Vevaud Kevin, Dallocchio Aymeric, Dumoitier Nathalie, Laspougeas Alban, Labrunie Anaïs, Belgacem Alexis, Fourcade Laurent, Ballouhey Quentin
Service de chirurgie pédiatrique, Hôpital des Enfants, Hôpital Universitaire de Limoges, 8 Avenue Dominique Larrey, Limoges Cedex, 87042, France.
Département universitaire de médecine Générale, Faculté de médecine de Limoges, 2 rue du Docteur Marcland, Limoges Cedex, 87042, France.
BMC Pediatr. 2024 Feb 19;24(1):131. doi: 10.1186/s12887-024-04619-z.
The objective of this study was to assess the likelihood of acute appendicitis (AA) in children presenting with abdominal symptoms at the emergency department (ED), based on their prior primary care (PC) consultation history.
Between February and June 2021, we prospectively enrolled all children presenting at the ED with acute abdominal pain indicative of possible acute appendicitis (AA). Subsequently, they were categorized into three groups: those assessed by a PC physician (PG), those brought in by their family without a prior consultation (FG), and those admitted after a PC consultation without being assessed as such. The primary objective was to assess the probability of AA diagnosis using the Pediatric Appendicitis Score (PAS). Secondary objectives included analyzing PAS and C-reactive protein (CRP) levels based on the duration of pain and final diagnoses.
124 children were enrolled in the study (PG, n = 56; FG, n = 55; NG, n = 13). Among them, 29 patients (23.4%) were diagnosed with AA, with 13 cases (23.2%) from the PG and 14 cases (25.4%) from the FG. The mean PAS scores for AA cases from the PG and FG were 6.69 ± 1.75 and 7.57 ± 1.6, respectively, (p = 0.3340). Both PAS scores and CRP levels showed a significant correlation with AA severity. No cases of AA were observed with PAS scores < 4.
There was no significant difference in PAS scores between patients addressed by PG and FG, even though PAS scores tended to be higher for patients with AA. We propose a new decision-making algorithm for PC practice, which incorporates inflammatory markers and pain duration.
Institutional Ethics Committee registration number: 447-2021-103 (10/01/2021).
ClinicalTrials.gov Identifier: NCT04885335 (Registered on 13/05/2021).
本研究的目的是根据儿童在急诊科(ED)出现腹部症状时的既往初级保健(PC)咨询病史,评估其患急性阑尾炎(AA)的可能性。
在2021年2月至6月期间,我们前瞻性纳入了所有因提示可能患有急性阑尾炎(AA)的急性腹痛而到急诊科就诊的儿童。随后,他们被分为三组:由初级保健医生评估的儿童(PG组)、未经事先咨询由家人带来的儿童(FG组)以及在初级保健咨询后入院但未得到此类评估的儿童(NG组)。主要目的是使用小儿阑尾炎评分(PAS)评估AA诊断的概率。次要目的包括根据疼痛持续时间和最终诊断分析PAS和C反应蛋白(CRP)水平。
124名儿童纳入研究(PG组,n = 56;FG组,n = 55;NG组,n = 13)。其中,29例患者(23.4%)被诊断为AA,PG组13例(23.2%),FG组14例(25.4%)。PG组和FG组AA病例的平均PAS评分分别为6.69±1.75和7.57±1.6,(p = 0.3340)。PAS评分和CRP水平均与AA严重程度显著相关。PAS评分<4时未观察到AA病例。
PG组和FG组患者的PAS评分无显著差异,尽管AA患者的PAS评分往往更高。我们提出了一种新的初级保健实践决策算法,该算法纳入了炎症标志物和疼痛持续时间。
机构伦理委员会注册号:447 - 2021 - 103(2021年1月10日)。
ClinicalTrials.gov标识符:NCT04885335(2021年5月13日注册)。