2024 article

Outcome of 21 dogs treated for the portocaval subtype of extrahepatic portosystemic shunts

Swieton, N., Weisse, C., Zwingenberger, A. L., Vilaplana Grosso, F. R., Carroll, K. A., Scharf, V. F., … Aly, A. M. (2024, October 30). VETERINARY SURGERY.

By: N. Swieton*, C. Weisse*, A. Zwingenberger*, F. Vilaplana Grosso*, K. Carroll n, V. Scharf n, K. Asano*, M. Wallace* ...

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Source: Web Of Science
Added: November 12, 2024

Abstract Objective To assess outcomes of dogs with side‐to‐side portocaval extrahepatic portosystemic shunts (PC‐EHPSS) and poor portal perfusion to the liver treated with medical management alone (MM) or surgical attenuation (SA). Study design Multi‐institutional retrospective study. Animals A total of 21 dogs with PC‐EHPSS (14/21 MM and 7/21 SA). Methods Medical records were reviewed, and data was collected on dogs <12 kg with PC‐EHPSS treated with MM or SA between June 2008 to June 2021. Signalment, clinical signs, postoperative complications, bloodwork values, long‐term clinical outcome, survival, and owner reported quality of life were recorded. Results Of 21 dogs included, 10 were mixed breeds and 14 were females. Median age at time of presenting clinical signs was 163 days. At final follow‐up examination (median 1119 days), all SA and 6/14 MM dogs were alive, with a median survival time of 2138 days following treatment onset. In surviving MM dogs, outcome was fair in 3/6 and poor in 3/6. In SA dogs with long‐term follow‐up, outcome was fair in 5/6, and poor in 1/6. A greater proportion of SA dogs had improved bloodwork parameter values at final follow‐up examination, and the mean relative change in final bloodwork values was higher when compared to MM dogs. Conclusion These findings demonstrate that SA has improved clinical outcomes to MM for PC‐EHPSS; however, SA clinical outcomes appear worse than those previously reported for other EHPSS. Clinical significance This information may have implications for expected outcomes in other EHPSS subtypes associated with severely diminished portal perfusion.