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Lactobacillus acidophilus and Bifidobacterium bifidum stored at ambient temperature are effective in the treatment of acute diarrhoea. 在环境温度下储存的嗜酸乳杆菌和两歧双歧杆菌对治疗急性腹泻有效。
Pub Date : 2010-01-01 DOI: 10.1179/146532810X12858955921159
S Rerksuppaphol, L Rerksuppaphol

Introduction: Probiotics have demonstrated potential to reduce duration of diarrhoea and frequency of watery stools. Probiotics such as Lactobacillus acidophilus and Bifidobacterium bifidum (Infloran(®)) are usually maintained at a storage temperature of 4°C which is generally not feasible in tropical or sub-tropical countries.

Aim: The efficacy of Infloran(®) for treatment of acute diarrhoea when stored at 28-32°C (room temperature) was evaluated.

Methods: This was a double-blind, randomised study of infants and children aged 2 months to 7 years with acute diarrhoea. Patients were randomly assigned to receive Infloran(®) stored at 4°C, at room temperature, or to a placebo group. Duration of diarrhoea was a primary outcome, while the number of stools, hospital stay and requirement for rehydration fluid were secondary outcomes.

Results: Probiotics shortened duration of diarrhoea (34.1 and 34.8 hrs when stored either at 4°C or at room temperature, respectively, and 58 hrs with placebo, p<0.01) and reduced the number of stools (7.3 and 8 vs 15.9 with placebo, p<0.01).

Conclusion: Administration of probiotics is beneficial as additional treatment of acute diarrhoea and efficacy is not affected by storage temperature.

益生菌已被证明具有减少腹泻持续时间和水样便频率的潜力。益生菌如嗜酸乳杆菌和两歧双歧杆菌(Infloran(®))通常保存在4°C的储存温度下,这在热带或亚热带国家通常是不可行的。目的:评价依芙兰(®)在28-32℃(室温)保存下治疗急性腹泻的疗效。方法:这是一项双盲、随机研究,研究对象为2个月至7岁急性腹泻的婴儿和儿童。患者被随机分配接受4°C、室温储存的Infloran(®)或安慰剂组。腹泻持续时间是主要结果,而大便次数、住院时间和补液需求是次要结果。结果:益生菌可缩短腹泻持续时间(在4℃和室温下分别为34.1和34.8小时,安慰剂组为58小时)。结论:益生菌作为急性腹泻的补充治疗是有益的,并且效果不受储存温度的影响。
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引用次数: 28
Neonatal brucellosis: rare and preventable. 新生儿布鲁氏菌病:罕见且可预防。
Pub Date : 2010-01-01 DOI: 10.1179/146532810X12786388978445
Pablo Yagupsky
In industrialised countries, brucellosis prevention is now under strict veterinarian control and is close to being eradicated. In developing countries, however, it continues to be an important zoonosis in many regions such as Latin America, the Mediterranean basin, the Middle East and central Asia. Brucellosis is mostly caused by Brucella melitensis, B. abortus and B. suis. It is maintained in nature among a variety of mammals, feral and domesticated, for which the different Brucella species exhibit a relative host preference. Brucellae are highly infective (infective dose between 10 and 100 organisms), and humans acquire the disease by exposure to infected animals and their products, usually through the gastro-intestinal tract, by aerosol inhalation and through abraded skin. Human-to-human transmission is rare and has been reported after blood transfusion, bone marrow transplantation and by the transplacental route, as in the infants described in the two reports in this issue. In endemic areas, brucellosis is particularly common in children who acquire the disease by ingesting contaminated dairy products, especially unpasteurised milk and soft cheese derived from unvaccinated bovines, sheep and goats. Neonates become infected congenitally by the transplacental route in the course of a maternal bacteraemic episode, by exposure to blood, urine or genital secretions during delivery, and by breastfeeding; these are also the main routes of dissemination of brucellae among mammalian reservoirs. Accidental acquisition of the disease through blood and exchange transfusion in the neonatal period has also been rarely reported. In animals, invasion of the trophoblast by circulating organisms is a frequent event in the course of the disease, and usually causes septic abortions. This tendency has been attributed to the high concentration of erythritol, an essential growth factor for the bacterium, in placental tissues of susceptible ungulates. Deliveries and abortions of infected animals also play an important role in the dissemination of brucellae within herds through contamination of pastures by infected blood, lochia and genital secretions, and the organism can survive in the soil for several weeks. The issue of whether brucellosis can also cause abortion or premature delivery in humans is subject to controversy. Brucella species have been isolated from human fetal or placental tissue but it has been suggested that the disease causes fewer spontaneous abortions in humans than it does in animals because of the absence of erythritol in human tissues. However, a study by Khan et al. demonstrated an excess of 1st and 2nd-trimester spontaneous abortions among pregnant women with active infection and Elshamy & Ahmed showed that Saudi women with positive serological tests for brucellosis have a higher incidence of miscarriage and intrauterine fetal death than control women with negative serology. Obviously, the observed poor outcome of pregnancy might not necess
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引用次数: 5
Ileal perforation in a child with abdominal tuberculosis. 腹部结核患儿回肠穿孔1例。
Pub Date : 2010-01-01 DOI: 10.1179/146532810X12786388978805
I Shah, A Rahangdale

