by
Julie A. E. Nelson;
Kristina De Paris;
Catalina Ramirez;
Andrew Edmonds;
Kate R. Mollan;
Camden P. Bay;
Kara Compliment;
Betsy C. Herold;
Kathryn Anastos;
Howard Minkoff;
Seble Kassaye;
Dominika L. Seidman;
Audrey French;
Elizabeth T. Golub;
Anandi Sheth;
Christina Ochsenbauer;
Ronald Swanstrom;
Joseph J. Eron;
Adaora A. Adimora
Objective: Determine the frequency of genital HIV-1 shedding in a large cohort of women on long-term suppressive antiretroviral therapy (ART) and its association with mucosal inflammation.Design:We measured levels of HIV-1 RNA and inflammation biomarkers in cervicovaginal lavage (CVL) from HIV-seropositive women enrolled in the Women's Interagency HIV Study (WIHS).Methods:HIV-1 was quantified (Abbott RealTime HIV-1 assay) from CVL samples of 332 WIHS participants with and without clinical evidence of genital inflammation at the time of CVL collection; participants had suppressed plasma viral load (PVL; limit of quantitation less than 20-4000copies/ml depending on year of collection) for a median of 7.1 years [interquartile range (IQR) 3.4-9.8, Group 1] or for a median of 1.0 years (IQR=0.5-1.0, Group 2). Twenty-two biomarkers of inflammation were measured in CVL to compare with clinical markers.Results:HIV-1 was detected in 47% of 38 pre-ART CVL samples (median 668copies/ml) and detection in CVL was associated with higher pre-ART PVL. HIV-1 was detected in only 1 of 38 CVL samples from these women on suppressive antiretroviral therapy for 1 year. No HIV-1 RNA was detected in 294 CVL samples from a cross-sectional set of women with suppressed PVL for a median of 7 years. Clinical inflammation markers were correlated with inflammatory biomarkers in CVL specimens, although genital inflammation was not associated with measurable genital HIV-1 shedding in these WIHS participants on ART.Conclusion:ART that suppresses HIV-1 in the plasma of women also prevents genital tract HIV-1 shedding, even in the presence of genital tract inflammation.
by
Monica Farley;
G Langley;
W Schaffner;
R Lynfield;
NM Bennett;
A Reingold;
A Thomas;
LH Harrison;
M Nichols;
S Petit;
L Miller;
MR Moore;
SJ Schrag;
FC Lessa;
TH Skoff;
JR MacNeil;
EC Briere;
EJ Weston;
C Van Beneden
Active Bacterial Core surveillance (ABCs) was established in 1995 as part of the Centers for Disease Control and Prevention Emerging Infections Program (EIP) network to assess the extent of invasive bacterial infections of public health importance. ABCs is distinctive among surveillance systems because of its large, population-based, geographically diverse catchment area; active laboratory-based identification of cases to ensure complete case capture; detailed collection of epidemiologic information paired with laboratory isolates; infrastructure that allows for more in-depth investigations; and sustained commitment of public health, academic, and clinical partners to maintain the system. ABCs has directly affected public health policies and practices through the development and evaluation of vaccines and other prevention strategies, the monitoring of antimicrobial drug resistance, and the response to public health emergencies and other emerging infections.
by
John Brooks;
Thibaut Davy-Mendez;
Sonia Napravnik;
Brenna C Hogan;
Keri N Althoff;
Kelly A Gebo;
Richard D Moore;
Michael A Horberg;
Michael J Silverberg;
John M Gill;
Heidi M Crane;
Vincent Marconi;
Ronald J Bosch;
Jonathan Colasanti;
Timothy R Sterling;
Christopher W Mathews;
Angel M Mayor;
Ni Gusti Ayu Nanditha;
Kate Buchacz;
Jun Li;
Peter F Rebeiro;
Jennifer E Thorne;
Ank Nijhawan;
David van Duin;
David A Wohl;
Joseph J Eron;
Stephn A Berry
Background: To assess the possible impact of antiretroviral therapy improvements, aging, and comorbidities, we examined trends in all-cause and cause-specific hospitalization rates among persons with HIV (PWH) from 2005 to 2015. Methods: In 6 clinical cohorts, we followed PWH in care (≥1 outpatient CD4 count or HIV load [VL] every 12 months) and categorized ICD codes of primary discharge diagnoses using modified Clinical Classifications Software. Poisson regression estimated hospitalization rate ratios for calendar time trends, adjusted for demographics, HIV risk factor, and annually updated age, CD4, and VL. Results: Among 28057 patients (125724 person-years), from 2005 to 2015, the median CD4 increased from 389 to 580 cells/μL and virologic suppression from 55% to 85% of patients. Unadjusted all-cause hospitalization rates decreased from 22.3 per 100 person-years in 2005 (95% confidence interval [CI], 20.6-24.1) to 13.0 in 2015 (95% CI, 12.2-14.0). Unadjusted rates decreased for almost all diagnostic categories. Adjusted rates decreased for all-cause, cardiovascular, and AIDS-defining conditions, increased for non-AIDS-defining infection, and were stable for most other categories. Conclusions: Among PWH with increasing CD4 counts and viral suppression, unadjusted hospitalization rates decreased for all-cause and most cause-specific hospitalizations, despite the potential effects of aging, comorbidities, and cumulative exposure to HIV and antiretrovirals.
