iron deficiency anemia (ida)

缺铁性贫血 ( ida )
  • 文章类型: Journal Article
    引言缺铁性贫血和β-地中海贫血性状是小细胞低色素性贫血的两个常见且重要的区别。自1973年以来,使用两个或更多个常见的全血细胞计数(CBC)参数的各种区分指数已用于区分这两者。最近,一个新的判别指数,CRUISE指数,是在2019年提出的。对我们地理区域的患者评估了各种旧指标以及CRUISE指数的疗效。材料和方法我们是以实验室为基础的,横断面研究,其中100名患者,根据纳入和排除标准,对小细胞性低色素性贫血患者的CBC参数以及血清铁蛋白和血红蛋白-高效液相色谱(HbHPLC)进行了评估。共有八个歧视指数,Mentzer,Srivastava,Shine&Lal,绿色与国王,RDWI,英格兰&弗雷泽,使用KermanI和CRUISE指数,并使用不同的统计参数评估其诊断功效。获得了ROC曲线,并为我们的种群提出了新的临界值。使用MicrosoftExcel(Microsoft®Corp.,雷德蒙德,WA,美国)和SPSSv29.0.2.0(20)(IBM公司,Armonk,NY,美国)。结果100例患者中,β-地中海贫血性状39例,缺铁性贫血61例。平均年龄为36.7(±12.7SD)岁。在73名女性中,43例诊断为缺铁性贫血(IDA),30例诊断为β-地中海贫血(BTT)。在27名男性中,18例诊断为IDA,9例诊断为BTT。IDA患者的平均红细胞体积(MCV)的平均值显着降低(p=.008),平均红细胞血红蛋白(MCH)(p=0.003),和平均红细胞血红蛋白浓度(MCHC)(p=.003),并且红细胞分布宽度(RDW)(p=.020)明显更高。IDA患者的平均铁蛋白水平为7.61(±3.75)mcg/L,BTT患者的平均铁蛋白水平为87.09(±66.77SD)mcg/L。IDA患者的平均HbA2水平为2.75%(±0.41%SD),BTT患者的平均HbA2水平为5.57%(±0.73%SD)。CRUISE指数显示出最高的AUC(0.934),YI(76.21)和准确性(90%),其次是Mentzer指数,诊断准确性为81%。Shine&Lal指数显示AUC最低(0.710),YI(3.28)和准确度(41%)。结论CRUISE指数,这是最近提出的,在AUC方面排名第一,YI,和准确性,在鉴别诊断这两种疾病的敏感性方面被认为是第二好的。Mentzer指数,常用的索引,在我们的研究中,BTT和IDA的诊断准确性也很高。CRUISE指数是一个新颖的指数,需要在其他各种地理设置中进行更多的研究工作,以评估该指数的有效性。
    Introduction Iron deficiency anemia and beta-thalassemia trait are two common and important differentials of microcytic hypochromic anemia. Various discrimination indices using two or more common complete blood cell count (CBC) parameters have been used to distinguish between the two since 1973. Recently, a new discriminant index, the CRUISE index, was proposed in the year 2019. The efficacy of various older indices along with the CRUISE index was evaluated for patients in our geographical area. Materials and method Ours was a laboratory-based, cross-sectional study where 100 patients, based on inclusion and exclusion criteria, with microcytic hypochromic anemia were evaluated for CBC parameters along with serum ferritin and hemoglobin-high performance liquid chromatography (Hb HPLC). A total of eight discrimination indices namely, Mentzer, Srivastava, Shine & Lal, Green & King, RDWI, England & Fraser, Kerman I and CRUISE index were used and evaluated for their diagnostic efficacy using different statistical parameters. ROC curves were obtained and a new cut-off value was proposed for our population. Data was analysed using Microsoft Excel (Microsoft® Corp., Redmond, WA, USA) and SPSS v29.0.2.0 (20) (IBM Corp., Armonk, NY, USA). Results Out of the total 100 cases, 39 were beta-thalassemia trait and 61 were iron deficiency anemia cases. The average age was 36.7 (±12.7 SD) years. Among the 73 females, 43 were diagnosed as iron deficiency anemia (IDA) and 30 as beta-thalassemia trait (BTT) cases. Among the 27 males, 18 were diagnosed as IDA and nine as BTT cases. The mean values were significantly lower in IDA patients for mean corpuscular volume (MCV) (p=.008), mean corpuscular haemoglobin (MCH) (p=.003), and mean corpuscular haemoglobin concentration (MCHC) (p=.003) and significantly higher for red cell distribution width (RDW) (p=.020). The mean ferritin levels in cases of IDA were 7.61 (±3.75) mcg/L and in BTT were 87.09 (±66.77 SD) mcg/L. The mean HbA2 levels in IDA cases were 2.75% (±0.41% SD) and BTT cases were 5.57% (±0.73% SD). CRUISE index revealed the highest AUC (0.934), YI (76.21) and accuracy (90%) followed by the Mentzer index with a diagnostic accuracy of 81%. Shine & Lal index revealed the lowest AUC (0.710), YI (3.28) and accuracy (41%). Conclusion CRUISE index, which was recently proposed, was ranked 1st in terms of AUC, YI, and accuracy and was considered 2nd best in terms of sensitivity for differentially diagnosing the two conditions. Mentzer index, a commonly used index, also revealed a high diagnostic accuracy in our study for differentiating BTT from IDA. CRUISE index being a novel index, more research work needs to be carried out in various other geographical setups to evaluate the efficacy of this index.
