Your browser doesn't support javascript.
loading
Menstrual Toxic Shock Syndrome: A French Nationwide Multicenter Retrospective Study.
Contou, Damien; Colin, Gwenhaël; Travert, Brendan; Jochmans, Sébastien; Conrad, Marie; Lascarrou, Jean-Baptiste; Painvin, Benoit; Ferré, Alexis; Schnell, David; La Combe, Beatrice; Coudroy, Rémi; Ehrmann, Stephan; Rambaud, Jérôme; Wiedemann, Arnaud; Asfar, Pierre; Kalfon, Pierre; Guérot, Emmanuel; Préau, Sébastien; Argaud, Laurent; Daviet, Florence; Dellamonica, Jean; Dupont, Audrey; Fartoukh, Muriel; Kamel, Toufik; Béduneau, Gaëtan; Canouï-Poitrine, Florence; Boutin, Emmanuelle; Lina, Gérard; Mekontso Dessap, Armand; Tristan, Anne; de Prost, Nicolas.
Afiliação
  • Contou D; Service de Réanimation Polyvalente, Centre Hospitalier Victor Dupouy, Argenteuil, France.
  • Colin G; Service de Médecine Intensive Réanimation, Centre Hospitalier Départemental de Vendée, Les Oudairies, Boulevard Stéphane Moreau, La Roche-sur-Yon, France.
  • Travert B; Service de Réanimation Pédiatrique, Centre Hospitalier Universitaire de Nantes, Nantes, France.
  • Jochmans S; Service de Médecine Intensive Réanimation, Groupe Hospitalier Sud Ile-de-France; Hôpital de Melun-Sénart, Melun, France.
  • Conrad M; Service de Réanimation, Centre Hospitalier Universitaire de Nancy, Nancy, France.
  • Lascarrou JB; Service de Médecine Intensive et Réanimation, Centre Hospitalier Universitaire de Nantes, Nantes, France.
  • Painvin B; Service des Maladies Infectieuses et Réanimation Médicale, Centre Hospitalier Universitaire de Rennes, Rennes, France.
  • Ferré A; Service de Réanimation Médico-Chirurgicale, Centre Hospitalier André Mignot de Versailles, Le Chesnay-Rocquencourt, France.
  • Schnell D; Service de Médecine Réanimation Polyvalente, Centre Hospitalier d'Angoulême, Angoulême, France.
  • La Combe B; Service de Réanimation Médico-Chirurgicale, Hôpital du Scorff-Groupe Hospitalier Bretagne Sud Lorient, Lorient, France.
  • Coudroy R; Service de Médecine Intensive et Réanimation, Centre Hospitalier Universitaire de Poitiers, Poitiers, France.
  • Ehrmann S; INSERM CIC1402, ALIVE Group, Université de Poitiers, France.
  • Rambaud J; Service de Médecine Intensive et Réanimation, CHRU de Tours, CIC 1415, CRICS-TriggerSEP, Centre d'Étude des Pathologies Respiratoires, INSERM U1100, Université de Tours, Tours, France.
  • Wiedemann A; Service de Réanimation Pédiatrique, Hôpital Trousseau, AP-HP, Paris, France.
  • Asfar P; INSERM u1256 N-GERE et Réanimation Pédiatrique Spécialisée-CHRU, Vandœuvre-lès-Nancy, France.
  • Kalfon P; Département de Médecine Intensive-Réanimation, Centre Hospitalier Universitaire d'Angers, Angers, France.
  • Guérot E; Service de Réanimation, Centre Hospitalier de Chartres, Le Coudray, France.
  • Préau S; Service de Médecine Intensive Réanimation, Hôpital Européen Georges Pompidou AP-HP, Paris, France.
  • Argaud L; Service de Réanimation, Centre Hospitalier Universitaire de Lille, Lille, France.
  • Daviet F; Service de Médecine Intensive-Réanimation, Hôpital Édouard-Herriot, Lyon, France.
  • Dellamonica J; Service de Médecine Intensive Réanimation, Hôpital Nord, Assistance Publique-Hôpitaux de Marseille, Aix-Marseille Université, Chemin des Bourrely, Marseille, France.
  • Dupont A; Service de Médecine Intensive Réanimation, Centre Hospitalier Universitaire de Nice, UR2CA Université Cote d'Azur, Nice, France.
  • Fartoukh M; Service de Réanimation Pédiatrique, Centre Hospitalier Universitaire de Nice, Nice, France.
  • Kamel T; Sorbonne Université, AP-HP, Service de Médecine Intensive Réanimation, Centre Hospitalier Universitaire Tenon AP-HP, Paris, France.
  • Béduneau G; Service de Médecine Intensive Réanimation, Centre Hospitalier Régional d'Orléans Hôpital de La Source, Orléans, France.
  • Canouï-Poitrine F; Universite de Normandie, UNIROUEN, EA3830, Service de Réanimation Médicale, Centre Hospitalier Universitaire de Rouen, Rouen, France.
  • Boutin E; Service de Santé Publique, Hôpital Henri-Mondor, AP-HP, Créteil, France.
  • Lina G; Service de Santé Publique, Hôpital Henri-Mondor, AP-HP, Créteil, France.
  • Mekontso Dessap A; Centre National de Référence des Staphylocoques, Institut des Agent Infectieux, Hôpital de la Croix Rousse, Hospices Civils de Lyon, Lyon, France.
  • Tristan A; Service de Médecine Intensive Réanimation, Groupe de Recherche CARMAS, Centre Hospitalier Universitaire Henri Mondor, Assistance Publique-Hôpitaux de Paris, Créteil, France.
  • de Prost N; Centre National de Référence des Staphylocoques, Institut des Agent Infectieux, Hôpital de la Croix Rousse, Hospices Civils de Lyon, Lyon, France.
Clin Infect Dis ; 74(2): 246-253, 2022 01 29.
Article em En | MEDLINE | ID: mdl-33906228
ABSTRACT

