Back to Search Start Over

Effect of oropharyngeal povidone-iodine preventive oral care on ventilator-associated pneumonia in severely brain-injured or cerebral hemorrhage patients: a multicenter, randomized controlled trial

Authors :
Philippe, Seguin
Bruno, Laviolle
Claire, Dahyot-Fizelier
Romain, Dumont
Benoit, Veber
Soizic, Gergaud
Karim, Asehnoune
Olivier, Mimoz
Pierre-Yves, Donnio
Eric, Bellissant
Yannick, Malledant
Eddy, Lebas
Foie, métabolismes et cancer
Université de Rennes (UR)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )
Centre d'Investigation Clinique [Rennes] (CIC)
Université de Rennes (UR)-Hôpital Pontchaillou-Institut National de la Santé et de la Recherche Médicale (INSERM)
Service de Pharmacologie [Rennes]
CHU Pontchaillou [Rennes]
Modélisations pharmacocinétiques-pharmacodynamiques pour un meilleur usage des anti-infectieux
Université de Poitiers-Institut National de la Santé et de la Recherche Médicale (INSERM)
Service d'Anesthésie-Réanimation [CHU Limoges]
CHU Limoges
Service de réanimation médicale [CHU Rouen]
Hôpital Charles Nicolle [Rouen]
CHU Rouen
Normandie Université (NU)-Normandie Université (NU)-CHU Rouen
Normandie Université (NU)-Normandie Université (NU)-Université de Rouen Normandie (UNIROUEN)
Normandie Université (NU)
Service d'anesthésie et réanimation chirurgicale
Centre Hospitalier Universitaire d'Angers (CHU Angers)
PRES Université Nantes Angers Le Mans (UNAM)-PRES Université Nantes Angers Le Mans (UNAM)
Unité de contrôle infectieux
Université de Rennes (UR)-Hôpital Pontchaillou-CHU Pontchaillou [Rennes]
Study of Povidone Iodine to Reduce Pulmonary Infection in Head Trauma and Cerebral Hemorrhage Patients (SPIRIT) ICU Study and AtlanRéa Groups.
Université de Rennes 1 (UR1)
Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Structure Fédérative de Recherche en Biologie et Santé de Rennes ( Biosit : Biologie - Santé - Innovation Technologique )
Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Hôpital Pontchaillou-Institut National de la Santé et de la Recherche Médicale (INSERM)
Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Poitiers
Hôpital Charles Nicolle [Rouen]-CHU Rouen
Université de Rennes (UNIV-RENNES)-Université de Rennes (UNIV-RENNES)-Hôpital Pontchaillou-CHU Pontchaillou [Rennes]
Source :
Critical Care Medicine, Critical Care Medicine, 2014, 42 (1), pp.1-8. ⟨10.1097/CCM.0b013e3182a2770f⟩, Critical Care Medicine, Lippincott, Williams & Wilkins, 2014, 42 (1), pp.1-8. ⟨10.1097/CCM.0b013e3182a2770f⟩
Publication Year :
2014
Publisher :
HAL CCSD, 2014.

Abstract

International audience; OBJECTIVE: To evaluate the efficacy and safety of oral care with povidone-iodine on the occurrence of ventilator-associated pneumonia in a high-risk population. DESIGN: A multicenter, placebo-controlled, randomized, double-blind, two-parallel-group trial performed between May 2008 and May 2011. SETTING: Six ICUs in France. PATIENTS: One hundred seventy-nine severely brain-injured patients (Glasgow Coma Scale ≤ 8) or cerebral hemorrhage expected to be mechanically ventilated for more than 24 hours. INTERVENTIONS: Participants were randomly assigned to receive oropharyngeal care with povidone-iodine (n = 91) or placebo (n = 88) six times daily until mechanical ventilation withdrawal. MEASUREMENTS AND MAIN RESULTS: Primary endpoint was the rate of ventilator-associated pneumonia. Secondary endpoint included the rates of ventilator-associated tracheobronchitis and acute respiratory distress syndrome and patient's outcome. The number of patients evaluable for the primary endpoint (preplanned modified intention-to-treat population) was 150 (78 in the povidone-iodine group, 72 in the placebo group). Ventilator-associated pneumonia occurred in 24 patients (31%) in the povidone-iodine group and 20 (28%) in the placebo group (relative risk, 1.11 [95% CI, 0.67-1.82]; p = 0.69). There was no significant difference between the two groups for ventilator-associated tracheobronchitis: eight patients (10%) in the povidone-iodine group and five patients (7%) in the placebo group (relative risk, 1.48 [95% CI, 0.51-4.31]; p = 0.47). Acute respiratory distress syndrome occurred in five patients in the povidone-iodine group but not in the placebo group (p = 0.06). There was no difference between groups for ICU and hospital lengths of stay, as well as ICU and 90-day mortality. CONCLUSIONS: There is no evidence to recommend oral care with povidone-iodine to prevent ventilator-associated pneumonia in high-risk patients. Furthermore, this strategy seems to increase the rate of acute respiratory distress syndrome.

Details

Language :
English
ISSN :
00903493 and 15300293
Database :
OpenAIRE
Journal :
Critical Care Medicine, Critical Care Medicine, 2014, 42 (1), pp.1-8. ⟨10.1097/CCM.0b013e3182a2770f⟩, Critical Care Medicine, Lippincott, Williams & Wilkins, 2014, 42 (1), pp.1-8. ⟨10.1097/CCM.0b013e3182a2770f⟩
Accession number :
edsair.doi.dedup.....8247a6a740c8d62d014c5bcefcc177ac
Full Text :
https://doi.org/10.1097/CCM.0b013e3182a2770f⟩