• 文章类型: Journal Article
    进行系统评价和荟萃分析以确定贫血的患病率。缺铁(ID),中国孕妇缺铁性贫血(IDA)。共收集了2010年1月至2020年12月期间发表的722篇关于妊娠期贫血的文章。对包括1,376,204名孕妇在内的57项符合条件的研究进行了系统评价和荟萃分析,以确定贫血的患病率和不同亚组的患病率.结果表明,贫血的患病率,ID,中国孕妇中的IDA为30.7%(95%CI:26.6%,34.7%),45.6%(95%CI:37.0%,54.2%),和17.3%(95%CI:13.9%,20.7%),分别。所有患病率随着妊娠的进展而增加。贫血的患病率有相当大的地区差异,ID,和IDA。一般来说,在该国经济较发达的东部地区,患病率较低,东部地区的ID患病率高于西部地区。农村地区贫血和IDA患病率高于城市地区,但城市地区的ID患病率较高。总之,贫血患病率的地区差异和城乡差异表明,需要更多针对具体环境的干预措施来预防和治疗贫血.研究发现,饮食因素是贫血的主要原因之一,含铁补充剂和营养咨询可以成为降低贫血患病率的有效干预措施,ID,和IDA在中国孕妇中。
    The systematic review and meta-analysis were conducted to ascertain the prevalence of anemia, iron deficiency (ID), and iron deficiency anemia (IDA) among Chinese pregnant women. A total of 722 articles on maternal anemia during pregnancy published between January 2010 and December 2020 were compiled, and a systematic review and meta-analysis were conducted on 57 eligible studies including 1,376,204 pregnant women to ascertain the prevalence of anemia and the prevalence in different subgroups. The results showed that the prevalence of anemia, ID, and IDA among pregnant women in China were 30.7% (95% CI: 26.6%, 34.7%), 45.6% (95% CI: 37.0%, 54.2%), and 17.3% (95% CI: 13.9%, 20.7%), respectively. All prevalence increased with the progression of the pregnancy. There were sizable regional variations in the prevalence of anemia, ID, and IDA. Generally, lower prevalence was observed in the economically more advanced eastern region of the country, while the prevalence of ID was higher in the eastern region than that in the western region. The prevalence of anemia and IDA in rural areas was higher than that in urban areas, but ID prevalence was higher in urban areas. In conclusion, the regional differences and urban-rural disparities in the prevalence of anemia indicate the need for more context-specific interventions to prevent and treat anemia. It was found that dietary factors were one of the major causes of anemia, and iron-containing supplements and nutrition counseling could be effective interventions to reduce the prevalence of anemia, ID, and IDA among Chinese pregnant women.
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  • 文章类型: Journal Article
    口腔疾病干预措施主要侧重于行为改变,如改善饮食和确保更好的口腔卫生。然而,认识到生物因素的影响,包括遗传学和早期营养,至关重要。缺铁(ID)及其高级形式,缺铁性贫血(IDA),影响全球近20亿人,尤其是儿童和孕妇。我们通过EndNote和WebofScience使用Medline进行了全面搜索,使用与缺铁性贫血(IDA)相关的关键词,我们确定了36项被认为与纳入本文献综述相关的研究.孕妇和幼儿的IDA患病率尤其高。IDA和幼儿龋齿(ECC)对贫困人口的影响不成比例,强调这个问题的社会经济层面。IDA表现出各种口腔粘膜变化,并与念珠菌病密切相关。此外,IDA可以阻碍牙齿发育并削弱免疫反应。多项人口调查显示,ECC和IDA之间存在显着关联。虽然一些研究探索了IDA与牙周病的联系,目前的证据在其稳健性上相对有限。总之,更全面的纵向研究对于加深我们对IDA-口腔疾病联系的理解至关重要.研究潜在的生物学机制对于开发有效的干预措施至关重要,特别是受国际开发协会影响的弱势群体。
    Oral disease interventions primarily focus on behavioral changes like dietary improvements and ensuring better oral hygiene. However, recognizing the influence of biological factors, including genetics and early-life nutrition, is crucial. Iron deficiency (ID) and its advanced form, iron deficiency anemia (IDA), affect nearly two billion people globally, especially children and pregnant women. We conducted a comprehensive search using Medline via EndNote and Web of Science, employing keywords related to iron deficiency anemia (IDA), and we identified 36 studies deemed relevant for inclusion in this literature review. IDA prevalence is notably high among pregnant women and young children. Both IDA and early-childhood caries (ECC) disproportionately affect impoverished populations, highlighting the socioeconomic dimension of this issue. IDA presents with various oral mucosal changes and is closely linked to candidiasis. Additionally, IDA can hinder tooth development and weaken the immune response. Multiple population surveys have revealed a significant association between ECC and IDA. While some studies have explored the IDA-periodontal disease link, the current evidence is relatively limited in its robustness. In conclusion, more comprehensive longitudinal studies are essential to deepen our understanding of the IDA-oral disease connection. Investigating the underlying biological mechanisms is critical to developing effective interventions, particularly for vulnerable populations affected by IDA.