BACKGROUND:

Studies describing the clinical features and short-term prognosis of patients admitted to the intensive care unit (ICU) for menstrual toxic shock syndrome (m-TSS) are lacking.

METHODS:

This was a multicenter retrospective cohort study of patients with a clinical diagnosis of m-TSS admitted between 1 January 2005 and 31 December 2020 in 43 French pediatric (n = 7) or adult (n = 36) ICUs. The aim of the study was to describe the clinical features and short-term prognosis, as well as to assess the 2011 Centers for Disease and Control (CDC) diagnostic criteria, in critically ill patients with m-TSS.

RESULTS:

In total, 102 patients with m-TSS (median age, 18 years; interquartile range, 16-24 years) were admitted to 1 of the participating ICUs. All blood cultures (n = 102) were sterile. Methicillin-sensitive Staphylococcus aureus grew from 92 of 96 vaginal samples. Screening for superantigenic toxin gene sequences was performed for 76 of the 92 vaginal samples positive for S. aureus (83%), and toxic shock syndrome toxin 1 was isolated from 66 strains (87%). At ICU admission, no patient met the 2011 CDC criteria for confirmed m-TSS, and only 53 (52%) fulfilled the criteria for probable m-TSS. Eighty-one patients (79%) were treated with antitoxin antibiotic therapy, and 8 (8%) received intravenous immunoglobulins. Eighty-six (84%) patients required vasopressors, and 21 (21%) tracheal intubation. No patient required limb amputation or died in the ICU.

CONCLUSIONS:

In this large multicenter series of patients included in ICUs for m-TSS, none died or required limb amputation. The CDC criteria should not be used for the clinical diagnosis of m-TSS at ICU admission.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Choque Séptico / Infecções Estafilocócicas Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans Idioma: En Revista: Clin Infect Dis Assunto da revista: DOENCAS TRANSMISSIVEIS Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Choque Séptico / Infecções Estafilocócicas Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Child / Female / Humans Idioma: En Revista: Clin Infect Dis Assunto da revista: DOENCAS TRANSMISSIVEIS Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França