Dong Hui, Li Hongwu, Zuo Yujie, Jiang Kaiwen, Ma Wentao, Zou Yubao, Ma Wenjun, Jiang Xiongjing
Department of Cardiology, Fuwai Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College/National Center for Cardiovascular Diseases, Beijing, China.
Int J Surg. 2025 Jul 1;111(7):4508-4515. doi: 10.1097/JS9.0000000000002452. Epub 2025 May 12.
Femoral vein access used to be the traditional approach for adrenal venous sampling (AVS) procedures, whereas antecubital vein access is the newly developed approach. Until now, no randomized trial for comparison of two approaches has been carried out.
To compare the success rate, safety, and procedural parameters of AVS via an antecubital approach versus femoral approach.
This randomized clinical trial (RCT) was conducted between January 2022 and December 2023. The patients with primary aldosteronism (PA) aged 18-60 years were randomly assigned to femoral vein access group (FV) or antecubital vein access group (AV). The intention-to-treat analysis included all randomized patients.
A total of 675 patients aged 18-60 years old with hypertension that were at increased risk for PA were screened, 183 of whom were confirmed with PA. Twenty-nine patients were excluded due to refusal of AVS, decline of participating in this trial, or contraindication to AVS. A total of 154 patients were recruited in this trial.
Patients were randomly assigned to undergo AVS via femoral approach or antecubital approach.
The primary end point was the success rate of bilateral AVS. Secondary end points included the success rate of right, left sampling, procedure duration, fluoroscopy time, contrast volume, incidence of complications, and postsurgical outcomes.
From January 2022 to December 2023, totally 154 patients with PA were randomized to FV group (77cases, mean age, 47.8 ± 8.1 years; 26 females [33.8%]) and AV group (77cases, mean age, 49.2 ± 8.6 years; 30 females [39%]). The baseline characteristics for the two groups were well balanced ( P > 0.05). There were no significant differences in the success rate of bilateral (89.6% vs 92.2%, P = 0.58),right (94.8% vs 97.4%, P = 0.68), and left (94.8% vs 94.8%, P = 1.00) sampling between two groups. The incidence of complications did not differ between the two groups (2.6% vs 0, P = 0.477). The incidence of arterial mis-puncture was significantly higher in FV group than that in AV group (0% vs 9.1%, P = 0.02). The fluoroscopy time and contrast volume did not significantly differ between two groups. The procedure duration in AV group was significantly shorter than that of FV group (18.0 [IQR, 15.0-23.0] versus 20.0 [IQR, 17.0-25.5], P = 0.011). There was no significant difference in the proportion of patients who achieved complete clinical success (50.0% vs 45.9%, P = 0.725) and complete biochemical success (92.1% vs 91.9%, P = 1.000) after adrenalectomy between FV group and AV group.
The trial showed AVS via AV approach or FV approach did not lead to significant differences in success rate and incidence of complications, as well as postsurgical outcomes. However, AV approach was associated with shorter procedure duration, no arterial mis-puncture and earlier ambulation after the procedure, which make it a better alternative to FV approach.
股静脉穿刺曾是肾上腺静脉采血(AVS)操作的传统方法,而肘前静脉穿刺是新开发的方法。到目前为止,尚未进行比较这两种方法的随机试验。
比较经肘前静脉途径与股静脉途径进行AVS的成功率、安全性和操作参数。
这项随机临床试验(RCT)于2022年1月至2023年12月进行。将年龄在18 - 60岁的原发性醛固酮增多症(PA)患者随机分配至股静脉穿刺组(FV)或肘前静脉穿刺组(AV)。意向性分析包括所有随机分组的患者。
共筛查了675例年龄在18 - 60岁、PA风险增加的高血压患者,其中183例确诊为PA。29例患者因拒绝AVS、拒绝参加本试验或存在AVS禁忌证而被排除。本试验共招募了154例患者。
患者被随机分配接受经股静脉途径或肘前静脉途径的AVS。
主要终点是双侧AVS的成功率。次要终点包括右侧、左侧采血成功率、操作持续时间、透视时间、造影剂用量、并发症发生率及术后结局。
2022年1月至2023年12月,共154例PA患者被随机分为FV组(77例,平均年龄47.8±8.1岁;26例女性[33.8%])和AV组(77例,平均年龄49.2±8.6岁;30例女性[39%])。两组的基线特征平衡良好(P>0.05)。两组之间双侧(89.6%对92.2%,P = 0.58)、右侧(94.8%对97.4%,P = 0.68)和左侧(94.8%对94.8%,P = 1.00)采血成功率无显著差异。两组并发症发生率无差异(2.6%对0,P = 0.477)。FV组动脉误穿发生率显著高于AV组(0%对9.1%,P = 0.02)。两组透视时间和造影剂用量无显著差异。AV组操作持续时间显著短于FV组(18.0[四分位间距,15.0 - 23.0]对20.0[四分位间距,17.0 - 25.5],P = 0.011)。肾上腺切除术后达到完全临床成功(50.0%对45.9%,P = 0.725)和完全生化成功(92.1%对91.9%,P = 1.000)的患者比例在FV组和AV组之间无显著差异。
该试验表明,经AV途径或FV途径进行AVS在成功率、并发症发生率及术后结局方面无显著差异。然而,AV途径操作持续时间较短,无动脉误穿且术后可更早活动,使其成为FV途径更好的替代方法。