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Red Blood Cells Alloimmunization and Autoimmunization in Multi-transfused Thalassemia Patients in South of Iran 伊朗南部多次输血地中海贫血患者的红细胞同种异体免疫和自身免疫
IF 0.3 Q4 PEDIATRICS Pub Date : 2019-01-10 DOI: 10.18502/ijpho.v9i1.295
Farogh Homeirani, M. Keramati, M. Sadeghian, Zeynab Mozafari, Azam Moradi Zarmehri
Background: Recurrent blood transfusion is a common treatment in patients with thalassemia. The development of antibodies against red blood cell (RBC) antigens complicates RBC cross-matching, enhances the in vivo destruction of transfused cells, accelerates tissue iron overloading, delays the provision of safe transfusion, and reduces health-related quality of life. Materials and Methods: In total, 516 thalassemia patients with a mean age of 18.5 years were included in this cross-sectional study in Mashhad University of Medical Sciences, Razavi Khorasan Province, Iran, in cooperation with the Abu Rayhan Special Medical Center and Hormozgan Blood Transfusion Organization between June 2015 and May 2016. The detection and identification of alloantibodies were done using 3 screen cells and 11 panel cells, respectively. To detect autoantibodies, auto-control was performed using polyspecific Coombs (IgG + C3d) standard method. Results: Alloantibodies and autoantibodies were observed in 16 (3.1%) and 21 (4.1%) patients, respectively. Among patients with alloantibodies, 2 patients (12.5%) developed 3 antibodies (Anti-c,E,P1; Anti-c,E,K), 1 patient (6.25%) developed 2 antibodies (Anti-D,C), and 13 patients developed 1 antibody (4 patients Anti-D (25%); 3 Anti-K (18.75%); 2 Anti-E (12.5%); 2 Anti-C (12.5%); 1 Anti-Jka (6.25%); and 1 Anti-Jkb (6.25%)). A statistically significant correlation between patient age (P = 0.031), age of splenectomy (P = 0.006), Rh(D) (P = 0.001), leukoreduction of RBCs (P = 0.043), and type of disease (P = 0.006) with RBC alloimmunization was seen. Conclusions: This study emphasized the need for the determination of RBC minor antigens, especially for Rh, Kell, and Kidd blood group systems, before the first transfusion and transfusion of antigen-matched blood. In addition, transfusion of prestorage leukoreduced packed cells is recommended for these patients. Keywords: Alloimmunization, Autoimmunization, Blood Transfusion, Thalassemia
背景:反复输血是地中海贫血患者的常用治疗方法。抗红细胞抗原抗体的产生使红细胞交叉配型复杂化,增强了输血细胞的体内破坏,加速了组织铁超载,延迟了安全输血的提供,并降低了与健康相关的生活质量。材料与方法:本横断面研究于2015年6月至2016年5月在伊朗拉扎维呼罗珊省马什哈德医科大学与Abu Rayhan特殊医疗中心和霍尔莫兹干输血组织合作,共纳入516例地中海贫血患者,平均年龄18.5岁。分别用3个筛选细胞和11个面板细胞对同种异体抗体进行检测和鉴定。检测自身抗体时,采用多特异性Coombs (IgG + C3d)标准法进行自动对照。结果:异体抗体16例(3.1%),自身抗体21例(4.1%)。在有同种异体抗体的患者中,2例(12.5%)出现3种抗体(Anti-c、E、P1;Anti-c、E、K), 1例(6.25%)出现2种抗体(Anti-D、C), 13例出现1种抗体(Anti-D 4例(25%);3 Anti-K (18.75%);2 Anti-E (12.5%);2抗c (12.5%);1 Anti-Jka (6.25%);1个Anti-Jkb(6.25%))。患者年龄(P = 0.031)、脾切除术年龄(P = 0.006)、Rh(D) (P = 0.001)、白细胞减少(P = 0.043)和疾病类型(P = 0.006)与红细胞同种异体免疫有统计学意义的相关性。结论:本研究强调在首次输血和输血抗原匹配血之前,需要检测红细胞次要抗原,特别是Rh、Kell和Kidd血型系统。此外,对于这些患者,建议输注储存前白细胞生成的填充细胞。关键词:同种异体免疫,自身免疫,输血,地中海贫血
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引用次数: 0
Primary kaposiform hemangioendothelioma of ulna 尺骨原发性卡泊样血管内皮瘤
IF 0.3 Q4 PEDIATRICS Pub Date : 2019-01-09 DOI: 10.18502/IJPHO.V9I1.297
Sami Sam Hajialiloo, A. Izanloo, M. Mirkazemi
