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Cardiovasc Intervent Radiol. 2022 Jan;45(1):29-40. doi: 10.1007/s00270-021-02954-7. Epub 2021 Sep 13.
2
Computed tomography image fusion, Coaxial guidewire technique, Fast intraprocedural cortisol testing technique improves success rate and decreases radiation exposure, procedure time, and contrast use for adrenal vein sampling.计算机断层扫描图像融合、同轴导丝技术、快速术中皮质醇检测技术提高了肾上腺静脉取样的成功率,降低了辐射暴露、手术时间和对比剂的使用。
J Hypertens. 2021 Sep 1;39(9):1918-1925. doi: 10.1097/HJH.0000000000002852.
3
Adrenocorticotropic Hormone-Stimulated Adrenal Venous Sampling Underestimates Surgically Curable Primary Aldosteronism: A Retrospective Cohort Study and Review of Contemporary Studies.促肾上腺皮质激素刺激的肾上腺静脉采样低估了可手术治愈的原发性醛固酮增多症:一项回顾性队列研究和对当代研究的综述。
Hypertension. 2021 Jul;78(1):94-103. doi: 10.1161/HYPERTENSIONAHA.121.17248. Epub 2021 May 17.
4
Aldosterone-induced cardiac damage in primary aldosteronism depends on its subtypes.原发性醛固酮增多症中醛固酮诱导的心脏损伤取决于其亚型。
Endocr Connect. 2021 Jan;10(1):29-36. doi: 10.1530/EC-20-0504.
5
Variability of Aldosterone Measurements During Adrenal Venous Sampling for Primary Aldosteronism.原发性醛固酮增多症肾上腺静脉采血中醛固酮测量的变异性。
Am J Hypertens. 2021 Feb 18;34(1):34-45. doi: 10.1093/ajh/hpaa151.
6
Association of Adrenal Venous Sampling With Outcomes in Primary Aldosteronism for Unilateral Adenomas.肾上腺静脉采血与原发性醛固酮增多症单侧腺瘤患者预后的相关性
JAMA Surg. 2021 Feb 1;156(2):165-171. doi: 10.1001/jamasurg.2020.5011.
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Utility of adrenocorticotropic hormone in adrenal vein sampling despite the occurrence of discordant lateralization.促肾上腺皮质激素在肾上腺静脉取样中的作用,尽管存在分歧的侧化。
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Preoperative non-stimulated adrenal venous sampling index for predicting outcomes of adrenalectomy for unilateral primary aldosteronism.术前非刺激肾上腺静脉采样指数预测单侧原发性醛固酮增多症肾上腺切除术的结果。
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The cardiovascular consequences of hyperaldosteronism.醛固酮增多症的心血管后果。
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Impact of cone beam - CT on adrenal vein sampling in primary aldosteronism.锥形束CT对原发性醛固酮增多症肾上腺静脉采血的影响。
Eur J Radiol. 2020 Mar;124:108792. doi: 10.1016/j.ejrad.2019.108792. Epub 2019 Dec 18.

原发性醛固酮增多症中单路与多路径肾上腺静脉采样的对比分析。

Comparative Analysis of Single-Path and Multipath Adrenal Venous Sampling in Primary Aldosteronism.

机构信息

Department of Geriatrics, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.

Fujian Hypertension Research Institute, The First Affiliated Hospital of Fujian Medical University, Fuzhou, China.

出版信息

J Interv Cardiol. 2023 Aug 12;2023:8670365. doi: 10.1155/2023/8670365. eCollection 2023.

DOI:10.1155/2023/8670365
PMID:37601238
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10439828/
Abstract

OBJECTIVE

To evaluate the safety and efficacy of adrenal venous sampling (AVS) via the cubital vein and femoral vein synchronously.

METHODS

A total of 200 patients with primary aldosteronism admitted to the First Hospital of Fujian Medical University were enrolled and randomly divided into a single-path AVS group (SP,  = 108) and a multipath AVS group (MP,  = 92). We analyzed the clinical characteristics, intubation success rate, procedure cost, total fluoroscopy time, complications, contrast dosage, and the number of catheters selected during AVS. A planar quadrant system was established to mark the direction of the adrenal opening, with the intersection of the right renal vein and the inferior vena cava defined as the origin. In digital subtraction angiography images, the RAV opening located in the 0-3 o'clock direction was the first quadrant (I), and the 3-6 o'clock direction was the third quadrant (III).

