A clinical prediction score for upper extremity deep venous thrombosis

被引:80
作者
Constans, Joel [1 ,2 ]
Salmi, Louis-Rachid [3 ,4 ]
Sevestre-Pietri, Marie-Antoinette [5 ]
Perusat, Sophie [1 ,2 ]
Nguon, Monika [1 ,2 ]
Degeilh, Maryse [5 ]
Labarere, Jose [6 ]
Gattolliat, Olivier [5 ]
Boulon, Carine [1 ,2 ]
Laroche, Jean-Pierre [5 ]
Le Roux, Philippe [5 ]
Pichot, Olivier [5 ]
Qu, Isabelle [5 ]
Conri, Claude [1 ,2 ]
Bosson, Jean-Luc [6 ]
机构
[1] Univ Bordeaux 2, Vasc & Internal Med Unit, F-33076 Bordeaux, France
[2] CHU Bordeaux, Bordeaux, France
[3] Univ Segalen Bordeaux 2, Inst Sante Publ Epidemiol & Dev, Bordeaux, France
[4] CHU Bordeaux, Serv Informat Med, Bordeaux, France
[5] OPTIMEV Study Sci Council, Grenoble, France
[6] CHU Grenoble, Clin Invest Ctr, F-38043 Grenoble, France
关键词
venous thrombosis; upper extremity deep vein thrombosis; clinical prediction;
D O I
10.1160/TH07-08-0485
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It was the objective of this study to design a clinical prediction score for the diagnosis of upper extremity deep venous thrombosis (UEDVT). A score was built by multivariate logistic regression in a sample of patients hospitalized for suspicion of UEDVT (derivation sample). It was validated in a second sample in the same university hospital, then in a sample from the multicenter OPTIMEV study that included both outpatients and inpatients. In these three samples, UEDVT diagnosis was objectively confirmed by ultrasound. The derivation sample included 140 patients among whom 50 had confirmed UEDVT, the validation sample included 103 patients among whom 46 had UEDVT and the OPTIMEV sample included 214 patients among whom 65 had UEDVT. The clinical score identified a combination of four items (venous material, localized pain, unilateral pitting edema and other diagnosis as plausible). One point was attributed to each item (positive for the first 3 and negative for the other diagnosis). A score of -1 or 0 characterized low probability patients, a score of I identified intermediate probability patients, and a score of 2 or 3 identified patients with high probability. Low probability score identified a prevalence of UEDVT of 12,9 and 13%, respectively, in the derivation, validation and OPTIMEV samples. High probability score identified a prevalence of UEDVT of 70, 64 and 69% respectively. In conclusion we propose a simple score to calculate clinical probability of UEDVT. This score might be a useful test in clinical trials as well as in clinical practice.
引用
收藏
页码:202 / 207
页数:6
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