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https://doi.org/10.1007/s00423-020-01884-1
Abstract
Purpose To compare the routine vs. selective use of computed tomography (CT) in patients presenting with non-traumatic acute
abdominal pain (AAP) to a surgical service.
Methods We conducted a systematic review of literature and meta-analysis of outcomes according to PRISMA statement
standards to compare the routine vs. selective use of CT in adult patients presenting with non-traumatic AAP.
Results Analysis of 722 patients from 4 randomised controlled trials showed no difference between the routine CT and selective
CT groups in terms of proportion of correct diagnoses (OR 1.36,95% CI 0.89, 2.07, P = 0.15), mortality (RD 0.03, 95% CI −
0.08, 0.02, P = 0.27] and length of hospital stay (LOS) [MD − 0.26, 95% CI − 2.07, 1.55, P = 0.78).
Conclusions The routine use of CT does not improve the proportion of correct diagnoses and mortality compared to selective use
of CT in adult patients with non-traumatic AAP. The available evidence regarding the influence of routine CT on LOS may be
subject to type 2 error. These findings, however, may not apply to the elderly patient with AAP and further studies are required.
Eligibility criteria The title and abstract of articles identified from the literature
searches were assessed independently by two authors (Shahab
We included RCTs comparing routine vs. selective use of CT in H, ML). The full texts of relevant reports were retrieved, and
adult patients of any gender presenting to hospital due to non- those articles that met the eligibility criteria of our review were
traumatic AAP. All patients who presented with AAP and selected. Any discrepancies in study selection were resolved
underwent CT scan or other imaging modalities while they by discussion between the authors. An independent third au-
were in emergency department or any other wards were con- thor (Shahin H) was consulted in the event of disagreement.
sidered eligible. The patients who had CT scan in emergency
department and were discharged due to normal findings were Data collection
also considered eligible. The exclusion criteria were age <
18 years, pregnancy, acute abdominal trauma, contraindication We created an electronic data extraction spreadsheet which
to iodinated contrast media and need for immediate surgery. was pilot-tested in randomly selected articles and adjusted
accordingly. This included study-related data (first author,
Intervention of interest year of publication, country of origin of the corresponding
author, journal, study design and sample size, and clinical
Routine CT was defined as CT within 24 h of presentation to condition of the study participants), baseline demographic
hospital with AAP regardless of clinical assessment. and clinical information of the study populations (age, gender,
Presentation to hospital was defined as either registration in diagnosis) and primary (correct diagnosis) and secondary
emergency department in case of direct presentation to emer- (mortality, LOS) outcomes. Data collection was performed
gency department or registration in surgical assessment unit in independently by two authors (Shahab H, ML), and disagree-
case of referral from community. ments were resolved by discussion. If no agreement could be
reached, a third author (Shahin H) was consulted.
Comparison of interest
Methodological quality and risk of bias assessment
Selective CT was the comparison of interest, defined as CT at
the discretion of physician based on clinical assessment. Any Two authors (Shahab H, ML) independently assessed the meth-
patient with abdominal pain allocated to this group would odological quality and risk of bias of the included articles using the
have initial plain radiographs or ultrasound, and, if necessary Cochrane tool for assessing the risk of bias of randomized con-
on clinical grounds as recognised by the on-call general sur- trolled trials [14]. The Cochrane tool assesses domains including
geon, CT within or after 24 h, or not at all. selection, performance, detection, attrition, reporting and other
sources of bias and, for each individual domain, classifies studies
Outcome measures into low, unclear and high risk of bias. Disagreements were re-
solved by discussion between the reviewers. If no agreement could
The proportion of correct diagnoses was the primary outcome be reached, a third author acted as an adjudicator.
measure. The final diagnosis established at maximum follow
up was used as reference for correct diagnosis. The secondary Data synthesis and statistical analyses
outcome measures included mortality and LOS.
