Critical Care Medicine Department, Clinical Center National Institutes of Health, (NIH, CC) Bethesda MD USA.
Division of Cardiology Duke University Medical Center Durham NC USA.
J Am Heart Assoc. 2024 Aug 6;13(15):e034026. doi: 10.1161/JAHA.123.034026. Epub 2024 Aug 5.
Septic shock is associated with increases in end-diastolic volume (EDV) and decreases in ejection fraction that reverse within 10 days. Nonsurvivors do not develop EDV increases. The mechanism is unknown.
Purpose-bred beagles (n=33) were randomized to receive intrabronchial or saline. Over 96 hours, cardiac magnetic resonance imaging and echocardiograms were performed. Tissue was obtained at 66 hours. From 0 to 96 hours after bacterial challenge, septic animals versus controls had significantly increased left ventricular wall edema (6%) and wall thinning with loss of mass (15%). On histology, the major finding was nonocclusive microvascular injury with edema in myocytes, the interstitium, and endothelial cells. Edema was associated with significant worsening of biventricular ejection fractions, ventricular-arterial coupling, and circumferential strain. Early during sepsis, (0-24 hours), the EDV decreased; significantly more in nonsurvivors (ie, greater diastolic dysfunction). From 24 to 48 hours, septic animals' biventricular chamber sizes increased; in survivors significantly greater than baseline and nonsurvivors, whose EDVs were not different from baseline. Preload, afterload, or heart rate differences did not explain these differential changes.
The cardiac dysfunction of sepsis is associated with wall edema. In nonsurvivors, at 0 to 24 hours, sepsis induces a more severe diastolic dysfunction, further decreasing chamber size. The loss of left ventricular mass with wall thinning in septic survivors may, in part, explain the EDV increases from 24 to 48 hours because of a potentially reparative process removing damaged wall tissue. Septic cardiomyopathy is most consistent with a nonocclusive microvascular injury resulting in edema causing reversible systolic and diastolic dysfunction with more severe diastolic dysfunction being associated with a decreased EDV and death.
脓毒性休克与舒张末期容积(EDV)增加和射血分数降低有关,这些变化在 10 天内逆转。未存活者不会出现 EDV 增加。其机制尚不清楚。
目的培育的比格犬(n=33)随机接受支气管内或生理盐水。在 96 小时内进行心脏磁共振成像和超声心动图检查。在 66 小时时获取组织。在细菌挑战后 0 至 96 小时,与对照组相比,脓毒症动物的左心室壁水肿(6%)和壁变薄伴质量损失(15%)明显增加。在组织学上,主要发现是非闭塞性微血管损伤,心肌细胞、间质和内皮细胞水肿。水肿与双心室射血分数、心室-动脉偶联和周向应变明显恶化有关。在脓毒症早期(0-24 小时),EDV 降低;未存活者(即,舒张功能障碍更严重)降低更为显著。从 24 至 48 小时,脓毒症动物的双心室腔大小增加;在存活者中明显大于基线,而非存活者的 EDV 与基线无差异。前负荷、后负荷或心率差异不能解释这些差异变化。
脓毒症的心脏功能障碍与壁水肿有关。在未存活者中,在 0 至 24 小时,脓毒症诱导更严重的舒张功能障碍,进一步减小腔室大小。脓毒症存活者的左心室质量损失伴壁变薄可能部分解释了从 24 至 48 小时的 EDV 增加,因为潜在的修复过程去除了受损的壁组织。脓毒性心肌病最符合非闭塞性微血管损伤导致水肿,引起可逆性收缩和舒张功能障碍,更严重的舒张功能障碍与 EDV 降低和死亡相关。