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Erythropoiesis in Malaria Infections and Factors Modifying the Erythropoietic Response 疟疾感染中的红细胞生成和改变红细胞生成反应的因素
IF 2.9 Q3 Medicine Pub Date : 2016-02-29 DOI: 10.1155/2016/9310905
V. Pathak, K. Ghosh
Anemia is the primary clinical manifestation of malarial infections and is responsible for the substantial rate of morbidity. The pathophysiology discussed till now catalogued several causes for malarial anemia among which ineffective erythropoiesis being remarkable one occurs silently in the bone marrow. A systematic literature search was performed and summarized information on erythropoietic response upon malaria infection and the factors responsible for the same. This review summarizes the clinical and experimental studies on patients, mouse models, and in vitro cell cultures reporting erythropoietic changes upon malaria infection as well as factors accountable for the same. Inadequate erythropoietic response during malaria infection may be the collective effect of various mediators generated by host immune response as well as parasite metabolites. The interplay between various modulators causing the pathophysiology needs to be explored further. Globin gene expression profiling upon malaria infection should also be looked into as abnormal production of globin chains could be a possible contributor to ineffective erythropoiesis.
贫血是疟疾感染的主要临床表现,也是疟疾发病率居高不下的原因。迄今为止讨论的病理生理学列出了疟疾性贫血的几种原因,其中红细胞生成无效是显著的,骨髓中静默发生。我们进行了系统的文献检索,总结了疟疾感染后红细胞生成反应及其相关因素的信息。本文综述了疟疾感染后红细胞生成变化的临床和实验研究、小鼠模型和体外细胞培养及其相关因素。疟疾感染期间红细胞生成反应不足可能是宿主免疫反应和寄生虫代谢物产生的各种介质的共同作用。引起病理生理的各种调节因子之间的相互作用有待进一步探讨。疟疾感染时的珠蛋白基因表达谱也应加以研究,因为珠蛋白链的异常产生可能是导致红细胞生成无效的一个可能因素。
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引用次数: 37
Prevalence of Anemia and Its Associated Factors among Pregnant Women Attending Antenatal Care in Health Institutions of Arba Minch Town, Gamo Gofa Zone, Ethiopia: A Cross-Sectional Study 埃塞俄比亚Gamo Gofa区Arba Minch镇卫生机构产前保健孕妇贫血患病率及其相关因素:一项横断面研究
IF 2.9 Q3 Medicine Pub Date : 2016-02-22 DOI: 10.1155/2016/1073192
A. Bekele, M. Tilahun, Aleme Mekuria
Background. Anemia during pregnancy is a major cause of morbidity and mortality of pregnant women in developing countries and has both maternal and fetal consequences. Despite its known serious effect on health, there is very little research based evidence on this vital public health problem in Gamo Gofa zone in general and in Arba Minch town of Southern Ethiopia in particular. Therefore, this study aims to assess the prevalence and factors associated with anemia among pregnant women attending antenatal care in health institutions of Arba Minch town, Gamo Gofa zone, Southern Ethiopia. Method. Institution-based, cross-sectional study was conducted from February 16 to April 8, 2015, among 332 pregnant women who attended antenatal care at government health institutions of Arba Minch town. Interviewer-administered questionnaire supplemented by laboratory tests was used to obtain the data. Bivariate and multivariate logistic regressions were used to identify predictors of anemia. Result. The prevalence of anemia among antenatal care attendant pregnant women of Arba Minch town was 32.8%. Low average monthly income of the family (AOR = 4.0; 95% CI: 5.62–11.01), having birth interval less than two years (AOR = 3.1; 95% CI: 6.01, 10.23), iron supplementation (AOR = 2.31; 95% CI: 7.21, 9.31), and family size >2 (AOR = 2.8; 95% CI: 1.17, 6.81) were found to be independent predictors of anemia in pregnancy. Conclusion. Anemia is found to be a moderate public health problem in the study area. Low average monthly income, birth interval less than two years, iron supplementation, and large family size were found to be risk factors for anemia in pregnancy. Awareness creation towards birth spacing, nutritional counselling on consumption of iron-rich foods, and iron supplementation are recommended to prevent anemia among pregnant women with special emphasis on those having low income and large family size.
