重症急性胆源性胰腺炎与2型糖尿病:哪种关系?

IF 0.1 Q4 GASTROENTEROLOGY & HEPATOLOGY
F. Lapolla, Immacolata Forlano, A. D. Lascia, M. Gorgoglione, Vincenzo Neri
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Furthermore, we evaluated the prevalence of diabetes by the criteria usually used to define the different severity grades of pancreatitis. Results The comparison between SAP and ESAP has shown the following results: impairment degree of pancreas (Balthazar CT score): SAP 2.3 vs . ESAP 3.85; abdominal compartment syndrome (ACS): ESAP 7.6% (1/13); multiorgan dysfunction syndrome (MODS): ESAP 46.1% (6/13); simple organ dysfunction: SAP 51% (24/47) vs . ESAP 53.8% (7/13); hypoxemia: SAP 65.9 % (31/47) vs . ESAP 76.9% (10/13); pancreatic infections: SAP 6.3% (3/47) vs . ESAP 23% (3/13); mortality: SAP 4.2% (2/47) vs . ESAP 15.4% (2/13). The prevalence of diabetes in AP patients was 19.5% (54/276), 31.7% (19/60) in all severe acute forms of pancreatitis group and 38.4% (5/13) in ESAP group (P<0.05 chi-square test). 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引用次数: 0

摘要

糖尿病可能增加急性胰腺炎的风险,也可能对急性胰腺炎(AP)的发展产生不利影响。目的:本研究的目的是评估糖尿病是否与严重急性胰腺炎和危重型(早期严重急性胰腺炎;此外,糖尿病如何改变急性胰腺炎的演变。方法2001 ~ 2012年收治急性胆源性胰腺炎276例。所有严重急性形式的胰腺炎为21.7% (n=60);SAP (n=47)和ESAP (n=13)的临床特征、器官衰竭、治疗选择和结果进行了比较。我们评估了每组糖尿病患者的患病率(AP、SAP和ESAP)。此外,我们通过通常用于定义胰腺炎不同严重程度等级的标准来评估糖尿病的患病率。结果SAP与ESAP的比较显示:胰腺损伤程度(Balthazar CT评分):SAP 2.3 vs . ESAP 2.3;ESAP 3.85;腹腔隔室综合征(ACS): ESAP 7.6% (1/13);多器官功能障碍综合征(MODS): ESAP 46.1% (6/13);单纯器官功能障碍:SAP 51% (24/47) vs。Esap 53.8% (7/13);低氧血症:SAP 65.9% (31/47);Esap 76.9% (10/13);胰腺感染:SAP 6.3% (3/47) vs。Esap 23% (3/13);死亡率:SAP 4.2% (2/47) vs。Esap 15.4%(2/13)。重症急性胰腺炎组糖尿病患病率分别为19.5%(54/276)、31.7%(19/60)和38.4% (5/13)(P<0.05卡方检验)。就严重程度标准而言,糖尿病单器官功能障碍患病率为23.3% (14/60),MODS患病率为23.1%(3/13),脓毒症积液坏死并发症患病率为6.6%(4/60)。结论急性胰腺炎与糖尿病的相关性是显而易见的:糖尿病增加了急性胰腺炎的风险,但也增加了重症胰腺炎的风险。根据我们的经验,糖尿病可能会在全身性炎症的第一阶段加重急性胰腺炎,否则它似乎与可能的晚期脓毒性并发症的演变没有很强的联系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Severe Acute Biliary Pancreatitis and Type 2 Diabetes: Which Kind of Connection?
Context Diabetes may increase the risk of acute pancreatitis and may also adversely affects the evolution of the acute pancreatitis (AP). Objective The aim of the study was to evaluate if diabetes is associated with higher incidence of severe acute pancreatitis and also of critical forms (early severe acute pancreatitis; ESAP) and, moreover, how diabetes may modify the evolution of acute pancreatitis. Methods Since 2001 to 2012 we treated 276 acute biliary pancreatitis. All severe acute forms of pancreatitis were 21.7% (n=60); 13 (21.7%) critical forms were identified among SAP. Clinical features, organ failure, therapeutic choices and results between SAP (n=47) and ESAP (n=13) were compared. We evaluated the prevalence of patients with diabetes in each group (AP, SAP, and ESAP). Furthermore, we evaluated the prevalence of diabetes by the criteria usually used to define the different severity grades of pancreatitis. Results The comparison between SAP and ESAP has shown the following results: impairment degree of pancreas (Balthazar CT score): SAP 2.3 vs . ESAP 3.85; abdominal compartment syndrome (ACS): ESAP 7.6% (1/13); multiorgan dysfunction syndrome (MODS): ESAP 46.1% (6/13); simple organ dysfunction: SAP 51% (24/47) vs . ESAP 53.8% (7/13); hypoxemia: SAP 65.9 % (31/47) vs . ESAP 76.9% (10/13); pancreatic infections: SAP 6.3% (3/47) vs . ESAP 23% (3/13); mortality: SAP 4.2% (2/47) vs . ESAP 15.4% (2/13). The prevalence of diabetes in AP patients was 19.5% (54/276), 31.7% (19/60) in all severe acute forms of pancreatitis group and 38.4% (5/13) in ESAP group (P<0.05 chi-square test). Regarding the severity criteria, diabetes had a prevalence of 23.3% (14/60) in single organ dysfunction and 23.1% (3/13) in MODS and 6.6% (4/60) in septic complications of fluid necrotic collections. Conclusion The association of AP with the diabetes is in evidence: the risk of acute pancreatitis is raised by diabetes, but also of critical forms. In our experience diabetes may worsen acute pancreatitis in the first phase of systemic inflammation, otherwise it seems to be not strongly connected to the evolution of possible late septic complications.
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Journal of the Pancreas
Journal of the Pancreas GASTROENTEROLOGY & HEPATOLOGY-
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