80岁以上老年急性胰腺炎患者的临床特征分析
DOI: 10.3969/j.issn.1001-5256.2021.01.028
Clinical features of elderly patients with acute pancreatitis aged ≥80 years
-
摘要:
目的 探讨≥80岁老年急性胰腺炎(AP)患者的临床特征。 方法 回顾性分析2013年1月—2019年12月西南医科大学附属医院消化内科收治的3642例AP患者,分为青年组(<65岁,n=2955)、中老年组(65~79岁, n=558)、老年组(≥80岁, n=129例)。收集并统计分析3组患者的资料信息,包括性别、年龄、病因、诱因、既往病史、病情严重程度、并发症和临床转归等。符合正态分布的计量资料3组间比较采用one-way ANOVA检验,进一步两两比较采用LSD-t检验; 不符合正态分布的计量资料3组间比较采用Mann-Whitney U检验; 计数资料3组间比较采用χ2检验或Fisher精确概率法,有序多分类变量比较采用Kruskal-Wallis H检验。 结果 中老年组和老年组女性比例均高于青年组(P值均<0.05);老年组并发高血压比例均高于中老年组和青年组(P值均<0.05);老年组并发高脂血症比例低于青年组(P<0.05)。3组AP患者均以高脂饮食为主要诱因,老年组因酒精、高脂饮食+酒精诱发AP比例均低于青年组(P值均<0.05);老年组以胆道疾病为病因的比例高于中老年、青年组(P值均<0.05),而高脂血症、酒精、胆道疾病+高脂血症比例均低于青年组(P值均<0.05)。老年组中发生轻症急性胰腺炎83例(64.3%),中度重症急性胰腺炎23例(17.8%),重症急性胰腺炎23例(17.8%),与中老年组及青年组相比,病情严重程度构成比例差异均有统计学意义(P值均<0.05);老年、中老年组复发比例均低于青年组(P值均<0.05)。在全身并发症方面,老年组发生肺炎、急性肾损伤、多器官功能障碍综合征的比例均高于青年组(P值均<0.05)。老年组治愈病例比例均低于中老年组和青年组(P值均<0.05),好转病例比例均高于中老年组和青年组(P值均<0.05)。老年组和中老年组放弃治疗比例均高于青年组(P值均<0.05)。老年组死亡1例(0.8%),中老年组死亡9例(1.6%)、青年组死亡16例(0.5%),3组间比较差异无统计学意义(P>0.05)。3组患者住院天数及住院费用比较差异均无统计学意义(P值均>0.05)。 结论 ≥80岁AP患者以女性为主,多由胆源性因素引起,易并发肺炎、急性肾损伤、多器官功能障碍综合征。 Abstract:Objective To investigate the clinical features of elderly patients with acute pancreatitis (AP) aged ≥80 years. Methods A retrospective analysis was performed for 3642 patients with pancreatitis who were admitted to Department of Gastroenterology in The Affiliated Hospital of Southwest Medical University from January 2013 to December 2019, and according to age, they were divided into young group (aged < 65 years) with 2955 patients, middle-aged group (aged 65-79 years) with 558 patients, and elderly group (aged ≥80 years) with 129 patients. Related clinical data were collected and analyzed, including sex, age, etiology, predisposing factors, past medical history, disease severity, complication, and clinical outcome. The independent samples one-way ANOVA-test was used for comparison of normally distributed continuous data between groups and the least significant difference t-test was used for comparison within each group; the Mann-Whitney U test was used for comparison of non-normally distributed continuous data between groups; the chi-square test or the Fisher's exact test was used for comparison of categorical data between groups; the Kruskal-Wallis H test was used for comparison of ordinal categorical variables. Results In the young group, there were 1721 male patients and 1234 female patients; in the middle-aged group, there were 214 male patients and 334 female patients; in the elderly group, there were 48 male patients and 81 female patients; the middle-aged group and the elderly group had a significantly higher proportion of female patients than the young group (62.8% vs 61.6% vs 41.8%, P < 0.05). High-fat diet was the main predisposing factor for all three