RESULTS

There was no statistical difference between the two groups at baseline. Multipath AVS had a significantly higher success rate of right-sided intubation than single-path AVS (success rate of right-sided intubation/%: SP 87.96 vs MP 95.65, = 0.043). Total fluoroscopy time was significantly reduced (fluoroscopy time/min: SP 9.80 ± 4.07 vs MP 7.42 ± 3.48, = 0.024) and the cost of the procedure was markedly lower (cost/yuan: SP 3,900.93 ± 1,191.12 vs MP 3,378.26 ± 399.40, < 0.001). There was no significant difference in postoperative complications between the two groups. In the group I, the procedure was completed mainly with an MPA catheter (catheter selection/%: MPA 98.19 vs TIG 17.65, < 0.001). In the group III, TIG catheters were used more frequently (catheter selection/%: MPA 1.81 vs TIG 82.35, < 0.001).

CONCLUSION

Multipath AVS via the cubital vein and femoral vein improves the success rate of AVS with comparable safety compared to single-path AVS. When the RAV is opened in the III quadrant, the TIG catheter improves the cannulation success rate. The multipath AVS method provides more catheter options. Patients diagnosed with PA at the First Hospital of Fujian Medical University from December 2019 to December 2021 were included. The collection of medical records of the included population was approved by the ethics committee (approval number: [2021] 311). This was a cross-sectional study in which some patients were treated surgically and some were treated with superselective adrenal artery embolization (SAAE). We conducted a cohort study of patients treated with SAAE. ClinicalTrials.gov Protocol Registration and Results System (PRS) receipt release date: January 11, 2022. This trial is registered with NCT05188872.

摘要

目的

评估经肘窝静脉和股静脉同步进行肾上腺静脉采样(AVS)的安全性和有效性。

方法

共纳入 200 例福建医科大学附属第一医院就诊的原发性醛固酮增多症患者,随机分为单路 AVS 组(SP,n=108)和多路 AVS 组(MP,n=92)。分析两组患者的临床特征、插管成功率、手术费用、总透视时间、并发症、造影剂用量及 AVS 时选择的导管数量。建立平面四分象限系统,以右肾静脉与下腔静脉的交点为原点。在数字减影血管造影图像中,RAV 开口位于 0-3 点钟方向的为第一象限(I),3-6 点钟方向的为第三象限(III)。

结果

两组患者基线资料比较差异无统计学意义。与单路 AVS 相比,多路 AVS 右侧插管成功率更高(右侧插管成功率/%:SP 87.96 vs MP 95.65, = 0.043)。总透视时间明显减少(透视时间/min:SP 9.80±4.07 vs MP 7.42±3.48, = 0.024),手术费用显著降低(手术费用/元:SP 3900.93±1191.12 vs MP 3378.26±399.40, <0.001)。两组患者术后并发症发生率比较差异无统计学意义。在象限 I 中,主要使用 MPA 导管完成手术(导管选择/%:MPA 98.19 vs TIG 17.65, <0.001)。在象限 III 中,TIG 导管的使用率更高(导管选择/%:MPA 1.81 vs TIG 82.35, <0.001)。

结论

与单路 AVS 相比,经肘窝静脉和股静脉的多路 AVS 可提高 AVS 成功率,且安全性相当。当 RAV 开口位于 III 象限时,TIG 导管可提高插管成功率。多路 AVS 方法提供了更多的导管选择。该研究纳入了 2019 年 12 月至 2021 年 12 月在福建医科大学附属第一医院诊断为 PA 的患者。纳入人群的病历收集经伦理委员会批准(批准文号:[2021]311)。这是一项横断面研究,部分患者接受了手术治疗,部分患者接受了超选择性肾上腺动脉栓塞术(SAAE)治疗。我们对接受 SAAE 治疗的患者进行了队列研究。ClinicalTrials.gov 方案注册和结果系统(PRS)发布日期:2022 年 1 月 11 日。该试验在 ClinicalTrials.gov 注册,编号为 NCT05188872。