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Prevalence of Malnutrition and Anaemia in Children ≤ 5 Years of Age in Some Conflict Hit Areas of Meme Division of the South West Region of Cameroon
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作者 Asoba Gillian Nkeudem Ebong Fidelis Sameh +3 位作者 Samuel Metuge Teh Rene Ning Ngede Laura Senge Sumbele Irene Ngole 《Food and Nutrition Sciences》 CAS 2024年第4期235-244,共10页
Malnutrition refers to the deficiency, imbalances, or excesses in a person’s intake of energy or nutrients [1]. Khan defines anaemia as below level of Haemoglobin in red blood shown by a lower number of functioning r... Malnutrition refers to the deficiency, imbalances, or excesses in a person’s intake of energy or nutrients [1]. Khan defines anaemia as below level of Haemoglobin in red blood shown by a lower number of functioning red blood cells [2]. The crisis in the North West and South West Regions of Cameroon has led to several negative effects on children’s living conditions. There has been an increase in malnutrition and anaemia in the South West Region and Kumba in particular. The main objective of this study was “to examine the prevalence of malnutrition and anaemia in children ≤ 5 years of age in some conflict-hit areas of Meme Division”. A descriptive cross-sectional study was conducted in 2023 from March to June. We recruited 200 children ≤ 5 years into the study from three hospitals. The regional hospital annex in Kumba, Presbyterian General Hospital Kumba and the Ntam Hospital in Kumba. Socio-demographic factors were assessed using questionnaire, nutritional status was assessed by the use anthropometric measurements and an auto haematology analyser was used to determine anaemia. The overall prevalence of malnutrition in the study area was 40.5%. The prevalence of malnutrition varied significantly (P < 0.001) with the study sites. The overall prevalence of anaemia in the study area was 70.5%. The prevalence of anaemia was not significantly associated with the study sites. The prevalence of Malnutrition and Anaemia in children ≤ 5 years of age is very high in the Kumba municipalities. This could be attributed to the ongoing crisis which has caused a lot of social migrations from rural areas to Urban areas which are safer. 展开更多
关键词 MALNUTRITION anaemia PREVALENCE Conflict Hit Areas
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Late Onset Combined Immune Deficiency (LOCID) Revealed by a Haemolytic Anaemia in a Child: A Case Report
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作者 Amal Hamami Maria Rkain +4 位作者 Madiha Benhachem Ayyad Ghannam Aziza Elouali Abdeladim Babakhoua Noufissa Benajiba 《Open Journal of Pediatrics》 CAS 2023年第3期347-351,共5页
Variable Common Immune Deficiency (VCID) is a very heterogeneous condition both clinically and immunologically. It is a group of molecular abnormalities responsible for a defect in antibody production leading to hypog... Variable Common Immune Deficiency (VCID) is a very heterogeneous condition both clinically and immunologically. It is a group of molecular abnormalities responsible for a defect in antibody production leading to hypogammaglobulinemia often associated with autoimmune and/or lymphoproliferative manifestations. Late Onset Combined Immune Deficiency (LOCID) is a type of Variable Common Immune Deficiency (VCID) defined by a defect in antibody production (IgG and IgA ± IgM type), profound CD4 T-cell lymphopenia and frequent opportunistic infections. LOCID has been considered as a distinct entity from VCID due to its particular clinical and immunological profile. 展开更多