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  • 文章类型: Journal Article
    地中海贫血是一种遗传性血液疾病,在一种称为血红蛋白的蛋白质的足够生产方面存在缺陷。我们旨在研究β地中海贫血(BTT)和缺铁性贫血(IDA)患者的简单血液指标,以提出使用逻辑回归来区分两种特征的新公式。
    在BTT咨询中心的702条记录中(Khoy,伊朗-2022),292例(219例缺铁性贫血(IDA)和73例BTT)符合研究条件。红细胞等血液指标,HGB,HbA2描述并用于诊断两种类型的参与者。血液指标具有高度的多重共线性,并进行了修改。用ROC曲线下面积(AUC)估计的血液指标拟合和拟合优度指数的逻辑回归。
    参与者的平均年龄为24.56岁。修改了自变量之间的多重共线性状态。HGB,MCV,模型中使用HbA2和HbA变量,仅HbA2状态显着(P<0.001)。根据模型的输出,HbA2每增加一个单位,患BTT的机会比IDA高约8.5倍。敏感性,特异性,AUC曲线,最终模型的准确度估计为97、72、84和93%,分别。提出了区分BTT和IDA的回归公式。
    在有关BTT与IDA的区别的研究中,HbA2指数在模型和预测中的存在是非常必要的。
    UNASSIGNED: Thalassemia is an inherited blood disorder with a defect in the sufficient production of a protein called hemoglobin. We aimed to investigate the simple blood indices of patients with Beta Thalassemia Trait (BTT) and Iron Deficiency Anemia (IDA) to propose a new formula using logistic regression for differentiate two characteristics from each other.
    UNASSIGNED: Among the 702 records of the BTT Counseling Center (Khoy, Iran-2022), 292 cases (219 iron deficiency anemia (IDA) and 73 BTT) were eligible for the study. Blood indices such as RBC, HGB, HbA2 described and used to diagnose two types of participants. Blood indices had high multicollinearity that was modified. Logistic regression for blood indices fitted and goodness of fit indices with Area Under ROC curve (AUC) estimated.
    UNASSIGNED: The average age of the participants was 24.56 yr. The status of Multicollinearity between independent variables was modified. The HGB, MCV, HbA2, and HbA variables were used in the model and only HbA2 status was significant (P<0.001). According to the output of the model, for each unit increase in HbA2, the chance of having BTT was about 8.5 times higher than IDA. The sensitivity, specificity, AUC curve, and accuracy of the final model were estimated to be 97, 72, 84, and 93%, respectively. A regression formula to differentiate BTT from IDA proposed.
    UNASSIGNED: In studies related to the differentiation of the BTT from IDA, the presence of the HbA2 index in the model and prediction is very necessary.
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  • 文章类型: Journal Article
    目的:本研究旨在研究缺铁性贫血中血小板功能的变化及其潜在机制。
    方法:最初,我们在IDA小鼠模型中评估了血小板功能.由于无法准确降低细胞内Fe2+浓度,我们通过引入不同浓度的Fe2+研究了Fe2+对血小板功能的影响。为了探究潜在的机制,我们同时检查了细胞质中钙的动力学,和整合素αIIbβ3在Fe2+处理的血小板中的激活。应用铁凋亡抑制剂Lip-1和Fer-1来确定铁凋亡是否参与该过程。
    结果:我们的研究表明,IDA小鼠的血小板功能受到抑制。Fe2浓度依赖性地促进血小板活化和体外功能。机械上,Fe2+促进钙动员,整合素αIIbβ3激活,和它的下游内外信号。此外,我们还证明了铁性凋亡可能在这一过程中发挥作用。
    结论:我们的数据表明铁和血小板活化之间存在关联,缺铁导致血小板功能受损,而高浓度的Fe2+通过促进钙动员促进血小板活化和功能,αIIbβ3活化,和铁中毒。
    OBJECTIVE: This research aimed to study the changes in platelet function and their underlying mechanisms in iron deficiency anemia.
