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. 2019 Nov 19;2019(11):CD009977. doi: 10.1002/14651858.CD009977.pub2

Summary of findings'. 'Summary of findings table.

Population Adults (> 14 years of age) with suspected acute appendicitis based on history, physical examination, and/or blood tests
Settings Emergency and Radiology Departments in secondary and tertiary care settings
Index test Computed tomography of the abdomen
Reference standard Histological examination of the resected appendix or intraoperative findings in persons who had surgery. Clinical follow‐up for persons who did not have surgery
Target condition Acute appendicitis
Number of studies 64 studies including 71 separate study populations with a total of 10,280 participants ‐ 4583 with and 5697 without acute appendicitis
Methodological concerns The methodological quality was generally poor, particularly with respect to the reference test and the flow and timing domains. For these domains, few studies were at low risk of bias. Differential verification was used in most studies because some of the participants with suspected acute appendicitis did not have surgery. Clinical follow‐up for these participants was inadequate, incomplete, or poorly described in most studies
Results Number of
studies
 (study populations)a
Summary
 sensitivity
 (95% CI) Summary
 specificity
 (95% CI) Prevalence of appendicitis
 (25% percentile
50% percentile
75% percentile)b
Post‐test probability
following a positive
 CT outcome
(95% CI)
Post‐test probability
following a negative
CT outcome
(95% CI)
CT overall 64
 (71) 0.95
 (0.93‐0.96) 0.94
(0.92‐0.95)
0.32
0.43
0.58
0.88 (0.85‐0.90)
0.92 (0.90‐0.94)
 0.96 (0.94‐0.96)
0.02 (0.02‐0.03)
0.04 (0.03‐0.05)
 0.07 (0.05‐0.09)
Unenhanced CT 19
(19)
0.91
 (0.87‐0.93) 0.94
 (0.90‐0.96) 0.32
0.43
0.58
0.87 (0.82‐0.92)
0.92 (0.88‐0.95)
0.95 (0.93‐0.97)
0.04 (0.03‐0.06)
0.07 (0.05‐0.09)
0.12 (0.09‐0.16)
CT with intravenous contrast enhancement 17
(18)
0.96
(0.92‐0.98)
0.93
 (0.90‐0.95) 0.32
0.43
0.58
0.87 (0.82‐0.90)
0.91 (0.88‐0.94)
0.95 (0.93‐0.96)
0.02 (0.01‐0.04)
0.03 (0.02‐0.06)
0.06 (0.03‐0.11)
CT with rectal contrast enhancement 9
(9)
0.97
 (0.93‐0.99) 0.95
 (0.90‐0.98) 0.32
0.43
0.58
0.91 (0.81‐0.96)
0.94 (0.87‐0.97)
0.97 (0.93‐0.99)
0.02 (0.01‐0.04)
0.03 (0.01‐0.06)
0.05 (0.02‐0.10)
CT with oral contrast enhancement 7
(7)
0.89
(0.81‐0.94)
0.94
(0.90‐0.97)
0.32
0.43
0.58
0.88 (0.81‐0.93)
0.92 (0.87‐0.96)
0.96 (0.92‐0.98)
0.05 (0.03‐0.09)
0.08 (0.04‐0.14)
0.14 (0.08‐0.22)
CT with oral and intravenous contrast enhancement 15
(15)
0.96
 (0.93‐0.98) 0.94
 (0.92‐0.96) 0.32
0.43
0.58
0.89 (0.85‐0.92)
0.93 (0.90‐0.95)
0.96 (0.94‐0.97)
0.02 (0.01‐0.03)
0.03 (0.02‐0.05)
0.05 (0.03‐0.09)
Low‐dose CT 7
(8)
0.94
(0.90‐0.97)
0.94
(0.91‐0.96)
0.32
0.43
0.58
0.88 (0.82‐0.92)
0.92 (0.88‐0.95)
0.96 (0.93‐0.97)
0.03 (0.02‐0.05)
0.04 (0.02‐0.08)
0.08 (0.04‐0.13)
Conclusion Sensitivity and specificity of CT for diagnosing acute appendicitis in adults are high. Unenhanced standard‐dose CT appears to have lower sensitivity than standard‐dose CT with intravenous, rectal, or oral+intravenous contrast enhancement. Use of different types of contrast enhancement or no enhancement does not appear to affect specificity. Differences in sensitivity and specificity between low‐dose and standard‐dose CT appear to be negligible. The results of this review should be interpreted with caution for 2 reasons. First, the results are based on studies of low methodological quality. Second, the comparisons between types of contrast enhancement and radiation dose may be unreliable because they are based on indirect comparisons that may be confounded by other factors

CI: confidence interval.
 CT: computed tomography.
 aIn five studies, participants were randomly allocated to two CT‐protocols, and in another study to three CT‐protocols. These protocols differed with respect to contrast enhancement and radiation dose. This generated seven additional study populations, which were included as separate studies in the meta‐analyses.

bThe distribution of the prevalence of appendicitis was roughly similar in the included studies across subgroups. Therefore, to facilitate comparison of post‐test probabilities between subgroups, these probabilities were calculated for the 25%, 50%, and 75% percentiles of prevalence for all 71 study populations.