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. 2017 Jul;14(7):1184–1196. doi: 10.1513/AnnalsATS.201701-062SR

Table 3.

Summary of findings, including the seven studies comparing nasal nitric oxide with an extended reference standard of electron microscopy and/or genetics*

Outcome Studies (n), Patients (n) Study Design Factors That May Decrease Quality of Evidence
Effect per 100 Patients Tested (Pretest Probability of 35%) Test accuracy QoE Importance
Risk of Bias Indirectness Inconsistency Imprecision Publication Bias
True positives (patients with PCD) 7 studies, 423 patients Cohort and case–control-type studies Serious Not serious Not serious Not serious None 34 (31–35) ⊕⊕⊕◯MODERATE Critical
False negatives (patients incorrectly classified as not having PCD)               1 (0–4)   Critical
True negatives (patients without PCD) 7 studies, 636 patients Cohort and case–control studies Serious Not serious Not serious Not serious None 63 (55–64) ⊕⊕⊕◯MODERATE Critical
False positives (patients incorrectly classified as having PCD)               2 (1–10)   Important
Inconclusive 7 studies, 27 patients   Important

Definition of abbreviations: PCD = primary ciliary dyskinesia; QOE = quality of evidence.

*

Sensitivity, 0.96 (95% confidence interval, 0.89–0.99); specificity, 0.96 (95% confidence interval, 0.85–0.99); prevalence 35%.

Four studies were case–control studies, among which one study included only healthy patients in the control group. Two studies did not prespecify the nasal nitric oxide cutoff before performing measurements and were not blinded to the reference standard.

Not downgraded for inconsistency since the residual heterogeneity was explained by the difference in the risk of bias between studies.