groups, and compared with the young group, the elderly group had a significantly lower proportion of patients with AP induced by alcohol or high-fat diet+alcohol (P < 0.05). The elderly group had a significantly higher proportion of patients with the etiology of biliary diseases than the middle-aged group and the young group (79.8% vs 69.2% vs 41.4%, χ2=204.127, P < 0.05), as well as a significantly lower proportion of patients with the etiology of hyperlipidemia, alcohol, or biliary diseases+hyperlipidemia (all P < 0.05). Among the 129 patients in the elderly group, 83 (64.3%) had mild AP, 23 (17.8%) had moderate-severe AP, and 23 (17.8%) had severe AP; there was a significant difference in the constituent ratio of disease severity between the elderly group and the middle-aged/young groups (H=1972.5, P < 0.05). The elderly group and the middle-aged group had a significantly lower proportion of patients with recurrence than the young group (both P < 0.05). There were no significant differences in local complications between the three groups (all P > 0.05), and as for systemic complications, compared with the young group, the elderly group had a significantly higher proportion of patients with pneumonia (3.9% vs 2.2%, P < 0.05), acute kidney injury (AKI) (6.2% vs 2.5%, P < 0.05), or multiple organ dysfunction syndrome (MODS) (7.8% vs 4.0%, P < 0.05). Compared with the middle-aged group and the young group, the elderly group had a significantly lower proportion of cured patients (67.4% vs 76.3% vs 82.0%, P < 0.05) and a significantly higher proportion of patients with improvement (23.3% vs 14.7%/12.7%, P < 0.05). The elderly group and the middle-aged group had a significantly higher proportion of patients withdrawn from treatment than the young group (8.5%/5.9% vs 3.4%, P < 0.05). There was 1 death in the elderly group (0.8%), 9 deaths in the middle-aged group (1.6%), and 16 deaths in the young group (0.5%), and there was no significant difference between the three groups (P > 0.05). There were no significant differences in length of hospital stay and hospital costs between the three groups (P > 0.05). Conclusion AP patients aged ≥80 years are mainly female and are often caused by biliary factors, and they are likely to develop the complications such as pneumonia, AKI, and MODS. -
Key words:
- Pancreatitis /
- Aged /
- Disease Attributes
-
表 1 3组患者一般资料比较
项目 青年组(n=2955) 中老年组(n=558) 老年组(n=129) 统计值 P值 年龄(岁) 45.1±10.5 71.2±4.21) 83.5±3.51)2) F=2 494.070 <0.001 性别[例(%)] χ2=90.884 <0.001 男 1721(58.2) 214(38.4)1) 48(37.2)1) 女 1234(41.8) 344(61.6) 81(62.8) 既往疾病史[例(%)] 胆道疾病 261(8.8) 45(8.1%) 11(8.5) χ2=0.367 0.832 高脂血症 109(3.7) 2(0.4)1) 01) χ2=21.858 <0.001 糖尿病 166(5.6) 19(3.4)1) 3(2.3) χ2=6.924 0.030 高血压 238(8.1) 100(17.9)1) 34(26.4)1)2) χ2=87.613 <0.001 混合因素 274(9.3) 70(12.5)1) 17(13.2) χ2=7.162 0.028 既往手术史[例(%)] 胆囊或胆道手术 223(7.5) 41(7.3) 15(11.6) χ2=3.009 0.222 ERCP 2(0.1) 2(0.4) 0 χ2=3.754 0.153 胃部手术 6(0.2) 1(0.2) 1(0.8) χ2=1.897 0.387 注:1)与青年组比较,P<0.05;2)与中老年组比较,P<0.05。ERCP,经内镜逆行胰胆管造影。 表 2 3组患者诱因与病因的差异性比较