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  • 文章类型: Journal Article
    目的:目的是研究在迪拜酋长国三级医院中,静脉(IV)铁输注在增加妊娠期缺铁性贫血(GIDA)患者血红蛋白水平中的有效性。阿拉伯联合酋长国(阿联酋)。
    方法:这是一项针对暴露于静脉补铁的GIDA患者的回顾性队列研究。分析了2018年至2019年阿联酋一家三级医院40例25-45岁患者的研究数据。变量占产妇年龄,静脉注射铁时的妊娠年龄,和IV铁剂量。
    结果:干预前的平均血红蛋白水平为9g/dL,干预后平均变化为10.4g/dL,干预前后平均差异为1.4g/dL。
    结论:GIDA患者在干预后补充静脉铁可以增加血红蛋白水平;然而,增加不符合12-16g/dL的推荐范围。
    OBJECTIVE: The objective is to investigate the effectiveness of intravenous (IV) iron infusion in increasing hemoglobin levels in gestational iron deficiency anemia (GIDA) patients in a tertiary-care hospital in Dubai emirate, United Arab Emirates (UAE).
    METHODS: This is a retrospective cohort study of GIDA patients who were exposed to IV iron infusion supplementation. Study data of 40 cases aged 25-45 in a tertiary-care hospital in the UAE between 2018 and 2019 were analyzed. Variables accounted for were maternal age, age of gestation when IV iron was administered, and IV iron dose.
    RESULTS: The average hemoglobin level before the intervention was 9 g/dL, and the average change after the intervention was 10.4 g/dL with a mean of 1.4 g/dL difference between before and after the intervention.
    CONCLUSIONS: Supplementation of IV iron infusion in GIDA patients was seen to have increased the hemoglobin level after the intervention; however, the increase did not meet the recommended range of 12-16 g/dL.