A 6-year-old boy presented with a 1-month history of fever followed by abdominal distension, constipation and bilious vomiting for 2 days. The clinical impression was of intestinal obstruction. At exploratory laparotomy, there was an ileal perforation secondary to tuberculosis. There are many case reports of tubercular ileal perforation in adults but in children it is very rare.

6岁男童,发热1个月后出现腹胀、便秘、胆汁性呕吐2天。临床表现为肠梗阻。在剖腹探查时,发现继发于肺结核的回肠穿孔。有许多病例报告结核性回肠穿孔在成人,但在儿童是非常罕见的。
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引用次数: 4
Locally produced ready-to-use supplementary food is an effective treatment of moderate acute malnutrition in an operational setting. 当地生产的即食补充食品是在业务环境中治疗中度急性营养不良的有效方法。
Pub Date : 2010-01-01 DOI: 10.1179/146532810X12703901870651
L Lagrone, S Cole, A Schondelmeyer, K Maleta, M J Manary

Background: Typical treatment of moderate acute malnutrition, simple wasting, in sub-Saharan Africa consists of dietary counselling and/or general or targeted distribution of corn/soy-blended flour (CSB). A randomised clinical effectiveness trial in 2007 showed CSB to be less effective than ready-to-use supplementary food (RUSF).

Aim: To determine the operational effectiveness of treating moderate acute malnutrition with RUSF.

Methods: Children aged 6-59 months were recruited in rural southern Malawi. Each child received 65 kcal/kg/d of locally produced soy/peanut RUSF, a product that provided about 1 RDA of each micronutrient. Anthropometric measurements were taken every 2 weeks and additional rations of RUSF were distributed at this time if the child remained wasted. Study participation lasted up to 8 weeks.

Results: Of the 2417 children enrolled, 80% recovered, 4% defaulted, 0.4% died, 12% remained moderately wasted and 3% developed severe acute malnutrition. Weight, length and MUAC gain were 2.6 g/kg/d, 0.2 mm/d and 0.1 mm/d respectively. Cost per child treated was $5.39.

Conclusions: This intervention proved to be robust, maintaining high recovery rates and low default rates when instituted without the additional supervision and beneficiary incentives of a research setting.

