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Aortic thrombosis in a neonate with COVID-19-related fetal inflammatory response syndrome requiring amputation of the leg: a case report. 患有covid -19相关胎儿炎症反应综合征的新生儿主动脉血栓形成,需要截肢:病例报告
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2021-08-01 Epub Date: 2021-09-07 DOI: 10.1080/20469047.2021.1968596
Priyanka S Amonkar, Jeetendra B Gavhane, Suhas N Kharche, Sameer S Kadam, Dattatray B Bhusare

Neonatal infection with SARS-CoV-2 is considered to have no major complications. A neonate with lower limb gangrene owing to spontaneous aortic thrombosis in the setting of a fetal inflammatory response syndrome (FIRS) post-intrauterine COVID-19 infection is presented. A healthy full-term newborn discharged from hospital on Day 3 developed irritability and progressive blackish discoloration of the toes of the right lower limb on Day 6 of life. Doppler imaging revealed acute thrombosis of the abdominal aorta with a critically ischaemic right lower limb. On Day 11 of life, SARS-CoV-2 RT-PCR was negative but total antibodies (IgG and IgM) were positive in both mother and neonate. The neonate showed raised inflammatory markers including CRP, ESR, interleukin-6, procalcitonin, ferritin and LDH along with elevated N-terminal pro-brain natriuretic peptide and D-dimer. In the absence of clinical signs of sepsis, FIRS was diagnosed. The neonate was treated with corticosteroids, heparin infusion and recombinant tissue plasminogen activator, and required surgical embolectomy followed by right limb amputation. By Day 31 of life, inflammatory markers showed serial return to normal and the neonate was discharged on oral steroids and aspirin. Intrauterine SARS-CoV-2 infection may trigger a systemic inflammatory response in some fetuses which is similar to post-COVID-19 multisystem inflammatory syndrome in children (MIS-C). Development of lower limb gangrene is a unique COVID-19-related neonatal complication and is attributed to thrombo-inflammation.ABBREVIATIONSCRP: C-reactive protein; FIRS: fetal inflammatory response syndrome; MIS-C: multisystem inflammatory syndrome in children; NT-proBNP: N-terminal pro-brain natriuretic peptide; RT-PCR: real-time polymerase chain reaction.

新生儿感染SARS-CoV-2被认为没有重大并发症。一例新生儿在宫内感染COVID-19后出现胎儿炎症反应综合征(FIRS),并发自发性主动脉血栓形成下肢坏疽。一个健康的足月新生儿在第3天出院,在出生第6天出现烦躁不安和右下肢脚趾逐渐变黑。多普勒显像显示急性腹主动脉血栓形成并伴有右下肢严重缺血。出生第11天,母亲和新生儿的SARS-CoV-2 RT-PCR均为阴性,但总抗体(IgG和IgM)均为阳性。新生儿炎症标志物CRP、ESR、白细胞介素-6、降钙素原、铁蛋白和LDH升高,n端脑钠肽前体和d -二聚体升高。在没有败血症临床症状的情况下,诊断为FIRS。新生儿给予皮质类固醇、肝素输注和重组组织型纤溶酶原激活剂治疗,并需要手术切除栓塞,随后截肢。到第31天,炎症指标显示连续恢复正常,新生儿出院时口服类固醇和阿司匹林。宫内SARS-CoV-2感染可能在一些胎儿中引发全身性炎症反应,这与儿童后covid -19多系统炎症综合征(MIS-C)相似。下肢坏疽的发展是一种独特的与covid -19相关的新生儿并发症,可归因于血栓炎症。scrp: c反应蛋白;FIRS:胎儿炎症反应综合征;misc:儿童多系统炎症综合征;NT-proBNP: n端前脑利钠肽;RT-PCR:实时聚合酶链反应。
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引用次数: 17
Efficacy of single phototherapy with low-cost reflective sheets versus single phototherapy alone in mild-to-moderate unconjugated hyperbilirubinaemia in full-term neonates. 低成本反射片单次光疗与单次光疗治疗足月新生儿轻至中度非共轭高胆红素血症的疗效比较
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2021-08-01 Epub Date: 2021-09-02 DOI: 10.1080/20469047.2021.1958603
Amira M Sabry, Mortada H F El-Shabrawi, Abdelrahman A Abdelrazek, Mahmoud F Ali

Background: An economical alternative method of increasing the light intensity of phototherapy for neonatal jaundice is the use of reflective sheets placed on the sides of the incubator.

