PT  - JOURNAL ARTICLE
AU  - Caliesch, Rahel
AU  - Sattelmayer, Martin
AU  - Reichenbach, Stephan
AU  - Zwahlen, Marcel
AU  - Hilfiker, Roger
TI  - Diagnostic accuracy of clinical tests for cam or pincer morphology in individuals with suspected FAI syndrome: a systematic review
AID  - 10.1136/bmjsem-2020-000772
DP  - 2020 Apr 01
TA  - BMJ Open Sport & Exercise Medicine
PG  - e000772
VI  - 6
IP  - 1
4099  - http://bmjopensem.bmj.com/content/6/1/e000772.short
4100  - http://bmjopensem.bmj.com/content/6/1/e000772.full
SO  - BMJ OPEN SP EX MED2020 Apr 01; 6
AB  - Objectives To determine the diagnostic accuracy of clinical tests for cam or pincer morphology in individuals with suspected femoroacetabular impingement (FAI) syndrome and to evaluate their clinical utility.Design A systematic review of studies investigating the diagnostic accuracy of clinical tests for cam and pincer morphology.Data sources PubMed, Embase, CINAHL and SPORTDiscus.Eligibility criteria for selecting studies Studies investigating the diagnostic accuracy of clinical tests for cam, pincer or mixed morphology in symptomatic patients. Patients had to undergo an index test and a reference test able to identify cam or pincer morphology. Study results have to allow the calculation of true or false positives and/or negatives to calculate sensitivity, specificity, likelihood ratios (LR) and post-test probabilities.Results Eight studies were included, investigating 17 tests and two test combinations. The studies reported a low specificity for all tests, ranging from 0.11 to 0.56. Sensitivity ranged from 0.11 to 1.00, with high sensitivities for the flexion-adduction-internal rotation (FADIR), foot progression angle walking (FPAW) and maximal squat tests. We estimated that negative test results on all of these three tests would result in a negative LR of 0.15. However, we judged the studies to provide low-quality evidence.Conclusion There is low-quality evidence that negative test results reduce the post-test probability of cam or mixed morphologies and that consecutive testing with the FADIR, FPAW and maximal squat tests might be used as a clinical test combination. We would not recommend their use to confirm the diagnosis of FAI syndrome.PROSPERO registration number CRD42018079116.