背景:在撒哈拉以南非洲,对中度急性营养不良(单纯消瘦)的典型治疗包括饮食咨询和/或普遍或有针对性地分发玉米/大豆混合面粉(CSB)。2007年的一项随机临床有效性试验表明,CSB的效果不如即食辅食(RUSF)。目的:探讨RUSF治疗中度急性营养不良的操作效果。方法:在马拉维南部农村招募6-59个月的儿童。每个儿童每天摄入65千卡的当地生产的大豆/花生RUSF,该产品为每种微量营养素提供约1 RDA。每两周进行一次人体测量,如果儿童仍然消瘦,则在此时分发额外的RUSF。研究参与时间长达8周。结果:在入选的2417名儿童中,80%康复,4%违约,0.4%死亡,12%中度消瘦,3%发展为严重急性营养不良。体重2.6 g/kg/d,体长0.2 mm/d, MUAC增重0.1 mm/d。每个儿童的治疗费用为5.39美元。结论:这种干预被证明是强有力的,在没有额外监督和研究设置的受益人激励的情况下,维持了高回收率和低违约率。
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引用次数: 46
Alopecia in vitamin D-dependent rickets type II responding to 1α-hydroxycholecalciferol. 1α-羟基胆钙化醇对维生素d依赖性佝偻病II型患者脱发的影响。
Pub Date : 2010-01-01 DOI: 10.1179/146532810X12858955921357
V Kumar, M Kumar, M Yadav

A 4-year-old boy presented with rickets, alopecia and macrocephaly along with elevated serum levels of 1,25(OH)₂D₃ which was diagnostic of vitamin D-dependent rickets type II. The rickets responded to conventional doses of 1α-hydroxycholecalciferol together with oral calcium supplement and there was also improvement in the alopecia. In patients with vitamin D-dependent rickets type II with alopecia, although rickets improves with treatment, improvement in alopecia has not been reported before.

一名4岁的男孩表现为佝偻病、脱发、大头畸形,并伴有血清125 (OH)₂D₃升高,诊断为维生素D依赖性佝偻病II型。佝偻病对常规剂量的1α-羟基胆钙化醇联合口服补钙有反应,脱发也有改善。对于伴有脱发的维生素d依赖性佝偻病II型患者,虽然佝偻病随着治疗而改善,但以前没有报道过脱发的改善。
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引用次数: 5
Ocular manifestations of sickle cell disease. 镰状细胞病的眼部表现。
Pub Date : 2010-01-01 DOI: 10.1179/146532810X12637745451870
A O Fadugbagbe, R Q Gurgel, C Q Mendonça, R Cipolotti, A M dos Santos, L E Cuevas

Sickle cell disease (SCD) is the most common genetic disease worldwide. The increase in life expectancy of SCD patients in recent years has led to the emergence of more complications of the disease, e.g. ocular, which in the past were uncommon. This review describes current knowledge of the ocular manifestations of patients with SCD. SCD can affect virtually every vascular bed in the eye and can cause blindness in the advanced stages. The most significant ocular changes are those which occur in the fundus, which can be grouped into proliferative sickle retinopathy, and non-proliferative retinal changes based on the presence of vascular proliferation. This distinction is important because the formation of new vessels is the single most important precursor of potentially blinding complications. Although various systemic complications of SCD are known to be more common in patients with the Hb SS genotype, visual impairment secondary to proliferative sickle retinopathy is more common in patients with the Hb SC genotype. There is also an increase with age in the incidence and prevalence rates of all ocular complications of SCD. It is therefore recommended that all patients with SCD undergo periodic ophthalmological screening from the age of 10 years.

镰状细胞病(SCD)是世界上最常见的遗传性疾病。近年来,SCD患者的预期寿命增加,导致出现更多的疾病并发症,例如眼部,这在过去是不常见的。本文综述了目前对SCD患者眼部表现的了解。SCD几乎可以影响眼睛的每一个血管床,并在晚期导致失明。最显著的眼部变化发生在眼底,可分为增殖性镰状视网膜病变和基于血管增生的非增殖性视网膜病变。这种区别很重要,因为新血管的形成是潜在致盲并发症的最重要的前兆。虽然已知SCD的各种全身并发症在Hb SS基因型患者中更为常见,但在Hb SC基因型患者中继发于增殖性镰状视网膜病变的视力损害更为常见。SCD的所有眼部并发症的发生率和患病率也随着年龄的增长而增加。因此,建议所有SCD患者从10岁开始进行定期眼科筛查。
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引用次数: 30
Growth in children and adolescents with sickle cell disease in Yemen. 也门镰状细胞病儿童和青少年的增长。
Pub Date : 2010-01-01 DOI: 10.1179/146532810X12858955921113
A-W M Al-Saqladi, H A Bin-Gadeen, B J Brabin

Background: Physical growth is known to be impaired in children with sickle cell disease (SCD) and the prevalence and severity vary with geographical location. The factors which contribute to this sub-optimal growth are poorly understood.