Aim: To determine whether reflective sheets in addition to phototherapy increase the reduction of bilirubin levels and the duration of hospital stay.

Methods: The study was undertaken in the neonatal intensive care unit of Cairo University Children's Hospital. There were two groups: a study group of 90 full-term neonates with neonatal jaundice who received single phototherapy in incubators covered with white plastic reflective sheets and a control group of 90 full-term neonates with neonatal jaundice who received single phototherapy without the reflective sheets.

Results: The mean (SD) rate of bilirubin decline in the first 24 hours of phototherapy was greater in the study group [3.7 (0.86) µmol/L/hr] than in the control group [2.2 (0.14) µmol/L/hr] (p<0.001).

Conclusion: Use of reflective sheets decreases the total duration of phototherapy and the cost and duration of hospitalisation without any added complications.Abbreviations: AAP: American Academy of Pediatrics; HIDS: high-intensity double-surface; LMIC: low- and middle-income countries; MCTP: mirror-covered tunnel phototherapy; NICU: neonatal intensive care unit; TSB: total serum bilirubin.

背景:增加新生儿黄疸光疗光强的一种经济的替代方法是在培养箱的两侧放置反射片。目的:探讨除光疗外,反射片是否能增加胆红素水平的降低和住院时间。方法:本研究在开罗大学儿童医院新生儿重症监护病房进行。有两组:研究组有90名患有新生儿黄疸的足月新生儿,他们在覆盖白色塑料反光片的孵育箱中接受单次光疗;对照组有90名患有新生儿黄疸的足月新生儿,他们接受单次光疗,不使用反光片。结果:研究组在光疗前24小时胆红素下降的平均(SD)率[3.7(0.86)µmol/L/hr]高于对照组[2.2(0.14)µmol/L/hr]。结论:使用反射片可减少光疗总时间,减少住院费用和住院时间,无任何并发症。缩写:AAP:美国儿科学会;HIDS:高强度双面;中低收入国家:低收入和中等收入国家;MCTP:镜面隧道光疗;NICU:新生儿重症监护病房;TSB:总血清胆红素。
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引用次数: 1
Incidence and predictive risk factors for ophthalmological complications in children with nephrotic syndrome receiving long-term oral corticosteroids: a cohort study. 长期口服皮质类固醇治疗的肾病综合征患儿眼科并发症的发生率和预测危险因素:一项队列研究
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2021-08-01 Epub Date: 2021-10-29 DOI: 10.1080/20469047.2021.1983315
Raja Hariharan, Sriram Krishnamurthy, Subashini Kaliaperumal, Pediredla Karunakar, Bobbity Deepthi

Background: There is a paucity of data from India on ophthalmological complications in children on long-term oral corticosteroids for idiopathic nephrotic syndrome.

Methods: All children aged 4-18 years with idiopathic nephrotic syndrome who had received long-term oral steroids for >6 months  and who attended the paediatric nephrology clinic between January 2019 and January 2021 were included. The majority of them (95/110) were being followed up in the paediatric nephrology clinic which was functioning from 2010.   The children were screened for ophthalmological complications at 6-month intervals.

