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. 2013 Sep 24;2013(9):CD009020. doi: 10.1002/14651858.CD009020.pub2

Swen 1998.

Clinical features and settings Inclusion criteria: Patients awaiting surgery because of clinically suspected of rotator cuff tears
The clinical diagnosis of rotator cuff tears was based on marked difficulty in initiating abduction of the arm with weakness and limitation of movement Lidocaine was injected below the acromion, if after the injection the strength of the rotator cuff was still decreased; this was considered to indicate rotator cuff tears
Exclusion criteria: Patients with neurologic origins of the weakness
Duration of symptoms: mean 2.3 years (range 0.3 to 10 years)
Previous treatments: Not reported
Care setting: Not reported, probably tertiary or secondary
Participants Place of study: The Netherlands
Period of study: January 1993 to December 1995
Number of participants eligible: 48 participants
Number of participants enrolled IT and RS:
‐ US and arthroscopy or open surgery: 48 participants
Data available for analyses:
‐ US and arthroscopy or open surgery: 48 participants
Age: mean 55 years (range 30 to 76 years)
Male/Female: 28/20
Dominant arm: Not reported
Nature of onset: Not reported
Study design Primary objective: To compare the diagnostic value of US performed by the rheumatologist with that of arthrography by a radiologist for otherwise healthy patients with suspected rotator cuff tears
Study design: Prospective consecutive accuracy cohort study
Language: English
Target condition and reference standard(s) Target conditions: Presence full thickness tears
Reference standard(s): Shoulder arthroscopy and open surgery
Description of technique: Not reported
Criteria for a positive result:
A full‐thickness was diagnosed if free communication was found between the bursal and humeral sides of the cuff
Index and comparator tests Index test(s): US
Description of technique:
Scanner: 7.5 MHz linear array and the 5.0 MHz curved array transducers
Technique: The shoulder was examined in the anterior, lateral, and posterior directions, in both the transverse and the longitudinal planes as described by Van Holsbeeck 1991
Patient position: The patients were seated
For the anterior approach, the patient’s upper arm was visualised in internal rotation, which was achieved by placing the patient’s hand behind the back
Criteria for a positive result:
Full thickness tears: a discontinuity in the rotator cuff extending from the bursal to the humeral side of the rotator cuff
Time from symptoms to index test: Not reported
Time from index test to reference standard: Not reported
Follow‐up Adverse events due to index test(s): Not reported
Adverse events due to reference standard test(s): Not reported
Notes A two‐by‐two table of the ITs and RS was given which tallied with the reported summary data
Table of Methodological Quality
Item Authors' judgement Description
Representative spectrum? 
 All tests Yes Tertiary or secondary care
Participants with suspected of having any rotator cuff tears The study was prospective and recruitment was consecutive
Acceptable reference standard? 
 All tests Yes The reference standard was arthroscopy or open surgery and the target conditions were presence of full thickness tears
Acceptable delay between tests? 
 All tests Unclear The study did not report the time elapsed between the index tests and reference standard
Partial verification avoided? 
 All tests Yes All patients who received the index test went on to receive verification of their disease status using a reference standard
Differential verification avoided? 
 All tests Yes All patients received the same reference standard, regardless of the result of their index test
Incorporation avoided? 
 All tests Yes The index test did not form part of the reference standard
Index test results blinded? 
 All tests Yes The study was prospective and the results of the index tests were interpreted before the reference standard
Reference standard results blinded? 
 All tests Unclear Insufficient information was given to permit judgement
Relevant clinical information? 
 All tests Unclear Not reported
Uninterpretable results reported? 
 All tests Yes The study was prospective, recruitment was consecutive and results were reported for all initially included participants
Withdrawals explained? 
 All tests Yes No participants were excluded from the analysis
Learning curve / training reported of index test? 
 All tests Yes The interpreter of index tests was a rheumatologist with experience in this technique
Learning curve / training reported of reference standard? 
 All tests Unclear Insufficient information was given to permit judgement
Index test criteria for a positive test result reported? 
 All tests Yes The study reported the definition of a positive index test result