Hypovolemic Shock And The Need For Invasive Mechanical Ventilation On A Patient With Congenital Heart Disease.

Marisa Simoes, Sergio Gaião
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Abstract

Techniques of venoarterial-extracorporeal membrane oxygenation (VA-ECMO) have improved over the decades, with numerous applications.1 Those with reversible low cardiac output benefit most from this support.1 Case of 21-year-old male, history of congenital heart disease (severe right ventricle hypoplasia and pulmonary artery stenosis with extracardiac cavo-pulmonary shunt (Fontan surgery), and atrial septal defect). Brought to the Emergency Department due to a Mallory-Weiss syndrome, upper-endoscopy "laceration at esophagogastric junction (EGJ) with active bleeding", clips were applied. However, worsening shock, repeated melenas and hematemesis, hemoglobin drop, lactate 2.8mmol/L, and needing noradrenaline (1.21mcg/kg/min). Due to active blood loss and worsening shock, the patient was intubated to maintain airway protection. Repeated upper-endoscopy "voluminous live red clot at EGJ, 4-clips and active bleeding of mucosa between, injection of polidocanol". Despite the implemented strategy, high risk of rebleeding remained. Following invasive mechanical ventilation (IMV), sustained hypotension having to increase noradrenaline (1.52mcg/kg/min) and lactate (5.8mmol/l), despite fluid resuscitation. Echocardiogram evidenced severe ventricular dysfunction, and fixed inferior vena cava (IVC) of 20mm. The heart defect combined with positive intrathoracic pressure, contributed to the worsened shock, as Fontan circulation is dependent on low vascular resistance to maintain output2. Needing VA-ECMO and admitted to ICU, volemia optimization, adjusting ventilation to lower intrathoracic pressure and started on milrinone and sildenafil. Another upper-endoscopy showed laceration at EGJ, with placement of clips. Echocardiogram revealed "Normal left ventricle. Hypoplastic right ventricle. Mild mitral regurgitation; aortic VTi 19cm. IVC 22mm. RV/RA gradient 70mmHg. Interatrial bidirectional shunt". Favorable evolution permitted extubation, suspension of milrinone and sildenafil, followed by decannulation. With rescue ECMO, congenital heart disease are salvageable despite sudden decompensation3. This case, positive intrathoracic pressure impairs the Fontan circulation, dependent on preload and higher central venous pressure to maintain cardiac output, as the ventricle is unable to compensate increased demands2, and worsening shock.

先天性心脏病患者的低血容量休克和对侵入性机械通气的需求。
1 该病例为 21 岁男性,有先天性心脏病史(严重右心室发育不良、肺动脉狭窄伴心外膜腔-肺分流(丰坦手术)和房间隔缺损)。因马洛里-魏斯综合征被送入急诊科,上内镜检查 "食管胃交界处撕裂伴活动性出血",使用了夹子。然而,休克加重,反复吐血,血红蛋白下降,乳酸 2.8mmol/L,需要去甲肾上腺素(1.21mcg/kg/min)。由于失血过多和休克恶化,患者被插管以维持气道保护。再次进行上内镜检查,发现 "EGJ 处有大量活的红色血块,4 个夹子之间的粘膜有出血现象,注射了聚多巴酚"。尽管采取了上述策略,但再次出血的风险仍然很高。有创机械通气(IMV)后,持续低血压导致去甲肾上腺素(1.52mcg/kg/min)和乳酸(5.8mmol/l)升高,尽管进行了液体复苏。超声心动图显示患者存在严重的心室功能障碍,下腔静脉(IVC)固定在20毫米处。心脏缺损加上胸内正压,导致休克恶化,因为丰坦循环依赖低血管阻力来维持输出量2。患者需要进行VA-ECMO,并被送入重症监护室,进行了血容量优化,调整通气以降低胸内压,并开始服用米力农和西地那非。另一次上内镜检查显示 EGJ 有裂口,放置了夹子。超声心动图显示 "左心室正常。右心室发育不良。二尖瓣轻度反流;主动脉瓣口 VTi 19 厘米。IVC 22 毫米。RV/RA 梯度 70mmHg。心房间双向分流"。由于病情发展良好,可以拔管、暂停米力农和西地那非,然后拔管。通过 ECMO 抢救,先天性心脏病尽管会突然失代偿,但仍可挽救3。本病例中,胸内正压损害了丰坦循环,由于心室无法补偿增加的需求2,心输出量依赖于前负荷和较高的中心静脉压来维持,并导致休克恶化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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