背景。妊娠期贫血是发展中国家孕妇发病和死亡的一个主要原因,对孕产妇和胎儿都有影响。尽管已知其对健康的严重影响,但在整个加莫戈法区,特别是在埃塞俄比亚南部的阿尔巴明奇镇,关于这一重大公共卫生问题的研究证据很少。因此,本研究旨在评估在埃塞俄比亚南部加莫戈法区阿尔巴明奇镇卫生机构接受产前保健的孕妇中贫血的患病率及其相关因素。方法。本研究于2015年2月16日至4月8日对在Arba Minch镇政府卫生机构接受产前保健的332名孕妇进行了基于机构的横断面研究。采用访谈者管理的问卷,辅以实验室测试来获取数据。使用双变量和多变量logistic回归来确定贫血的预测因子。结果。Arba Minch镇产前护理孕妇贫血患病率为32.8%。家庭平均月收入低(AOR = 4.0);95% CI: 5.62-11.01),生育间隔小于2年(AOR = 3.1;95% CI: 6.01, 10.23),补铁(AOR = 2.31;95% CI: 7.21, 9.31)和家庭规模(AOR = 2.8;95% CI: 1.17, 6.81)是妊娠期贫血的独立预测因子。结论。在研究地区,贫血被认为是一个中度的公共卫生问题。平均月收入低、生育间隔少于两年、补铁和家庭人口多是妊娠期贫血的危险因素。建议提高对生育间隔的认识,就食用富含铁的食物提供营养咨询,并补充铁,以预防孕妇贫血,特别强调低收入和大家庭的孕妇。
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引用次数: 94
Antianemic Treatment of Cancer Patients in German Routine Practice: Data from a Prospective Cohort Study—The Tumor Anemia Registry 德国常规实践中癌症患者的抗贫血治疗:来自肿瘤贫血登记的前瞻性队列研究的数据
IF 2.9 Q3 Medicine Pub Date : 2016-02-04 DOI: 10.1155/2016/8057650
T. Steinmetz, J. Schröder, M. Plath, H. Link, M. Vogt, M. Frank, N. Marschner
The aim of this prospective cohort study was to assess current antianemic treatment of cancer patients in German routine practice, including diagnostics, treatments, and quality of life (QoL). 88 study sites recruited 1018 patients at the start of antianemic treatment with hemoglobin (Hb) levels <11 g/dL (females) or <12 g/dL (males). Patients were followed up for 12 weeks. 63% of the patients had inoperable solid tumors, 22% operable solid tumors, and 15% hematological malignancies. Over 85% received chemotherapy. Median age was 67 years; 48% were male. Red blood cell transfusions (RBCTx) were given to 59% of all patients and to 55% of the patients with Hb ≥8 g/dL on day 1 of the observation period (day 1 treatment). Erythropoiesis-stimulating agents (ESAs) were the second most frequently applied day 1 treatment (20%), followed by intravenous (IV) iron (15%) and ESA + IV iron (6%). Only about a third of patients were tested for blood serum iron parameters at the start of treatment. Overall, more than half of the patients had long-term responses to antianemic therapy. Our data suggest that in routine practice diagnostics for treatable causes of anemia are underused. A high proportion of cancer patients receive RBCTx. It should be discussed whether thorough diagnostics and earlier intervention could decrease the need for RBCTx. This trial is registered with NCT01795690.