For dichotomous outcome variables, we calculated the odds ratio
Literature search strategy (OR) as the summary measure. We calculated the risk difference
(RD) when more than half of the studies had zero events in both
Two authors independently (Shahab H, ML) searched the fol- groups. For continuous parameters, we calculated the mean differ-
lowing electronic databases: MEDLINE, EMBASE, ence (MD) between the two groups. Individual patient was used as
CINAHL and the Cochrane Central Register of Controlled the unit of analysis. We used intention-to-treat data from the indi-
Trials (CENTRAL). The last search was run on 06 vidual clinical studies. We used the Review Manager 5.3 software
May 2019. Thesaurus headings, search operators and limits for data synthesis [14]. Random or fixed-effects modelling was
Langenbecks Arch Surg
1 Routine: TI,AB,KW
2 Routine near 2 ct: TI,AB,KW
3 Routine near 2 computed tomography: TI,AB,KW
4 Mandatory: TI,AB,KW
5 No. 1 OR no. 2 OR no. 3 OR no. 4
6 Selective: TI,AB,KW
7 Selective near 2 ct: TI,AB,KW
8 Selective near 2 computed tomography: TI,AB,KW
9 No. 6 OR no. 7 OR no. 8
10 MeSH descriptor: [computed tomography scanner, x-ray] explode all trees
11 Computed tomography: TI,AB,KW
12 ct: TI,AB,KW
13 No. 10 OR no. 11 OR no. 12
14 abdom* near 2 pain
15 MeSH descriptor: [acute abdomen] explode all trees
16 MeSH descriptor: [abdominal pain] explode all trees
17 No. 14 OR no. 15 OR no .16
18 No. 5 AND no. 9 AND no. 13 AND no. 17
a
This search strategy was adopted for following databases: MEDLINE, EMBASE, CINAHL and the Cochrane
Central Register of Controlled Trials (CENTRAL)
used as appropriate for analysis. We report the results in a Forest databases, 69 articles were not relevant to the topic of this
plot with 95% confidence intervals (CIs). Heterogeneity among study and were excluded directly. The remaining 7 studies
the studies was assessed using the Cochran Q test (χ2). We quan- were relevant to the topic of this study and, after assessing
tified inconsistency by calculating I2 and interpreted it using the their full texts, 3 more were excluded; two were additional
following guide: 0 to 50% may represent low heterogeneity, 50 to analyses of a previously published RCT, and one was exclud-
75% may represent moderate heterogeneity and 75 to 100% may ed, as the comparison group in the study did not undergo
represent high heterogeneity. selective CT. Therefore, 4 RCT studies [15–18] enrolling
722 patients were selected for this review. Overall, 369 pa-
Sensitivity analyses tients were included in the routine CT group and 353 patients
were included in the selective CT group. The included popu-
To explore potential sources of heterogeneity and assess the ro- lations in the individual studies were comparable by baseline
bustness of our results, additional analyses were conducted for characteristics. The literature search flow chart (PRISMA for-
outcomes that were reported by at least four studies. For each mat), baseline characteristics of the included studies and base-
outcome, we repeated the primary analysis using the random- line characteristics and final diagnoses of the included popu-
effects and fixed-effect model. In addition, we calculated the risk lation are shown in Fig. 1; Tables 2 and 3, respectively.
ratio (RR) and risk difference (RD) for each dichotomous vari-
able. We assessed the effect of each study on the overall effect Description of included studies
size and heterogeneity by repeating the analysis after removing
one study at a time. In order assess the consistency of our results, Lehtimäki 2013 [15]: This was an RCT from Finland that
we removed the studies including patients with right lower quad- included 254 patients presenting to the surgical emergency
rant pain or non-specific abdominal pain only. department with acute abdominal pain of unknown cause.
Patients were randomised to routine CT or selective CT.
Patients in routine CT group underwent abdominopelvic CT
Results imaging within 24 h of presentation to the emergency depart-
ment. Patients in selective CT group underwent initial diag-
Results of the search nostic imaging such as plain radiographs or ultrasound scans
and if necessary on clinical grounds CT scan.
