Aminoglycosides in Immunocompromised Critically Ill Patients With Bacterial Pneumonia and Septic Shock: A Post-Hoc Analysis of a Prospective Multicenter Multinational Cohort
Language English Country United States Media print
Document type Clinical Trial, Journal Article, Multicenter Study, Research Support, Non-U.S. Gov't
PubMed
32496415
DOI
10.1097/shk.0000000000001553
PII: 00024382-202012000-00005
Knihovny.cz E-resources
- MeSH
- Aminoglycosides administration & dosage MeSH
- Anti-Bacterial Agents administration & dosage MeSH
- Pneumonia, Bacterial * complications drug therapy mortality MeSH
- Immunocompromised Host * MeSH
- Critical Illness MeSH
- Middle Aged MeSH
- Humans MeSH
- Survival Rate MeSH
- Disease-Free Survival MeSH
- Prospective Studies MeSH
- Aged MeSH
- Shock, Septic * complications drug therapy mortality MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial MeSH
- Multicenter Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Aminoglycosides MeSH
- Anti-Bacterial Agents MeSH
BACKGROUND: The routine use of empiric combination therapy with aminoglycosides during critical illness is associated with uncertain benefit and increased risk of acute kidney injury. This study aimed to assess the benefits of aminoglycosides in immunocompromised patients with suspected bacterial pneumonia and sepsis. METHODS: Secondary analysis of a prospective multicenter study. Adult immunocompromised patients with suspected bacterial pneumonia and sepsis or septic shock were included. Primary outcome was hospital mortality. Secondary outcomes were needed for renal replacement therapy (RRT). Mortality was also assessed in neutropenic patients and in those with confirmed bacterial pneumonia. Results were further analyzed in a cohort matched on risk of receiving aminoglycosides combination. RESULTS: Five hundred thirty-five patients were included in this analysis, of whom 187 (35%) received aminoglycosides in addition to another antibiotic effective against gram-negative bacteria. Overall hospital mortality was 59.6% (58.3% vs. 60.3% in patients receiving and not receiving combination therapy; P = 0.71). Lack of association between mortality and aminoglycosides was confirmed after adjustment for confounders and center effect (adjusted OR 1.14 [0.69-1.89]) and in a propensity matched cohort (adjusted OR = 0.89 [0.49-1.61]). No association was found between aminoglycosides and need for RRT (adjusted OR = 0.83 [0.49-1.39], P = 0.477), nor between aminoglycoside use and outcome in neutropenic patients or in patients with confirmed bacterial pneumonia (adjusted OR 0.66 [0.23-1.85] and 1.25 [0.61-2.57], respectively). CONCLUSION: Aminoglycoside combination therapy was not associated with hospital mortality or need for renal replacement therapy in immunocompromised patients with pulmonary sepsis.
Agostino Gemelli University Hospital Università Cattolica del Sacro Cuore Rome Italy
Anesthesiology Department CHU Nîmes University of Nîmes Montpellier Nîmes France
Department of Critical Care King's College Hospital NHS Foundation Trust London UK
Department of Intensive Care Copenhagen University Hospital Rigshospitalet Copenhagen Denmark
Department of Intensive Care Hôpital Erasme Université Libre de Bruxelles Brussels Belgium
Department of Intensive Care Hospital Copa d'Or Rio de Janeiro Brazil
Department of Intensive Care Hospital Santa Rita Santa Casa de Misericordia Porte Allegre Brazil
Department of Medical Intensive Care Medicine University Hospital of Angers Angers France
Infectious Area Vall d'Hebron Institute of Research Barcelona Spain
Medical ICU Nantes University Hospital Nantes France
Medical Intensive Care Unit APHP Hôpital Cochin and University Paris Descartes Paris France
Medical Intensive Care Unit La Source Hospital CHR Orléans Orléans France
Medical Intensive Care Unit Montpellier University Hospital Montpellier France
Medical Surgical ICU Paoli Calmette Institute Marseille France
Medical Surgical Intensive Care Unit Andre Mignot Hospital Versailles France
Pulmonary and Critical Care Medicine Mayo Clinic Rochester Minnesota
The Department of Intensive Care Medicine Radboud University Medical Center Nijmegen The Netherlands
See more in PubMed
Pavon A, Binquet C, Kara F, Martinet O, Ganster F, Navellou J-C, Castelain V, Barraud D, Cousson J, Louis G, et al. Profile of the risk of death after septic shock in the present era: an epidemiologic study. Crit Care Med 41 (11):2600–2609, 2013.
Jamme M, Daviaud F, Charpentier J, Marin N, Thy M, Hourmant Y, Mira JP, Pène F. Time course of septic shock in immunocompromised and nonimmunocompromised patients. Crit Care Med 45 (12):2031–2039, 2017.
Tolsma V, Schwebel C, Azoulay E, Darmon M, Souweine B, Vesin A, Goldgran-Toledano D, Lugosi M, Jamali S, Cheval C, et al. Sepsis severe or septic shock: outcome according to immune status and immunodeficiency profile. Chest nov 146 (5):1205–1213, 2014.
Darmon M, Bourmaud A, Georges Q, Soares M, Jeon K, Oeyen S, Rhee CK, Gruber P, Ostermann M, Hill QA, et al. Changes in critically ill cancer patients’ short-term outcome over the last decades: results of systematic review with meta-analysis on individual data. Intensive Care Med 45 (7):977–987, 2019.
