pulmonary arterial hypertension: Pulmonary arterial hypertension (PAH) is a group of diseases characterized by elevated pulmonary arterial resistance leading to right heart failure. PAH is progressive and potentially fatal. PAH may be idiopathic and/ or familial, or induced by drug or toxin (drug-or toxin-induced PAH, see these terms) or associated with other diseases like congenital heart disease, connective tissue disease, HIV, schistosomiasis, portal hypertension (PAH associated with other disease, see this term).
| Name | I9_PULMOTHHD |
|---|---|
| Long name | Other pulmonary heart/vessel disease |
| Hospital Discharge registry | ICD-10: I28/I27, ICD-9: 416/417, ICD-8: 426 |
| Cause of Death registry | ICD-10: I28/I27, ICD-9: 416/417, ICD-8: 426 |
| Include | I9_SECONDRIGHT |
| Level in the ICD-hierarchy | 3 |
| First defined in version | DF2 |
| All | Female | Male | |
|---|---|---|---|
| Number of individuals | 493 | 261 | 232 |
| Unadjusted prevalence (%) | 0.23 | 0.21 | 0.25 |
| Mean age at first event (years) | 61.96 | 60.27 | 63.86 |
| Case fatality at 5-years (%) | 20.08 | 14.94 | 25.86 |
| All | Female | Male | |
|---|---|---|---|
| Median nb. of events per indiv. | 2.0 | 2.0 | 1.0 |
| Recurrence at 6 months (%) | 44.22 | 49.43 | 38.36 |
before Other pulmonary heart/vessel disease
after Other pulmonary heart/vessel disease
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