项目 青年组(n=2955) 中老年组(n=558) 老年组(n=129) χ2值 P值 诱因[例(%)] 高脂饮食 869(29.4) 136(24.3)1) 31(24.0) 7.234 0.027 酒精 239(8.0) 31(5.5)1) 4(3.1)1) 8.125 0.017 高脂饮食+酒精 155(5.2) 2(0.4)1) 01) 33.253 <0.001 其他因素 10(0.3) 2(0.4) 2(1.6) 4.755 0.093 病因[例(%)] 胆道疾病 1223(41.4) 387(69.2)1) 103(79.8)1)2) 204.127 <0.001 高脂血症 1002(33.9) 62(11.1)1) 12(9.3)1) 143.900 <0.001 胆道疾病+高脂血症 148(5.0) 7(1.3) 1(0.8) 20.194 <0.001 酒精 320(10.8) 35(6.3)1) 4(3.1)1) 17.908 <0.001 药物 11(0.4) 5(0.9) 0 3.522 0.172 特发及其他 251(8.5) 63(11.3)1) 8(6.2) 5.650 0.059 注:1)与青年组比较,P<0.05;2)与中年组比较,P<0.05。 表 3 3组患者病情及复发差异性比较
项目 青年组(n=2955) 中老年组(n=558) 老年组(n=129) 统计值 P值 分型[例(%)] H=1 972.50 <0.001 MAP 1898(64.23) 365(65.4)1) 83(64.3)1)2) MSAP 545(18.44) 82(14.6) 23(17.8) SAP 512(17.33) 111(19.8) 23(17.8) 复发[例(%)] 是 740(25.0) 74(13.3)1) 16(12.4)1) χ2=45.22 <0.001 否 2215(75.0) 484(86.7) 113(87.6) 注:1)与青年组比较,P<0.05;2)与中老年组比较,P<0.05。MAP,轻症急性胰腺炎; MSAP,中度重症急性胰腺炎。 表 4 3组患者并发症比较
项目 青年组(n=2955) 中老年组(n=558) 老年组(n=129) χ2值 P值 局部并发症[例(%)] 急性液体积聚 1111(37.6) 197(35.3) 50(38.8) 1.179 0.555 假性囊肿 92(3.1) 23(4.1) 4(3.1) 1.522 0.467 急性坏死物积聚 506(17.1) 125(18.8) 22(17.1) 0.948 0.623 包裹性坏死 97(3.3) 15(2.7) 3(2.3) 0.845 0.655 感染性胰腺坏死 44(1.5) 13(2.3) 0 4.280 0.118 腹腔出血 8(0.3) 1(0.2) 0 0.664 区域性门静脉高压 38(1.3) 4(0.7) 1(0.8) 1.491 0.474 消化道瘘 4(0.1) 0 0 0.433 胃流出道梗阻 2(0.1) 1(0.2) 0 0.681 全身并发症[例(%)] 肺炎 28(0.9) 12(2.2)1) 5(3.9)1) 13.207 0.001 SIRS 829(28.1) 145(26.0) 34(26.4) 1.120 0.571 ARDS 194(6.6) 39(7.0) 5(3.9) 1.686 0.430 AKI 75(2.5) 17(3.0) 8(6.2)1) 6.436 0.040 胰性脑病 1(0) 1(0.2) 1(0.8) 9.005 0.011 脓毒症 30(1.0) 5(0.9) 1(0.8) 0.130 0.937 MODS 118(4.0) 36(6.5)1) 10(7.8)1) 9.879 0.007 注:1)与青年组比较,P<0.05;2)与中老年组比较,P<0.05。SIRS,全身反应炎症综合征; ARDS,急性呼吸窘迫综合征; AKI,急性肾损伤; MODS,多器官功能障碍综合征。 表 5 3组患者临床转归、住院天数、住院费用比较
项目 青年组(n=2955) 中老年组(n=558) 老年组(n=129) 统计值 P值 临床转归[例(%)] 治愈 2423(82.0) 426(76.3)1) 87(67.4)1)2) χ2=24.448 <0.001 好转 375(12.7) 82(14.7) 30(23.3)1)2) χ2=12.908 0.002 转外科 40(1.4) 8(1.4) 0 χ2=1.809 0.405 放弃 101(3.4) 33(5.9)1) 11(8.5)1) χ2=14.879 <0.001 死亡 16(0.5) 9(1.6)1) 1(0.8) χ2=7.609 0.022 住院费用(元) 20 272.6 (14 619.9~33 548.8) 23 321.2 (14 905.2~33 780.9)1) 19 050.7 (12 570.6~32 938.5) H=1.055 0.348 住院天数(d) 12.38±7.64 12.86±8.23 12.07±8.39 F=7.059 0.290 注:1)与青年组比较,P<0.05;2)与中老年组比较,P<0.05。 -
