Local α-receptor antagonists as a targeted therapeutic approach in patients with vasopressor-induced symmetrical peripheral gangrene

Abstract Objectives Symmetrical peripheral gangrene (SPG) is a rare condition characterized by symmetrical gangrene affecting the acral regions of two or more extremities, without the presence of major vessel obstruction. The precise pathophysiology of SPG is unclear, but it is believed to involve various biochemical pathways and is often associated with vasopressor therapy. Despite various therapeutic attempts, there is no established standard treatment for SPG. Methods This study evaluated the efficacy of locally administered phentolamine, an alpha-receptor antagonist, in four critically ill patients undergoing catecholamine therapy and presenting with SPG. Tissue perfusion was assessed using clinical observation and indocyanine green-assisted laser angiography before and after phentolamine administration. Results All four patients demonstrated immediate improvement in tissue perfusion following phentolamine application, as evidenced by angiography. No amputations were necessary. The patients’ clinical outcomes suggest that phentolamine effectively counteracts vasopressor-induced ischemia. Conclusions Phentolamine offers a targeted therapeutic approach for vasopressor-induced SPG by mitigating vasoconstriction without systemic side effects. Its incorporation into clinical practice requires further validation to optimize its application and efficacy.

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Publication Details

Journal
Innovative Surgical Sciences
Published
2026-01-07
DOI
https://doi.org/10.1515/iss-2025-0044
Primary Topic
Chemotherapy-related skin toxicity
Type
article
Field-Weighted Citation Impact
0.00

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article

Local α-receptor antagonists as a targeted therapeutic approach in patients with vasopressor-induced symmetrical peripheral gangrene

Michael Pawlik, Jasmin Lenhard, Lukas Prantl, Vinzent Forstmeier et al.
Innovative Surgical Sciences
Chemotherapy-related skin toxicity
article

Local α-receptor antagonists as a targeted therapeutic approach in patients with vasopressor-induced symmetrical peripheral gangrene

Michael Pawlik, Jasmin Lenhard, Lukas Prantl, Vinzent Forstmeier, P. Lamby
article en

Abstract

Abstract Objectives Symmetrical peripheral gangrene (SPG) is a rare condition characterized by symmetrical gangrene affecting the acral regions of two or more extremities, without the presence of major vessel obstruction. The precise pathophysiology of SPG is unclear, but it is believed to involve various biochemical pathways and is often associated with vasopressor therapy. Despite various therapeutic attempts, there is no established standard treatment for SPG. Methods This study evaluated the efficacy of locally administered phentolamine, an alpha-receptor antagonist, in four critically ill patients undergoing catecholamine therapy and presenting with SPG. Tissue perfusion was assessed using clinical observation and indocyanine green-assisted laser angiography before and after phentolamine administration. Results All four patients demonstrated immediate improvement in tissue perfusion following phentolamine application, as evidenced by angiography. No amputations were necessary. The patients’ clinical outcomes suggest that phentolamine effectively counteracts vasopressor-induced ischemia. Conclusions Phentolamine offers a targeted therapeutic approach for vasopressor-induced SPG by mitigating vasoconstriction without systemic side effects. Its incorporation into clinical practice requires further validation to optimize its application and efficacy.

Innovative Surgical Sciences
University Hospital Regensburg (DE), Klinikum Passau (DE), Caritas-Krankenhaus St. Josef (DE), Bundeswehrkrankenhaus Ulm (DE)
Universität Regensburg
Good health and well-being
Openalex Percentile: Top 95%
Chemotherapy-related skin toxicity
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Local α-receptor antagonists as a targeted therapeutic approach in patients with vasopressor-induced symmetrical peripheral gangrene — Michael Pawlik, Jasmin Lenhard, et al. · Innovative Surgical Sciences (2026) | TGRS Research Map | TGRS