糖尿病患者贫血的患病率和相关因素

Wafaa Tahseen Mohammad Sawalmeh, Abeer Fayez Salem Habarneh, Mohammad Adnan Ayed Batayneh, Rawnaq Ahmad Marji Al-Masaeed, Balgees Mohammad Abdullah Al-Rawashdeh
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引用次数: 0

摘要

导言:糖尿病与一系列病理变化有关,如新陈代谢、细胞和血液紊乱,会导致长期的微血管和大血管并发症,因此是一项重大的全球性健康挑战。尽管文献报道的贫血患病率范围很广,但医疗服务提供者往往低估了贫血在糖尿病并发症中的作用。事实证明,及早解决糖尿病患者的贫血问题可以降低这些并发症的发病率:研究目的:本研究旨在估算 2 型糖尿病(T2DM)患者中贫血的患病率及其相关因素:这是一项横断面前瞻性研究,对皇家医疗服务部四家军事医院(侯赛因国王医疗中心、拉希德王子军事医院、阿利亚王后军事医院和哈希姆王子军事医院)家庭医学门诊的糖尿病患者病历进行了回顾性审查。被诊断患有 2 型糖尿病一年以上的 18 岁以上成年患者将被纳入研究范围。但是,患有可能导致贫血的疾病(如地中海贫血和白血病)或其他全身性疾病(如传染病)的患者、患有急性出血等急性疾病的患者、在过去三个月中接受过输血的患者、孕妇或 1 型糖尿病患者将被排除在外。贫血的定义是男性血红蛋白水平低于 13 g/dl,女性血红蛋白水平低于 12 g/dl(Harrison TR,2011 年)。2 型糖尿病将被定义为糖化血红蛋白(HbA1c > 6.5%)、空腹血糖(FBG > 126 mg/dl)、随机血糖(RBG > 200 mg/dl)(美国糖尿病协会,2012 年)。此外,还将排除任何患有排除标准中所述的一种或多种疾病的患者。同时,在患者同意参与研究后,研究人员将在门诊收集以下数据,包括:年龄、性别、婚姻状况、吸烟状况、合并症、人体测量数据,包括体重、身高和体重指数(BMI)。此外,患者将被要求提取全血细胞计数(CBC)血样,其中包括血红蛋白、平均血球容积(MCV)、平均血球血红蛋白(MCH)和平均血球血红蛋白浓度(MCHC),以诊断是否存在贫血。研究变量血糖控制将根据 HbA1c 结果分为两类(控制糖尿病组包括 HbA1c 水平等于或等于 7.5% 的患者)。体重指数将根据美国疾病控制中心(CDC)的标准进行分类,具体如下体重指数小于 18.5 千克/平方米为体重不足,18.5-24.9 千克/平方米为正常,25-29.9 千克/平方米为超重,体重指数≥30 千克/平方米为肥胖。 样本量将根据科兰的样本量公式计算:n=Z2 pq /e2。其中,p 为糖尿病人群贫血患病率的预期值,q=1 -p;e 为可接受误差(5%);Z= 1.96。将采用简单随机抽样(系统程序)来选择 2 型糖尿病患者,以减少选择偏差的可能性。采用这种方法时,我们先随机抽取第一名受试者,然后根据 K(间隔)定期抽取下一名受试者。K 将根据研究人员准备的抽样框架除以 n 来确定。对于正态分布的变量,将使用平均值(标准差)进行描述性分析;对于高度偏态分布的变量,将使用中位数(四分位间距)进行描述性分析。对于正态分布和高度偏态分布的变量,将分别使用 t 检验和 Mann-Whitney 检验来比较贫血组和非贫血组之间定量变量的基线特征。分类变量将使用卡方检验进行组间比较。将采用逻辑回归分析找出这些变量与贫血的关系。分析结果将以几率比(ORs)和 95% 置信区间(CI)的形式给出。我们将只选择单变量分析中 p 值小于 0.20 的协变量进入逻辑分析。
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Prevalence and associated Factors of Anemia in Diabetic Patients
Introduction: Diabetes presents a significant global health challenge due to its association with a range of pathological changes, such as metabolic, cellular, and blood disturbances, that lead to long-term microvascular and macrovascular complications. Healthcare providers often underestimate anemia as a co-morbidity in diabetes, despite the wide range of prevalence estimates reported in the literature. Addressing anemia in diabetes patients early can reduce the incidence of these complications, as has been demonstrated. Aim of the study: The study aimed to estimate the prevalence of anemia and its associated factors among patients with type 2 diabetes mellitus (T2DM). Methods: This is a cross-sectional prospective study with a retrospective review of diabetic patient medical records attending family medicine clinics at four military hospitals (King Hussien Medical Center, Prince Rashed Military Hospital, Queen Aliah Military Hospital, and Prince Hashem Military Hospital) at Royal Medical Services. Adult patients over the age of 18 diagnosed with type 2 diabetes mellitus for more than one year will be included in the study. However, those patients with diseases (such as thalassemia and leukemia) or other systemic disorders (such as infectious diseases) that could result in anemia, those with acute conditions such as acute hemorrhage, those who received blood transfusions in the last three months, pregnant women, or type 1 diabetes will be excluded.  