[1] LEPPÄNIEMI A, TOLONEN M, TARASCONI A, et al. 2019 WSES guidelines for the management of severe acute pancreatitis[J]. World J Emerg Surg, 2019, 14: 27. DOI: 10.1186/s13017-019-0247-0 [2] SANDZÉN B, ROSENMVLLER M, HAAPAMÄKI MM, et al. First attack of acute pancreatitis in Sweden 1988-2003: Incidence, aetiological classification, procedures and mortality-a register study[J]. BMC Gastroenterol, 2009, 9: 18. DOI: 10.1186/1471-230X-9-18 [3] ROBERTS SE, MORRISON-REES S, JOHN A, et al. The incidence and aetiology of acute pancreatitis across Europe[J]. Pancreatology, 2017, 17(2): 155-165. DOI: 10.1016/j.pan.2017.01.005 [4] BANKS PA, BOLLEN TL, DERVENIS C, et al. Classification of acute pancreatitis-2012: Revision of the Atlanta classification and definitions by international consensus[J]. Gut, 2013, 62(1): 102-111. DOI: 10.1136/gutjnl-2012-302779 [5] VLGER BV, GVL M, USLUKAYA Ö, et al. New hormones to predict the severity of gallstone-induced acute pancreatitis[J]. Turk J Gastroenterol, 2014, 25(6): 714-717. http://europepmc.org/abstract/med/25599787 [6] SCHERER J, SINGH VP, PITCHUMONI CS, et al. Issues in hypertriglyceridemic pancreatitis: An update[J]. J Clin Gastroenterol, 2014, 48(3): 195-203. DOI: 10.1097/01.mcg.0000436438.60145.5a [7] GAO YJ, LI YQ, WANG Q, et al. Analysis of the clinical features of recurrent acute pancreatitis in China[J]. J Gastroenterol, 2006, 41(7): 681-685. DOI: 10.1007/s00535-006-1820-3 [8] KOWALP, GOODKINDD, HEW. (2016) An Aging World: 2015, International Population Reports. U.S[EB/OL]. http://www.census.gov/library/publications/2016/demo/P95-16-1.html. [9] CLEGG A, YOUNG J, ILIFFE S, et al. Frailty in elderly people[J]. Lancet, 2013, 381(9868): 752-762. DOI: 10.1016/S0140-6736(12)62167-9 [10] ZHU Y, PAN X, ZENG H, et al. A study on the etiology, severity, and mortality of 3260 patients with acute pancreatitis according to the Revised Atlanta Classification in Jiangxi, China over an 8-year period[J]. Pancreas, 2017, 46(4): 504-509. DOI: 10.1097/MPA.0000000000000776 [11] QUERO G, COVINO M, OJETTI V, et al. Acute pancreatitis in oldest old: A 10-year retrospective analysis of patients referred to the emergency department of a large tertiary hospital[J]. Eur J Gastroenterol Hepatol, 2020, 32(2): 159-165. DOI: 10.1097/MEG.0000000000001570 [12] Editoral Board of Chinese Journal of Digestion, Cooperation Group of Hepatobiliary Disease of Chinese Society of Gastroenterology. Consensus on diagnosis and treatment of chronic cholecystitis and gallstones in China (2018)[J]. J Clin Hepatol, 2019, 35(6): 1231-1236. (in Chinese) DOI: 10.3969/j.issn.1001-5256.2019.06.011中华消化杂志编辑委员会, 中华医学会消化病学分会肝胆疾病协作组. 中国慢性胆囊炎、胆囊结石内科诊疗共识意见(2018年)[J]. 临床肝胆病杂志, 2019, 35(6): 1231-1236. DOI: 10.3969/j.issn.1001-5256.2019.06.011 [13] TAI WP, ZHANG NW, ZHU B, et al. Clinical characteristics and diagnosis and treatment efficiency of acute pancreatitis in the elderly[J]. Chin J Mult Organ Dis Elderly, 2018, 17(1): 57-60. (in Chinese) https://www.cnki.com.cn/Article/CJFDTOTAL-ZLQG201801015.htm台卫平, 张能维, 朱斌, 等. 老年急性胰腺炎患者的临床特征和诊疗效果分析[J]. 