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Randomized Controlled Trial
. 2020 Feb 1;180(2):263-272.
doi: 10.1001/jamainternmed.2019.5713.

Acyclovir for Mechanically Ventilated Patients With Herpes Simplex Virus Oropharyngeal Reactivation: A Randomized Clinical Trial

Charles-Edouard Luyt  1 , Jean-Marie Forel  2 , David Hajage  3 , Samir Jaber  4 , Sophie Cayot-Constantin  5 , Thomas Rimmelé  6 , Elisabeth Coupez  7 , Qin Lu  8 , Mamadou Hassimiou Diallo  9 , Christine Penot-Ragon  10 , Marc Clavel  11 , Carole Schwebel  12 , Jean-François Timsit  13 , Jean-Pierre Bedos  14 , Caroline Hauw-Berlemont  15 , Jérémy Bourenne  16 , Julien Mayaux  17 , Jean-Yves Lefrant  18 , Jean-Paul Mira  19 , Alain Combes  1 , Michel Wolff  20 , Jean Chastre  1 , Laurent Papazian  2 ; Preemptive Treatment for Herpesviridae Study Group, Réseau Européen de recherche en Ventilation Artificielle Network
Affiliations
Randomized Controlled Trial

Acyclovir for Mechanically Ventilated Patients With Herpes Simplex Virus Oropharyngeal Reactivation: A Randomized Clinical Trial

Charles-Edouard Luyt et al. JAMA Intern Med. .

Abstract

Importance: The role of herpes simplex virus (HSV) reactivation on morbidity and mortality in patients in the intensive care unit requiring mechanical ventilation remains unknown.

Objective: To determine whether preemptive treatment with intravenous acyclovir reduces the duration of mechanical ventilation in patients with HSV oropharyngeal reactivation.

Design, setting, and participants: A double-blind, placebo-controlled randomized clinical trial was conducted in 16 intensive care units in France. Participants included 239 adults (age, >18 years) who received mechanical ventilation for at least 96 hours and continued to receive mechanical ventilation for 48 hours or more, with HSV oropharyngeal reactivation. Patients were enrolled between February 2, 2014, and February 22, 2018.

Interventions: Participants were randomized to receive intravenous acyclovir, 5 mg/kg, 3 times daily for 14 days or a matching placebo.

Main outcomes and measures: The primary end point was ventilator-free days from randomization to day 60. Prespecified secondary outcomes included mortality at 60 days. Main analyses were conducted on an intention-to-treat basis.

Results: Of 239 patients enrolled and randomized, 1 patient withdrew consent, leaving 238 patients, with 119 patients in both the acyclovir and placebo (control) groups (median [IQR] age, 61 [50-70] years; 76 [32%] women) available for primary outcome measurement. On day 60, the median (IQR) numbers of ventilator-free days were 35 (0-53) for acyclovir recipients and 36 (0-50]) for controls (P = .17 for between-group comparison). Among secondary outcomes, 26 patients (22%) and 39 patients (33%) had died at day 60 (risk difference, 0.11, 95% CI, -0.004 to 0.22, P = .06). The adverse event frequency was similar for both groups (28% in the acyclovir group and 23% in the placebo group, P = .40), particularly acute renal failure post randomization affecting 3 acyclovir recipients (3%) and 2 controls (2%). Four patients (3%) in the acyclovir group vs none in the placebo group stopped the study drug for treatment-related adverse events.

Conclusions and relevance: In patients receiving mechanical ventilation for 96 hours or more with HSV reactivation in the throat, use of acyclovir, 5 mg/kg, 3 times daily for 14 days, did not increase the number of ventilator-free days at day 60, compared with placebo. These findings do not appear to support routine preemptive use of acyclovir in this setting.

Trial registration: ClinicalTrials.gov identifier: NCT02152358.

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Conflict of interest statement

Conflict of Interest Disclosures: Dr Luyt reported receiving grants from French Ministry of Health during the conduct of the study; personal fees from Bayer Healthcare, Carmat, Faron, Merck Sharp & Dohme, ThermoFischer Brahms, and Biomérieux; and grants from Bayer Healthcare outside the submitted work. Dr Forel reported receiving grants from DGOS PHRCN during the conduct of the study. Dr Hajage reported receiving grants from the Ministry of Health during the conduct of the study. Dr Samir reported receiving personal fees from Drager, Fisher-Paykel, Medtronic, Baxter, and Xenios-Fresenius outside the submitted work. Dr Rimmelé reported receiving grants from Baxter and personal fees from Fresenius Medical Care and Biomérieux outside the submitted work. Dr Timsit reported receiving grants and personal fees from Merck and Pfizer; personal fees from Gilead, Nabriva, and Paratek; grants from Biomerieux, and personal fees from Bayer outside the submitted work. Dr Combes reported receiving grants from Getinge and personal fees from Getinge and Baxter outside the submitted work. Dr Wolff reported receiving personal fees from Merck & Co, Pfizer, Correvio, and Inotrem outside the submitted work. Dr Chastre reported receiving grants from French Ministry of Health during the conduct of the study; personal fees from Bayer, Shionogi, Aridis, Merck, Polyphor, and Tigenix/Takeda; and grants and personal fees from AstraZeneca outside the submitted work. Dr Papazian reported receiving grants from French Ministry of Health during the conduct of the study. No other disclosures were reported.

Figures

Figure 1.
Figure 1.. Study Flowchart
The Simplified Acute Physiology Score (SAPS) II is assessed on a scale ranging from 0 to 163, with higher scores indicating greater disease severity. CMV indicates cytomegalovirus; HSV, herpes simplex virus.
Figure 2.
Figure 2.. Survival Analysis Through 60 Days
Survival estimates in the intention-to-treat population.
See this image and copyright information in PMC

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