Evidence map›Paper›PMID 19417581›Full record

ArticleAIDS (London, England)2009

Immune reconstitution inflammatory syndrome among HIV-infected South African infants initiating antiretroviral therapy.

Kelly Smith, Louise Kuhn, Ashraf Coovadia, Tammy Meyers, Chih-Chi Hu, Cordula Reitz, Gillian Barry, Renate Strehlau, Gayle Sherman, Elaine J Abrams

Open access · greenAbstract read
In one paragraph

Article in AIDS (London, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 7 pooled it
11.2field-weighted citation impact, top 1% 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

42 citing papers in PubMed, 7 syntheses or guidelines pooled it, 86 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Isoniazid for preventing tuberculosis in HIV-infected children.The Cochrane database of systematic reviews · 2017
    Pooled it
  5. Pooled it
  6. Guideline
  7. Guideline
  8. Trial
  9. Trial
  10. Trial
  11. Trial
  12. Early antiretroviral treatment reduces risk of bacille Calmette-Guérin immune reconstitution adenitis.The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease · 2011
    Trial
  13. Trial
  14. Trial
  15. Trial
  16. Trial
  17. Article
  18. Article
  19. Article
  20. BCG Vaccination and Mother-to-Infant Transmission of HIV.The Journal of infectious diseases · 2020
    Article
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

10 authors at 5 institutions in 2 countries.

Kelly SmithColumbia University College of Physicians & Surgeons, New York, New York, USA.
Louise Kuhn
Ashraf Coovadia
Tammy Meyers
Chih-Chi Hu
Cordula Reitz
Gillian Barry
Renate Strehlau
Gayle Sherman
Elaine J Abrams
Columbia University · USEmpilisweni District Hospital · ZAChris Hani Baragwanath Hospital · ZAMedical Care Development International · USUniversity of the Witwatersrand · ZA

Funding

Clinical Relevance of Transient Nevirapine ResistanceR01HD047177 · NICHD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI KUHN, LOUISE · 2004 to 2008
$2.6M
NICHD NIH HHS HD 47177NICHD NIH HHS R01 HD047177
6 · The paper itself

Abstract

objectivesTo determine the incidence, clinical manifestations and risk factors for immune reconstitution inflammatory syndrome (IRIS) in young children initiating highly active antiretroviral therapy (HAART).

designA prospective cohort of antiretroviral-naïve HIV-infected children less than 24 months of age enrolled in a treatment strategies trial in Johannesburg, South Africa.

methodsAmong 169 HIV-infected children initiating HAART, April 2005 to November 2006, the records of 83 children suspected to have IRIS within 6 months of starting treatment were reviewed to determine whether they met criteria for IRIS. Seven were excluded due to incomplete follow-up. Pretreatment and post-treatment characteristics of children with and without IRIS were compared.

resultsOverall, 34/162 (21%) children developed IRIS at a median of 16 days (range 7-115 days) post-HAART initiation. Bacille Calmette-Guérin reaction was most common occurring in 24/34 (71%) children, primarily injection site lesions and/or ipsilateral axillary lymphadenitis with abscess. Other IRIS conditions (not mutually exclusive) included Mycobacterium tuberculosis (n = 12), cytomegalovirus pneumonia (n = 1), Streptococcus pneumonia sepsis (n = 1), and severe seborrheic dermatitis (n = 1). Children with IRIS were younger (median age 7 vs. 10 months, P = 0.007) with a lower CD4 cell percentage (median 13.9 vs. 19.2, P = 0.009) at HAART initiation than controls. After 24 weeks on HAART, 62% of IRIS cases vs. 28% of controls had HIV RNA more than 400 copies/ml (P = 0.001), odds ratio = 2.88 (95% confidence interval = 1.14-7.29) after adjusting for baseline factors.

conclusionInfants and young children with advanced HIV disease initiating HAART are at high risk for developing IRIS, leading to additional morbidity and possibly impairing virologic response to antiretroviral treatment.

Indexed as

AIDS-Related Opportunistic InfectionsAntiretroviral Therapy, Highly ActiveBCG VaccineCD4 Lymphocyte CountCD4-Positive T-LymphocytesFemaleHIV-1HumansImmune Reconstitution Inflammatory SyndromeInfantMaleProspective StudiesRisk FactorsSouth AfricaViral LoadBCG Vaccine

Identifiers

PMID19417581
PMCPMC2810152
OpenAlexW2015545253

What OpenQuestion holds

Textmetadata
LicenceTDM
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.