Necrotizing Fasciitis Within 72 hours After Presentation with Skin and Skin Structure Infection.


Journal

The western journal of emergency medicine
ISSN: 1936-9018
Titre abrégé: West J Emerg Med
Pays: United States
ID NLM: 101476450

Informations de publication

Date de publication:
10 Jul 2020
Historique:
received: 08 12 2019
accepted: 05 05 2020
entrez: 30 7 2020
pubmed: 30 7 2020
medline: 15 12 2020
Statut: epublish

Résumé

A small percentage of patients with skin infections later develop necrotizing fasciitis (NF). Diagnostic testing is needed to identify patients with skin infections at low risk of NF who could be discharged from the emergency department (ED) after antibiotic initiation. Elevated lactate has been associated with NF; existing estimates of the frequency of NF are based on retrospective reviews, and cases often lack testing for lactate. We present the incidence of patients with skin infections who developed NF and their baseline lactates. In four phase-3 trials, 2883 adults with complicated or acute bacterial skin and skin structure infections were randomized to dalbavancin or comparator, with early and late follow-up visits through Day 28. We prospectively collected baseline plasma lactates in one trial to assess an association with NF. NF was diagnosed in 3/2883 patients (0.1%); all three survived. In the study with prospectively collected baseline lactates (n = 622), 15/622 (2.4%) had a lactate ≥4 millimoles per liter (mmol/L), including 3/622 (0.5%) with a lactate ≥7 mmol/L. NF was not seen in patients with a lactate <4 mmol/L; NF was seen in 1/15 (6.7%) with a lactate ≥4 mmol/L, including 1/3 (33.3%) with lactate ≥7 mmol/L. NF incidence within 72 hours of antibiotic initiation in patients with complicated or acute bacterial skin and skin structure infections was extremely low (0.1%) and occurred in 6.7% with a lactate ≥4 mmol/L. Lactate <4 mmol/L can be used to identify patients at low risk of NF who could be safely discharged from the ED after antibiotic initiation.

Identifiants

pubmed: 32726268
pii: westjem.2020.5.46046
doi: 10.5811/westjem.2020.5.46046
pmc: PMC7390563
doi:

Substances chimiques

Anti-Bacterial Agents 0
Lactic Acid 33X04XA5AT
Teicoplanin 61036-62-2
dalbavancin 808UI9MS5K

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

943-948

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Auteurs

Urania Rappo (U)

Allergan PLC, Madison, New Jersey.

H Bryant Nguyen (HB)

Loma Linda University, Division of Pulmonary, Critical Care, Hyperbaric, Allergy and Sleep Medicine Loma Linda, California.

Sailaja Puttagunta (S)

Allergan PLC, Madison, New Jersey.
BiomX Ltd, Ness Ziona, Israel.

Caroline Ojaimi (C)

Allergan PLC, Madison, New Jersey.
Novartis Pharmaceuticals Corp, East Hanover, New Jersey.

Karthik Akinapelli (K)

Independent consultant, Hamden, Connecticut.
Iterum Therapeutics, Old Saybrook, Connecticut.

Michael W Dunne (MW)

Allergan PLC, Madison, New Jersey.
Iterum Therapeutics, Old Saybrook, Connecticut.

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Classifications MeSH