Your browser doesn't support javascript.
loading
A risk score for prediction of venous thromboembolism in gynecologic cancer: The Thrombogyn score.
Norris, Lucy A; Ward, Mark P; O'Toole, Sharon A; Marchocki, Zibi; Ibrahim, Nadia; Khashan, Ali S; Abu Saadeh, Feras; Gleeson, Noreen.
Afiliação
  • Norris LA; Department of Obstetrics and Gynaecology Trinity College Dublin Trinity Centre for Health Sciences St. James's Hospital Dublin 8 Ireland.
  • Ward MP; Department of Obstetrics and Gynaecology Trinity College Dublin Trinity Centre for Health Sciences St. James's Hospital Dublin 8 Ireland.
  • O'Toole SA; Department of Obstetrics and Gynaecology Trinity College Dublin Trinity Centre for Health Sciences St. James's Hospital Dublin 8 Ireland.
  • Marchocki Z; Department of Obstetrics and Gynaecology Trinity College Dublin Trinity Centre for Health Sciences St. James's Hospital Dublin 8 Ireland.
  • Ibrahim N; Department of Gynaecology Oncology St James's Hospital Dublin 8 Ireland.
  • Khashan AS; Department of Obstetrics and Gynaecology Trinity College Dublin Trinity Centre for Health Sciences St. James's Hospital Dublin 8 Ireland.
  • Abu Saadeh F; Department of Gynaecology Oncology St James's Hospital Dublin 8 Ireland.
  • Gleeson N; School of Public Health University College Cork Cork Ireland.
Res Pract Thromb Haemost ; 4(5): 848-859, 2020 Jul.
Article em En | MEDLINE | ID: mdl-32685894
BACKGROUND: Gynecologic cancers are associated with high rates of venous thromboembolism (VTE), which is exacerbated by pelvic surgery and chemotherapy. OBJECTIVES: The aim of this study was to develop and validate a risk score for VTE in patients with gynecologic cancer and to test the predictive ability of the score following addition of procoagulant biomarker data. PATIENTS AND METHODS: Clinical and laboratory variables were used to develop a risk score for the prediction of VTE in patients with gynecological cancer (n = 616), which was validated in a separate cohort of patients (n = 406). Endogenous thrombin potential and D-dimer levels were determined in a subset (n = 290) of patients and used to produce an extended score in the validation cohort. RESULTS: Multivariable regression analysis identified BMI >30, hemoglobin <11.5 g/dL and chemotherapy as independent predictors of VTE, which formed the Thrombogyn score. Following competing risk regression analysis, subdistribution hazard ratios (SHRs), adjusted for cancer stage, were 8.16 (95% confidence interval [CI], 1.69-43.77) in the high-risk group (score = 2-3) and 4.12 (95% CI, 0.85-20.15) in the intermediate-risk group (score = 1) compared with the low-risk group (score = 0). SHRs for the validation cohort were 6.26 (95% CI, 1.24-31.39) and 3.00 (95% CI, 0.67-13.32), respectively. Cumulative incidence of VTE in the validation cohort high-risk group was 10.34% (95% CI, 6.51-16.41) per women-years compared with 1.06% (95% CI, 0.26-4.26) in the low-risk group. Using the extended Thrombogyn score, adjusted SHRs were 16.83 (95% CI, 4.20-67.37) in the high-risk group with a cumulative incidence of 21.15% (95% CI, 10.32-45.24). External validation of the score is required. CONCLUSIONS: The Thrombogyn score identifies patients with gynecologic cancer at high and low risk of VTE. Addition of biomarker data improves the predictive power of the score.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Res Pract Thromb Haemost Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Res Pract Thromb Haemost Ano de publicação: 2020 Tipo de documento: Article