关键词 Haemolytic anaemia LOCID Immune Deficiency CHILD
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Distortion product otoacoustic emissions in newborn babies with and without late-term maternal iron deficiency anaemia
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作者 Deepashree Somanahalli Ramachandra Ajith Kumar Uppunda Kumar Gavali Suryanarayana 《Journal of Otology》 CAS CSCD 2023年第3期132-138,共7页
Background:Studies on animals have demonstrated that maternal iron deficiency anaemia(IDA)could result in decreased cochlear sensory hair cells and reduced amplitudes of distortion-product otoacoustic emissions(DPOAEs... Background:Studies on animals have demonstrated that maternal iron deficiency anaemia(IDA)could result in decreased cochlear sensory hair cells and reduced amplitudes of distortion-product otoacoustic emissions(DPOAEs)of young guinea pigs.Thus,it is essential to study the functioning of cochlear hair cells using DPOAEs in human newborn babies with maternal IDA.The current study explores maternal IDA’s effect on DPOAEs in newborn babies.Method:A total of 110 newborn babies with gestational age≥34 weeks were considered and a‘betweensubjects’design was used.The participants were divided into 3 groups-“Normal”(61 babies without maternal IDA),“Mild”(28 babies with mild maternal IDA)and“Moderate”(21 babies with moderate maternal IDA).The cord blood was collected and the DPOAEs were recorded for each baby for a range of frequencies(1 k 8 kHz)and a range of intensities(7040 dB SPL in 10 dB steps).Results:The analysis of both DP-gram and DP input-output(I/O)function showed that there was no significant difference(p>0.05)across the normal,mild,and moderate groups in the overall presence of DPOAEs as well as the amplitude across frequencies or intensities(7040 dB SPL).Also,the overall correlation of RBC indices with DPOAE amplitude across frequencies as well as the slope of the I/O function showed no relationship.Conclusion:The current study concludes that there is no effect of late-term maternal IDA on the DPOAEs of newborn babies. 展开更多
关键词 Maternal iron deficiency anaemia Newborn babies Distortion product otoacoustic emissions Cochlear hair cell functioning Red blood cell indices HAEMOGLOBIN
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Factors Associated with Haemolytic Anaemia in the Internal Medicine Department of the Douala General Hospital in Cameroon
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作者 Eveline Ngouadjeu Dongho Brice Utrich Afana +5 位作者 Clémence Olemba Jean Pierre Nda Mefo’o Cécile Ebongue Okalla Abdou Temfomo Jules Clement Nguedia Assob Henry Namme Luma 《Open Journal of Blood Diseases》 2023年第2期83-91,共9页
Introduction: Haemolytic anaemia (HA) is defined as a decrease in haemoglobin (Hb) levels below baseline due to excessive and premature destruction of red blood cells (RBCs) in the periphery resulting in a shortened l... Introduction: Haemolytic anaemia (HA) is defined as a decrease in haemoglobin (Hb) levels below baseline due to excessive and premature destruction of red blood cells (RBCs) in the periphery resulting in a shortened life span of less than 120 days. Haemolysis can be corpuscular or extra-corpuscular. The