1 April 2016

Articles and Commentaries

Naomi J. Gadsby and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 817–823, https://doi.org/10.1093/cid/civ1214

This is the first time a comprehensive, multipathogen, quantitative and qualitative molecular approach for respiratory bacteria and viruses has been compared with traditional diagnostic methods on a large hospitalized pneumonia cohort, with estimation of potential effects on antibiotic prescribing.

Daniel M. Musher
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 824–825, https://doi.org/10.1093/cid/civ1216
Seema Jain and Andrew T. Pavia
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 826–828, https://doi.org/10.1093/cid/civ1219
Christiane S. Eberhardt and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 829–836, https://doi.org/10.1093/cid/ciw027

Guidelines recommend that pregnant women be vaccinated against pertussis between gestational weeks 26 and 36. We show that this narrow window can be widened, as optimal neonatal antibody concentrations and expected infant seropositivity rates are elicited between weeks 13 and 33.

John E. Williams and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 837–844, https://doi.org/10.1093/cid/civ1198

The sensitivity of a rapid diagnostic test (RDT) for malaria was compared with that of a polymerase chain reaction assay in pregnant West African women. The sensitivity of the RDT was high at enrollment but lower at delivery.

Gayle Langley and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 845–852, https://doi.org/10.1093/cid/civ1032

In a population-based analysis, diabetes in all races and extreme obesity in whites were associated with increased risk of invasive group A Streptococcus (iGAS). Obesity, but not diabetes, was associated with increased odds of death in persons with iGAS.

Grace A. McComsey and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 853–862, https://doi.org/10.1093/cid/ciw017

This randomized trial compared peripheral and central fat changes 96 weeks after a first-line regimen containing darunavir/ritonavir, atazanavir/ritonavir, or raltegravir. Similar and significant increases were seen in all arms. Pre-treatment HIV-1 RNA level was the strongest predictor of fat gains.

Fardou H. Heida and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 863–870, https://doi.org/10.1093/cid/ciw016

Development of necrotizing enterocolitis (NEC) has been associated with altered intestinal bacterial colonization. Via a prospective case-control study a NEC-associated gut microbiota was identified in meconium samples. Clostridium perfringens and Bacteroides dorei are associated with NEC development starting immediately after birth. In post-meconium samples increased numbers of staphylococci are negatively associated with NEC.

Christian Theilacker and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 871–878, https://doi.org/10.1093/cid/civ1195

In a prospective cohort study, pneumococci were the most frequent cause of severe sepsis or septic shock in asplenic patients, accounting for 42% of infections. Most patients with pneumococcal sepsis had not received pneumococcal vaccination and many developed purpura fulminans.

Alex Marzel and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 879–886, https://doi.org/10.1093/cid/civ1221

A subgroup of patients infected with nontyphoidal Salmonella develops a persistent infection. Most of these are presented as symptomatic relapse gastroenteritis, illuminating a previously overlooked manifestation. During persistence, Salmonella gains genetic and phenotypic changes, affecting antibiotic resistance, and host-pathogen interactions.

Gregory J. Fox and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 887–895, https://doi.org/10.1093/cid/ciw002

Partial lung resection, but not pneumonectomy, was associated with improved treatment success among patients with multidrug-resistant tuberculosis. Although improved outcomes may reflect patient selection, partial lung resection after culture conversion may improve treatment outcomes, alongside optimal medical therapy.

Sarah M. Richer and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 896–902, https://doi.org/10.1093/cid/ciw007

Detection of immunoglobulin M (IgM) and immunoglobulin G (IgG) antibodies by enzyme immunoassay improves the sensitivity for the diagnosis of acute pulmonary histoplasmosis. The highest sensitivity was achieved by testing for antigen and of IgM and IgG antibodies.

BRIEF REPORTS

Séverine Caluwaerts and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 903–905, https://doi.org/10.1093/cid/civ1024

Photo Quiz

Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 906–907, https://doi.org/10.1093/cid/ciw031

INVITED ARTICLES

Clinical Practice

Samuel P. Costello and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 908–914, https://doi.org/10.1093/cid/civ994

Although fecal microbiota transplant (FMT) is a highly effective therapy for recurrent Clostridium difficile infection, numerous technical, logistical, and regulatory issues have hampered development of FMT capability at many sites. We describe how to establish such a service using a frozen stool bank.

HIV/AIDS

Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 915–918, https://doi.org/10.1093/cid/civ1000

While the clinical case for tenofovir alafenamide (TAF) over tenofovir disoproxil fumarate (TDF) appears solid, we find that the increased cost that TAF might merit over TDF is modest, ~$1000. Under alternative assumptions where TDF toxicity leads to fewer events or better quality of life, or when TDF becomes generically available, the defensible price differential related to TAF may be even smaller.

HIV/AIDS

Sahar Saeed and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 919–926, https://doi.org/10.1093/cid/civ1222

Trial results are used to support licensure, inform cost-effectiveness analyses, and guide clinical decision making. We found the majority of coinfected patients were not included in clinical trials of direct-acting antivirals, raising concerns about the generalizability of these trial results.

Marianne Martinello and Gregory J. Dore
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 927–928, https://doi.org/10.1093/cid/civ1227
Will Garner and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 929–934, https://doi.org/10.1093/cid/civ1034

Discordant viremia results near human immunodeficiency virus type 1 RNA 50 copies/mL by the TaqMan 2.0 assay led to significantly lower efficacy rates in clinical trials and increased patient management decision points compared with the historical standard Amplicor assay.

Elvin H. Geng and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 935–944, https://doi.org/10.1093/cid/civ1004

Retention after starting antiretroviral therapy is best understood by examining multiple outcomes including stopping care, deaths in care, deaths out of care, and silent transfers.

Answer To The Photo Quiz

Ingrid Fernandes and Anandit Mu
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 945–946, https://doi.org/10.1093/cid/ciw033

Correspondence

Amélie Menard and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 947–949, https://doi.org/10.1093/cid/civ1215
Joseph S. Cervia
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Page 947, https://doi.org/10.1093/cid/ciw004
Stephen D. Shafran
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 949–950, https://doi.org/10.1093/cid/civ1217
Philippe Saliou and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 950–951, https://doi.org/10.1093/cid/civ1200
Hajime Kanamori and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Page 951, https://doi.org/10.1093/cid/civ1202
Rotraut Mössner and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 951–953, https://doi.org/10.1093/cid/ciw020
Joshua Fierer
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 953–954, https://doi.org/10.1093/cid/civ1225
Elie F. Berbari and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Page 954, https://doi.org/10.1093/cid/civ1226
Trond Bruun and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 954–955, https://doi.org/10.1093/cid/ciw003
David A. Talan and others
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages 955–956, https://doi.org/10.1093/cid/ciw005

Cover/Standing Material

Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Page NP, https://doi.org/10.1093/cid/civ1047
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Page NP, https://doi.org/10.1093/cid/civ1071
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Page NP, https://doi.org/10.1093/cid/civ1095
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Page NP, https://doi.org/10.1093/cid/civ1119
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Page NP, https://doi.org/10.1093/cid/civ1143
Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Page NP, https://doi.org/10.1093/cid/civ1167

News

Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages i–ii, https://doi.org/10.1093/cid/ciw034

In the Literature

Clinical Infectious Diseases, Volume 62, Issue 7, 1 April 2016, Pages iii–iv, https://doi.org/10.1093/cid/ciw068
Close
This Feature Is Available To Subscribers Only

Sign In or Create an Account

Close

This PDF is available to Subscribers Only

View Article Abstract & Purchase Options

For full access to this pdf, sign in to an existing account, or purchase an annual subscription.

Close