Kaposiform hemangioendothelioma (KHE) is a rare vascular neoplasm that can be potentially low malignant and mainly affects infants and adolescents. This tumor usually is seen in the skin, soft tissue, and retroperitoneum. This study is a case of KHE in the long bone of the ulna. The subject was a 7-year-old female patient with osteolytic lesion in the forearm without cutaneous lesions. Histologically, the neoplasms comprised of nodules of spindle-to oval-shaped cells that grew in an infiltrative fashion. The results of 2-year follow-up of the patient after enblec resection were desirable and no recurrence was observed. This is the first study to report a case of KHE of the bone in Iran. Keywords: Bone, Hemangioma, Hemangioendothelioma, Kaposiform
卡波西样血管内皮瘤(KHE)是一种罕见的血管性肿瘤,具有潜在的低度恶性,主要发生在婴儿和青少年。这种肿瘤通常见于皮肤、软组织和腹膜后。本研究是一例尺骨长骨KHE。研究对象是一名7岁的女性患者,前臂无皮肤病变,有溶骨性病变。组织学上,肿瘤由梭形至卵形细胞结节组成,浸润性生长。肿物切除后2年随访结果良好,未见复发。这是伊朗首次报道骨KHE病例的研究。关键词:骨;血管瘤;血管内皮瘤
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引用次数: 0
Pubertal status and its relation with serum ferritin level in thalassemia major patients 地中海贫血重症患者青春期状态及其与血清铁蛋白水平的关系
IF 0.3 Q4 PEDIATRICS Pub Date : 2019-01-09 DOI: 10.18502/IJPHO.V9I1.294
M. A. Aghamaleki, A. Tamaddoni, H. M. Nesheli, M. Hajiahmadi, Motahareh Amouzadeh Samakoush, Faeze Aghajanpour
Background: Thalassemia major (TM) is one of the most common hereditary anemia with multiple endocrinopathies (especially hypogonadism). So, we evaluated the rate of delayed puberty (DP) and its relation with serum ferritin level in patients. Materials and Methods: This cross-sectional (descriptive-analytical) study was conducted on 100 patients with TM between 14-64 years old, admitted to Amirkola Thalassemia Center, Babol, Iran, in 2016. The pubertal status, (Marshall-Tanner scale), existance of DP, and its different types were evaluated. Mean serum ferritin level was measured and the data were classified to three groups of <1500, 1500-2500, and >2500 ng/ml. Data were analyzed using SPSS (version20). Results: Out of 100 patients, 64 (64%) and 36 (36%) were female and male, respectively. Considering age, 23, 77 patients (%) were under and over 20 years old, respectively. Totally, 69 (69%) of them had DP, of whom 64 (92.8%) ones had secondary (central) hypogonadotropic hypogonadism. Mean serum ferritin level (±SD) was 2707.94±1683.42 ng/ml. In addition, 26, 29, and 45 patients had ferritin level <1500, 1500-2500, and >2500 ng/ml, respectively. Thirty two patients with DP (46.4%) had ferritin level above 2500 ng/ml (p-value= 0.623). Conclusion: The results showed a high frequency of DP in TM patients, requiring careful examination and follow-up in terms of puberty for early diagnosis and proper treatment to improve their quality of life, and prevention of the complications like osteoporosis. We couldn't find any significant relationship between serum ferritin level and hypogonadism, even for cases who received enough iron chelators. Keywords: Delayed Puberty, Ferritin, Hypergonadotropic Hypogonadism, Hypogonadotropic Hypogonadism, Thalassemia Major    
背景:地中海贫血(Thalassemia major, TM)是一种最常见的遗传性贫血,伴有多种内分泌疾病(尤其是性腺功能减退)。因此,我们评估了青春期延迟发生率及其与血清铁蛋白水平的关系。材料与方法:本横断面(描述性分析)研究对2016年在伊朗巴博勒Amirkola地中海贫血中心收治的100例14-64岁的TM患者进行了研究。评估青少年的青春期状态、Marshall-Tanner量表、DP的存在程度及其不同类型。测定血清平均铁蛋白水平,按2500 ng/ml分为3组。数据分析采用SPSS (version20)软件。结果:100例患者中,女性64例(64%),男性36例(36%)。年龄方面,20岁以下和20岁以上分别有23、77例(%)。DP 69例(69%),其中继发性(中枢性)促性腺功能减退64例(92.8%)。平均血清铁蛋白水平(±SD)为2707.94±1683.42 ng/ml。此外,26例、29例和45例患者铁蛋白水平分别为2500 ng/ml。32例(46.4%)DP患者铁蛋白水平高于2500 ng/ml (p值= 0.623)。结论:TM患者DP发生率高,需要在青春期进行仔细检查和随访,早期诊断,及时治疗,提高生活质量,预防骨质疏松等并发症的发生。我们没有发现血清铁蛋白水平与性腺功能减退有任何显著的关系,即使在服用足够的铁螯合剂的病例中也是如此。关键词:青春期延迟,铁蛋白,促性腺功能亢进症,促性腺功能亢进症,地中海贫血