aim of our study was to investigate the factors associated with it for optimal management of patients hospitalised in internal medicine at the Douala General Hospital (DGH). Methodology: We conducted an analytical cross-sectional study, including all patients admitted to the internal medicine department of the DGH from 11 February to 20 May 2022, and excluding patients with non-compliant samples. The search for haemolytic anaemia was carried out by means of blood count, reticulocyte count, blood smear, unconjugated bilirubin, lactate dehydrogenase and direct Coombs test. Sociodemographic, clinical and biological parameters were collected and analysed. Correlation was defined for a p value 0.05. Results: This study included 147 patients, 50.34% of whom were men, for a sex ratio of 1.01. The mean age was 52 ± 17.9 years. The most represented age group was 56 - 70 years (n = 49;33%) with extremes from 15 to 90 years. We counted 29.3% cases of haemolytic anaemia (HA) and 13.9% cases of autoimmune haemolytic anaemia (AIHA). Haemolytic anaemia (HA) was present in 54.14% of men for a sex ratio of 1.38;the most represented age group was 40 - 55 years, 37.2%. HA was associated with jaundice (OR: 3.74, CI: [1.70 - 8.22], p = 0.001), HIV - AIDS (OR: 2.72, CI: [0.98 - 7.53], p = 0.05), thrombocytopaenia (OR: 3.53, CI: [1.58 - 7.89], p = 0.02). LDH was elevated (OR: 2.86, CI: [1.30 - 6.26], p = 0.00) as well as elevated reticulocyte count (OR: 3.84, CI: [1.75 - 8.44], p = 0.01). Unconjugated bilirubin was elevated in all these patients. In multivariate analysis, factors associated with HA were a history of HIV/AIDS, jaundice, thrombocytopaenia and elevated reticulocyte count. Conclusion: Hemolytic anaemia is common in internal medicine and is significantly associated with thrombocytopenia, HIV/AIDS infection and jaundice. 展开更多
关键词 Haemolytic anaemia Internal Medicine DGH
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Use of iron in perinatal anaemia:Indications for women’s health care policies and procedure
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作者 Mike Etemady Melika Hajizadeh +3 位作者 Beata Gidaszewski Julie Ann Swain Seng Chai Chua Marjan Khajehei 《World Journal of Obstetrics and Gynecology》 2023年第4期33-44,共12页
This paper reviews management of obstetric anaemia and the role of intravenous iron for the treatment of obstetric anaemia.Red blood cell transfusions are routinely used for haemoglobin restoration in anaemic women.Th... This paper reviews management of obstetric anaemia and the role of intravenous iron for the treatment of obstetric anaemia.Red blood cell transfusions are routinely used for haemoglobin restoration in anaemic women.The decision for red blood cell transfusion is made on a combination of haemoglobin level and clinical status,and it is suggested that transfusions are not necessary in those who are well compensated or when alternative therapy is available.To reduce the risk,intravenous iron infusion is proposed as a bloodless therapeutic approach.There are a variety of iron preparations.Intravenous iron infusion can reduce the requirement for blood transfusion in hemodynamically stable women with perinatal anaemia,especially in resource-scarce settings.It a cost-effective bloodless approach for the treatment of anaemia than can enhance patient outcomes.According to the literature,when haemoglobin is greater than 90 g/L,blood transfusion is not often required.In perinatal women with anaemia,the decision whether to administer blood or iron is based on patient preferences,haemoglobin levels,clinical symptoms,past and present medical conditions and the clinician’s judgement.Nevertheless,due to the lack of rigid criteria for blood transfusions in the majority of clinical settings,it is considered the default treatment for anaemia in perinatal women. 展开更多
