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Clinical Infectious Diseases Cover Image for Volume 56, Issue 11
Volume 56, Issue 11
1 June 2013
ISSN 1058-4838
EISSN 1537-6591

Volume 56, Issue 11, 1 June 2013

NEWS

Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages i–ii, https://doi.org/10.1093/cid/cit190

IN THE LITERATURE

Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages iii–iv, https://doi.org/10.1093/cid/cit144

ARTICLES AND COMMENTARIES

Christian L. Coles and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1519–1526, https://doi.org/10.1093/cid/cit137

Mass therapy with azithromycin for trachoma is associated with increased risk of antibiotic-resistant Streptococcus pneumoniae carriage among young children in the 6 months following treatment. Studies are needed assess the clinical relevance of azithromycin-associated resistance on treatment of pediatric infections.

Surbhi Malhotra-Kumar and Herman Goossens
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1527–1529, https://doi.org/10.1093/cid/cit139
Suman Rijal and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1530–1538, https://doi.org/10.1093/cid/cit102

Relapse is observed in one fifth of miltefosine-treated visceral leishmaniasis (VL) patients in Nepal. The authors monitored clinical outcomes of VL treatment and here discuss the role of patient compliance, drug resistance, and reinfection.

Lindley A. Barbee and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1539–1545, https://doi.org/10.1093/cid/cit084

In this retrospective study, combination therapy with an oral cephalosporin and azithromycin was comparable to intramuscular ceftriaxone alone or with azithromycin for the treatment of pharyngeal gonorrhea. Combination therapy with doxycycline was associated with a higher risk of recurrent infection.

Raymund R. Razonable and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1546–1553, https://doi.org/10.1093/cid/cit096

This clinical trial of a cytomegalovirus (CMV) DNA test standardized to the First World Health Organization International Standard for CMV in solid organ transplant patients undergoing treatment for CMV disease found that viral suppression is predictive of shorter time to CMV disease resolution.

Stephanie A. Fritz and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1554–1561, https://doi.org/10.1093/cid/cit123

Serum antibody responses against Staphylococcus aureus α-hemolysin serve as a marker for protective immunity against recurrent communityonset disease, highlighting an opportunity to define and stratify risk for subsequent infection and to modify disease risk through development of immunization programs.

Kyle P. Murray and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1562–1569, https://doi.org/10.1093/cid/cit112

In the setting of methicillin-resistant Staphylococcus aureus bacteremia with a vancomycin minimum inhibitory concentration >1 µg/mL, an early switch to daptomycin based solely on vancomycin susceptibility was associated with significantly less clinical failure, compared to continued vancomycin.

Adam Weston and Helen W. Boucher
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1570–1572, https://doi.org/10.1093/cid/cit118
Emily R. Levy and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1573–1578, https://doi.org/10.1093/cid/cit113

We retrospectively describe successful outcomes in 8 of 9 children with refractory invasive coccidioidomycosis who were treated with combination voriconazole and caspofungin salvage therapy between January 2000 and June 2012 after failing conventional therapy.

James M. McCarty and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1579–1585, https://doi.org/10.1093/cid/cit114

A retrospective observational study of 33 children hospitalized with coccidioidomycosis identified 31 with various pulmonary manifestations, 5 with osteomyelitis, and 2 with meningitis. Mediastinitis with purulence and abscessed/necrotic lymph nodes occurred in 21% of patients and resulted in longer hospitalizations.

John N. Galgiani
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1586–1588, https://doi.org/10.1093/cid/cit117
A. Sarah Walker and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1589–1600, https://doi.org/10.1093/cid/cit127

Clostridium difficile genotype predicts 14-day mortality in 1893 enzyme immunoassay–positive/culture-positive adults. Excess mortality correlates with genotype-specific changes in biomarkers, strongly implicating inflammatory pathways as a major influence on poor outcome. Polymerase chain reaction ribotype 078/ST 11(clade 5) is associated with high mortality; ongoing surveillance remains essential.

Dale N. Gerding and Stuart Johnson
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1601–1603, https://doi.org/10.1093/cid/cit133

REVIEW ARTICLE

Julie E. Myers and Kent A. Sepkowitz
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1604–1612, https://doi.org/10.1093/cid/cit085

Recent FDA approval of tenofovir-emtricitabine for HIV prevention has led to concern about implementation of this approach. We review the social and medical history of the oral contraceptive pill, which has many parallels with the current debate about pre-exposure prophylaxis.