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引用次数: 2
Antibiotic induced hemolytic anemia and thrombocytopenia among pediatric patients admitted to intensive care unit 抗生素引起的溶血性贫血和血小板减少症儿科患者入住重症监护病房
IF 0.3 Q4 PEDIATRICS Pub Date : 2019-01-09 DOI: 10.18502/IJPHO.V9I1.291
Hassan Taherahmadi, Alireza Moradabadi, Ali Arjomand Shabestari, J. Nazari, M. Kahbazi
Background: Drug induced hemolytic anemia and thrombocytopenia (DIHA and DIT) are common drug adverse effects of antibiotics in patients admitted to hospital.  This reaction is important in patients who have a chronic disease especially in pediatrics. In this study, possible hemolytic anemia was investigated before and after the antibiotics administration. Materials and Methods: A total of 835 children were investigated in this retrospective study. The laboratory tests were performed before and at least one week after antibiotics administration. The red blood cell (RBC), platelet (plt), hematocrit (Hct), and hemoglobin (Hb) were measured. Results: With respect to age, 76.11% of studied patients were under 6 years old. The others were between 6-10 years (mean 5.38 years). The two tailed T tests results on the patients’ information showed  a difference between RBC, platelet, hematocrit, and hemoglobin values before and after antibiotics administration to the point where the RBC mean counts before and after administration were 4.53 to 3.82 *1012/L, respectively. These changes for plt, Hb, and Hct were 323.5 to 232.5 *109/L, 13.61 to 11.46 mg/dL, and 40.83 to 34.38 %, respectively. The p-values were 0.000025, 0.000051, 0.000061, and 0.000032 for RBC, platelet, hematocrit, and hemoglobin; respectively. This finding confirmed that antibiotics administration can decrease the platelets and RBC count. The antibiotics used in the children were ceftriaxone (38.2%), clindamycin (23.3%), Clarithromycin (19.6%), and acyclovir (12.1%); respectively. The dose of the ceftriaxone varied from 50 mg/kg to 70 mg/kg in shigelloses and pneumonia, respectively. Additionally, clindamycin, clarithromycin, and acyclovir were prescribed for 10 mg/kg, 5-10, and 10 mg/kg per day; respectively. Conclusion: This study showed that antibiotics administration had adverse effects and should be considered when they are prescribed to children with chronic diseases. The physicians should be awarded about proper dosing to decrease adverse effects. Keywords: Anti-Bacterial Agents, Drug-Related Side Effects, Adverse Reactions, Hemolytic Anemia, Pediatric, Thrombocytopenia  
背景:药物性溶血性贫血和血小板减少症(DIHA和DIT)是住院患者常见的抗生素药物不良反应。这种反应对患有慢性疾病的患者很重要,尤其是儿科患者。在这项研究中,可能的溶血性贫血的调查前后抗生素给药。材料与方法:对835名儿童进行回顾性研究。在使用抗生素之前和至少一周后进行实验室检查。测定红细胞(RBC)、血小板(plt)、红细胞压积(Hct)和血红蛋白(Hb)。结果:从年龄上看,76.11%的患者年龄在6岁以下。其余6 ~ 10岁,平均5.38岁。患者信息的双尾T检验结果显示,抗生素给药前后RBC、血小板、红细胞压积、血红蛋白值存在差异,给药前后RBC均值分别为4.53 ~ 3.82 *1012/L。plt、Hb和Hct的变化幅度分别为323.5 ~ 232.5 *109/L、13.61 ~ 11.46 mg/dL和40.83 ~ 34.38%。RBC、血小板、红细胞压积和血红蛋白的p值分别为0.000025、0.000051、0.000061和0.000032;分别。这一发现证实抗生素可以降低血小板和红细胞计数。儿童使用的抗生素为头孢曲松(38.2%)、克林霉素(23.3%)、克拉霉素(19.6%)、阿昔洛韦(12.1%);分别。头孢曲松对志贺菌和肺炎的剂量分别为50mg /kg至70mg /kg。此外,克林霉素、克拉霉素和阿昔洛韦的处方剂量为每天10mg /kg、5-10和10mg /kg;分别。结论:本研究表明抗生素给药有不良反应,在给患有慢性疾病的儿童开处方时应予以考虑。医生应该被告知适当的剂量以减少不良反应。关键词:抗菌药物,药物相关副作用,不良反应,溶血性贫血,儿童,血小板减少症