    METHODS: Initially, we evaluated platelet function in an IDA mice model. Due to the inability to accurately reduce intracellular Fe2+ concentrations, we investigated the impact of Fe2+ on platelet function by introducing varying concentrations of Fe2+. To probe the underlying mechanism, we simultaneously examined the dynamics of calcium in the cytosol, and integrin αIIbβ3 activation in Fe2+-treated platelets. Ferroptosis inhibitors Lip-1 and Fer-1 were applied to determine whether ferroptosis was involved in this process.
    RESULTS: Our study revealed that platelet function was suppressed in IDA mice. Fe2+ concentration-dependently facilitated platelet activation and function in vitro. Mechanistically, Fe2+ promoted calcium mobilization, integrin αIIbβ3 activation, and its downstream outside-in signaling. Additionally, we also demonstrated that ferroptosis might play a role in this process.
    CONCLUSIONS: Our data suggest an association between iron and platelet activation, with iron deficiency resulting in impaired platelet function, while high concentrations of Fe2+ contribute to platelet activation and function by promoting calcium mobilization, αIIbβ3 activation, and ferroptosis.
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  • 文章类型: Journal Article
    目的:缺铁性贫血常见于炎症性肠病(IBD)患者,导致生活质量下降,这可以通过增加铁储存和血红蛋白水平的治疗来逆转。当前的事后分析估计了用去异麦芽糖铁或羧基麦芽糖铁治疗后IBD患者的健康状况效用值,并评估了驱动变化的健康领域。
    方法:在基线和第14、35、49和70天,从随机纳入的97名患者中记录SF-36v2反应,双盲,PHOSPHARE-IBD试验(ClinicalTrials.govID:NCT03466983),其中五个欧洲国家的IBD患者被随机分配到去日麦芽糖铁或羧基麦芽糖铁。通过混合模型分析SF-36v2量表评分和SF-6Dv2健康效用值的变化。
    结果:在两个治疗组中,SF-6Dv2效用值和所有SF-36v2量表得分,除了身体疼痛,显著改善(p=<0.0001)。SF-6Dv2效用值的改良显示医治组差别无统计学意义。效用值的提高完全可以通过活力评分的提高来解释。活力评分显示出双麦芽糖铁比羧基麦芽糖铁有更大的改善(p=0.026)。磷酸盐下降最小的患者在每个时间点(所有比较p=<0.05)和总体(p=0.0006)的活力评分均有明显更大的改善。
    结论:静脉补铁治疗后效用值显著改善。效用值的提高主要是由活力得分推动的,这表明在铁脱异麦芽糖臂显著更大的改善。磷酸盐的较小减少与明显较高的活力评分相关,提示低磷酸盐血症降低了生活质量的改善。效用值可以为未来的成本效用分析提供信息。
    OBJECTIVE: Iron deficiency anemia is common in people with inflammatory bowel disease (IBD), causing deterioration in quality of life, which can be reversed by treatment that increases iron stores and hemoglobin levels. The present post hoc analyses estimate health state utility values for patients with IBD after treatment with ferric derisomaltose or ferric carboxymaltose and evaluate the health domains driving the changes.
    METHODS: SF-36v2 responses were recorded at baseline and day 14, 35, 49, and 70 from 97 patients enrolled in the randomized, double-blind, PHOSPHARE-IBD trial (ClinicalTrials.gov ID: NCT03466983), in which patients with IBD across five European countries were randomly allocated to either ferric derisomaltose or ferric carboxymaltose. Changes in SF-36v2 scale scores and SF-6Dv2 health utility values were analyzed by mixed models.
    RESULTS: In both treatment arms, SF-6Dv2 utility values and all SF-36v2 scale scores, except Bodily Pain, improved significantly (p =  < 0.0001). The improvement in SF-6Dv2 utility values showed no significant treatment group difference. The improvement in utility values was completely explained by improvement in Vitality scores. Vitality scores showed significantly larger improvement with ferric derisomaltose versus ferric carboxymaltose (p = 0.026). Patients with the smallest decrease in phosphate had significantly larger improvements in Vitality scores at each time point (p =  < 0.05 for all comparisons) and overall (p = 0.0006).