Anemia will be defined as hemoglobin level < 13 g/dl in men and 12g/dl in females (Harrison TR, 2011). Type 2 DM will be defined glycated hemoglobin (HbA1c > 6.5%), fasting blood glucose (FBG > 126 mg/dl), random blood glucose (RBG > 200 mg/dl) (American Diabetes Association, 2012). Patients’ medical records will be reviewed for patient medications, duration of diabetes, diabetic complications, and glycemic control. Furthermore, to exclude any patients who have one or more of the aforementioned conditions reported in the exclusion criteria. Meanwhile, researcher will collect the following data in the clinic after patients’ agreement to participate in the study which include: age, sex, marital status, smoking status, comorbidities, anthropometric measurements including weight, height and body mass index (BMI). Moreover, patient will ask to withdraw complete blood count (CBC) blood sample which include hemoglobin, mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH) and mean corpuscular hemoglobin concentration (MCHC) for diagnosing anemia if its present. Patients will be divided into two groups based on the presence of anemia; anemic group and non-anemic group. Regarding study variables. Glycemic control will be classified into two categories based on HbA1c result (controlled diabetic group comprised those whose HbA1c level was equal to or <7.5% and poorly controlled diabetic group comprised those whose HbA1c level was >7.5%). Body mass index will classify according to Center of Disease Control (CDC) as follow: BMI score < 18.5 Kg/m2 is underweight, 18.5–24.9 Kg/m2 is normal, 25–29.9 Kg/m2 is overweight and BMI ≥ 30 Kg/m2 is obese.     The sample size will be calculated based on Cohran’s sample size formula as: n=Z2 pq /e2. Here, p will be the anticipation of anemia prevalence in the diabetic population, q=1 - p; e is an acceptable error (5%); and Z= 1.96. A simple random sampling (systematic procedure) will be used to choose patients with type 2 diabetes in order to reduce the possibility of selection bias. With this technique, we randomly choose the first subject and then select the next subjects in a periodic manner according to K (interval). K will be determined based on the sampling frame prepared by researchers divided by n.  Descriptive analysis will be used with the mean (standard deviation) for normally distributed variables and the median (inter-quartile range) for highly skewed distributions. The t-test and the Mann-Whitney test will be used to compare the baseline characteristics of quantitative variables between anemic and non-anemic groups for variables with a normal and highly skewed distribution, respectively. Categorical variables will be compared between the groups using the chi-square test. Logistic regression analyses will be employed to find out how these variables are associated with anemia. The results will be given as odds ratios (ORs) with a 95% confidence interval (CI). We will select only covariates with a p-value <0.20 in the univariate analysis to enter the logistic analysis.
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