Legrand M, Max A, Schlemmer B, Azoulay E, Gachot B. The strategy of antibiotic use in critically ill neutropenic patients. Ann Intensive Care 1 (1):22, 2011.
Mokart D, Saillard C, Sannini A, Chow-Chine L, Brun J-P, Faucher M, Blache JL, Blaise D, Leone M. Neutropenic cancer patients with severe sepsis: need for antibiotics in the first hour. Intensive Care Med 40 (8):1173–1174, 2014.
Foster RA, Troficanto C, Bookstaver PB, Kohn J, Justo JA, Al-Hasan MN. Utility of combination antimicrobial therapy in adults with bloodstream infections due to enterobacteriaceae and non-fermenting gram-negative bacilli based on in vitro analysis at two community hospitals. Antibiotics (Basel) 8 (1):15, 2019.
Daniels LM, Durani U, Barreto JN, O’Horo JC, Siddiqui MA, Park JG, Tosh PK. Impact of time to antibiotic on hospital stay, intensive care unit admission, and mortality in febrile neutropenia. Support Care Cancer 27 (11):4171–4177, 2019.
Giamarellou H. Aminoglycosides plus beta-lactams against gram-negative organisms. Evaluation of in vitro synergy and chemical interactions. Am J Med 80 (6B):126–137, 2019.
Milatovic D, Braveny I. Development of resistance during antibiotic therapy. Eur J Clin Microbiol 6 (3):234–244, 1987.
Paul M, Dickstein Y, Schlesinger A, Grozinsky-Glasberg S, Soares-Weiser K, Leibovici L. Beta-lactam versus beta-lactam-aminoglycoside combination therapy in cancer patients with neutropenia. Cochrane Database Syst Rev 2013; (6):CD003038.
Paul M, Lador A, Grozinsky-Glasberg S, Leibovici L. Beta lactam antibiotic monotherapy versus beta lactam-aminoglycoside antibiotic combination therapy for sepsis. Cochrane Database Syst Rev 2014; (1):CD003344.
Ong DSY, Frencken JF, Klein Klouwenberg PMC, Juffermans N, van der Poll T, Bonten MJM, Cremer OL. Short-course adjunctive gentamicin as empirical therapy in patients with severe sepsis and septic shock: a prospective observational cohort study. Clin Infect Dis 64 (12):1731–1736, 2017.
Schnell D, Azoulay E, Benoit D, Clouzeau B, Demaret P, Ducassou S, Frange P, Lafaurie M, Legrand M, Meert AP. Management of neutropenic patients in the intensive care unit (NEWBORNS EXCLUDED) recommendations from an expert panel from the French Intensive Care Society (SRLF) with the French Group for Pediatric Intensive Care Emergencies (GFRUP), the French Society of Anesthesia and Intensive Care (SFAR), the French Society of Hematology (SFH), the French Society for Hospital Hygiene (SF2H), and the French Infectious Diseases Society (SPILF). Ann Intensive Care 6 (1):90, 2016.
Freifeld AG, Bow EJ, Sepkowitz KA, Boeckh MJ, Ito JI, Mullen CA, Raad II, Rolston KV, Young JA, Wingard JR. Clinical practice guideline for the use of antimicrobial agents in neutropenic patients with cancer: 2010 update by the infectious diseases society of America. Clin Infect Dis 52 (4):e56–e93, 2011.
Kochanek M, Schalk E, von Bergwelt-Baildon M, Beutel G, Buchheidt D, Hentrich M, Henze L, Kiehl M, Liebregts T, Von Lillienfeld-Toal M, et al. Management of sepsis in neutropenic cancer patients: 2018 guidelines from the Infectious Diseases Working Party (AGIHO) and Intensive Care Working Party (iCHOP) of the German Society of Hematology and Medical Oncology (DGHO). Ann Hematol 98 (5):1051–1069, 2019.
Azoulay E, Pickkers P, Soares M, Perner A, Rello J, Bauer PR, Van de Louw A, Hemelaar P, Lemiale V, Taccone FS, et al. Acute hypoxemic respiratory failure in immunocompromised patients: the Efraim multinational prospective cohort study. Intensive Care Med 43 (12):1808–1819, 2017.
Vincent JL, Moreno R, Takala J, Willatts S, De Mendonça A, Bruining H, Reinhart CK, Suter PM, Thijs LG. The SOFA (Sepsis-related Organ Failure Assessment) score to describe organ dysfunction/failure. On behalf of the Working Group on Sepsis-Related Problems of the European Society of Intensive Care Medicine. Intensive Care Med 22 (7):707–710, 1996.
Oken MM, Creech RH, Tormey DC, Horton J, Davis TE, McFadden ET, Carbone PP. Toxicity and response criteria of the Eastern Cooperative Oncology Group. Am J Clin Oncol 5 (6):649–655, 1982.
Leibovici L, Paul M, Poznanski O, Drucker M, Samra Z, Konigsberger H, Pitlik SD. Monotherapy versus beta-lactam-aminoglycoside combination treatment for gram-negative bacteremia: a prospective, observational study. Antimicrob Agents Chemother 41 (5):1127–1133, 1997.