    CONCLUSIONS: Utility values improved significantly with intravenous iron treatment. Improvement in utility values was primarily driven by Vitality scores, which showed significantly greater improvement in the ferric derisomaltose arm. Smaller decreases in phosphate were associated with significantly higher Vitality scores, suggesting that quality of life improvement is attenuated by hypophosphatemia. The utility values can inform future cost-utility analysis.
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  • 文章类型: Journal Article
    观察性研究表明缺铁性贫血(IDA)与哮喘之间存在关联,这可能会影响哮喘的发生。然而,IDA是否是哮喘新的治疗目标还有待确定.
    我们进行了双样本孟德尔随机化(MR)分析,以评估IDA与哮喘之间的关联。
    我们进行了双样本MR研究,以评估IDA(ncase=12,434,ncontrol=59,827)和哮喘(ncase=20,629,ncontrol=135,449)之间的因果关系。使用逆方差加权(IVW)作为分析的主要方法。此外,我们使用加权中位数和MR-Egger来增强鲁棒性。将遗传变异与IDA和哮喘相关的数据结合起来评估IDA对哮喘风险的影响。
    有五个单核苷酸多态性(SNP)被用作暴露因素的遗传工具变量。遗传确定的IDA与哮喘风险增加显著相关(OR=1.37,95%CI:1.09-1.72,p=0.007)。在MR研究中几乎没有异质性,也没有发现水平多效性的证据。
    在我们的MR研究中,我们的研究结果强调IDA可能与哮喘的高风险有关,表明IDA在哮喘发展中的潜在作用。未来的研究需要阐明其潜在的机制,为预防和治疗哮喘铺平道路。
    UNASSIGNED: Observational studies have suggested an association between iron deficiency anemia (IDA) and asthma, which may affect the occurrence of asthma. However, whether IDA is a new management goal for asthma remains to be determined.
    UNASSIGNED: We conducted a two-sample Mendelian randomization(MR)analysis to assess the association between IDA and asthma.
    UNASSIGNED: We performed a two-sample MR study to assess a causal relationship between IDA (ncase = 12,434, ncontrol = 59,827) and asthma (ncase = 20,629, ncontrol = 135,449). Inverse variance weighted (IVW) was used as the primary method for the analyses. Furthermore, we used weighted medians and MR-Egger to enhance robustness. Data linking genetic variation to IDA and asthma were combined to assess the impact of IDA on asthma risk.
    UNASSIGNED: There are five single nucleotide polymorphisms (SNPs) were used as genetic tool variables for exposure factors. Genetically determined IDA was significantly associated with an increased risk of asthma (OR = 1.37, 95% CI: 1.09-1.72, p = 0.007). There was little heterogeneity in the MR studies and no evidence of level pleiotropy was found.
    UNASSIGNED: In our MR study, our findings emphasize that IDA may be associated with a high risk of asthma, indicating a potential role for IDA in the development of asthma. Future research needs to elucidate its potential mechanisms to pave the way for the prevention and treatment of asthma.
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  • 文章类型: Journal Article
    目的:为了研究大剂量静脉(IV)铁的肝脏效应,包括肝功能和纤维化程度,在肝硬化的大鼠模型中。
    方法:我们将25只Sprague-Dawley大鼠均匀分为5组:正常大鼠(对照组),肝硬化大鼠接受静脉生理盐水(肝硬化[LC]组),和肝硬化大鼠接受20、40或80mg/kg静脉铁羧基麦芽糖(LC-iron20,LC-iron40和LC-iron80组,分别)。在0、7、14、21和28天比较生化参数。评估肝纤维化和铁沉积的程度。还比较了炎症和氧化应激标志物。
    结果:LC-iron20,LC-iron40和LC-iron80组的28天血清丙氨酸转氨酶水平没有显着差异(对照组为69±7、1003±127、1064±309、919±346和820±195/IU,LC,LC-iron20、LC-iron40和LC-iron80基团,分别)。肝脏铁积累以剂量依赖性方式增加,但各组之间的肝纤维化程度相当。根据IV铁剂量,炎症和氧化应激标志物水平没有显着差异。
    结论:在我们的肝硬化大鼠模型中,以各种高剂量给予静脉铁似乎是安全的。
    OBJECTIVE: To investigate the hepatic effects of high-dose intravenous (IV) iron, including those on liver function and the degree of fibrosis, in a rat model of cirrhosis.
