Fleming Nicole D, Alvarez-Secord Angeles, Von Gruenigen Vivian, Miller Michael J, Abernethy Amy P
Division of Gynecologic Oncology, Duke University Medical Center, Durham, NC 27710, USA.
J Pain Symptom Manage. 2009 Sep;38(3):341-9. doi: 10.1016/j.jpainsymman.2008.09.008. Epub 2009 Mar 28.
The safety and efficacy of indwelling intraperitoneal (IP) catheters for the management of refractory malignant ascites is unclear. A systematic literature overview and retrospective chart review of patients with malignant refractory ascites who underwent indwelling IP catheter placement was performed. Standardized literature abstraction and chart review templates were used to ensure that consistent information was collected. Fifteen publications met literature search criteria, representing 221 patients. Tenckhoff (Quinton Instrument Company, Seattle, WA, USA), Pleurex (Denver Biomedical Inc., Golden, CO, USA), and peritoneal catheters were used, along with IP ports. A median 5.9% of cases (range: 2.5%-34%) had documented peritonitis. In the literature, untunneled catheters were most commonly associated with infections. Our chart review added 19 cases from two academic institutions to this literature (median age: 60 years [range: 31-85]; females: 17 [89%]; gynecological malignancies: 14 [73%]). Palliative management before catheter placement included diuretics (n=4 [21%]) and multiple paracenteses (n=11 [58%] had two or more taps [range: 2-8]). Median time from diagnosis to catheter placement was 25 months (range: 1-77). Interventions were: French pigtail catheters (n=16 [84%]), Tenckhoff catheter (n=1 [5%]), and Port-A-Caths (Smith Medical MD, St. Paul, MN, USA) (n=2; 11%). Four (21%) catheters were tunneled. Prophylactic antibiotics were prescribed in six cases (32%). Two cases (11%) had documented infections, seven catheters (37%) became occluded, and two leaked (11%). The median time from catheter until death was 36 days (range: 4-660). Nine patients (47%) were admitted to hospice. In these retrospective studies, indwelling IP catheters appear to be a safe and effective palliative strategy to manage refractory malignant ascites, without overwhelming infection rates.
留置腹腔内(IP)导管用于治疗难治性恶性腹水的安全性和有效性尚不清楚。我们对接受留置IP导管置入术的恶性难治性腹水患者进行了系统的文献综述和回顾性病历审查。使用标准化的文献摘要和病历审查模板,以确保收集到一致的信息。15篇出版物符合文献检索标准,涵盖221例患者。使用了Tenckhoff导管(美国华盛顿州西雅图市的Quinton Instrument Company公司生产)、Pleurex导管(美国科罗拉多州戈尔登市的Denver Biomedical Inc.公司生产)以及腹腔导管,并配备了IP端口。有记录的腹膜炎病例占比中位数为5.9%(范围:2.5%-34%)。在文献中,非隧道式导管最常与感染相关。我们的病历审查为该文献补充了来自两个学术机构的19个病例(年龄中位数:60岁[范围:31-85岁];女性:17例[89%];妇科恶性肿瘤:14例[73%])。导管置入术前的姑息治疗包括利尿剂(n = 4 [21%])和多次腹腔穿刺术(n = 11 [58%]进行了两次或更多次穿刺[范围:2-8次])。从诊断到导管置入的中位时间为25个月(范围:1-77个月)。干预措施包括:法国猪尾导管(n = 16 [84%])、Tenckhoff导管(n = 1 [5%])以及Port-A-Caths导管(美国明尼苏达州圣保罗市的Smith Medical MD公司生产)(n = 2;11%)。4根(21%)导管为隧道式。6例(32%)患者使用了预防性抗生素。2例(11%)有记录的感染病例,7根导管(37%)发生堵塞,2根(11%)发生渗漏。从导管置入到死亡的中位时间为36天(范围:4-660天)。9例患者(47%)入住临终关怀机构。在这些回顾性研究中,留置IP导管似乎是一种安全有效的姑息治疗策略,可用于治疗难治性恶性腹水,且感染率并不高。