这项前瞻性队列研究的目的是评估目前德国常规实践中癌症患者的抗贫血治疗,包括诊断、治疗和生活质量(QoL)。88个研究地点招募了1018名抗贫血治疗开始时血红蛋白(Hb)水平<11 g/dL(女性)或<12 g/dL(男性)的患者。随访12周。不可手术的实体瘤占63%,可手术的实体瘤占22%,血液系统恶性肿瘤占15%。超过85%的患者接受了化疗。中位年龄67岁;48%是男性。在观察期第1天(治疗第1天),59%的患者和55%的Hb≥8 g/dL的患者接受红细胞输注(RBCTx)。促红细胞生成剂(ESA)是第1天最常用的治疗方法(20%),其次是静脉(IV)铁(15%)和ESA + IV铁(6%)。只有大约三分之一的患者在治疗开始时进行了血清铁参数检测。总的来说,超过一半的患者对抗贫血治疗有长期反应。我们的数据表明,在常规实践中,对可治疗的贫血病因的诊断未得到充分利用。接受RBCTx治疗的癌症患者比例很高。应该讨论彻底诊断和早期干预是否可以减少RBCTx的需求。本试验注册号为NCT01795690。
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引用次数: 8
Sickle-Cell Disease Healthcare Cost in Africa: Experience of the Congo 非洲镰状细胞病的医疗费用:刚果的经验
IF 2.9 Q3 Medicine Pub Date : 2016-02-02 DOI: 10.1155/2016/2046535
L. Ngolet, M. Moyen Engoba, I. Kocko, A. Elira Dokékias, J. Mombouli, G. Moyen
Background. Lack of medical coverage in Africa leads to inappropriate care that has an impact on the mortality rate. In this study, we aimed to evaluate the cost of severe acute sickle-cell related complications in Brazzaville. Methods. A retrospective study was conducted in 2014 in the Paediatric Intensive Care Unit. It concerned 94 homozygote sickle-cell children that developed severe acute sickle-cell disease related complications (average age 69 months). For each patient, we calculated the cost of care complication. Results. The household income was estimated as low (
背景。非洲缺乏医疗覆盖,导致护理不当,对死亡率产生影响。在这项研究中,我们旨在评估布拉柴维尔严重急性镰状细胞相关并发症的成本。方法。2014年在儿科重症监护室进行了一项回顾性研究。它涉及94名发生严重急性镰状细胞病相关并发症的纯合子镰状细胞儿童(平均年龄69个月)。对于每位患者,我们计算了护理并发症的成本。结果。27.7%的家庭收入估计较低(< 9万里亚尔/< 158.40美元)。镰状细胞相关急性并发症的住院总中位费用为65,460澳币/ 115.21美元。费用随严重急性并发症的发生因素而波动(p = 0.041)。细菌感染引起的并发症较高(从66,765 XAF / 117.50美元到135,271.50 XAF / 238.07美元),与疟疾相关的并发症较低(从28,305/49.82 XAF到64,891.63 XAF / 114.21美元)。死亡率为17%,与病例管理费用相关(p = 0.006)。结论。在刚果,儿童镰状细胞病严重急性并发症的病例管理费用很高。
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引用次数: 14
Magnitude of Anemia and Hematological Predictors among Children under 12 Years in Odisha, India. 印度奥迪沙 12 岁以下儿童贫血症的严重程度和血液学预测因素。
IF 2.9 Q3 Medicine Pub Date : 2016-01-01 Epub Date: 2016-04-04 DOI: 10.1155/2016/1729147
Shuchismita Behera, Gandham Bulliyya

Background. Anemia is a wide spread public health problem in India which affects children. The present study evaluates the prevalence of anemia and status of various hematological parameters among children of Khurda district, Odisha. Method. A total of 313 children aged 0-12 years were enrolled for the study which included preschool (0-5 years) and school aged (6-12 years) groups. Hematological indicators were measured by standard procedures, which include red blood cell (RBC) indicators, white blood cell (WBC) indicators, and plasma ferritin. Results. Mean hemoglobin (Hb) of the study population was 10.43 ± 3.33 g/dL and prevalence of anemia was 62%. In this population, boys had a lower mean Hb value than that of the girls. All grades of anemia were higher among school age children than preschool children. Mean plasma ferritin was found to be higher in school age boys than their counterpart girls. The mean level of WBC count was found to be higher among preschool age boys than among the school age boys (p = 0.025). Conclusion. The prevalence of anemia was higher with concomitant acute infection among study population, which is a matter of concern. Since the hematological parameters are interrelated with each other as well as with the age and gender, relevant intervention strategy and constant monitoring are needed while providing public health nutrition programs to eradicate anemia.