关键词 anaemia Blood transfusion Iron deficiency Iron infusion Postpartum haemorrhage PREGNANCY
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大量腹水伴多系统受累的TAFRO综合征一例并文献复习
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作者 饶芝国 刘音 薛晓艳 《北京医学》 CAS 2024年第2期112-117,共6页
目的 探讨大量腹水伴多系统受累TAFRO综合征患者的识别及临床表现。方法 选取2015年11月航天中心医院出现大量腹水并多系统损伤的患者1例,回顾性分析其入院资料及临床表现、实验室检查结果,并复习相关文献。结果 本例患者女性,39岁,急... 目的 探讨大量腹水伴多系统受累TAFRO综合征患者的识别及临床表现。方法 选取2015年11月航天中心医院出现大量腹水并多系统损伤的患者1例,回顾性分析其入院资料及临床表现、实验室检查结果,并复习相关文献。结果 本例患者女性,39岁,急性起病,发热后出现大量腹水,伴贫血、PLT减少,SCr升高伴少尿。查体:皮肤巩膜黄染,腹膨隆,无压痛及反跳痛,移动性浊音阳性,肠鸣音弱,右下腹留置腹腔引流管,引流液呈血性,双下肢水肿。实验室结果显示,WBC 8.45×10^(9)/L,RBC 1.73×10^(12)/L,Hb 53 g/L,PLT 11×10^(9)/L,BUN 51.6 mmol/L,SCr 232.9μmol/L,免疫球蛋白G 1 730 mg/dl(正常范围:751~1 560 mg/dl),乳酸脱氢酶569.0 IU/L。诊断考虑TAFRO综合征。给予肾脏替代及支持治疗,配合免疫抑制剂,患者临床症状好转。结论 TAFRO综合征与一些自身免疫性疾病背景相同,临床表现为多系统受累,起病急,发病罕见,鉴别比较困难,预后凶险。患者需紧急医疗处理,可以获得良好的临床效果。 展开更多
关键词 TAFRO综合征 腹腔积液 多系统受累 血小板减少 贫血
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儿童及青少年巨幼细胞性贫血病因及临床特点变化分析
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作者 谷文鑫 李春怀 +4 位作者 王玥 刘爽爽 常纯 姜昊旻 薛露 《中国小儿血液与肿瘤杂志》 CAS 2024年第3期209-213,共5页
目的 探讨及分析近年来儿童巨幼细胞性贫血(MA)的病因及临床特点的变化。方法 对本中心13例MA患儿的临床资料进行回顾性分析,总结及探讨病因构成及临床特点的变化。结果 病因方面,13例患儿中10例处于青春期生长过快(占77%),9例饮食结构... 目的 探讨及分析近年来儿童巨幼细胞性贫血(MA)的病因及临床特点的变化。方法 对本中心13例MA患儿的临床资料进行回顾性分析,总结及探讨病因构成及临床特点的变化。结果 病因方面,13例患儿中10例处于青春期生长过快(占77%),9例饮食结构不合理(占69%)。临床特点突出表现为发病年龄明显滞后,中位年龄14岁,最小年龄6岁;就诊原因多为急性感染和出血,而早期的贫血、巩膜黄染、神经系统损害症状并未引起重视;外周血象改变明显,红系改变为著,均为大细胞性贫血,其中7例(54%)为重度贫血,8例(62%)全血细胞减少。骨髓流式细胞学突出改变为幼红细胞表面CD71和CD36表达减低。结论 儿童MA的病因及临床特点近年来逐渐发生变化,早期易被漏诊和误诊,需引起儿科医生重新重视。 展开更多
关键词 巨幼细胞性贫血 全血细胞减少 病因 发病高峰年龄段 神经系统损害
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基于“温肾化气,利湿泻浊”理论探讨肾性贫血的辨治
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作者 杨思齐 张婧 +1 位作者 赵晰 王耀光 《天津中医药》 CAS 2024年第2期186-190,共5页
肾性贫血是慢性肾脏病的常见并发症之一。随着残存肾功能的恶化,贫血程度不断加重;严重贫血者可诱发心脑血管疾病的急性发作,影响患者生活质量。虚实夹杂、本虚标实的病机贯穿该病始终,脾肾亏虚为本,痰湿、浊毒阻络为标,主要累及脏腑为... 肾性贫血是慢性肾脏病的常见并发症之一。随着残存肾功能的恶化,贫血程度不断加重;严重贫血者可诱发心脑血管疾病的急性发作,影响患者生活质量。虚实夹杂、本虚标实的病机贯穿该病始终,脾肾亏虚为本,痰湿、浊毒阻络为标,主要累及脏腑为肝、脾、肾。治疗上当温补肾气与祛浊毒邪兼顾,益气补血并用,肝、脾、肾同治,补虚的同时不忘通腑利湿泻浊,以平补、轻补为主,调畅气机,补而不滞。 展开更多
关键词 慢性肾脏病 贫血 中西医结合 理论
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促红细胞生成素联合氨甲环酸改善股骨粗隆间骨折围手术期贫血及失血的疗效与安全性分析 被引量:1
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作者 马庆宏 张润 +1 位作者 严旭东 孙超 《南京医科大学学报(自然科学版)》 CAS 北大核心 2024年第6期826-831,共6页
目的:探究促红细胞生成素(erythropoietin,EPO)联合氨甲环酸(tranexamic acid,TXA)改善股骨粗隆间骨折(inter-trochantericfracture,IF)患者围手术期贫血及减少围术期失血的疗效及安全性。方法:分析2018年1月—2023年1月在南京医科大学... 目的:探究促红细胞生成素(erythropoietin,EPO)联合氨甲环酸(tranexamic acid,TXA)改善股骨粗隆间骨折(inter-trochantericfracture,IF)患者围手术期贫血及减少围术期失血的疗效及安全性。方法:分析2018年1月—2023年1月在南京医科大学附属江宁医院因IF手术的患者174例,依据治疗情况分为3组:对照组(A组)62例;仅使用TXA组(B组)57例;TXA联合EPO组(C组)55例。收集3组患者入院时及术前术后血红蛋白(haemoglobin,Hb)量、术中总失血量、显/隐性失血量、围手术期输血率及输血量、住院时间及血栓等并发症情况。结果:3组入院时Hb量差异无统计学意义;C组术前及术后2、5d的Hb量与A组及B组相比,明显改善;C组总失血量、输血率及输血量均低于A组,差异均有统计学意义(P<0.05)。术后3组血栓等并发症发生率比较,差异无统计学意义(P>0.05)。结论:术中静脉和局部联用TXA和EPO能有效减少IF患者围手术期失血及输血率,缩短住院时间及降低住院费用,且不增加血栓等并发症的风险。 展开更多