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  • 文章类型: Case Reports
    一名15个月大的非裔美国男性患者前往儿科诊所建立护理。该患者曾被一位先前的儿科医生看过并治疗,该儿科医生诊断为无法茁壮成长,贫血,和肝脾肿大,根据病人的父母。在体检时,患者身高低于第一百分位数,体重低于第八百分位数.还观察到正面凹陷。在办公室测量患者的血红蛋白水平以帮助确认先前的贫血诊断,并确定为6.3g/dL(正常:10.5-13.0g/dL)。在这一点上,患者被送往儿科急诊科继续治疗和检查.在急诊室,患者接受了广泛的实验室检查以评估贫血,提示缺铁性贫血(血红蛋白:5.6g/dL(正常:10.5-13g/dL),平均红细胞体积:51.4fl(正常:70-84fl),铁:18mcg/dL(正常:30-70mcg/dL),总铁结合能力:598mcg/dL(正常:100-400mcg/dL),和血细胞比容:23.7%(正常:33-38%)和维生素D水平降低(<6ng/mL,正常:>30ng/mL),离子钙(1.17mg/dL,正常:4.4-5.2mg/dL),和磷(2.4毫克/分升,正常:2.9-5.9mg/dL)。这些研究,与患者的肩膀和手腕的X射线图像配对,进一步证实了病的诊断。Rick病是儿科患者的一种疾病,定义为骨phy板矿化有缺陷的疾病。维生素D的营养缺乏,钙,或磷酸盐会导致后天的病。这种情况最常见于发展中国家;一些诱发因素包括阳光照射不良,高海拔,和母乳喂养。患者住院后在门诊儿科就诊,他接受了输血,在那里他接受了碳酸钙悬浮液的补充,多糖铁络合物/novaferrum滴剂,和胆钙化醇滴剂,转诊至内分泌学,血液学,和营养学。这个案例是如何诊断营养缺乏的一个例子,比如病,在美国等发达国家也可以找到。鉴别诊断中考虑的其他疾病是囊性纤维化,坏死性小肠结肠炎,代谢紊乱,吸收不足,和机械进料困难,必须排除其中的每一个,以确保即使是不太可能的发现也不会错过。
    A 15-month-old African American male patient presented to the pediatric clinic to establish care. The patient had been seen and treated by a previous pediatrician who had diagnosed him with failure to thrive, anemia, and hepatosplenomegaly, according to the patient\'s parents. Upon physical examination, the patient was determined to be less than the first percentile for height and in the eighth percentile for weight. Frontal bossing was also observed. The patient\'s hemoglobin level was measured in the office to help confirm the previous anemia diagnosis and was determined to be 6.3 g/dL (normal: 10.5-13.0 g/dL). At this point, the patient was sent to a pediatric emergency department for continued treatment and workup. At the emergency department, the patient received an extensive laboratory workup for the evaluation of anemia, revealing iron deficiency anemia (hemoglobin: 5.6 g/dL (normal: 10.5-13 g/dL), mean corpuscular volume: 51.4 fl (normal: 70-84 fl), iron: 18 mcg/dL (normal: 30-70 mcg/dL), total iron binding capacity: 598 mcg/dL (normal: 100-400 mcg/dL), and hematocrit: 23.7% (normal: 33-38%)) and decreased levels of vitamin D (<6 ng/mL, normal: >30 ng/mL), ionized calcium (1.17 mg/dL, normal: 4.4-5.2 mg/dL), and phosphorus (2.4 mg/dL, normal: 2.9-5.9 mg/dL). These studies, paired with X-ray images of the patient\'s shoulders and wrists, further confirmed the diagnosis of rickets. Rickets is a disease in pediatric patients defined as a condition in which the mineralization of epiphyseal plates is defective. A nutritional deficiency in vitamin D, calcium, or phosphate causes acquired rickets. This condition is most commonly found in developing countries; some predisposing factors include poor sun exposure, high altitude, and breastfeeding. The patient was seen in the outpatient pediatric setting after the hospitalization, in which he received a blood transfusion, where he was managed on supplementation of calcium carbonate suspension, polysaccharide iron complex/novaferrum drops, and cholecalciferol drops with referral to endocrinology, hematology, and dietetics. This case serves as an example of how the diagnosis of nutritional deficiencies, such as rickets, can also be found in developed countries like the United States. Other conditions considered in the differential diagnosis were cystic fibrosis, necrotizing enterocolitis, metabolic disorders, inadequate absorption, and mechanical feeding difficulties, each of which must be ruled out to ensure that even an unlikely finding was not missed.
