# Short-acting urapidil compared to long-acting phenoxybenzamine in the management of pheochromocytoma

## TL;DR

This study compares urapidil and phenoxybenzamine for treating pheochromocytoma, finding that urapidil allows shorter treatment and fewer side effects.

## Contribution

The study introduces oral urapidil as a viable alternative to phenoxybenzamine for preoperative management of pheochromocytoma.

## Key findings

- Oral urapidil treatment duration was significantly shorter than phenoxybenzamine.
- Patients on urapidil had fewer side effects and shorter hospital stays.
- No significant differences in hemodynamic instability or complications were observed between treatment groups.

## Abstract

In patients with pheochromocytoma current guidelines recommend preoperative alpha-adrenoceptor blockade with selective or nonselective antagonists for at least 7–14 days. To date, no information exists about orally administered urapidil retard, a short-acting selective antagonist.

The medical records of consecutive patients with pheochromocytoma between 2010 and 2023 were reviewed. Patients received phenoxybenzamine between 2010 and 2017, intravenous urapidil was given between 2017 and 2019. Orally administered urapidil retard has been used from 2019 until present.

Forty-nine patients with pheochromocytomas were included. Twenty-six patients received orally administered long-acting phenoxybenzamine and 23 patients were pretreated with short-acting intravenous (n = 8) or orally administered urapidil (n = 15). Treatment prior to surgery was significantly shorter with intravenously (3 days (IQR, 3–4), p = 0.015) or orally administered urapidil (2 days (IQR 2–3), p = 0.003) compared to phenoxybenzamine (7 days (IQR, 4–10)). Side effects were more often in the phenoxybenzamine group (17/26 vs 6/23, p = 0.02). The modified hemodynamic instability (HI) score was low and there was no significant difference between patients treated with phenoxybenzamine and those treated with intravenous or oral urapidil (29 (IQR 18.5–38); 26 (IQR 18–42); 31 (IQR 15–36) ns). No 30-day postoperative mortality or cardiovascular complications occurred in any of the three groups. The postoperative hospital stay was significantly shorter in the orally administered urapidil group compared to the phenoxybenzamine group (3 days (IQR 3–5)) vs 4 days (IQR 4–5)), p = 0.04).

Oral pretreatment with urapidil retard is well tolerated for patients with pheochromocytoma, enabling a safe intra- and postoperative course.