关键词 股骨粗隆间骨折 贫血 氨甲环酸 促红细胞生成素
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肉碱缺乏对透析患者相关并发症发生机制的研究
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作者 刘辰玲 樊建春 +2 位作者 孙姜华 谭煌 刘圣君 《中国医药导报》 CAS 2024年第12期185-188,共4页
肉碱作为游离脂肪酸进出线粒体的中间转运体,其在人体脂肪酸的β氧化和能量代谢中发挥重要作用。肉碱缺乏可因阻碍线粒体能量代谢而危及生命,肉碱缺乏的原因主要包括原发性合成不足及继发性丢失过多,透析治疗患者是肉碱继发性缺乏较为... 肉碱作为游离脂肪酸进出线粒体的中间转运体,其在人体脂肪酸的β氧化和能量代谢中发挥重要作用。肉碱缺乏可因阻碍线粒体能量代谢而危及生命,肉碱缺乏的原因主要包括原发性合成不足及继发性丢失过多,透析治疗患者是肉碱继发性缺乏较为常见的人群。肉碱缺乏的可能后果包括:细胞内游离脂肪酸积累产生毒性效应,透析过程中出现低血压及心脏病变;继发线粒体内某些关键酶代谢紊乱及改变细胞膜的稳定性,使红细胞变形性及渗透脆性增加进而加重贫血;骨骼肌氧供不足,肌肉含量下降导致患者出现肌病、肌无力、透析期间肌肉痉挛。本文概括了肉碱的生成、代谢途径、生物学功能及缺乏时对机体的影响,阐述了肉碱缺乏时透析患者并发心功能障碍、血流动力学不稳定、贫血、肌肉痉挛的发生机制,为肉碱治疗透析相关并发症提供参考。 展开更多
关键词 肉碱 透析治疗 低血压 贫血 心脏病变 肌肉功能
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高原地区不同时间结扎脐带对经阴道分娩早产儿的影响
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作者 张丹丹 仝海英 +2 位作者 怡萍 孙宝琳 肖海雪 《护理学杂志》 CSCD 北大核心 2024年第13期14-16,共3页
目的比较高原地区不同时间结扎脐带对早产儿短期预后的影响,为明确高原地区早产儿最佳的脐带结扎时间提供参考。方法将高原地区经阴道分娩的100例早产儿随机分为常规组、60 s组、120 s组及180 s组各25例,分别于早产儿娩出30 s、60 s、12... 目的比较高原地区不同时间结扎脐带对早产儿短期预后的影响,为明确高原地区早产儿最佳的脐带结扎时间提供参考。方法将高原地区经阴道分娩的100例早产儿随机分为常规组、60 s组、120 s组及180 s组各25例,分别于早产儿娩出30 s、60 s、120 s、180 s结扎脐带,比较四组早产儿出生5~7 d血红蛋白、血细胞比容、血清胆红素及相关并发症发生率。结果四组早产儿血细胞比容及喂养不耐受、高胆红素血症、红细胞增多症发生率比较,差异无统计学意义(均P>0.05);常规组血红蛋白显著低于其他三组,180 s组经皮胆红素显著高于其他三组(均P<0.05);四组贫血发生率比较,差异有统计学意义(均P<0.05)。结论高原地区早产儿脐带结扎延迟至60~120 s有助于提高早产儿出生5~7 d血红蛋白,降低贫血发生率,且不增加红细胞增多症、高胆红素血症等并发症的发生。 展开更多
关键词 高原地区 早产儿 延迟断脐 脐带结扎 贫血 高胆红素血症 喂养不耐受 红细胞增多症
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4种静脉铁剂治疗缺铁性贫血的快速卫生技术评估
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作者 邢质聪 孙福东 +3 位作者 薛青霞 张蓓 慕升君 赵泉 《药物流行病学杂志》 CAS 2024年第9期1030-1043,共14页
目的采用快速卫生技术评估方法评价4种静脉铁剂治疗缺铁性贫血(IDA)的有效性、安全性和经济性,为临床决策提供依据。方法计算机检索PubMed、Embase、Cochrane Library、CNKI、WanFang Data、SinoMed数据库和国外卫生技术评估机构官方网... 目的采用快速卫生技术评估方法评价4种静脉铁剂治疗缺铁性贫血(IDA)的有效性、安全性和经济性,为临床决策提供依据。方法计算机检索PubMed、Embase、Cochrane Library、CNKI、WanFang Data、SinoMed数据库和国外卫生技术评估机构官方网站,搜集蔗糖铁(IS)、右旋糖酐铁(ID)、羧基麦芽糖铁(FCM)和异麦芽糖酐铁(IIM)4种静脉铁剂治疗IDA的卫生技术评估报告、系统评价/Meta分析和药物经济学研究,检索时限均从建库至2024年8月15日。2名研究者独立筛选文献、提取资料并评价纳入研究的质量,对结果进行定性描述与分析。结果共纳入文献32篇,包括卫生技术评估报告1篇,系统评价/Meta分析16篇,药物经济学研究15篇。有效性方面,FCM的应答患者比例高于IS(P<0.05),FCM和IIM的应答患者比例差异无统计学意义(P>0.05);接受FCM补铁的患者比接受IS的患者具有更高的血红蛋白水平(P<0.05),IIM和FCM在血红蛋白水平改善方面尚无统一结论;对于铁蛋白变化值,FCM可能优于其他3种静脉铁剂。安全性方面,FCM、IS、ID和IIM的不良事件发生率分别为12.0%、15.3%、12.0%、17.0%;与FCM和IS相比,IIM导致的心血管不良事件发生率较低(P<0.05);在4种静脉铁剂中,FCM低磷血症发生率最高(P<0.05),且IIM、IS和ID之间低磷血症发生率差异无统计学意义(P>0.05);相对于FCM和IS,IIM发生严重或重度超敏反应的风险较低。经济性方面,相较于IS,FCM和IIM具有经济学优势;IS、ID和FCM按经济性优劣排序依次为FCM、ID、IS,FCM和IIM的经济性对比尚无定论。结论FCM和IIM在治疗IDA方面具有较好的有效性、安全性和经济性,但纳入的经济学研究多基于国外人群,国内经济学研究有待进一步论证。 展开更多
关键词 蔗糖铁 右旋糖酐铁 羧基麦芽糖铁 异麦芽糖酐铁 缺铁性贫血 快速卫生技术评估
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BIERMER’s Disease: About 4 Cases Diagnosed at Regional University Hospital of Ouahigouya (Chur/Ohg) and Literature Review
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作者 Zanga Damien Ouattara Stève Léonce Zoungrana +4 位作者 Saïdou Santi Emeline Agathe Carama Fabien Dembele Bafima Désiré Diarra Alain Bougouma 《Open Journal of Gastroenterology》 CAS 2024年第9期322-329,共8页
