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Desmopressin for prevention of bleeding for thrombocytopenic, critically ill patients undergoing invasive procedures: A randomised, double-blind, placebo-controlled feasibility trial.
Desborough, Michael J R; Laing, Emma; Kounali, Daphne; Mora, Ana; Hodge, Renate; Martin, Siobhan; Thomas, Helen; Hudson, Cara; Parsons, Joseph; Shah, Akshay; Hutton, Paula; Parke, Tim; Wise, Matthew P; Morgan, Matthew; McKechnie, Stuart; Stanworth, Simon J.
Afiliação
  • Desborough MJR; Department of Clinical Haematology Oxford University Hospitals NHS Foundation Trust Oxford UK.
  • Laing E; Radcliffe Department of Medicine University of Oxford Oxford UK.
  • Kounali D; NHS Blood and Transplant John Radcliffe Hospital Oxford UK.
  • Mora A; NHS Blood and Transplant Clinical Trials Unit Cambridge UK.
  • Hodge R; NHS Blood and Transplant Clinical Trials Unit Bristol UK.
  • Martin S; NHS Blood and Transplant Clinical Trials Unit Cambridge UK.
  • Thomas H; NHS Blood and Transplant Clinical Trials Unit Cambridge UK.
  • Hudson C; NHS Blood and Transplant Clinical Trials Unit Cambridge UK.
  • Parsons J; NHS Blood and Transplant Clinical Trials Unit Bristol UK.
  • Shah A; NHS Blood and Transplant Clinical Trials Unit Bristol UK.
  • Hutton P; NHS Blood and Transplant Clinical Trials Unit Bristol UK.
  • Parke T; Department of Critical Care Oxford University Hospitals NHS Foundation Trust Oxford UK.
  • Wise MP; Nuffield Department of Clinical Neurosciences University of Oxford Oxford UK.
  • Morgan M; Department of Critical Care Oxford University Hospitals NHS Foundation Trust Oxford UK.
  • McKechnie S; Department of Critical Care Royal Berkshire Hospital Reading UK.
  • Stanworth SJ; Department of Critical Care University Hospital of Wales Cardiff UK.
EJHaem ; 5(4): 772-777, 2024 Aug.
Article em En | MEDLINE | ID: mdl-39157598
ABSTRACT
Thrombocytopenic patients have an increased risk of bleeding when undergoing invasive procedures. In a multicentre, phase II, blinded, randomised, controlled feasibility trial, critically ill patients with platelet count 100 × 109/L or less were randomised 11 to intravenous desmopressin (0.3 µg/kg) or placebo before an invasive procedure. Forty-three participants (18.8% of those eligible) were recruited, with 41 eligible for analysis. Post-procedure bleeding occurred in one of 22 (4.5%) in the placebo arm and zero of 19 in the desmopressin arm. Despite liberal inclusion criteria, there were significant feasibility challenges recruiting patients in the critical care setting prior to invasive procedures.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: EJHaem Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: EJHaem Ano de publicação: 2024 Tipo de documento: Article País de publicação: Estados Unidos