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  • 文章类型: Case Reports
    胃癌转移到不典型部位会使治疗复杂化,经常导致临床医生严重依赖化疗。当胃癌扩散到肝脏时,腹膜,淋巴系统在文献中有很好的记载,有有限的证据表明它传播到肠内器官,尤其是结肠。报告的稀缺性使诊断变得复杂,鉴于组织病理学的变化。该病例报告重点介绍了一名35岁的遗传性弥漫性胃癌(HDGC)被诊断为结肠转移的患者,同时正在评估缺铁性贫血的潜在原因。E-cadherin(CDH1)肿瘤抑制基因中的突变与HDGC相关。CDH1的失调导致肿瘤增殖,入侵,迁移,和转移。胃癌的治疗选择包括新辅助或辅助化疗的手术切除或转移性疾病的化疗姑息治疗。尽管胃癌的结肠转移很少见,记录在案的事件可以提供有价值的见解,避免误诊原发性肿瘤,并有助于指导进一步的管理。
    Metastasis of gastric carcinoma to atypical locations can complicate management, often leading clinicians to rely heavily on chemotherapy. While instances of gastric carcinoma spreading to the liver, peritoneum, and lymphatics are well documented in the literature, there is limited evidence of its spread to intraintestinal organs, particularly the colon. This scarcity of reports complicates diagnosis, given the variations in histopathology. This case report highlights a 35-year-old patient diagnosed with colonic metastasis from hereditary diffuse gastric cancer (HDGC) while being evaluated for potential causes of iron deficiency anemia. A mutation in the E-cadherin (CDH1) tumor suppressor gene is associated with HDGC. Dysregulation of CDH1 leads to tumor proliferation, invasion, migration, and metastasis. Treatment options for gastric cancer include surgical resection with neoadjuvant or adjuvant chemotherapy or palliative care with chemotherapy in metastatic disease. Although colonic metastasis from gastric cancer is rare, documented incidents can offer valuable insights that avoid misdiagnosing primary tumors and help guide further management.
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  • 文章类型: Journal Article
    背景:地球上几乎四分之一的人贫血,他们中的大多数居住在撒哈拉以南非洲和南亚地区。儿童贫血与认知和运动发育受损有关,并影响未来的收入能力。贫血最常见的原因是缺铁。印度政府已经启动了多个根除贫血的计划。尽管该国经济有所改善,但贫血的患病率并未下降。儿童的比例从2015-16年的58.7%上升到2019-21年的67.1%,孕妇的比例从2015-16年的50.4%上升到2019-21年的52.2%。产妇教育,社会经济地位,家庭中儿童的数量是影响贫血患病率的一些因素。由于这些因素不能在短时间内得到改善,我们旨在通过针对来自农村/半城市背景的学生来提高对这一问题的认识。
    方法:这项试点研究旨在促进学生在社区中成为公共卫生倡导者。贫血意识计划是在郊区的一所当地中学进行的,有153名八班学生(72名女性)参加。使用了包含20个多项选择/真假类型问题的测试前和测试后问卷。获得测试前和测试后的分数。研究的第二部分是对贫血学生的鉴定。从静脉血样本中测量了127名学生(58名女性)的血液血红蛋白水平。学生还被要求告知他们的朋友/亲戚贫血,并将有贫血症状的人送到医学院附属医院组织的为期两天的免费贫血意识营进行检查。
    结果:测试后的平均评分(15.68/20)远高于测试前的评分(2.99/20)。127名学生中有38名(25名女性)患有轻度/中度小细胞性低色素性贫血,提示缺铁.三十二人参观免费健康营,接受学生的资讯,其中四人血红蛋白水平正常。
    结论:这项初步研究表明,在印度,由医生进行的贫血意识计划是在普通人群中传播信息的相对低成本的方法。
    BACKGROUND: Almost a quarter of the people on earth are anemic, and most of them reside in regions of sub-Saharan Africa and South Asia. Anemia in children is linked with impaired cognitive and motor development and affects the future earning capacity. The most common cause of anemia is iron deficiency. The Indian Government has initiated multiple programs for the eradication of anemia. The prevalence of anemia has not decreased despite the improvements in the country\'s economy. It increased from 58.7% in 2015-16 to 67.1% in 2019-21 in children and from 50.4% in 2015-16 to 52.2% in 2019-21 in pregnant women. Maternal education, socioeconomic status, and number of children in the family are some factors that influence the prevalence of anemia. As these factors cannot be improved in a short time, we aimed to increase awareness about this issue by targeting school students from rural/semi-urban backgrounds.
    METHODS: This pilot study aimed at promoting school students as public health advocates in their community. Anemia Awareness Program was conducted in a local middle school in the suburban area, which was attended by 153 class eight students (72 female). Pre- and post-test questionnaires comprising 20 multiple-choice/true-false type questions were used. Pre- and post-test scores were obtained. The second part of the study was the identification of students with anemia. Blood hemoglobin levels of 127 students (58 female) were measured from venous blood samples. The students were also asked to inform their friends/relatives about anemia and to send people with symptoms of anemia to the free two-day Anemia Awareness Camp organized by the Medical College Hospital for check-ups.
