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. 2019 Aug 1;2019(8):CD011871. doi: 10.1002/14651858.CD011871.pub2

Chandrasiri 2010.

Study characteristics
Patient sampling Study assessment based only on the abstract. Cross‐sectional design with unclear sampling method.
Patient characteristics and setting Sample size: 7 cases, 52 non‐cases (total 59)
Clinical presentation: NR ("suspected of leptospirosis")
Risk factors: NR
Region: Sri Lanka
Clinical setting: teaching hospital
Prevalence of leptospirosis: 11.8%
DPO of disease at moment of enrolment: NR
Index tests Index test: PCR
Target gene: G1 and G2 primers (original reference unknown)
Timing of sample collection at # DPO of disease: NR
Cut‐off value: not applicable
Patient material: blood product (not specified which)
Company/brand: inhouse
Frozen samples: NR
Target condition and reference standard(s) Target condition: leptospirosis
Case definition: MAT positive
Timing of sample collection at # DPO of disease (MAT): NR
Single or paired sera (MAT): single
Cut‐off value (MAT): ≥ 1:800
Patient material (MAT): blood product, most likely serum
Flow and timing All people were included in the analysis.
Comparative  
Notes This study was reported as a meeting abstract.
Methodological quality
Item Authors' judgement Risk of bias Applicability concerns
DOMAIN 1: Patient Selection
Was a consecutive or random sample of patients enrolled? Unclear    
Was a 2‐gate case‐control design avoided? Yes    
Did the study avoid inappropriate exclusions? Unclear    
    Unclear Unclear
DOMAIN 2: Index Test PCR
Were the index test results interpreted without knowledge of the results of the reference standard? Unclear    
If a threshold was used, was it pre‐specified? Yes    
Does the index test, its conduct and interpretation, match the review question? Unclear    
Is the execution of the test reported in such detail that reproduction is possible? No    
    Unclear High
DOMAIN 3: Reference Standard
Is this the type of test that is likely to correctly classify the target condition? No    
Did the execution of the MAT include paired samples? No    
Were the reference standard results interpreted without knowledge of the results of the index tests? Unclear    
Does the case definition match the review question? Yes    
Is the execution of the test reported in such detail that reproduction is possible? No    
    High High
DOMAIN 4: Flow and Timing
Was there an appropriate interval between index test and reference standard? Unclear    
Did all patients receive a reference standard? Yes    
Did all patients receive the same reference standard? Yes    
Were all patients included in the analysis? Yes    
    Low