Objectives: To describe the growth status of children and adolescents with SCD in Yemen using the new WHO reference values and to assess correlation of growth indicators with disease severity and with haematological and biochemical parameters.

Methods: A cross-sectional study of children <16 years with SCD was conducted at Al-Wahda General Teaching Hospital, Aden. Anthropometric measurements of weight, length/height, mid-upper-arm circumference (MUAC) and body mass index (BMI) were collected. Disease severity was assessed using a severity index (SI) score.

Results: A total of 102 children (56 male) were included and their mean age was 7.2 years (range 6 months to 15 years). Low weight, height and BMI-for-age Z-scores (<-2 SD) were observed in 45%, 54% and 35% of children, respectively. Regression analyses indicated an association of low height-for-age with male gender (p=0.02), low weight-for-age and weight-for-height with increased age (both p<0.001), low weight-for-age with raised alkaline phosphatase (p=0.04), and low BMI with reduced plasma albumin (p=0.04). There was no correlation between growth deficits and SI or anaemia severity.

Conclusion: Growth is severely impaired in children and adolescents with SCD in Yemen. Growth monitoring and nutritional support should be included in their comprehensive care package.

背景:已知镰状细胞病(SCD)儿童的身体发育受损,其患病率和严重程度因地理位置而异。人们对导致这种次优增长的因素了解甚少。目的:利用新的WHO参考值描述也门儿童和青少年SCD的生长状况,并评估生长指标与疾病严重程度以及血液学和生化参数的相关性。方法:儿童横断面研究结果:共纳入102例儿童,其中男56例,平均年龄7.2岁(6个月~ 15岁)。结论:也门儿童和青少年SCD患者的生长严重受损。生长监测和营养支持应包括在他们的综合护理包中。
{"title":"Growth in children and adolescents with sickle cell disease in Yemen.","authors":"A-W M Al-Saqladi,&nbsp;H A Bin-Gadeen,&nbsp;B J Brabin","doi":"10.1179/146532810X12858955921113","DOIUrl":"https://doi.org/10.1179/146532810X12858955921113","url":null,"abstract":"<p><strong>Background: </strong>Physical growth is known to be impaired in children with sickle cell disease (SCD) and the prevalence and severity vary with geographical location. The factors which contribute to this sub-optimal growth are poorly understood.</p><p><strong>Objectives: </strong>To describe the growth status of children and adolescents with SCD in Yemen using the new WHO reference values and to assess correlation of growth indicators with disease severity and with haematological and biochemical parameters.</p><p><strong>Methods: </strong>A cross-sectional study of children <16 years with SCD was conducted at Al-Wahda General Teaching Hospital, Aden. Anthropometric measurements of weight, length/height, mid-upper-arm circumference (MUAC) and body mass index (BMI) were collected. Disease severity was assessed using a severity index (SI) score.</p><p><strong>Results: </strong>A total of 102 children (56 male) were included and their mean age was 7.2 years (range 6 months to 15 years). Low weight, height and BMI-for-age Z-scores (<-2 SD) were observed in 45%, 54% and 35% of children, respectively. Regression analyses indicated an association of low height-for-age with male gender (p=0.02), low weight-for-age and weight-for-height with increased age (both p<0.001), low weight-for-age with raised alkaline phosphatase (p=0.04), and low BMI with reduced plasma albumin (p=0.04). There was no correlation between growth deficits and SI or anaemia severity.</p><p><strong>Conclusion: </strong>Growth is severely impaired in children and adolescents with SCD in Yemen. Growth monitoring and nutritional support should be included in their comprehensive care package.</p>","PeriodicalId":50759,"journal":{"name":"Annals of Tropical Paediatrics","volume":"30 4","pages":"287-98"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1179/146532810X12858955921113","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"29502788","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 30
Bacteraemia with pleural effusions complicating typhoid fever caused by high-level ciprofloxacin-resistant Salmonella enterica serotype Typhi. 高水平环丙沙星耐药肠炎沙门氏菌血清型伤寒引起的菌血症伴胸腔积液并发伤寒。
Pub Date : 2010-01-01 DOI: 10.1179/146532810X12786388978760
S Mohanty, R Gaind, B Paglietti, P Paul, S Rubino, M Deb