by
Ighovwerha Ofotokun;
ER Cedarbaum;
Y Ma;
AA Adimora;
M Bamman;
MH Cohen;
MA Fischl;
D Gustafson;
K Matsushita;
M Plankey;
EC Seaberg;
A Sharma;
PC Tien
Objectives: Peripheral artery disease (PAD) is associated with decreased physical function and increased mortality in the general population. We previously found that PAD is common in middle-aged women with and without HIV infection, but its association with functional decline is unclear. We examine the contribution of PAD to functional decline in the Women’s Interagency HIV Study, controlling for traditional cardiovascular risk factors and HIV-related factors. Methods: Analysis included 1839 participants (72% with HIV) with measured ankle – brachial index (ABI) and 4 m gait speed. ABI values categorized PAD severity. Linear models with repeated measures estimated the association of PAD severity with log-transformed gait speed after controlling for demographic, behavioral, and metabolic risk factors, and HIV/hepatitis C virus status. Results: Median age was 50 years and more than 70% were Black. Compared with normal ABI, there was a dose – response relationship between increasing PAD severity and slower gait speed in univariable analyses: 6% slower gait speed for low-normal ABI [95% confidence interval (CI): 4 – 9%], 10% for borderline PAD (95% CI: 6 – 13%), 14% for mild PAD (95% CI: 9 – 18%), and 16% for moderate – severe PAD (95% CI: 5 – 25%). PAD severity remained associated with slower gait speed in multivariable analyses. HIV/hepatitis C virus co-infection was independently associated with 9% (95% CI: 4 – 14%) slower gait speed compared with those with neither infection. Among women with HIV, neither CD4þ cell count nor HIV-RNA level was associated with gait speed. Conclusion: In middle-aged women with and without HIV infection, greater PAD severity is associated with progressively slower gait speed. Early detection of subclinical PAD may decrease the risk of lower extremity functional impairment and its long-term health consequences.
by
Nadine Rouphael;
G Wang;
JT Stapleton;
AW Baker;
CB Creech;
HM El Sahly;
JE Stout;
L Jackson;
E Charbek;
FJ Leyva;
KM Tomashek;
M Tibbals;
A Miller;
S Frey;
S Niemotka;
TL Wiemken;
N Beydoun;
G Alaaeddine;
N Turner;
EB Walter;
R Chamberland;
G Abate
Coinfections are more common in patients with cystic fibrosis and bronchiectasis. Infiltrates on imaging studies are seen more commonly in patients with coinfections, but coinfections did not affect treatment outcomes of pulmonary Mycobacterium avium complex.
Toxoplasma gondii can cause severe opportunistic infection in immunocompromised individuals, but diagnosis is often delayed. We conducted a retrospective review of solid organ transplant (SOT) and hematopoietic stem cell transplant (HSCT) recipients with toxoplasmosis between 2002 and 2018 at two large US academic transplant centers. Patients were identified by ICD-9 or ICD-10 toxoplasmosis codes, positive Toxoplasma polymerase chain reaction test result, or pathologic diagnosis. Data were collected regarding transplant type, time from transplant to toxoplasmosis diagnosis, clinical and radiographic features, and mortality at 30 and 90 days. Twenty patients were identified: 10 HSCT recipients (80% allogeneic HSCT) and 10 SOT recipients (60% deceased donor renal transplants). Rejection among SOT recipients (70%) and graft-versus-host disease (GVHD) prophylaxis among HSCT recipients (50%) were frequent. Median time from transplant to toxoplasmosis diagnosis was longer for SOT than HSCT (1385 vs. 5 days, P-value.002). Clinical manifestations most commonly were encephalitis (65%), respiratory failure (40%), renal failure (40%), and distributive shock (40%). Cohort 30-day mortality was 45%, and 90-day mortality was 55%. Diagnosis was postmortem in 25% of the cohort. Further evaluation of toxoplasmosis screening is needed for noncardiac SOT recipients, HSCT recipients with GVHD, and periods of increased net immunosuppression.
