Hsia Daniel S, Tarai Sarah G, Alimi Amir, Coss-Bu Jorge A, Haymond Morey W
Division of Pediatric Diabetes and Endocrinology, Department of Pediatrics, Baylor College of Medicine, Texas Children's Hospital, Houston, TX 77030, USA.
Baylor College of Medicine, Medical School, Houston, TX 77030, USA.
Pediatr Diabetes. 2015 Aug;16(5):338-44. doi: 10.1111/pedi.12268. Epub 2015 Mar 19.
To compare outcomes of diabetic ketoacidosis (DKA) 6 yrs before and 6 yrs after changing rehydration fluids from ½ normal saline to Lactated Ringer's and decreasing the total intended fluid volume administered in the first 24 hrs from 3500 mL/m(2) /d to ≤ 2500 mL/m(2) /d at Texas Children's Hospital (TCH) in response to recommendations by the ESPE, LWPES, and ISPAD in 2004.
SUBJECTS/METHODS: A retrospective cohort study was conducted in which 1868 admissions for DKA were identified and reviewed. The cohort was divided into two groups: Group A, 1998-2004, and Group B, 2004-2010. Subjects with suspected clinical cerebral edema and adverse outcomes were identified.
Although not statistically significant, there was an equal number (n = 3) of adverse outcomes (death or neurological damage) in each group despite more than double the admissions in Group B (1264) compared with those in Group A (604). Overall, the incidence of suspected clinical cerebral edema was more than double for those admissions in which fluid resuscitation was initiated at an outside hospital (OSH) vs. at TCH (13.6 vs. 5.3%, p < 0.001).
Decreasing the intended fluid rate during the initial 24 hrs to 2500 mL/m(2) /d and increasing the IV fluid sodium content did not significantly decrease the incidence of adverse outcomes in children with DKA. However, children transferred from an OSH had a higher incidence of suspected clinical cerebral edema. Thus, we need to more readily share our management protocols with the emergency rooms of local referring hospitals to potentially decrease the incidence of suspected clinical cerebral edema and adverse outcomes in children transferred with DKA.
根据2004年欧洲儿科内分泌学会(ESPE)、欧洲儿科液体治疗学会(LWPES)和国际儿童糖尿病学会(ISPAD)的建议,比较德克萨斯儿童医院(TCH)将补液从1/2生理盐水改为乳酸林格氏液,并将最初24小时内计划给予的总液体量从3500 mL/m²/d降至≤2500 mL/m²/d前后6年糖尿病酮症酸中毒(DKA)的治疗结果。
受试者/方法:进行了一项回顾性队列研究,确定并审查了1868例DKA住院病例。该队列分为两组:A组,1998 - 2004年;B组,2004 - 2010年。确定有疑似临床脑水肿和不良结局的受试者。
尽管无统计学意义,但两组的不良结局(死亡或神经损伤)数量相等(n = 3),尽管B组(1264例)的住院人数是A组(604例)的两倍多。总体而言,与在TCH开始液体复苏的住院患者相比,在外部医院(OSH)开始液体复苏的患者疑似临床脑水肿的发生率高出一倍多(13.6%对5.3%,p < 0.001)。
将最初24小时内的液体输注速率降至2500 mL/m²/d并增加静脉输液的钠含量,并未显著降低DKA患儿不良结局的发生率。然而,从OSH转诊的儿童疑似临床脑水肿的发生率较高。因此,我们需要更及时地与当地转诊医院的急诊室分享我们的管理方案,以潜在降低DKA转诊儿童疑似临床脑水肿和不良结局的发生率。