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引用次数: 7
Obesity, Dyslipidemia and Insulin Resistance in Survivors of Childhood Cancer 儿童癌症幸存者的肥胖、血脂异常和胰岛素抵抗
IF 0.3 Q4 PEDIATRICS Pub Date : 2019-01-01 DOI: 10.18502/ijpho.v9i1.290
Soundarya Mahalingam MD, K. G. Md, Anita Dhulipalli Mbbs, Saravanan Ramaswamy MD
Abstract Background: With the increased survival rates following the treatment of childhood cancer, it becomes equally important that the need for evidence based surveillance of long term effects of cancer therapy is addressed. This includes the risk of development of metabolic syndrome features like obesity, altered lipid and sugar profile, which was attempted in the present study. Materials and Methods: In this cross sectional case study, 50 survivors of childhood cancer aged between 5 – 18 years were recruited. Positive history of obesity, diabetes mellitus, dyslipidemia, and stroke in family were recorded and their anthropometry was noted with calculation of their Body Mass Index (BMI). Fasting lipid profile, blood sugar, and serum insulin levels were tested; the Homeostatic model assessment of Insulin Resistance (HOMA IR) value and the Fasting Glucose to Insulin Ratio(FGIR) were derived as markers of insulin sensitivity.  The data were analyzed using SPSS (version 17.0). Results: In these fifty children, the risk factors studied for dyslipidemia and insulin resistance due to chemotherapy were: age at diagnosis, sex, radiation exposure, steroid, and L-asparaginase use during the treatment for cancer. Among the fifty survivors, 7 were found obese, 32 normal, and 11 underweight as per the age specific BMI charts. Their metabolic parameters showed that 12 had raised cholesterol levels, 8 had raised triglyceride levels, and 4 had lowered HDL-C levels. Nine survivors also had raised HOMA-IR levels. However, these metabolic derangements were not found to be statistically significant (p value>0.05) and no correlation was found between the risk factors and obesity, dyslipidemia, or insulin resistance. Conclusion: As against the prior evidence, there was no risk of developing obesity, dyslipidemia, and insulin resistance in survivors of childhood cancers.  Keywords: Dyslipidemias, Insulin Resistance, Obesity, Survivors of childhood cancer
背景:随着儿童癌症治疗后生存率的提高,对癌症治疗长期效果的循证监测变得同样重要。这包括发展代谢综合征特征的风险,如肥胖、脂质和糖谱的改变,这是本研究的尝试。材料和方法:在这个横断面病例研究中,招募了50名年龄在5 - 18岁之间的儿童癌症幸存者。记录家族中肥胖、糖尿病、血脂异常、脑卒中的阳性病史,并对其进行人体测量,计算其身体质量指数(BMI)。检测空腹血脂、血糖和血清胰岛素水平;胰岛素抵抗的稳态模型评估(HOMA IR)值和空腹葡萄糖胰岛素比(FGIR)作为胰岛素敏感性的标志物。数据采用SPSS(17.0版)分析。结果:在这50名儿童中,研究了化疗引起的血脂异常和胰岛素抵抗的危险因素:诊断时年龄、性别、辐射暴露、类固醇和l -天冬酰胺酶在癌症治疗期间的使用。在50名幸存者中,根据年龄特定的BMI图表,发现7人肥胖,32人正常,11人体重不足。他们的代谢参数显示,12人的胆固醇水平升高,8人的甘油三酯水平升高,4人的HDL-C水平降低。9名幸存者的HOMA-IR水平也有所升高。然而,这些代谢紊乱没有统计学意义(p值为0.05),危险因素与肥胖、血脂异常或胰岛素抵抗之间没有相关性。结论:与先前的证据相反,儿童癌症幸存者没有发生肥胖、血脂异常和胰岛素抵抗的风险。关键词:血脂异常,胰岛素抵抗,肥胖,儿童癌症幸存者
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引用次数: 2
Evaluation Efficacy of Ferrous Sulfate Therapy on Headaches of 5-15 Years Old Iron Deficient Children with Migraine. 硫酸亚铁治疗5 ~ 15岁缺铁儿童偏头痛的疗效评价。
IF 0.3 Q4 PEDIATRICS Pub Date : 2016-01-01 Epub Date: 2016-03-15
R Fallah, S Zare Bidoki, M Ordooei