    METHODS: We evenly allocated 25 Sprague-Dawley rats into five groups: normal rats (control group), cirrhotic rats receiving IV normal saline (liver cirrhosis [LC] group), and cirrhotic rats receiving 20, 40, or 80 mg/kg IV ferric carboxymaltose (LC-iron20, LC-iron40, and LC-iron80 group, respectively). Biochemical parameters were compared at 0, 7, 14, 21, and 28 days. The degrees of hepatic fibrosis and iron deposition were evaluated. Inflammatory and oxidative stress markers were also compared.
    RESULTS: There were no significant differences in the 28-day serum alanine aminotransferase levels among the LC-iron20, LC-iron40, and LC-iron80 groups (69 ± 7, 1003 ± 127, 1064 ± 309, 919 ± 346, and 820 ± 195 IU/L in the control, LC, LC-iron20, LC-iron40, and LC-iron80 groups, respectively). Hepatic iron accumulation increased in a dose-dependent manner, but the degree of hepatic fibrosis was comparable among the groups. The inflammatory and oxidative stress marker levels did not differ significantly according to the IV iron dose.
    CONCLUSIONS: Administration of IV iron at various high doses appears safe in our rat model of cirrhosis.
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  • 文章类型: Editorial
    缺铁性贫血(IDA)仍然是一个全球性的公共卫生问题。口服铁剂是普遍接受的一线疗法,大多数儿童对口服制剂有迅速和良好的反应。在由于不容忍而无法做出反应的儿童中,依从性差,或者肠道吸收不足,肠外铁的指示。尽管在患有IDA的成年人中进行了大量不同病因的研究,关于肠胃外使用铁的儿科研究非常有限.虽然大多是回顾性的和小的,这些研究记录了静脉注射铁制剂的有效性和安全性.在这篇社论中,作者评论了最重要的已发表数据,并强调需要认真考虑对口服治疗无反应的儿童使用肠胃外铁剂。
    Iron deficiency anemia (IDA) continues to be a global public health problem. Oral iron is the universally accepted first-line therapy, and most children have a prompt and favorable response to oral formulations. In subsets of children who fail to respond due to intolerance, poor adherence, or inadequate intestinal absorption, parenteral iron is indicated. Despite numerous studies in adults with IDA of diverse etiologies, pediatric studies on parenteral iron use are very limited. Although mostly retrospective and small, these studies have documented the efficacy and safety profile of intravenous iron formulations. In this editorial the author comments on the most important published data and underscores the need to seriously consider parenteral iron use in children unresponsive to oral therapy.
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  • 文章类型: Journal Article
    缺铁性贫血是最常见的贫血类型之一,但日本的实际临床管理实践尚不清楚.这项研究回顾性地探索了铁的处方模式,治疗效果,和评估。纳入2020年9月至2022年9月至少有一个治疗期的患者,并将其分为三组(羧基麦芽糖铁[FCM]:7437例患者,糖化氧化铁[SFO]:98,648名患者,和口服铁:359,547例患者)。评估随时间变化的与铁相关的实验室值和测试比例。FCM的基线血红蛋白水平中位数最低(FCM:8.10g/dL,SFO:8.70g/dL,口服铁:9.70g/dL),但是FCM在12周时血红蛋白水平的变化最大(FCM:3.20g/dL,SFO:2.60g/dL,口服铁:1.70g/dL)。FCM治疗后8周的中位血清铁蛋白水平为43.70ng/mL,≤500mg,与>500至≤1500mg的123.30ng/mL相比。诊断时,所有组的血清铁蛋白和转铁蛋白饱和度(TSAT)检测比例均较低(<38%),在治疗后评估中进一步下降(<24%)。这项研究表明,根据包装说明书开出适当的总铁累积剂量的重要性,以及基于血清铁蛋白/TSAT的诊断和评估。
    Iron deficiency anemia is one of the most common types of anemia, but real-world clinical management practices in Japan are unclear. This study retrospectively explored iron prescription patterns, treatment effectiveness, and assessments. Patients with at least one treatment period between September 2020 and September 2022 were included and classified into three groups (ferric carboxymaltose [FCM]: 7437 patients, saccharated ferric oxide [SFO]: 98,648 patients, and oral iron: 359,547 patients). Iron-related laboratory values over time and testing proportions were evaluated. Median baseline hemoglobin levels were lowest with FCM (FCM: 8.10 g/dL, SFO: 8.70 g/dL, oral iron: 9.70 g/dL), but changes in hemoglobin levels by 12 weeks were greatest with FCM (FCM: 3.20 g/dL, SFO: 2.60 g/dL, oral iron: 1.70 g/dL). The median serum ferritin level at 8 weeks after FCM treatment was 43.70 ng/mL for ≤500 mg, versus 123.30 ng/mL for >500 to ≤1500 mg. All groups had a low proportion of serum ferritin and transferrin saturation (TSAT) testing at diagnosis (<38%), which decreased further for post-treatment assessment (<24%). This study suggests the importance of prescribing an appropriate total iron cumulative dose per the package insert, along with diagnosis and assessments based on serum ferritin/TSAT.