Megaloblastic pernicious anemia is an autoimmune disorder, considered rare in African context. The objective of this study was to report four clinical cases collected at the CHUR/OHG, and to review the literature. The... Megaloblastic pernicious anemia is an autoimmune disorder, considered rare in African context. The objective of this study was to report four clinical cases collected at the CHUR/OHG, and to review the literature. The study population consisted of two men and two women. The clinical manifestations were mainly neurological and hematological. The neurological signs were mainly paresthesia. One patient presented memory problems. On the biological level, macrocytic anemia and vitamin B12 deficiency were reported in two cases prior to treatment while the other two without serological assay of vitamin B12 were put on trial treatment. Anti-intrinsic factor antibodies were positive in three patients. The Schilling test was not used. Upper gastrointestinal endoscopy revealed atrophic fundic gastritis in all four patients who received treatment through intramuscular injection of hydroxocobalamin (vitamin B12). The evolution was favorable after one month of treatment in all cases. The literature review is dominated by clinical case reports, the largest cohorts of which are from the Maghreb. 展开更多
关键词 ANEMIA Pernicious megaloblastic Vitamin B12
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Impact of Regular Blood Donation on Body Iron Stores at Saudi Blood Donors
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作者 Mohammed Qassadi Saleh Mohammed Abdullah 《Open Journal of Blood Diseases》 2024年第3期65-80,共16页
Introduction: One of the most frequent observations in long-term blood donation is chronic iron deficiency, which can develop into anaemia. The majority of blood screening methods employed by blood banks do not incorp... Introduction: One of the most frequent observations in long-term blood donation is chronic iron deficiency, which can develop into anaemia. The majority of blood screening methods employed by blood banks do not incorporate iron-status markers, which may result in potential subclinical iron deficiency. The aim of this study was to evaluate the effects of repeated blood donation on the levels of iron in the body and to guide blood donors in preventing the depletion of iron stores. Methods: Regular blood donors were categorised into distinct groups according to the number of donations they gave, and then the correlation between these groups and their bodies’ iron levels was examined. Different parameters were employed to identify iron deficiency and iron depletion in blood donors: serum ferritin, mean corpuscular volume (MCV), mean corpuscular haemoglobin (MCH), mean corpuscular haemoglobin concentration (MCHC), total iron-binding capacity (TIBC), and serum iron. Results: The study included 300 individuals who regularly and willingly donated blood. There were no iron insufficiency cases among those donating blood for the first time (Group I). However, 15.5% of individuals who had donated once before (Group II) had ferritin levels of 15 - 30 μg/dl (ng/ml), indicating reduced iron stores. The rate increased to 18% (37 out of 206 individuals) among regular blood donors (Groups III, IV, and V). Iron deficiency (depletion) prevalence among regular blood donors in Groups III, IV, and V was 5.9% (12 out of 206) and 50.4% (100 out of 206). Donors who had donated blood most frequently had the lowest levels of haematological markers MCH, MCHC, and TIBC. Provide the p-values representing the differences between the means of MCV, MCH, iron, TIBC, and ferritin levels when comparing donor groups with the control group (Group I) based on the frequency of