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. 2014 Apr 3;9(4):e93702.
doi: 10.1371/journal.pone.0093702. eCollection 2014.

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

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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 et al. PLoS One. .

Abstract

Background: Cytomegalovirus (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.

Method: This 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.

Results: After 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).

Conclusion: This 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.

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Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Algorithm showing the selection of study participants.
Study participants were selected after a review of records and laboratory results for all the patients who had CMV VL results during ICU stay, within the study period. CMV VL = cytomegalovirus viral load.
Figure 2
Figure 2
Kaplan-Meier curve analysis showing survival probalities between the groups of patients: (A) who had CMV viral loads <1000 copies/ml compared to those who had viral loads >1000 copies/ml at baseline testing, (B) who had CMV viral loads <5000 copies/ml compared to those who had viral loads >5000 copies/ml at baseline testing, (C) who had CMV viral loads <10000 copies/ml compared to those who had viral loads >10000 copies/ml at baseline testing. HR = hazard ratio, CI = confidence interval.

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References

    1. Atkinson C, Emery VC (2011) Cytomegalovirus quantification: Where to next in optimising patient management? J Clin Virol 51: 223–8. - PubMed
    1. Sundar IK (2004) Update: cytomegalovirus infection in HIV-infected patients – a review. Clin Microbiol Newsl 26: 137–44.
    1. Mocarski Jr ES, Shenk T, Pass RF (2007) Cytomegaloviruses. In: Knipe DM, Howley PM, Griffin DE, Lamb RA, Martin MA, Roizman B, et al.., editors. Fields Virology. 5th ed. Philadelphia: Lippincot Williams & Wilkins, a Wolters Kluwer business. pp. 2701–72.
    1. Barron MA, Weinberg A (2005) Common viral infections in transplant recipients, part 1. Herpesviruses. Clin Microbiol Newsl 27: 99–106.
    1. De la Hoz RE, Stephens G, Sherlock C (2002) Diagnosis and treatment approaches of CMV infections in adult patients. J Clin Virol 25: 1–12. - PubMed

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The authors have no support or funding to report.