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. 2020 Dec 21;18(12):1005–1018. doi: 10.18502/ijrm.v18i12.8022

Table 2.

JBI critical appraisal checklist applied to the included studies


Author name/year (Ref) Q1 Q2 Q3 Q4 Q5 Q6 Q7 Q8 Q9 Q10 Overall quality
Case series
Liu et al. , 2020-a (27) Yes Yes Yes Yes Yes No Yes N/A No Yes 7/10
Liu et al. , 2020-c (28) Yes Yes Yes Yes N/A Yes Yes Yes N/A Yes 8/10
Zhu et al. , 2020 (31) Yes Yes Yes Yes No Yes Yes Yes No Yes 8/10
Yu et al. , 2020 (30) Yes Yes Yes Yes No No Yes Yes N/A Yes 7/10
Khan et al. , 2020 (25) Yes Yes N/A Yes No Yes N/A No No Yes 5/10
Chen et al. , 2020-a (13) Yes Yes N/A Yes No Yes N/A Yes No Yes 6/10
Chen et al. , 2020-b (22) Yes Yes Yes Yes Yes N/A N/A Yes No Yes 7/10
Chen et al. , 2020-c (14) Yes Yes Yes Yes No No Yes Yes No Yes 7/10
Case-control
Liu et al. , 2020-b (26) Yes Yes Yes Yes Yes Yes N/A Yes Yes No 8/10
Li et al. , 2020 (24) Yes Yes Yes Yes No Yes N/A N/A Yes No 6/10
Case series design questions: Q1. Were there clear criteria for inclusion in the case series? Q2. Was the condition measured in a standard, reliable way for all participants included in the case series? Q3. Were valid methods used for identification of the condition for all participants included in the case series? Q4. Did the case series have consecutive inclusion of participants? Q5. Did the case series have complete inclusion of participants? Q6. Was there clear reporting of the demographics of the participants in the study? Q7. Was there clear reporting of the clinical information of the participants? Q8. Were the outcomes or follow-up results of cases reported? Q9. Was there clear reporting of the presenting site(s)/clinic(s) demographic information? Q10. Was the statistical analysis appropriate? Case-control design questions: Q1. Were the groups comparable other than the presence of disease in cases of the absence of disease in controls? Q2. Were cases and controls matched appropriately? Q3. Were the same criteria used for the identification of cases and controls? Q4. Was exposure measured in a standard, valid, and reliable way? Q5. Was exposure measured in the same way for cases and controls? Q6. Were confounding factors identified? Q7. Were strategies to deal with confounding factors stated? Q8. Were outcomes assessed in a standard, valid, and reliable way for cases and controls? Q9. Was the exposure period of interest long enough to be meaningful? Q10. Was an appropriate statistical analysis used?