    RESULTS: The mean post-test score (15.68/20) was much higher than the pretest score (2.99/20). Thirty-eight (25 female) out of 127 students had mild/moderate microcytic hypochromic anemia, suggesting iron deficiency. Thirty-two persons visited the free health camp to receive information from the students, of whom four had normal hemoglobin levels.
    CONCLUSIONS: This pilot study showed that physician-conducted anemia awareness programs are relatively low-cost methods to spread information among the general population in India.
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  • 文章类型: Journal Article
    背景和客观贫血,特别是缺铁性贫血(IDA),提出了重大的全球卫生挑战,特别是在发展中国家五岁以下的儿童中。同时,高热惊厥(FC)影响多达5%的6-60个月的神经系统健康儿童,在父母中造成相当大的困扰。有一个提示发烧和缺铁之间的相关性,这可能会加剧神经系统风险,可能降低癫痫发作阈值并增加FC的风险。然而,调查IDA和FC之间关系的研究显示出相互矛盾的结果。鉴于此,这项研究旨在探讨印度东部6-60个月儿童之间的这种关系,该协会尚未进行彻底调查的领域。材料与方法病例对照研究包括6-60个月的儿童。这些案件包括出现在FC的儿童,而对照组包括患有高热疾病但没有癫痫发作的同年龄组儿童。获得知情同意,详细的历史记录,并对两组进行临床检查。根据WHO标准进行血液检查以诊断IDA:血红蛋白<11gm/dl,具有低平均红细胞体积(MCV)的经典三联征,低平均红细胞血红蛋白(MCH),和低平均红细胞血红蛋白浓度(MCHC)的年龄。使用基于R的软件Jamovi2.4.8进行数据分析。适当的统计检验。结果81例,80例对照。该研究发现IDA和FC之间的统计学显著关联,比值比(OR)为2.25[95%置信区间(CI):1.03-4.91;p=0.039]。此外,研究显示血红蛋白水平,MCH,MCV,与对照组相比,病例中的MCHC较低,而红细胞分布宽度(RDW)较高。关于RBC指数的这些发现均具有统计学意义(p<0.05)。结论我们的发现表明,在5岁以下儿童中,IDA和FC之间存在统计学上的显着关联。实施预防IDA的措施和加强现有战略可能有助于减轻FC在这一弱势群体中的负担。
    Background and objective Anemia, particularly iron deficiency anemia (IDA), presents a significant global health challenge, particularly among children under the age of five years in developing nations. Concurrently, febrile convulsions (FC) affect up to 5% of neurologically healthy children aged 6-60 months, causing considerable distress among parents. There is a suggested correlation between fever and iron deficiency, which may exacerbate neurological risks, potentially lowering seizure thresholds and increasing the risk of FC. However, studies investigating the relationship between IDA and FC have shown conflicting results. In light of this, this study aimed to explore this relationship among children aged 6-60 months in Eastern India, an area where this association has yet to be thoroughly investigated. Materials and methods The case-control study included children aged 6-60 months. The cases consisted of children presenting with FC, while controls comprised children in the same age group presenting with febrile illness but without seizures. Informed consent was obtained, a detailed history was taken, and clinical examinations were conducted for both groups. Blood investigations were performed to diagnose IDA according to WHO criteria: hemoglobin <11 gm/dl with the classical triad of low mean corpuscular volume (MCV), low mean corpuscular hemoglobin (MCH), and low mean corpuscular hemoglobin concentration (MCHC) for age. Data analysis was performed using the R-based software Jamovi 2.4.8. with appropriate statistical tests. Results We included 81 cases and 80 controls. The study found a statistically significant association between IDA and FC with an odds ratio (OR) of 2.25 [95% confidence interval (CI): 1.03-4.91; p=0.039]. Additionally, the study revealed that hemoglobin levels, MCH, MCV, and MCHC were lower among cases compared to controls, while the red cell distribution width (RDW) was higher. Both these findings regarding RBC indices were statistically significant (p<0.05). Conclusions Our findings indicate a statistically significant association between IDA and FC among children under five years of age. Implementing measures to prevent IDA and strengthening existing strategies may help alleviate the burden of FC in this vulnerable population.
