Evidence map›Paper›PMID 26349907›Full record

SynthesisBMJ (Clinical research ed.)2015

Diagnostic prediction models for suspected pulmonary embolism: systematic review and independent external validation in primary care.

Janneke M T Hendriksen, Geert-Jan Geersing, Wim A M Lucassen, Petra M G Erkens, Henri E J H Stoffers, Henk C P M van Weert, Harry R Büller, Arno W Hoes, Karel G M Moons

Abstract readSystematic ReviewValidation Study
In one paragraph

Synthesis in BMJ (Clinical research ed.), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 4 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

42 citing papers in PubMed, 4 syntheses or guidelines pooled it.

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  4. Fatal recurrent VTE after anticoagulant treatment for unprovoked VTE: a systematic review.European respiratory review : an official journal of the European Respiratory Society · 2018
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  16. Excluding pregnancy-associated deep vein thrombosis with whole-leg ultrasound.Research and practice in thrombosis and haemostasis · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Janneke M T HendriksenDepartment of Epidemiology, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, 3508 GA Utrecht, Netherlands j.m.t.hendriksen-9@umcutrecht.nl.
Geert-Jan GeersingDepartment of Epidemiology, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, 3508 GA Utrecht, Netherlands.
Wim A M LucassenDepartment of General Practice, Academic Medical Center, Amsterdam, Netherlands.
Petra M G ErkensDepartment of Family Medicine, CAHPRI School for Public Health and Primary Care, Maastricht University, Maastricht, Netherlands.
Henri E J H StoffersDepartment of Family Medicine, CAHPRI School for Public Health and Primary Care, Maastricht University, Maastricht, Netherlands.
Henk C P M van WeertDepartment of General Practice, Academic Medical Center, Amsterdam, Netherlands.
Harry R BüllerDepartment of Vascular Medicine, Academic Medical Center, Amsterdam, Netherlands.
Arno W HoesDepartment of Epidemiology, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, 3508 GA Utrecht, Netherlands.
Karel G M MoonsDepartment of Epidemiology, Julius Center for Health Sciences and Primary Care, University Medical Center Utrecht, 3508 GA Utrecht, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo validate all diagnostic prediction models for ruling out pulmonary embolism that are easily applicable in primary care.

designSystematic review followed by independent external validation study to assess transportability of retrieved models to primary care medicine.

setting300 general practices in the Netherlands.

participantsIndividual patient dataset of 598 patients with suspected acute pulmonary embolism in primary care.

main outcome measuresDiscriminative ability of all models retrieved by systematic literature search, assessed by calculation and comparison of C statistics. After stratification into groups with high and low probability of pulmonary embolism according to pre-specified model cut-offs combined with qualitative D-dimer test, sensitivity, specificity, efficiency (overall proportion of patients with low probability of pulmonary embolism), and failure rate (proportion of pulmonary embolism cases in group of patients with low probability) were calculated for all models.

resultsTen published prediction models for the diagnosis of pulmonary embolism were found. Five of these models could be validated in the primary care dataset: the original Wells, modified Wells, simplified Wells, revised Geneva, and simplified revised Geneva models. Discriminative ability was comparable for all models (range of C statistic 0.75-0.80). Sensitivity ranged from 88% (simplified revised Geneva) to 96% (simplified Wells) and specificity from 48% (revised Geneva) to 53% (simplified revised Geneva). Efficiency of all models was between 43% and 48%. Differences were observed between failure rates, especially between the simplified Wells and the simplified revised Geneva models (failure rates 1.2% (95% confidence interval 0.2% to 3.3%) and 3.1% (1.4% to 5.9%), respectively; absolute difference -1.98% (-3.33% to -0.74%)). Irrespective of the diagnostic prediction model used, three patients were incorrectly classified as having low probability of pulmonary embolism; pulmonary embolism was diagnosed only after referral to secondary care.

conclusionsFive diagnostic pulmonary embolism prediction models that are easily applicable in primary care were validated in this setting. Whereas efficiency was comparable for all rules, the Wells rules gave the best performance in terms of lower failure rates.

Indexed as

Decision Support TechniquesFemaleFibrin Fibrinogen Degradation ProductsHumansMaleMiddle AgedPrimary Health CarePulmonary EmbolismRisk FactorsSensitivity and SpecificityFibrin Fibrinogen Degradation Productsfibrin fragment D

Identifiers

PMID26349907
PMCPMC4561760

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.