An unusual case of bacteraemia with bilateral pleural effusion caused by Salmonella enterica serotype Typhi in a 10-year-old previously healthy girl is reported. The organism was isolated from pleural fluid aspirate and from blood, and exhibited high-level ciprofloxacin resistance (MIC 16 μg/ml) associated with triple mutations in the QRDRs of the gyrA and parC genes leading to the amino-acid changes Ser83→Phe and Asp87→Asn in gyrA and Ser80→Ile in parC. The patient was successfully treated with parenteral ceftriaxone and intercostal chest tube drainage. The case is notable because of the important issue of antimicrobial resistance in S. Typhi and the therapeutic dilemma faced by clinicians regarding the empirical use of ciprofloxacin and newer fluoroquinolones.

一例罕见的菌血症与双侧胸腔积液引起的伤寒沙门氏菌在一个10岁以前健康的女孩报告。从吸出的胸膜液和血液中分离出该菌,显示出高水平的环丙沙星耐药性(MIC为16 μg/ml),与gyrA和parC基因QRDRs的三重突变相关,导致gyrA中Ser83→Phe和Asp87→Asn和parC中Ser80→Ile的氨基酸变化。患者经肠外头孢曲松及肋间胸管引流治疗成功。该病例值得注意,因为伤寒沙门氏菌的抗微生物药物耐药性的重要问题,以及临床医生在经验性使用环丙沙星和较新的氟喹诺酮类药物方面面临的治疗困境。
{"title":"Bacteraemia with pleural effusions complicating typhoid fever caused by high-level ciprofloxacin-resistant Salmonella enterica serotype Typhi.","authors":"S Mohanty,&nbsp;R Gaind,&nbsp;B Paglietti,&nbsp;P Paul,&nbsp;S Rubino,&nbsp;M Deb","doi":"10.1179/146532810X12786388978760","DOIUrl":"https://doi.org/10.1179/146532810X12786388978760","url":null,"abstract":"<p><p>An unusual case of bacteraemia with bilateral pleural effusion caused by Salmonella enterica serotype Typhi in a 10-year-old previously healthy girl is reported. The organism was isolated from pleural fluid aspirate and from blood, and exhibited high-level ciprofloxacin resistance (MIC 16 μg/ml) associated with triple mutations in the QRDRs of the gyrA and parC genes leading to the amino-acid changes Ser83→Phe and Asp87→Asn in gyrA and Ser80→Ile in parC. The patient was successfully treated with parenteral ceftriaxone and intercostal chest tube drainage. The case is notable because of the important issue of antimicrobial resistance in S. Typhi and the therapeutic dilemma faced by clinicians regarding the empirical use of ciprofloxacin and newer fluoroquinolones.</p>","PeriodicalId":50759,"journal":{"name":"Annals of Tropical Paediatrics","volume":"30 3","pages":"233-40"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1179/146532810X12786388978760","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40058024","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Coeliac disease presenting as acute pancreatitis in a 3-year-old. 乳糜泻表现为急性胰腺炎在3岁。
Pub Date : 2010-01-01 DOI: 10.1179/146532810X12786388978887
I M Halabi

A 3-year-old boy presented with a history of intermittent abdominal pain and vomiting from the age of 1 year. Raised serum amylase and lipase levels supported a diagnosis of acute pancreatitis. Subsequent investigation confirmed coeliac disease. This is the youngest patient to be reported with this combination.