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  • 文章类型: Case Reports
    尤因肉瘤传统上是骨恶性肿瘤,它可能罕见地出现在骨骼外,导致一系列令人费解的表现,这取决于所涉及的组织。这里,我们描述了一例66岁的男子,他向初级保健办公室进行间歇性黑便评估。他最终接受了胶囊内窥镜检查,并出现了继发性小肠梗阻,揭开他的肿瘤。然后切除肿瘤并仅在监视下进行管理,4年随访后,患者仍无疾病迹象。
    While Ewing sarcoma is traditionally a malignant tumor of bone, it may uncommonly present extra-skeletally, leading to an array of puzzling presentations depending on the tissue involved. Here, we describe the case of a 66-year-old man who presented to the primary care office for evaluation of intermittent melena. He ultimately underwent capsule endoscopy and developed a secondary small bowel obstruction, unveiling his neoplasm. The tumor was then resected and managed with surveillance only, and the patient remains without evidence of disease after four years of follow-up.
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  • 文章类型: Journal Article
    高热惊厥(FS)常见于年轻年龄组。癫痫发作的原因是多方面的,包括病毒性疾病,某些疫苗,如MMR(麻疹,腮腺炎,风疹),FS家族史,和某些矿物质缺乏,如锌。缺铁性贫血(IDA)是同一年龄段儿童贫血的最常见原因。根据系统评价和荟萃分析(PRISMA)指南的首选报告项目进行系统评价。本文旨在探讨IDA与发热惊厥的相关性。使用PubMed和GoogleScholar数据库对2013年1月至2023年9月之间发表的研究进行了系统的文献检索。以下关键字用于搜索文章:\"children\",“高热惊厥”,和“缺铁性贫血”,使用所有可能的组合,并在它们之间使用单词\"和\"。在纳入和排除标准应用之后,在这项研究中,我们纳入了23项以英语编写的病例对照研究.使用纽卡斯尔渥太华量表进行研究质量评估。
    Febrile seizures (FS) are commonly seen in younger age groups. The cause of seizures is multifactorial, including viral illnesses, certain vaccines such as MMR (measles, mumps, rubella), family history of FS, and certain mineral deficiencies like zinc. Iron deficiency anemia (IDA) is the most common cause of anemia in children of the same age group. The systematic review was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines. This review aimed to investigate the correlation between IDA and fever convulsions. A systematic literature search was conducted using PubMed and Google Scholar databases for studies published between January 2013 and September 2023. The following keywords were used to search the articles: \"children\", \"febrile seizures\", and \"iron deficiency anemia\", using all possible combinations and using the word \"and\" between them. Following the inclusion and exclusion criteria application, we included 23 case-control studies written in the English language in this study. Quality assessment of studies was done using the Newcastle Ottawa Scale.
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  • 文章类型: Journal Article
    背景:甲状腺激素显著影响整个人体代谢的生理平衡。亚临床甲状腺功能减退症,这通常是隐藏的,与缺铁性贫血和各种其他血液系统疾病有关。在本研究中,我们试图确定缺铁性贫血的患病率和严重程度,并研究亚临床甲状腺功能减退与铁缺乏的相关性。
    方法:将纳入研究的100名受试者分为两组。第1组包括50例亚临床甲状腺功能减退症,第2组包括50名年龄和性别匹配的健康对照。使用Sysmex自动细胞计数器(神户,兵库县,日本)。甲状腺激素(游离三碘甲状腺原氨酸(fT3),游离甲状腺素(fT4),测量促甲状腺激素(TSH)。
    结果:在50例中,48(96%)有缺铁性贫血,52(104%)患有亚临床甲状腺功能减退症。在缺铁性贫血的病例中,43(86%)也有亚临床甲减。促甲状腺激素(TSH)与Hb水平呈负相关。皮尔逊相关系数“r”值为-0.86408。与健康对照组相比,病例的血清铁蛋白水平降低,病例和对照组在血清铁蛋白方面的均值差异也具有统计学意义。
    结论:亚临床甲状腺功能减退症的贫血患病率显著升高,考虑到早期没有明显的临床表现,建议定期进行调查以及早发现,促进及时管理。因此,我们的研究强调,明显和亚临床甲状腺功能减退症都应被视为缺铁性贫血的危险因素。
    BACKGROUND: The physiological equilibrium of the entire human body\'s metabolism is significantly influenced by thyroid hormones. Subclinical hypothyroidism, which is often concealed, is connected to iron deficiency anemia and various other hematological disorders. We in the current study tried to determine the prevalence and severity of iron deficiency anemia and investigate the correlation of subclinical hypothyroidism with iron deficiency.