背景。贫血是印度广泛存在的公共卫生问题,对儿童的影响很大。本研究评估了奥迪沙邦库尔达地区儿童的贫血患病率和各种血液学参数的状况。研究方法研究共招募了 313 名 0-12 岁的儿童,包括学龄前(0-5 岁)和学龄期(6-12 岁)儿童。采用标准程序测量血液指标,包括红细胞(RBC)指标、白细胞(WBC)指标和血浆铁蛋白。结果显示研究人群的平均血红蛋白(Hb)为 10.43 ± 3.33 g/dL,贫血发生率为 62%。男孩的平均血红蛋白值低于女孩。学龄儿童的各等级贫血率均高于学龄前儿童。学龄男孩的平均血浆铁蛋白高于女孩。学龄前男孩的白细胞计数平均水平高于学龄前男孩(p = 0.025)。结论在研究人群中,伴随急性感染的贫血发生率较高,这是一个值得关注的问题。由于血液学参数与年龄和性别相互关联,因此在提供公共卫生营养计划以消除贫血的同时,还需要相关的干预策略和持续监测。
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引用次数: 0
Evaluation of Serum Leptin Levels and Growth in Patients with β-Thalassaemia Major. β-地中海贫血患者血清瘦素水平和生长的评价。
IF 2.9 Q3 Medicine Pub Date : 2016-01-01 Epub Date: 2016-03-21 DOI: 10.1155/2016/8454286
Lamia Mustafa Al-Naama, Meaad Kadum Hassan, Muhannad Maki Abdul Karim

Background. Iron deposition in the body can damage the endocrine glands of patients with β-thalassaemia major (β-TM). Leptin plays a key role in the regulation of appetite, body fat mass, and endocrine function. Objectives. This study aimed to evaluate the relationship between serum leptin and growth and pubertal development in patients with β-TM, as well as whether serum leptin can predict growth retardation and delayed puberty in these patients. Methods. Fifty β-TM patients (aged 8-20 years) and 75 age-matched healthy controls were recruited. Anthropometric data and sexual maturity ratings were assessed. Serum leptin was measured by ELISA. Results. Serum leptin levels were significantly lower in patients with β-TM than in healthy individuals (P < 0.001). Leptin levels were also significantly reduced in female patients with short stature (P < 0.002) and in patients who displayed delayed puberty (P = 0.032) compared to those with normal stature who had reached puberty. The sensitivity of leptin for predicting short stature and delayed puberty among patients was 84.6% and 92.3%, respectively. Conclusion. Low serum leptin is sensitive to predict short stature and significant in β-TM females only. This link could thus be used as a guide for further therapeutic or hormonal modulation.

背景。β-地中海贫血(β-TM)患者体内的铁沉积会损害内分泌腺体。瘦素在调节食欲、体脂量和内分泌功能方面起着关键作用。目标。本研究旨在探讨血清瘦素与β-TM患者生长发育和青春期发育的关系,以及血清瘦素是否可以预测这些患者的生长发育迟缓和青春期延迟。方法。招募了50例β-TM患者(8-20岁)和75名年龄匹配的健康对照。评估了人体测量数据和性成熟评分。ELISA法测定血清瘦素水平。结果。β-TM患者血清瘦素水平明显低于健康人群(P < 0.001)。身材矮小的女性患者(P < 0.002)和青春期延迟的女性患者(P = 0.032)的瘦素水平也明显低于已经进入青春期的正常身材患者。瘦素预测患者身材矮小和青春期延迟的敏感性分别为84.6%和92.3%。结论。低血清瘦素仅在β-TM女性中对身材矮小敏感。因此,这种联系可以作为进一步治疗或激素调节的指导。
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引用次数: 9
Absolute Reticulocyte Count and Reticulocyte Hemoglobin Content as Predictors of Early Response to Exclusive Oral Iron in Children with Iron Deficiency Anemia. 绝对网织红细胞计数和网织红细胞血红蛋白含量作为缺铁性贫血儿童口服铁治疗早期反应的预测指标。
IF 2.9 Q3 Medicine Pub Date : 2016-01-01 Epub Date: 2016-03-22 DOI: 10.1155/2016/7345835
Emilia Parodi, Maria Teresa Giraudo, Fulvio Ricceri, Maria Luigia Aurucci, Raffaela Mazzone, Ugo Ramenghi
We report data regarding kinetic of response to oral iron in 34 iron deficiency anemia children. Twenty-four/34 patients (70.5%) reached reference value of hemoglobin (Hb) concentration for age and sex at day + 30 from the beginning of treatment (complete early responders (CERs)), and 4/34 (12%) reached an Hb concentration at least 50% higher than the original (partial early responders (PERs)). CHr at T1 (within 7 days from the beginning of treatment) was significantly different in the different groups (22.95 in CERs versus 18.41 in other patients; p = 0.001; 22.42 in early responders versus 18.07 in NERs; p = 0.001). Relative increase of CHr from T0 to T1 resulted significantly higher in CERs than in other patients (0.21 versus 0.11, p = 0.042) and in early responders than in NERs (0.22 versus 0.004, p = 0.006). Multivariate logistic models revealed a higher probability of being a complete early responder due to relative increase of ARC from T0 to T1 [OR (95% CI) = 44.95 (1.54–1311.98)] and to CHr at T1 [OR (95% CI) =3.18 (1.24–8.17)]. Our preliminary data confirm CHr as early and accurate predictor of hematological response to oral iron.
