Shahrin Lubaba, Sarmin Monira, Parvin Irin, Al Hasan Md Maksud, Nahar Mst Arifun, Mohammad Sayeem Bin Shahid Abu Sadat, Shaima Shamsun Nahar, Salahuddin Mamun Gazi Md, Nasrin Shajeda, Ahmed Tahmeed, Chisti Mohammod Jobayer
Clinical and Diagnostic Services, icddr,b, Dhaka, Bangladesh.
Nutrition Research Division, icddr,b, Dhaka, Bangladesh.
Lancet Reg Health Southeast Asia. 2024 Oct 21;30:100500. doi: 10.1016/j.lansea.2024.100500. eCollection 2024 Nov.
Septic shock and hypovolemic shock are life-threatening illnesses that necessitate immediate recognition and intervention, as they can result in deadly consequences. While the underlying processes may vary, both entities can exhibit hypotension and organ dysfunction. No studies have been conducted on bedside testing to differentiate between these illnesses. Lactate measurement has been established as a viable option for early detection of septic shock. However, its role in diagnosing hypovolemic shock has yet to be evaluated. The aim of the study was to investigate alterations in lactate levels among diarrheal patients with septic shock and hypovolemic shock following the administration of first fluid resuscitation.
We conducted a prospective observational study in critically ill diarrheal adults aged ≥18 years in the emergency ward in Dhaka Hospital of icddr,b from 21st October 2021 to 31st May 2023 (total 19 months). The enrollment process was operational between 8:30 AM and 5:00 PM. Diarrheal adults with a diagnosis of sepsis with shock featured with poor peripheral perfusion (characterized by cold periphery and weak or absent pulse and capillary refill time >3 s) or hypotension (characterized by mean arterial pressure <65 mm-Hg) were enrolled as cases and consecutive diarrheal patients without any obvious features of sepsis with hypovolemic shock (due to severe dehydration) comprised the comparison group. POC lactate test was done at hours 0, 1st and 6th by StatStrip Lactate meters (Nova Biomedical, US) to all enrolled patients. For comparison of POC lactate levels, we used paired t-test for comparing the lactate samples drawn at hour 0, hour 1 and 6 with the septic shock and hypovolemic shock group. Odds ratio (OR) and their 95% confidence intervals (CIs) were used to demonstrate the strength of association. The study was registered at Clinicaltrials.gov (NCT05108467) and received institutional ethical approval (PR-21097).
Of 435 patients, 135 had septic shock and 141 had hypovolemic shock, rest 41 patient responded with fluid bolus. 25% (34/135) of the people in the septic shock group died whereas there is no mortality in the hypovolemic shock group. The number of patients visiting from outside Dhaka city had more septic shock than from inside were higher in comparison with (55% vs. 28%; p < 0.001). Statistically significant difference was observed between septic shock and hypovolemic shock group for a median POC lactate in 0, 1st and 6th hours with an OR of 1.07 (95% CI: 0.99, 1.17; p = 0.039); 1.48, (95% CI: 1.28, 1.70; p < 0.001) and 2.36 (95% CI: 1.85, 3.00; p < 0.001), respectively. The gradient of 1st to 2nd sample between septic shock and hypovolemic shock was found to be significantly different (OR: 0.74, 95% CI: 0.64, 0.85; p < 0.001).
POC lactate test can detect septic shock by differentiating hypovolemic shock in diarrheal patients. By providing quick, reliable and accurate result this test can help clinicians quickly diagnose and treat time-sensitive condition, like septic shock.
The study was funded by Global Affairs of Canada (GR-01726). The donors had no role in the design, implementation, analysis, data interpretation or writing manuscript, or decision to publish. The corresponding author had access to all data and takes responsibility for the final approval and submission of the manuscript.
感染性休克和低血容量性休克是危及生命的疾病,需要立即识别和干预,因为它们可能导致致命后果。虽然潜在过程可能有所不同,但这两种情况都可能出现低血压和器官功能障碍。尚未进行关于床边检测以区分这些疾病的研究。乳酸测量已被确立为早期检测感染性休克的可行选择。然而,其在诊断低血容量性休克中的作用尚未得到评估。本研究的目的是调查感染性休克和低血容量性休克腹泻患者在首次液体复苏后乳酸水平的变化。
我们于2021年10月21日至2023年5月31日(共19个月)在达卡医院国际腹泻病研究中心的急诊病房对年龄≥18岁的重症腹泻成年患者进行了一项前瞻性观察研究。入组过程在上午8:30至下午5:00之间进行。诊断为感染性休克且伴有外周灌注不良(表现为四肢冰冷、脉搏微弱或无脉且毛细血管再充盈时间>3秒)或低血压(表现为平均动脉压<65mmHg)的腹泻成年患者被纳入病例组,而连续的无任何明显感染性休克特征(因严重脱水导致低血容量性休克)的腹泻患者组成对照组。对所有入组患者在第0小时、第1小时和第6小时使用StatStrip乳酸仪(美国Nova Biomedical公司)进行即时检验(POC)乳酸检测。为比较POC乳酸水平,我们使用配对t检验比较感染性休克组和低血容量性休克组在第0小时、第1小时和第6小时采集的乳酸样本。比值比(OR)及其95%置信区间(CI)用于表明关联强度。该研究已在Clinicaltrials.gov注册(NCT05108467)并获得机构伦理批准(PR - 21097)。
435例患者中,135例患有感染性休克,141例患有低血容量性休克,其余41例患者经快速补液后有反应。感染性休克组25%(34/135)的患者死亡,而低血容量性休克组无死亡病例。来自达卡市以外的患者中感染性休克的人数比来自市内的患者更多(55%对28%;p<0.001)。在第0小时、第1小时和第6小时,感染性休克组和低血容量性休克组的POC乳酸中位数存在统计学显著差异,OR分别为1.07(95%CI:0.99,1.17;p = 0.039);1.48(95%CI:1.28,1.70;p<0.001)和2.36(95%CI:1.85,3.00;p<0.001)。发现感染性休克组和低血容量性休克组第1次与第2次样本之间的梯度有显著差异(OR:0.74,95%CI:0.64,0.85;p<0.001)。
POC乳酸检测可通过区分腹泻患者的低血容量性休克来检测感染性休克。通过提供快速且可靠准确的结果,该检测可帮助临床医生快速诊断和治疗像感染性休克这样对时间敏感的病症。
本研究由加拿大全球事务部资助(GR - 01726)。资助者在研究设计、实施、分析、数据解读、撰写稿件或决定发表方面均无作用。通讯作者有权获取所有数据,并对稿件的最终批准和提交负责。