Chitwood W R, Lyerly H K, Sabiston D C
Ann Surg. 1985 Jan;201(1):11-26.
Recurrent pulmonary emboli ultimately may produce respiratory insufficiency, severe hypoxemia, and progressive pulmonary hypertension. In many patients this syndrome is silent in its initial phases, and when thrombophlebitis is present it is often unresponsive to anticoagulant therapy. Unless pulmonary embolectomy is undertaken, most of these patients characteristically succumb with severe respiratory insufficiency. Twenty-five patients with this syndrome have been evaluated at the Duke University Medical Center, and 14 were selected for elective pulmonary embolectomy for relief of severe and incapacitating pulmonary insufficiency. In each patient preoperative pulmonary scans and arteriography demonstrated a high degree of vascular occlusion. The obstructing lesions affected both lungs in the majority of patients. Bronchial arteriography was found to be a very valuable method for demonstrating patency of the pulmonary arteries distal to occluding lesions by retrograde filling through collateral vessels joining the bronchial and pulmonary circulations. Preoperatively radionuclide angiocardiography revealed severe right ventricular dysfunction with significantly depressed ejection fractions at rest and during exercise. Retrograde pulmonary arterial flow as shown by selective bronchial arteriography was excellent in ten patients, fair in three, and absent in one. Long term follow-up indicated a clear relationship between the magnitude of arterial backflow at the time of embolectomy and the degree of clinical improvement. There were two perioperative deaths, one from massive reperfusion pulmonary hemorrhage and another from intractable right ventricular failure. Eleven patients with this syndrome were unsuitable candidates for embolectomy and of these, nine had severe distal emboli diffusely spread in the small pulmonary arteries and not amenable to direct removal. One patient had severe right ventricular failure with extreme pulmonary hypertension (145/45 mmHg) and another was massively obese with severe congestive heart failure and expired in the hospital a week later. In this group of 11 patients, three succumbed and most of the others are currently totally debilitated at rest (NYHA Class IV). Long-term follow-up of the surgically managed patients (1 to 15 years) shows that ten patients improved from NYHA functional Class IV to either I or II, another patient from Class III to Class I, and a final patient was only minimally improved.(ABSTRACT TRUNCATED AT 400 WORDS)
复发性肺栓塞最终可能导致呼吸功能不全、严重低氧血症和进行性肺动脉高压。在许多患者中,该综合征在初始阶段并无明显症状,而且当存在血栓性静脉炎时,往往对抗凝治疗无反应。除非进行肺栓子切除术,否则这些患者大多会因严重呼吸功能不全而死亡。杜克大学医学中心对25例患有该综合征的患者进行了评估,其中14例被选行选择性肺栓子切除术,以缓解严重且使人丧失能力的肺功能不全。在每例患者中,术前肺部扫描和动脉造影均显示高度血管阻塞。大多数患者的阻塞性病变累及双肺。发现支气管动脉造影是一种非常有价值的方法,可通过与支气管和肺循环相连的侧支血管逆行充盈来显示阻塞性病变远端肺动脉的通畅情况。术前放射性核素血管造影显示严重右心室功能障碍,静息和运动时射血分数明显降低。选择性支气管动脉造影显示的逆行肺动脉血流,10例患者良好,3例尚可,1例无血流。长期随访表明,栓子切除术时动脉逆流的程度与临床改善程度之间存在明显关系。围手术期有2例死亡,1例死于大量再灌注性肺出血,另1例死于顽固性右心室衰竭。11例患有该综合征的患者不适合行栓子切除术,其中9例有严重的远端栓子广泛散布于小肺动脉,无法直接清除。1例患者有严重右心室衰竭伴极重度肺动脉高压(145/45 mmHg),另1例极度肥胖,伴有严重充血性心力衰竭,1周后在医院死亡。在这11例患者中,3例死亡,其他大多数患者目前静息时完全失能(纽约心脏协会IV级)。接受手术治疗患者的长期随访(1至15年)显示,10例患者从纽约心脏协会功能IV级改善为I级或II级,另1例从III级改善为I级,最后1例仅略有改善。(摘要截取自400字)