    METHODS: A total of 100 subjects included in the study were divided into two groups. Group 1 included 50 cases with subclinical hypothyroidism, and Group 2 included 50 healthy age- and sex-matched controls. Hemoglobin (Hb) levels were measured within 24 hours of sample collection using a Sysmex automated cell counter (Kobe, Hyogo, Japan). Thyroid hormones (free triiodothyronine (fT3), free thyroxine (fT4), and thyroid-stimulating hormone (TSH)) were measured.
    RESULTS: Out of 50 cases, 48 (96%) have iron deficiency anemia, and 52 (104%) have subclinical hypothyroidism. Among the cases with iron deficiency anemia, 43 (86%) also have subclinical hypothyroidism. There was a negative correlation between thyrotropin (TSH) and Hb levels. Pearson\'s correlation coefficient \"r\" values were -0.86408. The serum ferritin levels of cases were decreased as compared to the healthy controls, and the difference in means for cases and controls in terms of serum ferritin is also statistically significant.
    CONCLUSIONS: The prevalence of anemia in subclinical hypothyroidism is significantly elevated, and considering the absence of significant clinical manifestations in the early stages, it is recommended to routinely conduct investigations for early detection, facilitating prompt management. Consequently, our study emphasizes that both overt and subclinical hypothyroidism should be recognized as risk factors for the development of iron deficiency anemia.
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  • 文章类型: Journal Article
    患者越来越依赖在线健康信息来了解和管理他们的疾病。文献中已经报道了对这些材料的质量和可读性的担忧。质量差和难以阅读的信息导致延迟诊断和不良结果。我们在Google上评估了有关缺铁性贫血(IDA)的在线健康信息的质量和可读性。方法我们在Google上使用术语“缺铁性贫血”搜索在线网页。包括200个网页中的112个。我们评估了网页类型,可读性,美国医学会杂志(JAMA)评分,DiscERN得分,以及网络健康基金会认证(HONcode)。用R版本4.2.2进行统计学分析。结果非营利和科学期刊网页是最常见的。科学期刊网页的质量最高。新闻网页是最可读性的。第一个GooglePage网页没有更高的JAMA分数或更低的Flesch-Kinkaid阅读等级(FKGL)和简单的Gobbledygo度量(SMOG)分数。所有网页中有46%是高质量的。第一个Google页面上的网页更有可能获得HONCode认证。结论我们强调了有关IDA的在线信息的可读性和质量方面的差距。在线网页超出了患者的推荐阅读水平。大多数网页的质量都很低;只有四分之一的网页获得了HONcode认证;第一个谷歌网页的质量并不比后来的搜索网页高。
    Introduction Patients increasingly rely on online health information to understand and manage their diseases. Concerns about the quality and readability of these materials have been reported in the literature. Poor quality and difficult-to-read information lead to delayed diagnoses and adverse outcomes. We assessed the quality and readability of online health information about iron deficiency anemia (IDA) on Google. Method We searched for online web pages using the term \"iron deficiency anemia\"on Google. One hundred and twelve out of 200 web pages were included. We assessed web page typology, readability, the Journal of the American Medical Association (JAMA) score, the DISCERN score, and the Health on the Net Foundation certification (HONcode). Statistical analysis was performed with R version 4.2.2. Result Non-profit and scientific journal web pages were the most common. Scientific journal web pages were of the highest quality. News web pages were the most readable. The first Google Page web pages did not have greater JAMA scores or lower Flesch-Kinkaid Reading Grade Level (FKGL) and Simple Measure of Gobbledygook (SMOG) scores. Forty-six percent of all web pages were high-quality. Web pages on the first Google page were more likely to have HONCode certification. Conclusion We highlight gaps in the readability and quality of online information about IDA. Online web pages exceeded the recommended reading level for patients. Most web pages were low quality; only a quarter were HONcode-certified; and the first Google page web pages were not higher in quality than the later web pages on search.
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