The global coronavirus pandemic we now confront has led to unprecedented mortality, strained our medical systems, disrupted our daily lives, and created economic stress unlike any other event in our lifetime. The origin is a novel virus that has swept across the globe with surprising speed, aided by air travel and a complete absence of population immunity. There can be no clearer reminder of the importance of immunization to modern civilization.
by
Jorge Salinas;
Christopher Rentsch;
Vincent Marconi;
Janet Tate;
Matthew Budoff;
Adeel A. Butt;
Matthew S. Freiberg;
Cynthia L. Gibert;
Matthew Bidwell Goetz;
David Leaf;
Maria C. Rodriguez-Barradas;
Amy C. Justice;
David Rimland
Background. After adjustment for cardiovascular risk factors and despite higher mortality, those with human immunodeficiency virus (HIV+) have a greater risk of acute myocardial infarction (AMI) than uninfected individuals. Methods. We included HIV+ individuals who started combination antiretroviral therapy (cART) in the Veterans Aging Cohort Study (VACS) from 1996 to 2012. We fit multivariable proportional hazards models for baseline, time-updated and cumulative measures of HIV-1 RNA, CD4 counts, and the VACS Index. We used the trapezoidal rule to build the following cumulative measures: viremia copy-years, CD4-years, and VACS Index score-years, captured 180 days after cART initiation until AMI, death, last clinic visit, or 30 September 2012. The primary outcomes were incident AMI (Medicaid, Medicare, and Veterans Affairs International Classification of Diseases-9 codes) and death. Results. A total of 8168 HIV+ individuals (53 861 person-years) were analyzed with 196 incident AMIs and 1710 deaths. Controlling for known cardiovascular risk factors, 6 of the 9 metrics predicted AMI and all metrics predicted mortality. Time-updated VACS Index had the lowest Akaike information criterion among all models for both outcomes. A time-updated VACS Index score of 55+ was associated with a hazard ratio (HR) of 3.31 (95% confidence interval [CI], 2.11-5.20) for AMI and a HR of 31.77 (95% CI, 26.17-38.57) for mortality. Conclusions. Time-updated VACS Index provided better AMI and mortality prediction than CD4 count and HIV-1 RNA, suggesting that current health determines risk more accurately than prior history and that risk assessment can be improved by biomarkers of organ injury.
Background:
Safety net family planning (FP) clinics provide vital care for women in high HIV-burden areas and may be ideal preexposure prophylaxis (PrEP) delivery sites. Yet, many FP providers lack knowledge about PrEP.
Setting:
Four safety net FP clinics in Atlanta, Georgia.
Methods:
We provided a 1.5-hour PrEP informational training for 28 providers working in these sites. To assess the training’s impact on PrEP counseling, we enrolled 500 female patients after training (47% ≤ 28 years; 69% black; 12% Hispanic) and determined their PrEP indication based on CDC guidelines. We conducted a postvisit survey to assess provider counseling and patients’ interest in PrEP and acceptance of off-site PrEP referral.
Results:
From pre-training to post-training, provider PrEP knowledge and confidence to identify women who may benefit from PrEP significantly increased. Only 19% of women knew about PrEP before the visit. Among 376 sexually active women, 29% had risk consistent with PrEP indication. Among PrEP-indicated women, 66% reported the provider discussed PrEP, 29% were interested in taking PrEP, but only 18% accepted off-site PrEP referral. Most (76%) were more willing to take PrEP if provided by the FP clinic.
Conclusions:
After a brief PrEP training, most women with HIV-risk indicators received PrEP counseling during their visits. Once counseled, women expressed interest if it were offered at the FP clinic rather than through off-site referral. Findings highlight the potential impact that PrEP capacity building within safety net FP clinics in high HIV-burden areas may have on PrEP scale-up for women.
by
Mark J. Sotir;
Douglas H. Esposito;
Elizabeth Barnett;
Karen Leder;
Phyllis E Kozarsky;
Poh L. Lim;
Effrossyni Gkrania-Klotsas;
Davidson H. Hamer;
Susan Kuhn;
Bradley A. Connor;
Rashila Pradhan;
Eric Caumes
This work is written by (a) US Government employee(s) and is in the public domain in the US. Measles remains a risk for travelers, with 94 measles diagnoses reported to the GeoSentinel network from 2000 to 2014, two-thirds since 2010. Asia was the most common exposure region, then Africa and Europe. Efforts to reduce travel-associated measles should target all vaccine-eligible travelers, including catch-up vaccination of susceptible adults.