PHOTO QUIZ

Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Page 1613, https://doi.org/10.1093/cid/cit076

INVITED ARTICLES

HEALTHCARE EPIDEMIOLOGY

Daniel J. Diekema and Michael A. Pfaller
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1614–1620, https://doi.org/10.1093/cid/cit038

Rapid detection of multidrug-resistant organism (MDRO) carriers remains a work in progress. Future efforts should be on developing rapid tests to detect gram-negative MDROs and on performing studies to determine how to incorporate rapid MDRO detection into infection prevention efforts.

IMMUNOCOMPROMISED HOSTS

Marta Bodro and David L. Paterson
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1621–1628, https://doi.org/10.1093/cid/cit071

We propose that a multinational case-control study be performed on incident patients with infections with trimethoprim-sulfamethoxazole (TMP-SMZ)–susceptible organisms occurring in patients receiving biologics. Such a study could identify high-risk patients who may benefit from TMP-SMZ prophylaxis.

VIRAL HEPATITIS

Naveen Gara and Marc G. Ghany
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1629–1636, https://doi.org/10.1093/cid/cit074

This review summarizes the relevant issues with pegylated interferon and ribavirin, with a particular focus on side effects profile and management, as well as their continued role in therapy given the emergence of interferon-free regimens.

HIV/AIDS

R. Campo and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1637–1645, https://doi.org/10.1093/cid/cis1203

Virologic suppression was well maintained when HIV patients receiving 3TC/ABC with a boosted protease inhibitor were switched to emtricitabine/tenofovir disoproxil fumarate (FTC/TDF). Subjects randomized to FTC/TDF) had fewer virologic failures; in addition, improvements in lipids and Framingham risk scores were noted, while slight declines in estimated GFR were observed.

José A. Mira and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1646–1653, https://doi.org/10.1093/cid/cit103

The achievement of sustained virologic response following pegylated interferon plus ribavirin treatment is associated with a marked reduction of the risk of hepatic decompensations and overall mortality in HIVinfected patients with compensated hepatitis C virus–related cirrhosis.

Charlotte Charpentier and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1654–1658, https://doi.org/10.1093/cid/cit104

Considering HIV-2 phenotypic data and experience from HIV-1 and from the follow-up of HIV-2–infected patients, European experts developed a rule set and an automated tool for HIV-2 drug resistance analyses freely available on the Internet.

Luke C. Swenson and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1659–1666, https://doi.org/10.1093/cid/cit105

This study offers a framework by which patients can be switched to a maraviroc-containing regimen while maintaining an undetectable viral load. Patients confirmed as having CCR5-tropic HIV according to DNAbased tropism methods had significantly better responses to maraviroc compared to those where CXCR4-using virus was detected in cells.

Jonathan Z. Li and Daniel R. Kuritzkes
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1667–1674, https://doi.org/10.1093/cid/cit125

Low-frequency HIV variants are increasingly recognized as a key factor that increases the risk of HIV treatment failure. This article will provide a review of HIV minority variants, including their demonstrated clinical impact and areas of controversy.

ANSWER TO THE PHOTO QUIZ

Tiffany J. Lieu and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1675–1676, https://doi.org/10.1093/cid/cit082

CORRESPONDENCE

Andrea Calcagno and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1677–1678, https://doi.org/10.1093/cid/cit087
Jennifer A. Kieran and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1678–1679, https://doi.org/10.1093/cid/cit092
Esteban C. Nannini and Cesar A. Arias
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Page 1679, https://doi.org/10.1093/cid/cit088
Wen-Pin Tseng and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1679–1680, https://doi.org/10.1093/cid/cit091
Nicole E. Stoesser and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1680–1681, https://doi.org/10.1093/cid/cit089
Clotilde Rousseau and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1681–1682, https://doi.org/10.1093/cid/cit093
Fan Ding and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages 1682–1683, https://doi.org/10.1093/cid/cit100

ERRATUM

Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Page 1685, https://doi.org/10.1093/cid/cit181

ELECTRONIC ARTICLE

Patrick Belton and others
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Pages e102–e104, https://doi.org/10.1093/cid/cit095

The street drug “bath salts” is a psychoactive mixture of cathinone derivatives. We report 3 cases of disseminated Staphylococcus aureus infection with cardiac involvement (2 endocarditis and 1 pericarditis), secondary to intravenous bath salts use.

COVER/STANDING MATERIAL

Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Page NP, https://doi.org/10.1093/cid/cis1056
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Page NP, https://doi.org/10.1093/cid/cis1091
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Page NP, https://doi.org/10.1093/cid/cis1102
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Page NP, https://doi.org/10.1093/cid/cis1125
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Page NP, https://doi.org/10.1093/cid/cis1148
Clinical Infectious Diseases, Volume 56, Issue 11, 1 June 2013, Page NP, https://doi.org/10.1093/cid/cis1171
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