Hellenkamp 2018.
Study characteristics | |||
Patient Sampling | Retrospective | ||
Patient characteristics and setting |
Study location: UK and Germany Study periods: between 2011 and 2016 Care setting: the Clinic for Cardiology and Pneumology, University Medical Center Göttingen; King's College Hospital, London; and the Department of Internal Medicine II, University of Regensburg Participants enrolled: 90: 43 males and 47 females Participants included in analysis: 90: 43 males and 47 females Age: mean age 64.8 years (IQR: 55‐79 years) BMI: not reported Classification of PH defined by WHO (diagnosis from right‐heart catheterisation): not reported Number of patients with asymptomatic or mild symptom: 24 (16%) Number of participants with COPD: not reported Number of intubated participants: 0 Inclusion criteria: patients who underwent echocardiography and right‐heart catheterisation within 24 hours Exclusion criteria: not reported |
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Index tests |
Description of index test: continuous‐wave Doppler ultrasonography of tricuspid regurgitation in apical four‐chamber and parasternal short‐axis views was applied, and the tricuspid regurgitation time‐velocity tracing was determined to obtain the time‐velocity integral, tricuspid regurgitation max velocity, mean tricuspid regurgitation velocity, maximal right atrial–right ventricular gradient, and TRP mean. Description of method to estimate right atrial pressure: Right atrial pressure was estimated by measuring the diameter of the IVC at end expiration and the inspiratory collapsibility in the subcostal view as follows: when the IVC diameter was #21 mm and the collapsibility with a sniff was > 50%, right atrial pressure was estimated to be 3 mmHg; when the IVC diameter was > 21 mm and the collapsibility was < 50%, right atrial pressure was estimated to be 15 mmHg. In all other cases (either IVC diameter > 21 mm and collapse > 50% or IVC diameter #21 mm and collapse < 50%), right atrial pressure was estimated to be 8 mmHg. Cut‐off value to declare PH: 31 mmHg Estimated systolic pulmonary arterial pressure: not reported Sonographer qualification: not reported How to handle the uninterpretable results: not applicable |
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Target condition and reference standard(s) |
Target condition: pulmonary hypertension Description of reference standard: not reported Mean pulmonary arterial pressure: median 35 mmHg (IQR: 24.7‐46.2 mmHg) |
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Flow and timing | The interval between the index test and reference standard: within 24 hours Number of indeterminates for whom the results of reference standard was available: 0 (0%) Number of patients who were excluded from the analysis: 0 (0%) |
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Comparative | |||
Notes | |||
Methodological quality | |||
Item | Authors' judgement | Risk of bias | Applicability concerns |
DOMAIN 1: Patient Selection | |||
Was a consecutive or random sample of patients enrolled? | Yes | ||
Did the study avoid inappropriate exclusions? | Yes | ||
Could the selection of patients have introduced bias? | Low risk | ||
Are there concerns that the included patients and setting do not match the review question? | Unclear | ||
DOMAIN 2: Index Test (All tests) | |||
Were the index test results interpreted without knowledge of the results of the reference standard? | Yes | ||
If a threshold was used, was it pre‐specified? | Unclear | ||
Could the conduct or interpretation of the index test have introduced bias? | Low risk | ||
Are there concerns that the index test, its conduct, or interpretation differ from the review question? | Low concern | ||
DOMAIN 3: Reference Standard | |||
Were the reference standard results interpreted without knowledge of the results of the index tests? | Yes | ||
Were the criteria of reference standard for target condition prespecified? | Unclear | ||
Could the reference standard, its conduct, or its interpretation have introduced bias? | Low risk | ||
Are there concerns that the target condition as defined by the reference standard does not match the question? | Low concern | ||
DOMAIN 4: Flow and Timing | |||
Was the interval between the index test and reference standard less than one day? | Yes | ||
Did all patients receive the same reference standard? | Yes | ||
Were all patients included in the analysis? | Yes | ||
Could the patient flow have introduced bias? | Low risk |