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本文引用的文献

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Hydroxyurea for Children and Adults with Hemoglobin SC Disease.羟基脲用于患有血红蛋白SC病的儿童和成人。
NEJM Evid. 2025 Feb;4(2):EVIDoa2400402. doi: 10.1056/EVIDoa2400402. Epub 2024 Dec 8.
2
Hydroxyurea dose optimisation for children with sickle cell anaemia in sub-Saharan Africa (REACH): extended follow-up of a multicentre, open-label, phase 1/2 trial.撒哈拉以南非洲镰状细胞贫血儿童羟脲剂量优化(REACH):一项多中心、开放性、1/2 期试验的扩展随访。
Lancet Haematol. 2024 Jun;11(6):e425-e435. doi: 10.1016/S2352-3026(24)00078-4. Epub 2024 Apr 30.
3
Sex and frequency of pain episodes are associated with acute pain trajectories in adolescents with sickle cell disease.性别和疼痛发作频率与镰状细胞病青少年的急性疼痛轨迹相关。
Pain Rep. 2023 Aug 7;8(5):e1084. doi: 10.1097/PR9.0000000000001084. eCollection 2023 Sep.
4
Estimating the risk of child mortality attributable to sickle cell anaemia in sub-Saharan Africa: a retrospective, multicentre, case-control study.估算撒哈拉以南非洲地区镰状细胞贫血导致儿童死亡的风险:一项回顾性、多中心、病例对照研究。
Lancet Haematol. 2022 Mar;9(3):e208-e216. doi: 10.1016/S2352-3026(22)00004-7.
5
Sickle cell disease as an accelerated aging syndrome.镰状细胞病作为一种加速衰老综合征。
Exp Biol Med (Maywood). 2022 Feb;247(4):368-374. doi: 10.1177/15353702211068522. Epub 2022 Feb 16.
6
Sickle Cell Disease-Genetics, Pathophysiology, Clinical Presentation and Treatment.镰状细胞病——遗传学、病理生理学、临床表现与治疗
Int J Neonatal Screen. 2019 May 7;5(2):20. doi: 10.3390/ijns5020020. eCollection 2019 Jun.
7
Sickle cell disease and malaria: decreased exposure and asplenia can modulate the risk from Plasmodium falciparum.镰状细胞病和疟疾:减少接触和脾切除可调节疟原虫感染的风险。
Malar J. 2020 Apr 25;19(1):165. doi: 10.1186/s12936-020-03212-w.
8
Sickle cell disease: A primary care update.镰状细胞病:初级保健更新。
Cleve Clin J Med. 2020 Jan;87(1):19-27. doi: 10.3949/ccjm.87a.18051. Epub 2020 Jan 2.
9
Chronic pain as a symptom or a disease: the IASP Classification of Chronic Pain for the International Classification of Diseases (ICD-11).慢性疼痛:作为一种症状或疾病——国际疼痛学会(IASP)对《国际疾病分类》第 11 版(ICD-11)中慢性疼痛的分类。
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10
Hydroxyurea for Children with Sickle Cell Anemia in Sub-Saharan Africa.在撒哈拉以南非洲,用羟脲治疗镰状细胞贫血儿童。
N Engl J Med. 2019 Jan 10;380(2):121-131. doi: 10.1056/NEJMoa1813598. Epub 2018 Dec 1.

到访乌干达穆拉戈国家转诊医院的镰状细胞病患者中与疼痛发作相关的危险因素。

Risk factors associated with pain episodes among sickle cell patients that visited Mulago National Referral Hospital-Uganda.

作者信息

Shamira Nassiwa, Bosco Asiimwe John, Dick Nsimbe, Lwanga Charles

机构信息

Department of Statistical Methods & Actuarial Sciences, School of Statistics & Planning, College of Business & Management Sciences, Makerere University, Kampala, Uganda.

Department of Planning, School of Statistics & Planning, College of Business & Management Sciences, Makerere University, Kampala, Uganda.

