Evidence map›Paper›PMID 24699683›Full record

ArticlePloS one2014

Cytomegalovirus viral load kinetics in patients with HIV/AIDS admitted to a medical intensive care unit: a case for pre-emptive therapy.

Simnikiwe H Mayaphi, Marieke Brauer, Daniel M Morobadi, Ahmad H Mazanderani, Rendani T Mafuyeka, Steve A S Olorunju, Gregory R Tintinger, Anton Stoltz

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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

8 authors at 3 institutions in 1 country.

Simnikiwe H MayaphiDepartment of Medical Virology, University of Pretoria/National Health Laboratory Service - Tshwane Academic Division (NHLS-TAD), Pretoria, South Africa.
Marieke BrauerDepartment of Medical Virology, University of Pretoria/National Health Laboratory Service - Tshwane Academic Division (NHLS-TAD), Pretoria, South Africa.
Daniel M MorobadiDepartment of Medical Virology, University of Pretoria/National Health Laboratory Service - Tshwane Academic Division (NHLS-TAD), Pretoria, South Africa.
Ahmad H MazanderaniDepartment of Medical Virology, University of Pretoria/National Health Laboratory Service - Tshwane Academic Division (NHLS-TAD), Pretoria, South Africa.
Rendani T MafuyekaDepartment of Medical Virology, University of Pretoria/National Health Laboratory Service - Tshwane Academic Division (NHLS-TAD), Pretoria, South Africa.
Steve A S OlorunjuBiostatistics unit, Medical Research Council, Pretoria, South Africa.
Gregory R TintingerDepartment of Internal Medicine, University of Pretoria, Pretoria, South Africa.
Anton StoltzDepartment of Internal Medicine, University of Pretoria, Pretoria, South Africa.
University of Pretoria · ZANational Health Laboratory Service · ZASouth African Medical Research Council · ZA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCytomegalovirus (CMV) infection is associated with severe diseases in immunosuppressed patients; however, there is a lack of data for pre-emptive therapy in patients with HIV/AIDS.

methodThis was a retrospective study, which enrolled patients diagnosed with HIV/AIDS (CD4<200 cells/μl), who had detectable CMV viral load (VL) during their stay in an adult medical intensive care unit between 2009-2012.

resultsAfter screening 82 patients' records, 41 patients met the enrolment criteria. Their median age was 37 (interquartile range [IQR]: 31-46), and median CD4 count was 29 cells/μl (IQR: 5-55). Sixteen patients (39%) had serial measurements of CMV VL before treatment with ganciclovir. Patients whose baseline CMV VL values were between 1,000-3,000 copies/ml had significantly higher values (median of 14,650 copies/ml) on follow-up testing done 4-12 days later. Those with undetectable VLs at baseline testing had detectable VLs (median of 1,590 copies/ml) mostly within 20 days of follow-up testing. Patients who had VLs >1,000 copies/ml at baseline testing had significantly higher mortality compared to those who had <1,000 copies/ml {hazard ratio of 3.46, p = 0.003 [95% confidence interval (CI): 1.55-7.71]}. Analysis of the highest CMV VL per patient showed that patients who had VLs of >5,100 copies/ml and did not receive ganciclovir had 100% mortality compared to 58% mortality in those who received ganciclovir at VLs of >5,100 copies/ml, 50% mortality in those who were not treated and had low VLs of <5,100 copies/ml, and 44% mortality in those who had ganciclovir treatment at VLs of <5,100 copies/ml (p = 0.084, 0.046, 0.037, respectively).

conclusionThis study showed a significantly increased mortality in patients with HIV/AIDS who had high CMV VLs, and suggests that a threshold value of 1,000 copies/ml may be appropriate for pre-emptive treatment in this group.

Indexed as

Intensive Care UnitsViral LoadAdultAntiviral AgentsCD4 Lymphocyte CountCytomegalovirusCytomegalovirus InfectionsGanciclovirHIV InfectionsHumansMiddle AgedAntiviral AgentsGanciclovir

Identifiers

PMID24699683
PMCPMC3974798
OpenAlexW1969839089

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.