Portal vein thrombosis following elective laparoscopic splenectomy: incidence and analysis of risk factors

被引:12
|
作者
Swinson, Benjamin [1 ]
Waters, Peadar S. [1 ]
Webber, Laurence [1 ]
Nathanson, Les [1 ,2 ]
Cavallucci, David J. [1 ,2 ,3 ]
O'Rourke, Nicholas [1 ,2 ,3 ]
Bryant, Richard D. [1 ,3 ,4 ]
机构
[1] Royal Brisbane & Womens Hosp, Dept Surg, Herston, Qld 4029, Australia
[2] Wesley Hosp, Dept Surg, Auchenflower, Qld 4066, Australia
[3] Univ Queensland, Fac Med, Brisbane, Qld, Australia
[4] St Vincents Private Hosp Northside, St Vincents Northside Med Ctr, 627 Rode Rd, Chermside, Qld 4032, Australia
来源
SURGICAL ENDOSCOPY AND OTHER INTERVENTIONAL TECHNIQUES | 2022年 / 36卷 / 05期
关键词
Laparoscopic splenectomy; Portal vein thrombosis; Myelofibrosis; Thrombocytosis; Minimally invasive splenectomy; MESENTERIC VENOUS THROMBOSIS; HEMATOLOGIC DISEASE; SYSTEM THROMBOSIS; PREVENTION; CIRRHOSIS; STILL;
D O I
10.1007/s00464-021-08649-x
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background Minimally invasive splenectomy is now well established for a wide range of pathologies. Portal vein thrombosis (PVT) is increasingly being recognised as a complication of splenectomy. The aim was to determine the incidence and risk factors for PVT after laparoscopic splenectomy. Methods All cases of elective laparoscopic splenectomy performed from 1993 to 2020 were reviewed. Parameters recorded included demographics, diagnostic criterion and post-operative outcomes. Data were analysed using Minitab V18 with a p < 0.05 considered significant. Results 210 patients (103 female, 107 male) underwent laparoscopic splenectomy (14 to 85 years). A major proportion of cases were performed for ITP (n = 77, p = 0.012) followed by lymphoma (n = 28), indeterminate lesions (n = 21) and myelofibrosis (n = 19). Ten patients developed symptomatic portal vein thrombosis (4.8%). Patients presented most commonly with pain and fever and diagnosis was confirmed by computed tomography (CT) or ultrasonography (USS). There were 10 conversions (4.8%) to open and two postoperative deaths, one from PVT and one from pneumonia. The remaining nine patients were successfully treated with anticoagulation. Of 19 patients with myelofibrosis, six patients developed PVT (p = 0.0002). Patients who developed PVT had significantly greater specimen weights (1773 g vs 348 g, p < 0.001). Forty-three patients had a specimen weight of 1 kg or greater, and of these 9 developed portal vein thrombosis (21%), versus one with PVT of 155 with a specimen weight of less than 1 kg (p < 0.0001). Myelofibrosis (p = 0.0039), specimen weight (p < 0.001) and mean platelet count (p = 0.0049) were predictive of PVT. Conclusion A high index of suspicion for this complication should be maintained and prompt treatment with anticoagulation. High-risk patients should be considered for prophylactic anticoagulation and routine imaging of the portal vein.
引用
收藏
页码:3332 / 3339
页数:8
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