Background: Some researches have shown the association between iron deficiency and migraine headache in adults. The aim of present study was to evaluate efficacy of ferrous sulfate treatment on migraine headaches of 5-15 years old migraineur children with iron deficiency.

Materials and methods: In a quasi- experimental study, monthly frequency, severity, duration and disability of headaches of 5-15 years old migraineur children that prophylactic therapy was indicated in them and had iron deficiency who were referred to Pediatric Neurology Clinic of Shahid Sadoughi University of Medical Sciences, Yazd, Iran between 2013 and 2015 and were treated with 2mg/kg/day topiramate plus 4mg/kg/day of ferrous sulfate for three consecutive months, were evaluated and headache characteristics before and after treatment were compared.

Results: In this study, 98 children with mean age of 9.72±3.19 were evaluated that 31children (31.6%) had iron deficiency. Monthly frequency (22.89±7.18 vs.14.5±4.56, P= 0.02), severity score (8.12± 1.76 vs. 5.03±1.15, P= 0.02) and disability score of headache (38.23±10.7vs. 30.12±7.46, P= 0.03) were more in children with iron deficiency. Iron therapy was effective in decreasing of monthlyfrequency 22.89± 7.18 vs. 10.13±4.51, P = 0.001), severity score (8.12±1.76 vs. 5.11±1.62, P =0.001), duration (2.14±1.23 vs.1.14±1.01, P= 0.001) and disability score of headache (38.23±10.7 vs. 22.87±8.65, P= 0.01).