Results: Overall, 110 children with nephrotic syndrome  were enrolled. Their median (IQR) age was 9.4 (7.0-12.8) years, and the median (range) duration of follow-up following onset of nephrotic syndrome was 5 years (1.0-16). The incidence of cataract was 18.1% (20 of 110 cases).  Visual acuity was impaired in seven (35%) of the children with cataract.  Children with cataract were younger as compared to those without cataract [Median (IQR) age at onset of nephrotic syndrome [2.5 (2.0-4.0) yrs vs 4 (2.1-6.0) yrs] (p=0.03)]. Children with cataract also had higher cumulative dose of prednisolone intake (mg/m2) [28,669 (21,329-33,500) vs 14,995 (10,492-19,687)] (p<0.01)] and greater cumulative duration of prednisolone intake [4.3 (3.1-5.2) vs 2.25 (1.3-3.7) yrs] (p<0.01). The incidence of raised IOP was 9.1% (10 of 110 cases).

Conclusions: The incidence of cataract and raised IOP was high. The risk factors for the development of cataract were age at onset of nephrotic syndrome, cumulative dose and cumulative duration of steroid intake.

背景:印度缺乏关于长期口服皮质类固醇治疗特发性肾病综合征的儿童眼科并发症的数据。方法:纳入所有患有特发性肾病综合征的4-18岁儿童,这些儿童长期口服类固醇治疗>6个月,并于2019年1月至2021年1月期间在儿科肾病诊所就诊。他们中的大多数(95/110)在2010年开始运作的儿科肾病诊所接受了随访。每隔6个月对患儿进行眼科并发症筛查。结果:总共纳入了110名肾病综合征患儿。他们的中位(IQR)年龄为9.4(7.0-12.8)岁,肾病综合征发病后随访的中位(范围)时间为5年(1.0-16)。白内障发生率为18.1%(20 / 110)。7例(35%)白内障患儿视力受损。有白内障的儿童比无白内障的儿童更年轻[肾病综合征发病的中位年龄(IQR)[2.5(2.0-4.0)岁对4(2.1-6.0)岁](p=0.03)]。白内障患儿的泼尼松龙累积剂量(mg/m2)也较高[28,669 (21,329-33,500)vs 14,995 (10,492-19,687)] (vs 2.25(1.3-3.7)年](结论:白内障和IOP升高的发生率较高。白内障发生的危险因素是肾病综合征发病年龄、累积剂量和累积类固醇摄入时间。
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引用次数: 3
Prevalence, risk factors and outcome of Mycoplasma pneumoniae infection among children in Uganda: a prospective study. 乌干达儿童肺炎支原体感染的流行、危险因素和结果:一项前瞻性研究。
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2021-08-01 Epub Date: 2021-11-08 DOI: 10.1080/20469047.2021.1980698
Rebecca Nantanda, Freddie Bwanga, Irene Najjingo, Grace Ndeezi, James K Tumwine

Background: : Atypical bacteria cause 10-40% of all childhood pneumonia.. Data on the burden of atypical pneumonia in sub-Saharan Africa are limited.

Aim: : To determine the prevalence, associated factors, and outcome of Mycoplasma pneumoniae infection in children with respiratory symptoms at Mulago National Referral Hospital, Kampala.

Methods: : Children aged 2 months to 12 years with cough and/or difficult breathing and fast breathing were recruited. A clinical history and physical examination were undertaken. Blood samples for Mycoplasma pneumoniae IgM antibodies were taken at enrolment and Day 21 and induced sputum for DNA-PCR. Admitted participants were followed for a maximum of 7 days or until discharge or death, whichever came first.

Results: : A total of 385 children were enrolled, and, of these, 368 (95.6%) were <5 years. Overall, 60/385 (15.6%) participants tested positive for M. pneumoniae IgM and/or DNA-PCR. Of these, 56/60 (93.3%) were <5 years of age. Wheezing was present in 21/60 (35.0%) of the children with atypical pneumonia and in 128/325 (39.4%) with typical pneumonia. The factors associated with M. pneumonia were female sex (AOR 1.94, 95% CI 1.22-3.08, p < 0.001), age ≥12 months (AOR 2.73, 95% CI 1.53-4.87, p = 0.01) and a history of prematurity (AOR 2.07, 95% CI 1.23-3.49, p = 0.01). Mortality was 17/352 (4.8%) and, of these, 4/17 (23.5%) had M. pneumonia.

