Prognostic models in acute pulmonary embolism: a systematic review and meta-analysis

被引:155
作者
Elias, Antoine [1 ,2 ]
Mallett, Susan [3 ]
Daoud-Elias, Marie [1 ]
Poggi, Jean-Noel [1 ]
Clarke, Mike [4 ]
机构
[1] Toulon La Seyne Hosp Ctr, St Musse Hosp, Dept Vasc Med, Toulon, France
[2] Univ Oxford, DPhil Programme Evidence Based Healthcare, Oxford, England
[3] Univ Oxford, Dept Primary Care Hlth Sci, Oxford, England
[4] Queens Univ Belfast, Northern Ireland Network Trials Methodol Res, Belfast, Antrim, North Ireland
关键词
LOW-RISK PATIENTS; HEMODYNAMICALLY STABLE PATIENTS; RIGHT-VENTRICULAR DYSFUNCTION; HELICAL COMPUTED-TOMOGRAPHY; CHARLSON COMORBIDITY INDEX; CLINICAL-PREDICTION RULES; OF-HOSPITAL TREATMENT; ACID-BINDING PROTEIN; DEEP-VEIN THROMBOSIS; SHORT-TERM MORTALITY;
D O I
10.1136/bmjopen-2015-010324
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To review the evidence for existing prognostic models in acute pulmonary embolism (PE) and determine how valid and useful they are for predicting patient outcomes. Design: Systematic review and meta-analysis. Data sources: OVID MEDLINE and EMBASE, and The Cochrane Library from inception to July 2014, and sources of grey literature. Eligibility criteria: Studies aiming at constructing, validating, updating or studying the impact of prognostic models to predict all-cause death, PE-related death or venous thromboembolic events up to a 3-month follow-up in patients with an acute symptomatic PE. Data extraction: Study characteristics and study quality using prognostic criteria. Studies were selected and data extracted by 2 reviewers. Data analysis: Summary estimates (95% CI) for proportion of risk groups and event rates within risk groups, and accuracy. Results: We included 71 studies (44 298 patients). Among them, 17 were model construction studies specific to PE prognosis. The most validated models were the PE Severity Index (PESI) and its simplified version (sPESI). The overall 30-day mortality rate was 2.3% (1.7% to 2.9%) in the low-risk group and 11.4% (9.9% to 13.1%) in the high-risk group for PESI (9 studies), and 1.5% (0.9% to 2.5%) in the low-risk group and 10.7% (8.8% to12.9%) in the high-risk group for sPESI (11 studies). PESI has proved clinically useful in an impact study. Shifting the cut-off or using novel and updated models specifically developed for normotensive PE improves the ability for identifying patients at lower risk for early death or adverse outcome (0.5-1%) and those at higher risk (up to 20-29% of event rate). Conclusions: We provide evidence-based information about the validity and utility of the existing prognostic models in acute PE that may be helpful for identifying patients at low risk. Novel models seem attractive for the high-risk normotensive PE but need to be externally validated then be assessed in impact studies.
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