donations. Indicate statistically significant differences where the p-value is less than 0.0125. This significance level is adjusted based on the Bonferroni method, considering multiple independent tests. The result shows that the Iron parameter for the comparison between Group I and Group III and Group I and Group IV suggests a statistically significant difference in iron levels between these donor groups. Conclusion: The findings of this study show that a higher times of donations lads to a higher occurrence of depleted iron stores and subsequent erythropoiesis with iron deficiency by one donor from every three healthy donors. The iron and ferritin concentrations were within the normal range in group one (Control group) and reduced in the other four groups (G-2 to G-5). However, the level of haemoglobin remained within an acceptable range for blood donation. This outcome suggests that it may be necessary to reassess the criteria for accepting blood donors. The average serum ferritin levels were examined in all five groups (G-1 to G-5), both for males and females, and significant variations were seen among the groups under study. This study found that 35% of the individuals who regularly donate blood have iron-deficient anaemia (sideropenia). This suggests that it would be beneficial to test for serum ferritin at an earlier stage, ideally after three donations. 展开更多
关键词 Iron Deficiency anaemia Regular Blood Donors anaemia Volunteer Blood Donor Blood Donation
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罗沙司他与重组人促红细胞生成素治疗慢性肾脏病5期贫血效果对比
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作者 涂强 汤小飞 余效辉 《中国医学创新》 CAS 2024年第13期121-125,共5页
目的:观察并比较罗沙司他与重组人促红细胞生成素(rHuEPO)对慢性肾脏病(CKD)5期贫血患者的治疗效果。方法:回顾性选取2021年7月—2022年8月于景德镇市第三人民医院治疗的CKD5期贫血患者60例的临床资料,根据用药方案不同分为罗沙司他组和... 目的:观察并比较罗沙司他与重组人促红细胞生成素(rHuEPO)对慢性肾脏病(CKD)5期贫血患者的治疗效果。方法:回顾性选取2021年7月—2022年8月于景德镇市第三人民医院治疗的CKD5期贫血患者60例的临床资料,根据用药方案不同分为罗沙司他组和rHuEPO组,各30例。比较两组临床疗效、血常规、铁代谢情况、炎症指标及不良反应发生率。结果:罗沙司他组治疗总有效率显著高于rHuEPO组(P<0.05)。治疗后,两组红细胞压积(Hct)、血红蛋白(Hb)、血清铁(Fe)较治疗前均升高,且罗沙司他组上述指标均高于rHuEPO组,差异均有统计学意义(P<0.05)。两组治疗前后转铁蛋白饱和度(TSAT)比较,差异均无统计学意义(P>0.05);治疗后,两组血清铁蛋白(SF)、白细胞介素-6(IL-6)、C反应蛋白(CRP)及肿瘤坏死因子(TNF-α)水平较治疗前均明显下降,且罗沙司他组更低,差异均有统计学意义(P<0.05)。观察期间罗沙司他组不良反应总发生率与rHuEPO组比较,差异无统计学意义(P>0.05)。结论:对于慢性肾脏病5期贫血患者,罗沙司他可显著提高其血红蛋白水平,调节患者铁代谢,减轻炎症反应,降低不良反应率,改善CKD5期贫血的效果显著高于rHuEPO。 展开更多
关键词 罗沙司他 重组人促红细胞生成素 慢性肾脏病 贫血
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老年患者全身麻醉腹腔镜下子宫切除术中低体温发生情况及危险因素
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作者 何学梁 王秋英 《中国医学创新》 CAS 2024年第27期166-170,共5页
目的:探讨老年患者全身麻醉腹腔镜下子宫切除术中低体温发生情况及危险因素。方法:回顾性选取2021年7月—2023年7月于广州市番禺区市桥医院进行全身麻醉腹腔镜下子宫切除术的老年患者200例,通过单因素及多因素分析的应用明确患者发生低... 目的:探讨老年患者全身麻醉腹腔镜下子宫切除术中低体温发生情况及危险因素。方法:回顾性选取2021年7月—2023年7月于广州市番禺区市桥医院进行全身麻醉腹腔镜下子宫切除术的老年患者200例,通过单因素及多因素分析的应用明确患者发生低体温的情况及相关危险因素。200例患者,发生低体温的纳入A组,未发生的纳入B组。结果:A组和B组美国麻醉医师协会(American stroke association,ASA)分级Ⅲ级对比,差异无统计学意义(P>0.05);两组的术中静脉输液量>1000 mL、年龄≥70岁、术中腹腔冲洗液量>1500 mL、术前存在焦虑情况、术中二氧化碳气腹时间>120 min、术中出血量>150 mL、术中二氧化碳加温到37℃、体重指数(body mass index,BMI)<24 kg/m^(2)、术中二氧化碳灌注量>200 L、术前存在轻中度贫血占比情况比较,差异均有统计学意义(P<0.05)。多因素结果显示,术中二氧化碳加温到37℃为保护性因素;而术前存在中轻度贫血情况、术中腹腔冲洗液量>1500 mL、年龄≥70岁、术中二氧化碳气腹时间>120 min、术中二氧化碳灌注量>200 L、术中静脉输液量>1000 mL、术前存在焦虑情况、BMI<24 kg/m^(2)、术中出血量>150 mL是导致全身麻醉腹腔镜下子宫切除术老年患者发生低体温的危险因素。结论:老年全身麻醉腹腔镜下子宫切除术患者低体温的发生率较高,而发生原因与术中二氧化碳加温、患者年龄、腹腔冲洗液量、术前有无贫血、气腹时间及二氧化碳灌注情况等存在密切关系,因此实际中需要以此进行指定性措施的制订,以此降低低体温的发生率。 展开更多
关键词 老年患者 全身麻醉 腹腔镜下子宫切除术 低体温 危险因素 贫血