我们报告了34例缺铁性贫血儿童口服铁反应动力学的数据。24 /34例患者(70.5%)在治疗开始后第30天达到年龄和性别血红蛋白(Hb)浓度参考值(完全早期反应者(CERs)), 4/34例(12%)的Hb浓度比原始(部分早期反应者(PERs))至少高出50%。不同组T1时(治疗开始后7天内)的CHr有显著差异(CERs组22.95,其他组18.41;P = 0.001;早期响应者为22.42,晚期响应者为18.07;P = 0.001)。从T0到T1的CHr相对升高导致cer患者显著高于其他患者(0.21比0.11,p = 0.042),早期应答者显著高于ner患者(0.22比0.004,p = 0.006)。多变量logistic模型显示,由于ARC从T0到T1的相对增加[OR (95% CI) = 44.95(1.54-1311.98)]和T1时的CHr [OR (95% CI) =3.18(1.24-8.17)],成为完全早期应答者的可能性更高。我们的初步数据证实CHr是口服铁的血液学反应的早期和准确的预测因子。
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引用次数: 22
Using Soluble Transferrin Receptor and Taking Inflammation into Account When Defining Serum Ferritin Cutoffs Improved the Diagnosis of Iron Deficiency in a Group of Canadian Preschool Inuit Children from Nunavik. 在确定血清铁蛋白切断时,使用可溶性转铁蛋白受体并考虑炎症改善了一组来自努那维克的加拿大学龄前因纽特儿童缺铁的诊断。
IF 2.9 Q3 Medicine Pub Date : 2016-01-01 Epub Date: 2016-06-13 DOI: 10.1155/2016/6430214
Huguette Turgeon O'Brien, Rosanne Blanchet, Doris Gagné, Julie Lauzière, Carole Vézina

The prevalence of iron depletion, iron deficient erythropoiesis (IDE), and iron deficiency anemia (IDA) was assessed in preschool Inuit children using soluble transferrin receptor (sTfR) and traditional indicators of iron status while disregarding or taking inflammation into account when defining SF cutoffs. Iron depletion was defined as follows: (1) SF < 15 μg/L regardless of the C-reactive protein (CRP) level and (2) SF < 15 or <50 μg/L with CRP ≤ 5 or >5 mg/L, respectively. IDE corresponded to iron depletion combined with total iron binding capacity > 72 μmol/L and/or transferrin saturation < 16%. Iron depletion and IDE affected almost half of the children when accounting for inflammation, compared to one-third when the SF cutoff was defined regardless of CRP level (P < 0.0001). The prevalence of IDE adjusted for inflammation (45.1%) was very similar to the prevalence observed when sTfR was used as a sole marker of IDE (47.4%). The prevalence of anemia was 15%. The prevalence of IDA (IDE + hemoglobin < 110 g/L) was higher when accounting for than when disregarding inflammation (8.0% versus 6.2%, P = 0.083). Using sTfR and different SF cutoffs for children with versus without inflammation improved the diagnosis of iron depletion and IDE. Our results confirm that Inuit children are at particularly high risk for iron deficiency.

使用可溶性转铁蛋白受体(sTfR)和传统的铁状态指标评估因纽特学龄前儿童中铁耗尽、铁缺乏性红细胞(IDE)和缺铁性贫血(IDA)的患病率,在定义SF截止时忽略或考虑炎症。铁耗尽的定义如下:(1)无论c反应蛋白(CRP)水平如何,SF < 15 μg/L; (2) SF分别< 15或5 mg/L。IDE对应铁耗尽,总铁结合容量> 72 μmol/L和/或转铁蛋白饱和度< 16%。当考虑到炎症时,铁缺乏和IDE影响了几乎一半的儿童,而当定义SF截止时,无论CRP水平如何,这一比例为三分之一(P < 0.0001)。经炎症调整的IDE患病率(45.1%)与使用sTfR作为IDE的唯一标志物时观察到的患病率(47.4%)非常相似。贫血的患病率为15%。考虑炎症时,IDA (IDE +血红蛋白< 110 g/L)的患病率高于不考虑炎症时(8.0%对6.2%,P = 0.083)。对有无炎症的儿童使用sTfR和不同的SF截止值可改善铁耗尽和IDE的诊断。我们的研究结果证实,因纽特儿童缺铁的风险特别高。
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引用次数: 16
Transfusion Thresholds, Quality of Life, and Current Approaches in Myelodysplastic Syndromes. 骨髓增生异常综合征的输血阈值、生活质量和当前治疗方法。
IF 2.9 Q3 Medicine Pub Date : 2016-01-01 Epub Date: 2016-04-19 DOI: 10.1155/2016/8494738
Ioannis Koutsavlis

Hemoglobin thresholds and triggers for blood transfusions have changed over the years moving from a higher to a lower level. This review article summarizes the current evidence of transfusion thresholds in the hospitalized as well as in the outpatient setting and particularly in myelodysplasia. Fatigue is the main reported symptom in this group of patients and current clinical trials are looking for a more liberal approach of red cell transfusion and the effect on quality of life as opposed to the restrictive strategy used in the critical care setting. Practical considerations, the cost effectiveness of this strategy in addition to the possible complications, and the use of quality of life questionnaires have also been reviewed.

