Postcardiotomy right ventricular failure
- Type
- Particular clinical situation in a disease or syndrome
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
A rare cardiac condition characterized by acute severe right ventricular failure with subsequent hemodynamic instability following a cardiac surgical procedure. Predisposing factors include suboptimal myocardial protection during surgery, long cardiopulmonary bypass time, right ventricular myocardial ischemia or infarction, atrial arrhythmias, reperfusion lung injury with secondary pulmonary hypertension, post-operative pulmonary micro- or macro-embolism, and pre-existing pulmonary vascular disease, among others.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Postcardiotomy right ventricular failure | |
| fr | Insuffisance cardiaque droite post-cardiotomie | |
| de | Postkardiotomie-Syndrom mit rechtsventrikulären Versagen | |
| es | Insuficiencia ventricular derecha postcardiotomía | |
| it | Insufficienza ventricolare destra post-cardiotomica | |
| nl | Postcardiotomie-rechterventrikelfalen | |
| pt | Falência do ventrículo direito pós-cardiotomia | |
| pl | Pokardiotomijna niewydolność prawej komory | |
| cs | Postkardiotomické selhání pravé komory | |
| uk | Посткардіохірургічна правошлуночкова недостатність | |
| zh | 心脏术后右心衰竭 | |
| tr | Postkardiyotomi sağ ventrikül yetmezliği |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | I97.1 | NTBT | attributed | validated |
| UMLS | C5680731 | E | validated | |
| GARD | 20898 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:97929Rare cardiac disease
rare cardiac diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-9 / 100 000 | — | Europe | Class only | Validated | European Medicines Agency 2010[OTHER] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/263352
- This record as JSON: /data/d/263352.json