一名3岁男孩自1岁起出现间歇性腹痛和呕吐史。血清淀粉酶和脂肪酶水平升高支持急性胰腺炎的诊断。随后的调查证实为乳糜泻。这是报道中最年轻的联合用药患者。
{"title":"Coeliac disease presenting as acute pancreatitis in a 3-year-old.","authors":"I M Halabi","doi":"10.1179/146532810X12786388978887","DOIUrl":"https://doi.org/10.1179/146532810X12786388978887","url":null,"abstract":"<p><p>A 3-year-old boy presented with a history of intermittent abdominal pain and vomiting from the age of 1 year. Raised serum amylase and lipase levels supported a diagnosis of acute pancreatitis. Subsequent investigation confirmed coeliac disease. This is the youngest patient to be reported with this combination.</p>","PeriodicalId":50759,"journal":{"name":"Annals of Tropical Paediatrics","volume":"30 3","pages":"255-7"},"PeriodicalIF":0.0,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1179/146532810X12786388978887","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40058028","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Immunity to hepatitis B vaccine in Tanzanian under-5 children. 坦桑尼亚5岁以下儿童对乙型肝炎疫苗的免疫力。
Pub Date : 2010-01-01 DOI: 10.1179/146532810X12703902516167
J Metodi, S Aboud, R Mpembeni, E Munubhi

Background: Hepatitis B vaccine was introduced in Tanzania in 2002 and is administered as DPT-hepatitis B at 4, 8 and 12 weeks of life.

Aim: To determine immunity to hepatitis B virus in children under 5 years attending reproductive and child health (RCH) clinics.

Methods: A cross-sectional, health facility-based study was conducted between July and December 2007 at Temeke, Amana and Mwananyamala municipal hospitals in Dar es Salaam, Tanzania. Children under 5 years who had received DPT-HB vaccine as evidenced by RCH card number 1 were included. Blood samples were collected to determine hepatitis B surface antigen (HB(s)Ag) and antibodies to hepatitis B surface antigen (anti-HB(s)) and hepatitis B core antigen (Anti-HB(c)). An anti-HB(s) level of > or =10 mIU/ml is regarded as protective. Nutritional and HIV status were also determined.

Results: A total of 296 children under 5 years vaccinated with DPT-HB were recruited, 153 (51.7%) of whom were male. Altogether, 205 (69.3%) children had anti-HB(s) levels > or =10 mIU/ml. The number of DPT-HB vaccine doses, time interval since last DPT-HB dose and HIV status were significant predictors of anti-HB(s) levels. Five children (1.7%) were positive for HB(s)Ag, suggesting possible vertical transmission. No child had anti-HB(c) antibodies.

Conclusion: More than two-thirds of children under 5 years had protective anti-HB(s) levels. A change in the hepatitis B immunisation schedule to include a dose immediately after birth should improve immunity.

背景:2002年,坦桑尼亚引进了乙型肝炎疫苗,在出生后4周、8周和12周以白喉-百白破-乙型肝炎疫苗的形式接种。目的:了解在生殖和儿童健康(RCH)诊所就诊的5岁以下儿童对乙型肝炎病毒的免疫力。方法:2007年7月至12月在坦桑尼亚达累斯萨拉姆的Temeke、Amana和Mwananyamala市立医院进行了一项以卫生设施为基础的横断面研究。包括接种过RCH卡号1证明的DPT-HB疫苗的5岁以下儿童。采集血样检测乙型肝炎表面抗原(HB(s)Ag)、乙型肝炎表面抗原抗体(抗HB(s))和乙型肝炎核心抗原抗体(抗HB(c))。抗hb (s)水平>或=10 mIU/ml被认为具有保护作用。还测定了营养状况和艾滋病毒状况。结果:共有296名5岁以下儿童接种了DPT-HB,其中153名(51.7%)为男性。总共有205名(69.3%)儿童的抗hb (s)水平>或=10 mIU/ml。接种DPT-HB疫苗的次数、上一次DPT-HB疫苗的时间间隔和HIV状态是抗hb (s)水平的重要预测因子。5名儿童(1.7%)HB(s)Ag阳性,提示可能存在垂直传播。没有孩子有抗hb (c)抗体。结论:超过三分之二的5岁以下儿童具有保护性的抗hb (s)水平。改变乙肝免疫接种计划,包括在出生后立即接种一剂,应能提高免疫力。
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引用次数: 22
期刊
Annals of Tropical Paediatrics
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