多年来,血红蛋白阈值和输血触发因素发生了变化,从较高的水平到较低的水平。这篇综述文章总结了输血阈值在住院和门诊的现有证据,特别是在骨髓增生异常。疲劳是这组患者报告的主要症状,目前的临床试验正在寻找一种更自由的红细胞输注方法及其对生活质量的影响,而不是在重症监护环境中使用的限制性策略。还审查了实际考虑因素、这一战略的成本效益以及可能的并发症和生活质量调查表的使用。
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引用次数: 25
The Cost-Effectiveness of Continuous Erythropoiesis Receptor Activator Once Monthly versus Epoetin Thrice Weekly for Anaemia Management in Chronic Haemodialysis Patients 慢性血液透析患者每月1次连续使用红细胞生成受体激活剂与每周3次生成素治疗贫血的成本-效果比较
IF 2.9 Q3 Medicine Pub Date : 2015-12-30 DOI: 10.1155/2015/189404
O. Maoujoud, S. Ahid, H. Dkhissi, Z. Oualim, Y. Cherrah
Introduction. The aim of this study was to compare the cost-effectiveness of continuous erythropoietin receptor activator (CERA) once monthly to epoetin beta (EpoB) thrice weekly to maintain haemoglobin (Hb) within the range 10.5–12 g/dL. Methods. Prospective cohort study and cost-effectiveness analysis. Chronic haemodialysis patients (CHP), being treated with EpoB, were selected for two periods of follow-up: period 1, maintaining prior treatment with EpoB, and period 2, conversion to CERA once monthly. Hb concentrations and costs were measured monthly. Health care payer perspective for one year was adopted. Results. 75 CHP completed the study, with a mean age of 52.9 ± 14.3 years. Baseline Hb was 11.14 ± 1.18 g/dL in EpoB phase and 11.46 ± 0.79 g/dL in CERA phase; we observed a significant increase in the proportion of patients successfully treated (Hb within the recommended range), 65.3% versus 70.7%, p: 0.008, and in the average effectiveness by 4% (0.55 versus 0.59). Average cost-effectiveness ratios were 6013.86 and 5173.64$, with an ICER CERA to EpoB at −6457.5$. Conclusion. Our health economic evaluation of ESA use in haemodialysis patients suggests that the use of CERA is cost-effective compared with EpoB.
介绍。本研究的目的是比较每月1次的持续促红细胞生成素受体激活剂(CERA)和每周3次的促红细胞生成素β (EpoB)的成本-效果,以维持血红蛋白(Hb)在10.5-12 g/dL范围内。方法。前瞻性队列研究及成本-效果分析。选择接受EpoB治疗的慢性血液透析患者(CHP)进行两期随访:第一期,维持先前的EpoB治疗,第二期,转换为CERA每月一次。每月测量Hb浓度和成本。采用为期一年的医疗保健支付者视角。结果:75例CHP完成研究,平均年龄52.9±14.3岁。EpoB期基线Hb为11.14±1.18 g/dL, CERA期基线Hb为11.46±0.79 g/dL;我们观察到成功治疗的患者比例(Hb在推荐范围内)显著增加,65.3%对70.7%,p: 0.008,平均有效性增加4%(0.55对0.59)。平均成本效益比为6013.86美元和5173.64美元,ICER CERA与EpoB的成本效益比为- 6457.5美元。结论。我们对血液透析患者使用ESA的健康经济评估表明,与EpoB相比,使用CERA具有成本效益。
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引用次数: 5
期刊
Anemia
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