Key result
Pulse methylprednisolone shows no benefit over non-pulse therapy for 5-week CMV-DNAemia clearance.
Why the study?
To investigate the impact of corticosteroids on the outcome of antiviral therapy in rheumatic patients with cytomegalovirus-emia.
Does pulse methylprednisolone affect CMV-DNAemia clearance in rheumatic disease patients receiving antiviral therapy?
Cohort (n=62)
Does pulse methylprednisolone affect CMV-DNAemia clearance in rheumatic disease patients receiving antiviral therapy?
Odds Ratio: 1.6 (95% CI 0.168–15.273)
Absolute Event Rate: 88.9% vs 83.3%
p-value: p=>0.05
Pulse methylprednisolone does not significantly impact the final clearance of CMV-DNAemia in rheumatic disease patients receiving effective antiviral therapy, though it may slightly prolong the duration of viremia in those with high baseline titers.
Corticosteroids showed no association with antiviral clearance in rheumatic CMV-emia; hypothesis-generating and should not yet change practice.
AIM: To investigate the impact of corticosteroids on the outcome of antiviral therapy in rheumatic patients with cytomegalovirus (CMV)-emia. METHOD: Sixty-two patients with rheumatic disease complicated by CMV infection from 2011 to 2014 were retrospectively analyzed. RESULTS: Fifty-five of 62 patients were diagnosed with CMV-DNAemia. Most patients (43/55, 78.2%) achieved viral clearance within 5 weeks. It was shown that, while undergoing active antiviral therapy, there was no significant difference in the CMV-DNAemia clearance rate between the pulse methylprednisolone (MPSL) therapy group and non-pulse group (8/9, 88.9% vs 30/36, 83.3%; OR = 1.600, 95% CI 0.168-15.273, P > 0.05) at the end of the 5-week follow-up. However, pulse MPSL might slightly prolong duration of CMV-DNAemia than non-pulse MPSL patients (20.78 ± 19.18 days vs 14.33 ± 9.01 days, P = 0.1430), especially in the high baseline titer group (33.7 ± 29.1 days in pulse MPSL group vs 18.3 ± 13.1 days in non-pulse group, P = 0.457). But in the low baseline titer group, CMVemia duration in the pulse MPSL group (14.3 ± 10.0 days) was about the same as that in the non-pulse MPSL group (13.4 ± 7.8 days). CONCLUSION: With effective antiviral therapy, pulse MPSL is acceptable in rheumatic disease patients with CMV-DNAemia, without significant impact on final clearance of virus. However, duration of CMV-DNAemia may be prolonged, especially in patients with high CMV-DNA titer at baseline.
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Li et al. (2019) conducted a cohort in Rheumatic disease complicated by cytomegalovirus (CMV) infection (n=62). Pulse methylprednisolone (MPSL) therapy vs. Non-pulse MPSL therapy was evaluated on CMV-DNAemia clearance rate at the end of 5-week follow-up (OR 1.600, 95% CI 0.168-15.273, p=>0.05). Pulse methylprednisolone therapy did not significantly affect the 5-week CMV-DNAemia clearance rate compared to non-pulse therapy (88.9% vs 83.3%; OR 1.600; 95% CI 0.168-15.273; P>0.05).
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