Evidence map›Paper›PMID 34017984›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2022

Genetic and Epidemiologic Analyses of an Outbreak of Pneumocystis jirovecii Pneumonia Among Kidney Transplant Recipients in the United States.

Marwan M Azar, Elizabeth Cohen, Liang Ma, Ousmane H Cissé, Geliang Gan, Yanhong Deng, Kristen Belfield, William Asch, Matthew Grant, Shana Gleeson and 7 more

Open access · greenAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.0field-weighted citation impact, top 14% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Unanticipated Global Emergence of MultiplemedRxiv : the preprint server for health sciences · 2025
    Article
  3. Review
  4. Axenic Long-Term Cultivation ofJournal of fungi (Basel, Switzerland) · 2023
    Article
  5. Article
  6. Trends in the Epidemiology ofJournal of fungi (Basel, Switzerland) · 2023
    Review
  7. The Pathogenesis and Diagnosis ofJournal of fungi (Basel, Switzerland) · 2022
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 5 institutions in 1 country.

Marwan M AzarDepartment of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, Connecticut,USA.ORCID 0000-0001-5498-5042
Elizabeth CohenKidney Transplantation Program, Yale-New Haven Hospital, New Haven, Connecticut, USA.
Liang MaCritical Care Medicine Department, NIH Clinical Center, Bethesda, Maryland, USA.
Ousmane H CisséCritical Care Medicine Department, NIH Clinical Center, Bethesda, Maryland, USA.
Geliang GanYale Center for Analytical Sciences, Yale School of Public Health, New Haven, Connecticut, USA.
Yanhong DengYale Center for Analytical Sciences, Yale School of Public Health, New Haven, Connecticut, USA.
Kristen BelfieldDepartment of Internal Medicine, Section of Nephrology, Yale School of Medicine, New Haven, Connecticut, USA.
William AschKidney Transplantation Program, Yale-New Haven Hospital, New Haven, Connecticut, USA.
Matthew GrantDepartment of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, Connecticut,USA.
Shana GleesonDepartment of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, Connecticut,USA.
Alan KoffDepartment of Internal Medicine, Section of Infectious Diseases, UC Davis School of Medicine, Sacramento, California, USA.
David C GastonDepartment of Pathology, Division of Medical Microbiology, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Jeffrey TopalDepartment of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, Connecticut,USA.
Shelly CurranCritical Care Medicine Department, NIH Clinical Center, Bethesda, Maryland, USA.
Sanjay KulkarniKidney Transplantation Program, Yale-New Haven Hospital, New Haven, Connecticut, USA.
Joseph A KovacsCritical Care Medicine Department, NIH Clinical Center, Bethesda, Maryland, USA.
Maricar MalinisDepartment of Internal Medicine, Section of Infectious Diseases, Yale School of Medicine, New Haven, Connecticut,USA.
Yale University · USNational Institutes of Health Clinical Center · USYale New Haven Hospital · USJohns Hopkins University · USUniversity of California, Davis · US

Funding

Molecular Studies Of Human Pneumocystis CariniiZIACL000192 · CLC · CLINICAL CENTER · PI KOVACS, JOSEPH A · 2009 to 2025
$0k
National Institute of Health Clinical Center
6 · The paper itself

Abstract

backgroundPneumocystis jirovecii is an opportunistic fungus that causes Pneumocystis pneumonia (PCP) in immunocompromised hosts. Over an 11-month period, we observed a rise in cases of PCP among kidney-transplant recipients (KTR), prompting an outbreak investigation.

methodsClinical and epidemiologic data were collected for KTR diagnosed with PCP between July 2019 and May 2020. Pneumocystis strain typing was performed using restriction fragment length polymorphism analyses and multilocus sequence typing in combination with next-generation sequencing. A transmission map was drawn, and a case-control analysis was performed to determine risk factors associated with PCP.

resultsNineteen cases of PCP in KTR were diagnosed at a median of 79 months post-transplantation; 8 received monthly belatacept infusions. Baseline characteristics were similar for KTR on belatacept versus other regimens; the number of clinic visits was numerically higher for the belatacept group during the study period (median 7.5 vs 3). Molecular typing of respiratory specimens from 9 patients revealed coinfection with up to 7 P. jirovecii strains per patient. A transmission map suggested multiple clusters of interhuman transmission. In a case-control univariate analysis, belatacept, lower absolute lymphocyte count, non-White race, and more transplant clinic visits were associated with an increased risk of PCP. In multivariate and prediction power estimate analyses, frequent clinic visits was the strongest risk factor for PCP.

conclusionsIncreased clinic exposure appeared to facilitate multiple clusters of nosocomial PCP transmission among KTR. Belatacept was a risk factor for PCP, possibly by increasing clinic exposure through the need for frequent visits for monthly infusions.

Indexed as

Kidney TransplantationPneumocystis cariniiPneumonia, PneumocystisDisease OutbreaksHumansMultilocus Sequence TypingTransplant RecipientsUnited Statesbelataceptkidney transplantnext-generation sequencingoutbreakPneumocystis jirovecii

Identifiers

PMID34017984
PMCPMC9012955
OpenAlexW3160370205

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.