Conclusion: In children, iron deficiency increased monthly frequency, severity and disability of migraine headache and ferrous sulfate can be used as a safe and effective drug in migraine prophylaxis.

背景:一些研究表明成人缺铁与偏头痛之间存在关联。本研究的目的是评价硫酸亚铁治疗5-15岁偏头痛缺铁儿童偏头痛的疗效。材料和方法:在一项准实验研究中,2013年至2015年,在伊朗亚兹德Shahid Sadoughi医科大学儿童神经病学门诊就诊的5-15岁偏头痛患儿,经预防治疗后,每月头痛的频率、严重程度、持续时间和残疾情况,连续3个月给予2mg/kg/天托吡酯加4mg/kg/天硫酸亚铁治疗。对治疗前后的头痛特征进行评价和比较。结果:98例儿童,平均年龄(9.72±3.19)岁,缺铁31例(31.6%)。月频次(22.89±7.18 vs.14.5±4.56,P= 0.02)、严重程度评分(8.12±1.76 vs. 5.03±1.15,P= 0.02)、头痛失能评分(38.23±10.7vs.)。(30.12±7.46,P= 0.03)。铁治疗在降低头痛月频次(22.89±7.18比10.13±4.51,P= 0.001)、严重程度评分(8.12±1.76比5.11±1.62,P= 0.001)、持续时间(2.14±1.23比1.14±1.01,P= 0.001)和失能评分(38.23±10.7比22.87±8.65,P= 0.01)方面均有效。结论:儿童缺铁可增加偏头痛的发生率、严重程度和致残性,硫酸亚铁可作为一种安全有效的预防偏头痛药物。
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引用次数: 0
Clinical Features and Treatment Outcomes of Primary Immune Thrombocytopenic Purpura in Hospitalized Children Under 2-Years Old. 2岁以下住院儿童原发性免疫性血小板减少性紫癜的临床特点及治疗效果
IF 0.3 Q4 PEDIATRICS Pub Date : 2016-01-01 Epub Date: 2016-03-15
H Farhangi, A Ghasemi, A Banihashem, Z Badiei, L Jarahi, G Eslami, T Langaee

Background: Immune thrombocytopenic purpura (ITP) is the most prevalent cause of thrombocytopenia in children. Despite the importance of ITP in children under 2-years old, only a few publications are available in the literature.ITP usually presents itself as isolated thrombocytopenia and mucocutaneous bleeding.

Materials and methods: This study was conducted on 187 under 2-year-old children diagnosed with ITP and treated at Dr. Sheikh Hospital from 2004 to 2011.In this retrospective study, clinical symptoms, laboratory findings, history of viral infections, vaccination history, and treatment efficacy in children under 2-years old with ITP were investigated.Patients were followed for one year after being discharged from the hospital.

Results: The risk of the disease developing into chronic form was higher in older children (0.001). ITP in children under 3-months old was significantly associated with vaccination (p=0.007). There was no significant differences between male and female patients in regards to newly diagnosed ITP, persistent, and chronic disease status (p = 0.21). No significant difference in bleeding symptoms was observed between patients under 3-months old and 3 to 24-months old (p=0.18).

Conclusion: Infantile ITP respond favorably to treatment. The risk of the disease developing into chronic form is higher in 3-to-24-month-old children compared to under-three-month olds.

背景:免疫性血小板减少性紫癜(ITP)是儿童血小板减少最常见的原因。尽管ITP对2岁以下儿童很重要,但文献中只有少数出版物。ITP通常表现为孤立性血小板减少和皮肤粘膜出血。材料与方法:本研究选取2004 - 2011年在Dr. Sheikh医院诊断为ITP并治疗的187名2岁以下儿童为研究对象。在这项回顾性研究中,研究了2岁以下ITP儿童的临床症状、实验室结果、病毒感染史、疫苗接种史和治疗效果。患者出院后随访一年。结果:年龄较大的儿童疾病发展为慢性形式的风险更高(0.001)。3个月以下儿童ITP与疫苗接种显著相关(p=0.007)。在新诊断ITP、持续性和慢性疾病状态方面,男性和女性患者无显著差异(p = 0.21)。3月龄以下患者与3 ~ 24月龄患者出血症状无显著差异(p=0.18)。结论:婴幼儿ITP治疗效果良好。与三个月以下的婴儿相比,3至24个月大的儿童患慢性疾病的风险更高。
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引用次数: 0
Severe Anemia and Helicobacter Pylori Infection in school age Children; A case reports. 学龄期儿童重度贫血与幽门螺杆菌感染一个案例报告。
IF 0.3 Q4 PEDIATRICS Pub Date : 2016-01-01 Epub Date: 2016-03-15
Sh Gheibi, M Noroozi, S Hejazi, M Karamyyar, H Farrokh-Eslamlou

Background: Iron-deficiency anemia is a widespread public health problem with major consequences for human health especially, children. However, in a fraction of patients an underlying cause is never found during routine investigation. Recent studies have suggested an association between Helicobacter pylori (H. Pylori) infection and iron-deficiency anemia.

