Abstract
Objective:
To evaluate short‐ and long‐term outcomes and health‐related quality of life (Hr‐QoL) in dogs with congenital intrahepatic portosystemic shunts (cIHPSS) treated using percutaneous transcatheter embolization (PTCE).
Study design:
Single center retrospective and prospective study.
Animals:
Sixty‐one client‐owned dogs.
Methods:
Medical records were reviewed, and owners completed validated Hr‐QoL and congenital portosystemic shunt scoring (Hr‐CPSS) questionnaires. Hr‐QoL scores ranged from 0 (worst) to 100 (best), and Hr‐CPSS from 0 (best) to 100 (worst). Survival was assessed using Kaplan–Meier analysis. Medical or dietary management at final follow‐up were recorded.
Results:
Median follow‐up time was 769 days (interquartile range [IQR]: 297–1865). Median survival time was 1496 days. At last follow‐up, 33 of 59 dogs remained on medical management and/or a specialized diet. Median Hr‐CPSS significantly decreased from prediagnosis (25 [IQR: 18–51.3]) to post‐PTCE (5 [IQR: 3–11]; p < .001), but not between post‐medical and post‐PTCE (p = .68). Median Hr‐QoL scores improved post‐PTCE (100 [IQR: 80–100]) compared to prediagnosis (35 [IQR: 10–50], p < .0001), and post‐medical (75 [IQR: 40–90], p = .005) as well as between prediagnosis and post‐medical (p = .038). One‐, two‐, and five‐year survival rates were 83%, 66%, and 54%, respectively.
Conclusion:
Treatment of cIHPSS with PTCE in dogs was associated with a good long‐term survival and significant improvement in QoL and clinical signs. Impact: The combination of PTCE and targeted medical management provides an effective minimally invasive treatment option for dogs with cIHPSS, supporting improved longevity and quality of life.
To evaluate short‐ and long‐term outcomes and health‐related quality of life (Hr‐QoL) in dogs with congenital intrahepatic portosystemic shunts (cIHPSS) treated using percutaneous transcatheter embolization (PTCE).
Study design:
Single center retrospective and prospective study.
Animals:
Sixty‐one client‐owned dogs.
Methods:
Medical records were reviewed, and owners completed validated Hr‐QoL and congenital portosystemic shunt scoring (Hr‐CPSS) questionnaires. Hr‐QoL scores ranged from 0 (worst) to 100 (best), and Hr‐CPSS from 0 (best) to 100 (worst). Survival was assessed using Kaplan–Meier analysis. Medical or dietary management at final follow‐up were recorded.
Results:
Median follow‐up time was 769 days (interquartile range [IQR]: 297–1865). Median survival time was 1496 days. At last follow‐up, 33 of 59 dogs remained on medical management and/or a specialized diet. Median Hr‐CPSS significantly decreased from prediagnosis (25 [IQR: 18–51.3]) to post‐PTCE (5 [IQR: 3–11]; p < .001), but not between post‐medical and post‐PTCE (p = .68). Median Hr‐QoL scores improved post‐PTCE (100 [IQR: 80–100]) compared to prediagnosis (35 [IQR: 10–50], p < .0001), and post‐medical (75 [IQR: 40–90], p = .005) as well as between prediagnosis and post‐medical (p = .038). One‐, two‐, and five‐year survival rates were 83%, 66%, and 54%, respectively.
Conclusion:
Treatment of cIHPSS with PTCE in dogs was associated with a good long‐term survival and significant improvement in QoL and clinical signs. Impact: The combination of PTCE and targeted medical management provides an effective minimally invasive treatment option for dogs with cIHPSS, supporting improved longevity and quality of life.
| Original language | English |
|---|---|
| Number of pages | 11 |
| Journal | Veterinary Surgery |
| Early online date | 13 Apr 2026 |
| DOIs | |
| Publication status | E-pub ahead of print - 13 Apr 2026 |
Bibliographical note
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