Witteveen Esther, Wieske Luuk, de Beer Friso M, Juffermans Nicole P, Verhamme Camiel, Schultz Marcus J, van Schaik Ivo N, Horn Janneke
Department of Intensive Care Medicine, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Laboratory of Experimental Intensive Care and Anesthesiology (LEICA), Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Ann Transl Med. 2018 Apr;6(7):115. doi: 10.21037/atm.2018.01.30.
The main risk factors for intensive care unit-acquired weakness (ICU-AW) are sepsis, the systemic inflammatory response syndrome (SIRS) and multiple organ dysfunction. These risk factors are associated with systemic complement activation. We hypothesized that critically ill patients who develop ICU-AW have increased systemic complement activation compared to critically ill patients who do not develop ICU-AW.
Complement activation products C3b/c, C4b/c and C5a were measured in plasma of ICU patients with mechanical ventilation for ≥48 hours. Samples were collected at admission to the ICU and for 6 consecutive days. ICU-AW was defined by a mean Medical Research Council (MRC) score <4. We compared the level of complement activation products between patients who did and who did not develop ICU-AW.
Muscle strength measurements and complement assays were available in 27 ICU patients, of whom 13 patients developed ICU-AW. Increased levels of C4b/c were seen in all patients. Neither admission levels, nor maximum, minimum and mean levels of complement activation products were different between patients who did and did not develop ICU-AW.
Complement activation is seen in critically ill patients, but is not different between patients who did and who did not develop ICU-AW.
重症监护病房获得性肌无力(ICU-AW)的主要危险因素是脓毒症、全身炎症反应综合征(SIRS)和多器官功能障碍。这些危险因素与全身补体激活有关。我们假设,与未发生ICU-AW的危重症患者相比,发生ICU-AW的危重症患者全身补体激活增加。
在机械通气≥48小时的ICU患者血浆中测量补体激活产物C3b/c、C4b/c和C5a。在入住ICU时及连续6天采集样本。ICU-AW定义为平均医学研究委员会(MRC)评分<4。我们比较了发生和未发生ICU-AW的患者之间补体激活产物水平。
27例ICU患者有肌肉力量测量值和补体检测结果,其中13例发生ICU-AW。所有患者的C4b/c水平均升高。发生和未发生ICU-AW的患者之间,补体激活产物的入院水平、最高水平、最低水平及平均水平均无差异。
危重症患者存在补体激活,但发生和未发生ICU-AW的患者之间无差异。