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通过格林菲尔德滤器中断腔静脉:扩大适应证

Interruption of the vena cava by means of the Greenfield filter: expanding the indications.

作者信息

Golueke P J, Garrett W V, Thompson J E, Smith B L, Talkington C M

机构信息

Department of Surgery, Baylor University Medical Center, Dallas, Texas.

出版信息

Surgery. 1988 Jan;103(1):111-7.

PMID:3336860
Abstract

Between 1978 and 1985, 88 patients underwent insertion of the Greenfield vena cava filter. In 21 of the 88 patients (23.9%) the filter was inserted prophylactically. Sixteen of the 21 prophylactic insertions were performed before total joint replacement in patients with a history of venous thromboembolism. Operative morbidity (4.6%) was minor and occurred only early in the series. The operative mortality rate was 4.6%. None of the deaths were related to filter insertion or pulmonary embolism. Follow-up in 65 patients (73.9%) ranged from 1 to 60 months (mean, 16.4 months). Leg edema developed in 9.2% (6/65), stasis ulceration in 3.1% (2/65), caval occlusion in 7.5% (3/40), and recurrent nonfatal embolism in 3.1% (2/65) of the patients. In the patients who received prophylactic filters before total joint replacement, there were no filter-related complications or episodes of pulmonary embolism. This series confirms the safety and effectiveness of the Greenfield filter and suggests that the indications for its use might be liberalized to include prophylactic insertion of the device in certain high-risk patients.

摘要

1978年至1985年间,88例患者接受了格林菲尔德下腔静脉滤器植入术。88例患者中有21例(23.9%)为预防性植入滤器。21例预防性植入中有16例是在有静脉血栓栓塞病史的患者进行全关节置换术前进行的。手术并发症发生率为4.6%,且仅在该系列早期出现,程度较轻。手术死亡率为4.6%。所有死亡均与滤器植入或肺栓塞无关。65例患者(73.9%)的随访时间为1至60个月(平均16.4个月)。9.2%(6/65)的患者出现腿部水肿,3.1%(2/65)的患者出现淤积性溃疡,7.5%(3/40)的患者出现腔静脉阻塞,3.1%(2/65)的患者出现复发性非致命性栓塞。在全关节置换术前接受预防性滤器植入的患者中,未出现与滤器相关的并发症或肺栓塞事件。该系列研究证实了格林菲尔德滤器的安全性和有效性,并表明其使用指征可能可以放宽,将该装置的预防性植入纳入某些高危患者。

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