Bloom Matthew B, Zaw Andrea A, Hoang David M, Mason Russell, Alban Rodrigo F, Chung Rex, Melo Nicolas, Volod Oksana, Ley Eric J, Margulies Daniel R
From the Division of Trauma and Critical Care (M.B.B., A.A.Z., D.M.H., R.F.A., R.C., N.M., E.J.L., D.R.M.), Department of Surgery, Department of Pharmacy (R.M.), and Division of Coagulation Service (O.V.), Department of Hematology, Cedars-Sinai Medical Center, Los Angeles, California.
J Trauma Acute Care Surg. 2016 Mar;80(3):398-403; discussion 403-4. doi: 10.1097/TA.0000000000000952.
The obese state has been linked to several immune-mediated conditions. Our objective was to examine the association of body mass index (BMI) with the diagnosis of heparin-induced thrombocytopenia (HIT).
Prospectively collected data on patients in the surgical and cardiac intensive care unit suspected of having HIT between January 2007 and August 2014 were analyzed. Patients were categorized into five discrete BMI (kg/m) groups and compared. Data collected included Warkentin 4-T scores, antiplatelet factor 4 (anti-PF4OD) values, serotonin release assay values, and thromboembolic diseases. HIT positivity was defined as serotonin release assay value greater than 20%.
Of 304 patients meeting inclusion criteria, mean (SD) age was 62.1 (16.5) years, 59% were male, and mean (SD) BMI was 27 (6) kg/m. Thirty-six (12%) were positive for HIT. Incidence of HIT increased progressively with BMI (0%, 8%, 11%, 19%, 36%; p < 0.001). Compared with patients with normal BMI, patients with a BMI of 30 kg/m to 39.9 kg/m had a 200% increase in the odds for HIT (odds ratio [OR], 2.94; 95% confidence interval [CI], 1.20-7.54; p = 0.019), while patients with a BMI of 40 kg/m or greater had a 600% increase (OR, 6.98; 95% CI, 1.59-28.2; p = 0.012). After regression analysis, BMI remained an independent predictor of the development of HIT (adjusted OR per kg/m, 1.08; 95% CI, 1.02-1.14; p = 0.010). Anti-PF4OD values greater than or equal to 2.0 also increased with BMI (p < 0.001). In-hospital mortality increased significantly with BMI above normal (p = 0.026). Warkentin 4-T scores, deep venous thrombosis, pulmonary embolism, and stroke incidence did not correlate with changes in BMI.
Increasing BMI seems to be strongly associated with increased rates of HIT in intensive care unit patients. Obesity is an important new clinical variable for estimating the pretest probability of HIT, and patient "thickness" could be considered a fifth "T" of the 4-T scoring system. Additional biochemical work is indicated to decipher the role of obesity in this immune-mediated condition.
Prognostic/epidemiologic study, level III.
肥胖状态与多种免疫介导的疾病相关。我们的目的是研究体重指数(BMI)与肝素诱导的血小板减少症(HIT)诊断之间的关联。
分析了2007年1月至2014年8月期间在外科和心脏重症监护病房疑似患有HIT的患者的前瞻性收集数据。患者被分为五个离散的BMI(kg/m)组并进行比较。收集的数据包括华法林4 - T评分、抗血小板因子4(抗PF4OD)值、血清素释放试验值和血栓栓塞性疾病。HIT阳性定义为血清素释放试验值大于20%。
在304例符合纳入标准的患者中,平均(标准差)年龄为62.1(16.5)岁,59%为男性,平均(标准差)BMI为27(6)kg/m。36例(12%)HIT呈阳性。HIT的发生率随BMI的增加而逐渐升高(0%,8%,11%,19%,36%;p < 0.001)。与BMI正常的患者相比,BMI为30 kg/m至39.9 kg/m的患者发生HIT的几率增加了200%(优势比[OR],2.94;95%置信区间[CI],1.20 - 7.54;p = 0.019),而BMI为40 kg/m或更高的患者增加了600%(OR,6.98;95% CI,1.59 - 28.2;p = 0.012)。经过回归分析,BMI仍然是HIT发生发展 的独立预测因素(每kg/m的调整OR,1.08;95% CI,1.02 - 1.14;p = 0.010)。抗PF4OD值大于或等于2.0也随BMI增加(p < 0.001)。BMI高于正常时,院内死亡率显著增加(p = 0.026)。华法林4 - T评分、深静脉血栓形成、肺栓塞和中风发生率与BMI的变化无关。
BMI升高似乎与重症监护病房患者HIT发生率增加密切相关。肥胖是估计HIT预测试验概率的一个重要新临床变量,患者的“肥胖程度”可被视为4 - T评分系统的第五个“T”。需要更多的生化研究来阐明肥胖在这种免疫介导疾病中的作用。
预后/流行病学研究,III级。