Huval W V, Lelcuk S, Shepro D, Hechtman H B
Ann Surg. 1984 Aug;200(2):166-72. doi: 10.1097/00000658-198408000-00008.
An early event in the evolution of acute respiratory failure (ARF) is thought to be the activation of platelets, their pulmonary entrapment and subsequent release of the smooth muscle constrictor serotonin (5HT). This study tests the thesis that inhibition of 5HT will improve lung function. The etiology of ARF in the 18 study patients was sepsis (N = 10), aspiration (N = 3), pancreatitis (N = 1), embolism (N = 2), and abdominal aortic aneurysm surgery (N = 2). Patients were divided into two groups determined by whether their period of endotracheal intubation was less than or equal to 4 days (early ARF, N = 12) or greater than 4 days (late ARF, N = 6). Transpulmonary platelet counts in the early group showed entrapment of 26,300 +/- 5900 platelets/mm3 in contrast to the late group where there was no entrapment (p less than 0.05). The platelet 5HT levels in the early group were 55 +/- 5 ng/10(9) platelets, values lower than 95 +/- 15 ng/10(9) platelets in the late ARF group (p less than 0.05), and 290 +/- 70 ng/10(9) platelets in normals. The selective 5HT receptor antagonist, ketanserin was given as an intravenous bolus over 3 minutes in a dose of 0.1 mg/kg, followed by a 30-minute infusion of 0.08 mg/kg. During this period mean arterial pressure (MAP) fell from 87 +/- 5 to 74 +/- 6 mmHg (mean +/- SEM) (p less than 0.05). One and one-half hours following the start of therapy, MAP returned to baseline. At this time, patients with early ARF showed decreases in: physiologic shunt (Qs/QT) from 26 +/- 3 to 19 +/- 3 (p less than 0.05); peak inspiratory pressure from 35 +/- 2 to 32 +/- 2 cmH2O (p less than 0.05) and in mean pulmonary arterial pressure from 32 +/- 2 to 29 +/- 1 mmHg (p less than 0.05). At 4 hours all changes returned to baseline levels. In early ARF ketanserin did not alter pretreatment values of: pulmonary arterial wedge pressure, 17 +/- 3 mmHg; cardiac index, 2.8 +/- 0.3 L/min X m2; platelet count, 219,000 +/- 45,000/mm3; platelet 5HT, 55 +/- 5 ng/10(9) platelets; plasma 5HT, 142 +/- 21 ng/ml; plasma thromboxane B2, 190 +/- 30 pg/ml; or plasma 6-keto-PGF1 alpha, 40 +/- 10 pg/ml. Ketanserin infusion in patients with late ARF yielded no benefit. In both ARF groups the decreases in QS/QT were inversely related to the duration of intubation (r = 0.70; p less than 0.05).(ABSTRACT TRUNCATED AT 400 WORDS)
急性呼吸衰竭(ARF)演变过程中的一个早期事件被认为是血小板的激活、其在肺部的滞留以及随后平滑肌收缩剂5-羟色胺(5HT)的释放。本研究检验了抑制5HT将改善肺功能这一论点。18例研究患者中ARF的病因包括败血症(N = 10)、误吸(N = 3)、胰腺炎(N = 1)、栓塞(N = 2)和腹主动脉瘤手术(N = 2)。患者根据气管插管时间是否小于或等于4天(早期ARF,N = 12)或大于4天(晚期ARF,N = 6)分为两组。早期组的经肺血小板计数显示每立方毫米有26,300±5900个血小板滞留,而晚期组无滞留(p<0.05)。早期组血小板5HT水平为55±5纳克/10⁹个血小板,低于晚期ARF组的95±15纳克/10⁹个血小板(p<0.05),正常人为290±70纳克/10⁹个血小板。选择性5HT受体拮抗剂酮色林以0.1毫克/千克的剂量在3分钟内静脉推注,随后以0.08毫克/千克的剂量输注30分钟。在此期间,平均动脉压(MAP)从87±5降至74±6毫米汞柱(平均值±标准误)(p<0.05)。治疗开始后一个半小时,MAP恢复到基线水平。此时,早期ARF患者出现以下降低:生理分流(Qs/QT)从26±3降至19±3(p<0.05);吸气峰压从35±2降至32±2厘米水柱(p<0.05),平均肺动脉压从32±2降至29±1毫米汞柱(p<0.05)。4小时时,所有变化均恢复到基线水平。在早期ARF中,酮色林未改变以下治疗前值:肺动脉楔压,17±3毫米汞柱;心脏指数,2.8±0.3升/分钟×平方米;血小板计数,219,000±45,000/立方毫米;血小板5HT,55±5纳克/10⁹个血小板;血浆5HT,142±21纳克/毫升;血浆血栓素B2,190±30皮克/毫升;或血浆6-酮-PGF1α,40±10皮克/毫升。晚期ARF患者输注酮色林无益处。在两个ARF组中,QS/QT的降低与插管持续时间呈负相关(r = 0.70;p<0.05)。(摘要截短至400字)