出版信息

BMC Health Serv Res. 2025 Apr 21;25(1):571. doi: 10.1186/s12913-025-12753-2.

DOI:10.1186/s12913-025-12753-2
PMID:40259337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12010511/
Abstract

BACKGROUND

Sickle cell disease (SCD) is a chronic hematologic disease associated with increased morbidity and mortality. The study aims to investigate the suggested socio-economic and clinical factors and their contribution to the frequency of pain episodes among sickle cell patients in Uganda.

METHOD

We used pre-existing secondary data from sickle cell clinic records at Mulago referral hospital collected in 2019, with a sample of 2532 sickle cell patients. In support of the outcome being count data, the Negative Binomial Regression model was utilized to estimate how the independent factors affected the frequency of pain episodes among the patients.

RESULTS

The frequency of pain episodes was different among age groups as age group (16/24) experienced the highest number of pain episodes on average (Incidence Rate Ratio = 1.39; 95% CI = 1.277-1.522; p = 0.000) compared to young children because as individuals age, pain management declines, and repeated episodes can lead to increased sensitivity, making them more prone to pain. While increased temperature (°C) (fever) increased the frequency of pain episodes by 24% (Incidence Rate Ratio = 1.243; 95% CI = 1.147-1.348; p = 0.000), infection by 27% (Incidence Rate Ratio = 1.27; 95% CI = 1.191-1.354; p < 0.000), other chronic diseases by 11% (Incidence Rate Ratio = 1.11; 95% CI = 1.038-1.188; p < 0.002), malaria by 38% (Incidence Rate Ratio = 1.38; 95% CI = 1.036-1.836; p < 0.027). The rate of hydroxyurea usage was very high at 90%. The intake of the drug reduced the frequency of pain episodes by 34% (Incidence Rate Ratio = 0.662; 95% CI = 0.584-0.750; p < 0.000). According to the observations, there is a high chance that hydroxyurea also had a strong protective against malaria in SCD patients. Nevertheless, there was no evidence that being a male or female would influence the frequency of pain episodes among sickle cell patients.

CONCLUSIONS

These findings are expected to add to the body of knowledge in the health sector, assist in advocacy programs, inform policy, and aid in tailored interventions.

摘要

背景

镰状细胞病(SCD)是一种慢性血液疾病,与发病率和死亡率增加相关。本研究旨在调查乌干达镰状细胞病患者中社会经济和临床因素及其对疼痛发作频率的影响。

方法

我们使用了2019年在穆拉戈转诊医院镰状细胞病门诊记录中已有的二手数据,样本为2532例镰状细胞病患者。为支持结果为计数数据,采用负二项回归模型来估计独立因素如何影响患者疼痛发作的频率。

结果

各年龄组的疼痛发作频率不同,年龄组(16/24岁)平均经历的疼痛发作次数最多(发病率比=1.39;95%置信区间=1.277 - 1.522;p = 0.000),与幼儿相比,随着个体年龄增长,疼痛管理能力下降,反复发作会导致敏感性增加,使他们更容易疼痛。温度升高(摄氏度)(发热)使疼痛发作频率增加24%(发病率比=1.243;95%置信区间=1.147 - 1.348;p = 0.000),感染使发作频率增加27%(发病率比=1.27;95%置信区间=1.191 - 1.354;p < 0.000),其他慢性病使发作频率增加11%(发病率比=1.11;95%置信区间=1.038 - 1.188;p < 0.002),疟疾使发作频率增加38%(发病率比=1.38;95%置信区间=1.036 - 1.836;p < 0.027)。羟基脲的使用率非常高,为90%。服用该药物使疼痛发作频率降低34%(发病率比=0.662;95%置信区间=0.584 - 0.750;p < 0.000)。根据观察结果,羟基脲在镰状细胞病患者中很有可能对疟疾也有很强的保护作用。然而,没有证据表明性别会影响镰状细胞病患者的疼痛发作频率。

结论

这些发现有望增加卫生部门的知识体系,有助于宣传项目,为政策提供信息,并有助于制定针对性的干预措施。