Case presentation: Here is reported four school aged children (two male, two female) with refractory severe iron-deficiency anemia associated H. Pylori gastritis. Mean age of the patients was 13.62 years old and they were admitted with chief complaints of abdominal, chest pain weakness, headache and respiratory distress. Mean hemoglobin level in patients was 6.2 g/dl with persistence to iron therapy. After the diagnosis and therapy of H. pylori infection, clinical complaints, hemoglobin level and iron profiles were being normal and they gained weight.

Conclusion: This study suggests screening of H. pylori infection and appropriate treatment in any case of refractory moderate to severe iron-deficiency anemia, especially with clinical manifestations of gastrointestinal tract in children.

背景:缺铁性贫血是一个广泛存在的公共卫生问题,对人类健康特别是儿童健康产生重大影响。然而,在一小部分患者中,在常规调查中从未发现根本原因。最近的研究表明幽门螺杆菌感染与缺铁性贫血有关。病例介绍:这里报告了4名学龄儿童(2男2女)患有难治性严重缺铁性贫血伴幽门螺杆菌胃炎。患者平均年龄13.62岁,主诉为腹痛、胸痛、乏力、头痛、呼吸窘迫。坚持铁治疗的患者平均血红蛋白水平为6.2 g/dl。诊断和治疗幽门螺杆菌感染后,临床主诉、血红蛋白水平和铁谱均正常,体重增加。结论:本研究建议对任何难治性中重度缺铁性贫血,特别是有胃肠道临床表现的儿童,均应筛查幽门螺杆菌感染并给予适当治疗。
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引用次数: 0
Hematological Indices in Children with Non-organic Failure to Thrive: a Case-Control Study. 非器质性发育不良儿童的血液学指标:一项病例对照研究。
IF 0.3 Q4 PEDIATRICS Pub Date : 2016-01-01 Epub Date: 2016-03-15
A H Jafari Nodoshan, A Hashemi, A Golzar, F Karami, R Akhondzaraini

Background: Non-organic failure to thrive (NFTT) is the most common cause of failure to thrive (FTT) which is attributed to inadequate nutrition due to economic factors or parental neglect . NFTT can lead to a vicious cycle of poor and inadequate eating and severity of anemia. The aim of this study was to determine the hematological indices in children with NFTT.

Materials and methods: In a cross sectional case control study, iron status and blood indices of forty five aged 6-60 months children with NFTT were evaluated and compared with 45 healthy control children (with matching of age and sex).

Results: In this study, the prevalence of anemia was 48.9% in NFTT compared to 11.4% in the control group (p<0.001). Microcytic anemia was significantly more prevalent among the subjects than the controls (77.8% versus 27.3%; p<0. 001). The serum iron level was 73.2 and 62.8 mcg/dl for the case and control groups (P=0.29). The ferritin level in the study group was 29.8 versus 35.47 ng/ml in the control group (p=0.227). The prevalence of iron deficiency anemia among children with mild, moderate, and severe underweight was 44.4%, 45.5%, and 48%, respectively. The highest prevalence of iron-deficiency anemia was seen between age group of 12 and 24 months (p<0.05).

Conclusion: Based on the results of this study, a correlation between malnutrition and anemia was found. However, further studies are needed to assess and confirm the current outcomes.