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网织红细胞、血清铁蛋白、VitB_(12)联合检测在MDS与MA鉴别诊断中的应用价值
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作者 徐小津 丁益群 +1 位作者 刘苏琴 杨子东 《中国医学创新》 CAS 2024年第27期148-152,共5页
目的:探讨网织红细胞、血清铁蛋白(SF)、维生素B_(12)(VitB_(12))联合检测在骨髓增生异常综合征(MDS)与巨幼细胞贫血(MA)鉴别诊断中的应用价值。方法:选取2020年7月—2023年11月吉安市中心人民医院收治的MDS患者43例纳入MDS组,MA患者43... 目的:探讨网织红细胞、血清铁蛋白(SF)、维生素B_(12)(VitB_(12))联合检测在骨髓增生异常综合征(MDS)与巨幼细胞贫血(MA)鉴别诊断中的应用价值。方法:选取2020年7月—2023年11月吉安市中心人民医院收治的MDS患者43例纳入MDS组,MA患者43例纳入MA组,另选取于本院体检的健康体检者43例纳入对照组,比较三组血浆网织红细胞、SF及血清VitB_(12)水平,通过受试者操作特征(ROC)曲线分析三项指标单独或联合检测对MDS的诊断效能。结果:MDS组、MA组网织红细胞血红蛋白(Ret-He)、未成熟网织红细胞指数(IRF)、中荧光强度网织红细胞比率(MFR)、高荧光强度网织红细胞比率(HFR)水平均高于对照组,差异均有统计学意义(P<0.05);MDS组、MA组的低荧光强度网织红细胞比率(LFR)均低于对照组(P<0.05);两组IRF、LFR、MFR、HFR水平比较,差异均无统计学意义(P>0.05);MDS组Ret-He水平低于MA组,差异有统计学意义(P<0.05);MDS组、MA组SF水平均高于对照组,差异均有统计学意义(P<0.05);MDS组血清VitB_(12)水平高于对照组,MA组血清VitB_(12)水平低于对照组,差异均有统计学意义(P<0.05);MDS组SF、VitB_(12)水平均高于MA组,差异均有统计学意义(P<0.05)。网织红细胞参数Ret-He与SF、VitB_(12)联合检测诊断MDS时ROC曲线下面积为0.942,高于三项指标单独检测曲线下面积0.755、0.813、0.830,差异均有统计学意义(P<0.05)。结论:网织红细胞联合SF和VitB_(12)对于指导MDS诊断具有一定的价值,MDS的SF、VitB_(12)均高于MA,Ret-He低于MA,可作为临床疾病鉴别的重要参考指标。 展开更多
关键词 骨髓增生异常综合征 再生障碍性贫血 网织红细胞 血清铁蛋白 维生素B_(12)
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妊娠期贫血患者的血常规检验结果分析
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作者 许婷 陈磊 《中国医药指南》 2024年第21期84-87,共4页
目的分析妊娠期贫血患者的血常规检验结果。方法研究按照是否有贫血症状分组,选择2023年1月至2023年11月我院收治的48例妊娠期贫血患者为观察组,选择同期接受体检的48名身体健康的孕妇为对照组(未见贫血问题)。比较两组血常规检验结果... 目的分析妊娠期贫血患者的血常规检验结果。方法研究按照是否有贫血症状分组,选择2023年1月至2023年11月我院收治的48例妊娠期贫血患者为观察组,选择同期接受体检的48名身体健康的孕妇为对照组(未见贫血问题)。比较两组血常规检验结果。结果观察组红细胞计数、平均红细胞体积(MCV)、血红蛋白(Hb)及平均红细胞血红蛋白浓度(MCHC)水平均低于对照组,平均红细胞血红蛋白量(MCH)、红细胞分布宽度(RDW)水平均高于对照组,差异有统计学意义(P<0.05);不同孕期贫血孕妇,在红细胞计数、MCV、Hb、MCHC、RDW方面也存在差异,且差异有统计学意义(P<0.05)。结论血常规检查可以用于诊断妊娠期贫血,对于判断病情和指导治疗具有重要意义。产妇应当关注血常规检查的各项数值,关注孕期健康。 展开更多
关键词 妊娠期贫血 血常规 检验结果
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八珍汤联合肠内营养治疗长期卧床伴气血亏虚型贫血患者的临床疗效分析
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作者 何佳澄 李晨 《黑龙江医药》 CAS 2024年第1期35-38,共4页
目的:探讨八珍汤在治疗长期卧床伴气血亏虚型贫血患者中的价值。方法:将入组患者随机分为八珍汤组和对照组,对照组予常规治疗+肠内营养支持治疗,八珍汤组在此基础上增加八珍汤益气养血,所有患者疗程均为14天。观察两组患者治疗后的总有... 目的:探讨八珍汤在治疗长期卧床伴气血亏虚型贫血患者中的价值。方法:将入组患者随机分为八珍汤组和对照组,对照组予常规治疗+肠内营养支持治疗,八珍汤组在此基础上增加八珍汤益气养血,所有患者疗程均为14天。观察两组患者治疗后的总有效率,将治疗后RBC、Hb、SI、SF等各项指标进行比较,并对治疗后出现的气血亏虚证和消化道不良反应进行综合评价。结果:八珍汤组的临床疗效为86.67%,对照组的临床疗效为60.00%,八珍汤组显著优于对照组。两组患者治疗后的气血亏虚证的中医证候分数较治疗前有所下降,八珍汤组和对照组之间存在显著差别(P<0.05);治疗14天后,八珍汤组在消化道不良反应方面的中医证候分数显著低于对照组(P<0.05);治疗后,两组患者的贫血指标均较治疗前有所改善,且八珍汤组较对照组有明显统计学差异(P<0.05)。结论:八珍汤联合肠内营养对治疗长期卧床伴气血亏虚型贫血有较理想的疗效,值得临床推广。 展开更多
关键词 八珍汤 肠内营养 气血亏虚 贫血
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罗沙司他联合重组人促红素治疗尿毒症肾性贫血维持性血液透析患者的效果分析
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作者 林建锋 《中国医药指南》 2024年第8期38-41,共4页
目的 探究罗沙司他联合重组人促红素治疗尿毒症肾性贫血维持性血液透析患者的效果。方法 选择2021年4月至2023年4月在我院治疗的尿毒症肾性贫血患者86例,应用随机数字表法将其分为对照组(重组人促红素)及观察组(联合罗沙司他)各43例,对... 目的 探究罗沙司他联合重组人促红素治疗尿毒症肾性贫血维持性血液透析患者的效果。方法 选择2021年4月至2023年4月在我院治疗的尿毒症肾性贫血患者86例,应用随机数字表法将其分为对照组(重组人促红素)及观察组(联合罗沙司他)各43例,对比两组营养指标[血红蛋白(Hb)、铁蛋白(SF)、转铁蛋白(TF)]、肾功能指标[尿素氮(BUN)、血肌酐(Scr)、β2-微球蛋白(β2-MG)]、炎症因子[单核细胞趋化因子(MCP-1)、缺氧诱导因子2α(HIF-2α)、基质金属蛋白酶抑制酶(TIMP-1)]及不良反应发生率。结果 观察组Hb、SF、TF水平高于对照组(均P<0.05)。观察组BUN、Scr、β2-MG水平低于对照组(均P <0.05)。观察组MCP-1、HIF-2α、TIMP-1水平低于对照组(均P <0.05)。观察组不良反应发生率与对照组比较差异无统计学意义(P> 0.05)。结论 罗沙司他联合重组人促红素,可改善肾性贫血患者机体营养状况、肾功能,纠正铁代谢功能,减轻炎症反应,且不增加不良反应。 展开更多
关键词 罗沙司他 重组人促红素 尿毒症肾性贫血 维持性血液透析
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