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  • 文章类型: Journal Article
    营养性贫血非常普遍,并在全球范围内引发了全球公认的公共卫生问题。
    为了更好地了解发达国家贫血的患病率和营养健康状况,以告知全球营养健康并更好地管理疾病。
    我们采用了医疗保健成本和利用项目(HCUP)-2020年全国住院医疗保健数据(NIS),由医疗保健研究和质量机构管理。营养性贫血是根据国际疾病分类诊断的,第十次修订(ICD-10)。使用匹配分析和多变量回归来调整患者和医院的特征。通过年龄和性别的分层和匹配获得对照。
    2020年HCUP-NIS数据库包含了对640万住院患者的调查,其中1,745,350例患者诊断为贫血,约占住院人口的26.97%,超过31万人被诊断为营养性贫血,13,150例患者以营养性贫血为主要诊断。营养性贫血的住院率在全国范围内表现出年龄依赖性增加,尤其是女性,比男性高1.87倍。值得注意的是,与对照组相比,黑人个体表现出更高的营养性贫血患病率(病例组:21.7%,对照组:13.0%,p<0.001)。此外,低收入人群的住院率较高,私人保险费率较低(病例组:18.7%,对照组:23.5%,p<0.001)和更高的医疗补助保险费率(病例组:15.4%,对照组:13.9%,p<0.001)。在城市中心较大,城乡分布内经济条件先进的地区,观察到患者住院频率增加.缺铁性贫血是营养性贫血的主要亚型,占12214(92.88%)。因营养性贫血住院的患者的二次诊断显示,相当多的患者面临高血压和肾衰竭等并发重大疾病。
    在经济繁荣的地区,应该更加关注低收入个人和老年人的健康。我们的研究结果为制定有针对性的公共卫生政策提供了宝贵的见解,以有效解决基于总体人口健康的营养性贫血的患病率和后果。
    UNASSIGNED: Nutritional anemia is highly prevalent and has triggered a globally recognized public health concern worldwide.
    UNASSIGNED: To better understand the prevalence of anemia and the state of nutritional health in developed countries to inform global nutritional health and better manage the disease.
    UNASSIGNED: We employed the Healthcare Cost and Utilization Project (HCUP)-2020 National Inpatient Health Care Data (NIS), administered by The Agency for Healthcare Research and Quality. Nutritional anemia was diagnosed according to the International Classification of Diseases, 10th Revision (ICD-10). Matching analysis and multivariate regression were used to adjust for patient and hospital characteristics. Controls were obtained by stratifying and matching for age and sex.
    UNASSIGNED: The 2020 HCUP-NIS database encompassed a survey over 6.4 million hospitalized patients, among which 1,745,350 patients diagnosed with anemia, representing approximately 26.97% of the hospitalized population, over 310,000 were diagnosed with nutritional anemia, and 13,150 patients were hospitalized for nutritional anemia as primary diagnosis. Hospitalization rate for nutritional anemia exhibited an increased age-dependent increase nationwide, especially among females, who displayed 1.87 times higher than males. Notably, in comparison to the control group, individuals of the Black race exhibit a higher prevalence of nutritional anemia (case group: 21.7%, control group: 13.0%, p < 0.001). In addition, hospitalization rates were higher among low-income populations, with lower rates of private insurance (case group: 18.7%, control group: 23.5%, p < 0.001) and higher rates of Medicaid insurance (case group: 15.4%, control group: 13.9%, p < 0.001). In areas characterized by larger urban centers and advanced economic conditions within the urban-rural distribution, there was an observed increase in the frequency of patient hospitalizations. Iron deficiency anemia emerged as the predominant subtype of nutritional anemia, accounting for 12,214 (92.88%). Secondary diagnosis among patients hospitalized for nutritional anemia revealed that a significant number faced concurrent major conditions like hypertension and renal failure.
    UNASSIGNED: In economically prosperous areas, greater attention should be given to the health of low-income individuals and the older adult. Our findings hold valuable insights for shaping targeted public health policies to effectively address the prevalence and consequences of nutritional anemia based on a overall population health.
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