背景:非有机发育不良(NFTT)是发育不良(FTT)最常见的原因,由于经济因素或父母忽视导致营养不足。NFTT会导致不良和不充分饮食和严重贫血的恶性循环。本研究的目的是确定NFTT患儿的血液学指标。材料与方法:采用横断面病例对照研究,评价45例6-60月龄NFTT患儿的铁状态和血液指标,并与45例年龄、性别匹配的健康对照患儿进行比较。结果:本研究中,NFTT组的贫血患病率为48.9%,而对照组为11.4% (p结论:根据本研究结果,发现营养不良与贫血之间存在相关性。然而,需要进一步的研究来评估和确认目前的结果。
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引用次数: 0
Implantable Port Devices, Complications and outcome in Pediatric Cancer, a Retrospective Study. 一项回顾性研究:儿童癌症的可植入端口装置、并发症和预后。
IF 0.3 Q4 PEDIATRICS Pub Date : 2016-01-01 Epub Date: 2016-03-15
H Esfahani, M Ghorbanpor, A Tanasan

Background: Peripheral blood vessels, due to availability are used for many years in cancer patients, however in patients with potentially harmful drugs to skin (vesicant drugs) or difficult accessibility to vessels, the use of implantable port (totally implantable venous access port-TIVAP) devices with central vascular access are important.

Materials and methods: In this retrospective study, 85 pediatric cancer patients younger than 16 years, with TIVAP implantation, were followed for their complications and outcome. In addition to demographic data, patients' port complications were assessed and compared with published articles.

Results: Mean days of implanted port usage were 531 ± 358 days in all patients. This period was 287 ±194 days in complicated patients. Complications included as infection (tunnel infection and catheter related blood-stream infection), malfunction and thrombosis, skin erosion, tube avulsion, and tube adhesion to the adjacent vessels were seen in 30.6% of patients.

Conclusion: According to the published data and this experience, the most common complications in TIVAP are infection and catheter malfunction. It is important to notice that in order to prolong its efficacious life, effective sterilization methods, prevention of clot formation and trauma, are the most useful measures.

背景:外周血管,由于其可获得性,在癌症患者中使用多年,然而,对于皮肤有潜在有害药物(泡状药物)或血管难以接近的患者,使用具有中心血管通路的植入式静脉通道(完全植入式静脉通道- tivap)装置是重要的。材料与方法:回顾性研究85例年龄小于16岁的儿童肿瘤患者,采用TIVAP植入术,观察其并发症及预后。除了人口统计数据外,还评估了患者的港口并发症,并与已发表的文章进行了比较。结果:所有患者的平均移植口使用天数为531±358天。并发症患者为287±194 d。并发症包括感染(隧道感染和导管相关血流感染)、功能障碍和血栓形成、皮肤糜烂、管撕脱、管与邻近血管粘连(30.6%)。结论:根据已发表的资料和本经验,TIVAP最常见的并发症是感染和导管故障。重要的是要注意,为了延长其有效寿命,有效的灭菌方法,防止血栓形成和创伤,是最有用的措施。
{"title":"Implantable Port Devices, Complications and outcome in Pediatric Cancer, a Retrospective Study.","authors":"H Esfahani,&nbsp;M Ghorbanpor,&nbsp;A Tanasan","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Peripheral blood vessels, due to availability are used for many years in cancer patients, however in patients with potentially harmful drugs to skin (vesicant drugs) or difficult accessibility to vessels, the use of implantable port (totally implantable venous access port-TIVAP) devices with central vascular access are important.</p><p><strong>Materials and methods: </strong>In this retrospective study, 85 pediatric cancer patients younger than 16 years, with TIVAP implantation, were followed for their complications and outcome. In addition to demographic data, patients' port complications were assessed and compared with published articles.</p><p><strong>Results: </strong>Mean days of implanted port usage were 531 ± 358 days in all patients. This period was 287 ±194 days in complicated patients. Complications included as infection (tunnel infection and catheter related blood-stream infection), malfunction and thrombosis, skin erosion, tube avulsion, and tube adhesion to the adjacent vessels were seen in 30.6% of patients.</p><p><strong>Conclusion: </strong>According to the published data and this experience, the most common complications in TIVAP are infection and catheter malfunction. It is important to notice that in order to prolong its efficacious life, effective sterilization methods, prevention of clot formation and trauma, are the most useful measures.</p>","PeriodicalId":44212,"journal":{"name":"Iranian Journal of Pediatric Hematology and Oncology","volume":"6 1","pages":"1-8"},"PeriodicalIF":0.3,"publicationDate":"2016-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4867165/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34515532","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Iranian Journal of Pediatric Hematology and Oncology
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