Searches of electronic databases identified 76 articles. Among Sala 2007 [16]: This was an RCT from UK that included
the studies that were identified through search of electronic 198 patients presenting to the on-call general surgeons with a
Langenbecks Arch Surg
Outcome synthesis
Study Journal Design Clinical Intervention Comparison Definition Definition of Sample size Methodological
presentation of routine selective CT quality
CT
Total Routine Selective
CT CT
Ng 2002 BMJ RCT Patients with Routine CT Standard Early CT CT requested 118 55 63 Moderate
acute scan practice within at
abdominal with 24 h of discretion
pain selective admis- of
presenting CT sion physician
to hospital imaging based on
clinical
assess-
ment
Lee 2007 Academic RCT Patients with Routine CT Standard Early CT CT requested 152 72 80 Moderate
emer- acute right scan practice within at
gency lower with 24 h of discretion
medi- quadrant selective admis- of
cine pain CT sion physician
presenting imaging based on
to hospital clinical
assess-
ment
Lehtmiki European RCT Patients with Routine CT Standard Early CT CT requested 254 143 111 Moderate
2013 radiolo- acute scan practice within at
gy abdominal with 24 h of discretion
pain selective admis- of
presenting CT sion physician
to hospital imaging based on
clinical
assess-
ment
Sala 2007 Clinical RCT Patients with Routine CT Standard Early CT CT requested 198 99 99 Moderate
radiolo- acute scan practice within at
gy abdominal with 24 h of discretion
pain selective admis- of
presenting CT sion physician
to hospital imaging based on
clinical
assess-
ment
Mean/median age (SD/range) 53 (17) 54 (17) 59 (42–73) 57 (43–75) 35.1 (14.5) 33.3 (12.6) NR NR
Male gender 68/143 53/111 42/99 30/99 24/72 31/80 NR NR
Female gender 75/143 58/111 57/99 69/99 48/72 49/80 NR NR
Final diagnosis:
Acute appendicitis 30/143 20/111 10/99 7/99 39/72 38/80 6/55 3/63
Acute diverticulitis 22/143 14/111 12/99 12/99 NR NR 10/55 12/63
Acute pancreatitis 13/143 10/111 4/99 6/99 NR NR 4/55 4/63
Biliary disease 9/143 10/111 5/99 1/99 NR NR 4/55 7/63
Bowel obstruction 10/143 4/111 8/99 5/99 NR NR 5/55 4/63
Urological disease 6/143 7/111 3/99 6/99 NR NR 1/55 1/63
Non-specific abdominal pain 27/143 33/111 20/99 18/99 NR NR 10/55 8/63
Inflammatory bowel disease 3/143 3/111 NR NR NR NR NR NR
Colitis NR NR 4/99 4/99 NR NR NR NR
Gastroenteritis NR NR 1/99 2/99 NR NR 1/55 2/63
Malignancy 3/143 1/111 8/99 14/99 NR NR 1/55 1/63
Perforated viscus NR NR 0/99 2/99 NR NR 1/55 3/63
Vascular disease 4/143 0/111 1/99 0/99 NR NR 0/55 1/63
Thoracic disease 2/143 3/111 1/99 0/99 NR NR 2/55 2/63
Gynaecological disease NR NR 4/99 2/99 NR NR 1/55 1/63
The reported outcomes of our review should be viewed and conclusions for these subgroups. The number of eligible stud-
interpreted in the context of inherent limitations. The sample ies for this review was less than 10, not allowing for formal
size of this study was adequate for robust conclusions regard- assessment of publication bias as planned in our protocol. The
ing the correct diagnosis rate and mortality; however, the sam- available data was not adequate to synthesise some clinically
ple size was not adequate for LOS, subjecting our results to important outcomes such as non-therapeutic surgery and
type 2 error for this outcome. One of the included studies missed diagnoses. Moreover, the available data from the in-
included patients with acute right lower quadrant pain and cluded studies was not adequate to determine what proportion
excluded patients with other forms of acute abdominal pain, of patients in the selective group already had a correct diag-
subjecting our results to potential selection bias. The included nosis by other imaging. Finally, the available data did not
studies had some differences in their design in terms of includ- allow for subgroup analysis based on the age of the patients;
ed population (one study included patients with right-sided therefore, we were not able to define a subgroup of patients
abdominal pain and one study included patients with non- who may benefit from routine use of CT.
specific abdominal pain) and time frame for performing CT
scan (one study performed CT scan within 1 h of presentation
and other 3 RCTs within 24 h of presentation). All of these can Conclusions
potentially subject the results of this study to bias. Moreover,
we excluded cases that were pregnant and cases with acute The best available evidence suggests that routine use of CT
abdominal trauma, contraindication to iodinated contrast me- does not improve the proportion of correct diagnoses and
dia and need for immediate surgery without delay; therefore, mortality compared to selective use of CT in adult patients
the results of current study cannot be used for definite with non-traumatic AAP. The available evidence regarding
Langenbecks Arch Surg
a) Correct diagnosis
b) Mortality
Fig. 3 Forest plots of the comparisons of outcomes between routine CT death, M-H Mantel-Haenszel methods, random random-effects model,
and selective CT groups. a Correct diagnosis: event = correct diagnosis, weight: the amount of information that each study contributes. c Length
M-H Mantel-Haenszel methods, fixed fixed-effect model, weight: the of hospital stay: IV Inverse variance; random random-effects model;
amount of information that each study contributes. b Mortality: event = weight: the amount of information that each study contributes
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