Ha 1994.
Study characteristics | |||
Patient sampling |
Primary objectives: to compare fat‐suppressed T1‐w MRI with conventional MR images for diagnosis of endometriosis, focusing on detectability of peritoneal implants Study population: patients with suspected endometriosis Selection criteria: not specified Study design: prospective, observational; non‐consecutive enrolment |
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Patient characteristics and setting |
Clinical presentation: not specified Age: mean 35 years, range 20 to 52 years Number enrolled: 31 women Number available for analysis: 31 women Setting: University Hospital, Catholic University Medical College Place of study: Seoul, Korea Period of study: 12‐month period, dates not specified Language: English |
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Index tests |
Index test:MRI 2 types (T1/T2‐w MRI; fat‐suppressed T1‐w MRI) Description of positive case definition by index test as reported: diagnostic criteria as previously published (referenced to Arrive et al.,1989; Togashi et al., 1991; Nishimura ey al., 1987; Zawin et al., 1989) and described; pelvic adhesions excluded from analysis because fat‐suppressed images were not useful in detecting fibrotic lesions; conventional and fat‐suppressed images evaluated separately in random order Examiners: images reviewed independently by 2 radiologists; level of expertise not reported. Observer knew only that patients had suspected endometriosis Interobserver variability: not provided; consensus findings used if interpretations differed |
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Target condition and reference standard(s) |
Target condition: pelvic endometriosis Prevalence of target condition in the sample: pelvic endometriosis 29/31 (94%): rASRM stage I 7/29 (24%), stage II 7/29 (24%), stage Ill 4/29 (14%), stage IV 11/29 (38%) Reference standard: laparoscopy 31/31 (100%) Description of positive case definition by reference test as reported: endometriosis diagnosed on the basis of visualisation of pelvic cavity at laparoscopy as endometrial cysts or peritoneal implants (rASRM classification); anatomical sites of involvement divided into 6 categories: right or left ovary, right or left uterine surface or uterosacral ligament, cul‐de sac and other anatomic sites (most often, rectum) Examiners: numbers or level of expertise of surgeons not reported; unclear whether blinded to results of the index test |
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Flow and timing |
Time interval between index test and reference standard: within 2 weeks Withdrawals: none reported |
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Comparative | |||
Key conclusions by the authors | Results show fat‐suppressed MR imaging as more accurate in the diagnosis of pelvic endometriosis and better than conventional MR imaging for predicting severity of disease | ||
Conflict of interests | Not reported | ||
Notes | Reported accuracy estimates for MRI, both conventional and fat‐suppressed, for diagnosis of pelvic endometriosis not confirmed Accuracy estimates for specific sites of endometriosis as well as for peritoneal and ovarian disease not included in this review as calculated per number of lesions rather than number of patients Data on accuracy of MRI in predicting severity of disease also presented – not included in this review |
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Methodological quality | |||
Item | Authors' judgement | Risk of bias | Applicability concerns |
DOMAIN 1: Patient Selection | |||
Was a consecutive or random sample of patients enrolled? | No | ||
Did the study avoid inappropriate exclusions? | Unclear | ||
Was a 'two‐gate' design avoided? | Yes | ||
High | Low | ||
DOMAIN 2: Index Test Any test | |||
Were the index test results interpreted without knowledge of the results of the reference standard? | Yes | ||
Did the study provide a clear pre‐specified definition of what was considered to be a “positive” result of index test? | Yes | ||
Was the index test performed by a single operator or interpreted by consensus in a joint session? | Yes | ||
Were the same clinical data available when the index test results were interpreted as would be available when the test is used in practice? | Yes | ||
Low | Low | ||
DOMAIN 3: Reference Standard | |||
Is the reference standards likely to correctly classify the target condition? | Unclear | ||
Were the reference standard results interpreted without knowledge of the results of the index tests? | Unclear | ||
Unclear | Low | ||
DOMAIN 4: Flow and Timing | |||
Was there an appropriate interval between index test and reference standard? | Yes | ||
Did all patients receive the same reference standard? | Yes | ||
Were all patients included in the analysis? | Yes | ||
Low |