中华老年多器官疾病杂志, 2018, 17(1): 57-60. https://www.cnki.com.cn/Article/CJFDTOTAL-ZLQG201801015.htm [14] BARBEIRO DF, KOIKE MK, COELHO AM, et al. Intestinal barrier dysfunction and increased COX-2 gene expression in the gut of elderly rats with acute pancreatitis[J]. Pancreatology, 2016, 16(1): 52-56. DOI: 10.1016/j.pan.2015.10.012 [15] CARVALHO JR, FERNANDES SR, SANTOS P, et al. Acute pancreatitis in the elderly: A cause for increased concern?[J]. Eur J Gastroenterol Hepatol, 2018, 30(3): 337-341. DOI: 10.1097/MEG.0000000000001028 [16] MIN A, LI H, XIANG HP, et al. Comparison of three classification systems for acute pancreatitis[J]. Chin J Emerge Med, 2019, 28(5): 625-629. (in Chinese) DOI: 10.3760/cma.j.issn.1671-0282.2019.05.018闵安, 李贺, 项和平, 等. 急性胰腺炎三种分类标准的比较[J]. 中华急诊医学杂志, 2019, 28(5): 625-629. DOI: 10.3760/cma.j.issn.1671-0282.2019.05.018 [17] JIANG X, XU H, YAN YF, et al. Clinical and prognostic characteristics of alcoholic pancreatitis[J]. J Clin Hepatol, 2019, 35(11): 2528-2532. (in Chinese) DOI: 10.3969/j.issn.1001-5256.2019.11.027蒋鑫, 徐欢, 严永峰, 等. 酒精性急性胰腺炎的临床及预后特征分析[J]. 临床肝胆病杂志, 2019, 35(11): 2528-2532. DOI: 10.3969/j.issn.1001-5256.2019.11.027 [18] TANG YL, FANG CG, WU WW, et al. Analysis of high risk factors and predictive models of secondary pancreatic necrosis in acute biliary pancreatitis[J]. Trauma and Crit Medicine, 2020, 8(2): 104-106, 109.(in Chinese) https://www.cnki.com.cn/Article/CJFDTOTAL-CSJB202002012.htm唐义龙, 方晨光, 吴文伟, 等. 急性胆源性胰腺炎继发胰腺坏死高危因素及预测模型分析[J]. 创伤与急危重病医学, 2020, 8(2): 104-106, 109. https://www.cnki.com.cn/Article/CJFDTOTAL-CSJB202002012.htm [19] LÖHR JM, PANIC N, VUJASINOVIC M, et al. The ageing pancreas: A systematic review of the evidence and analysis of the consequences[J]. J Intern Med, 2018, 283(5): 446-460. DOI: 10.1111/joim.12745 [20] SHEN XZ, WU SD. Pathogenesis and progress of diagnosis and treatment of severe acute pancreatitis-associated kidney injury[J]. Chin J Dig, 2019, 39(5): 300-303. (in Chinese) DOI: 10.3760/cma.j.issn.0254-1432.2019.05.005沈锡中, 吴盛迪. 重症急性胰腺炎相关肾损伤的发病机制和诊疗进展[J]. 中华消化杂志, 2019, 39(5): 300-303. DOI: 10.3760/cma.j.issn.0254-1432.2019.05.005 [21] PATEL K, LI F, LUTHRA A, et al. Acute biliary pancreatitis is associated with adverse outcomes in the elderly: A propensity score-matched analysis[J]. J Clin Gastroenterol, 2019, 53(7): e291-e297. DOI: 10.1097/MCG.0000000000001108 [22] KOZIEL D, GLUSZEK-OSUCH M, SULIGA E, et al. Elderly persons with acute pancreatitis - specifics of the clinical course of the disease[J]. Clin Interv Aging, 2019, 14: 33-41. http://www.researchgate.net/publication/329820494_Elderly_persons_with_acute_pancreatitis_-_specifics_of_the_clinical_course_of_the_disease [23] MÁRTA K, LAZARESCU AM, FARKAS N, et al. Aging and comorbidities in acute pancreatitis I: A Meta-analysis and systematic review based on 194, 702 patients[J]. Front Physiol, 2019, 10: 328. DOI: 10.3389/fphys.2019.00328
计量
- 文章访问数: 915
- HTML全文浏览量: 176
- PDF下载量: 48
- 被引次数: 0