Conclusion: : M. pneumonia is common in young children , especially females above 2 years and those with history of prematurity. It presents with severe symptoms. The results of the study highlight the importance of considering atypical bacteria in under-5s with the symptoms of pneumonia.

背景:非典型细菌引起的所有儿童肺炎的10-40%。关于撒哈拉以南非洲非典型肺炎负担的数据有限。目的:确定坎帕拉穆拉戈国家转诊医院有呼吸道症状的儿童肺炎支原体感染的流行情况、相关因素和结局。方法:招募年龄为2个月~ 12岁、咳嗽和/或呼吸困难、呼吸急促的患儿。进行了临床病史和体格检查。在入组和第21天采集肺炎支原体IgM抗体血样和诱导痰进行DNA-PCR检测。入院的参与者最多随访7天或直到出院或死亡,以先到者为准。结果:共纳入385名儿童,其中368名(95.6%)为肺炎支原体IgM和/或DNA-PCR。其中56/60(93.3%)为肺炎支原体、女性(AOR 1.94, 95% CI 1.22 ~ 3.08, p p = 0.01)和早产史(AOR 2.07, 95% CI 1.23 ~ 3.49, p = 0.01)。死亡率为17/352(4.8%),其中4/17(23.5%)为肺炎支原体。结论:肺炎支原体常见于幼儿,尤其是2岁以上的女性和有早产史的儿童。它的症状很严重。研究结果强调了在5岁以下有肺炎症状的儿童中考虑非典型细菌的重要性。
{"title":"Prevalence, risk factors and outcome of Mycoplasma pneumoniae infection among children in Uganda: a prospective study.","authors":"Rebecca Nantanda,&nbsp;Freddie Bwanga,&nbsp;Irene Najjingo,&nbsp;Grace Ndeezi,&nbsp;James K Tumwine","doi":"10.1080/20469047.2021.1980698","DOIUrl":"https://doi.org/10.1080/20469047.2021.1980698","url":null,"abstract":"<p><strong>Background: </strong>: Atypical bacteria cause 10-40% of all childhood pneumonia.. Data on the burden of atypical pneumonia in sub-Saharan Africa are limited.</p><p><strong>Aim: </strong>: To determine the prevalence, associated factors, and outcome of <i>Mycoplasma pneumoniae</i> infection in children with respiratory symptoms at Mulago National Referral Hospital, Kampala.</p><p><strong>Methods: </strong>: Children aged 2 months to 12 years with cough and/or difficult breathing and fast breathing were recruited. A clinical history and physical examination were undertaken. Blood samples for <i>Mycoplasma pneumoniae</i> IgM antibodies were taken at enrolment and Day 21 and induced sputum for DNA-PCR. Admitted participants were followed for a maximum of 7 days or until discharge or death, whichever came first.</p><p><strong>Results: </strong>: A total of 385 children were enrolled, and, of these, 368 (95.6%) were <5 years. Overall, 60/385 (15.6%) participants tested positive for <i>M. pneumoniae</i> IgM and/or DNA-PCR. Of these, 56/60 (93.3%) were <5 years of age. Wheezing was present in 21/60 (35.0%) of the children with atypical pneumonia and in 128/325 (39.4%) with typical pneumonia. The factors associated with <i>M. pneumonia</i> were female sex (AOR 1.94, 95% CI 1.22-3.08, <i>p</i> < 0.001), age ≥12 months (AOR 2.73, 95% CI 1.53-4.87, <i>p</i> = 0.01) and a history of prematurity (AOR 2.07, 95% CI 1.23-3.49, <i>p</i> = 0.01). Mortality was 17/352 (4.8%) and, of these, 4/17 (23.5%) had <i>M. pneumonia</i>.</p><p><strong>Conclusion: </strong>: <i>M. pneumonia</i> is common in young children , especially females above 2 years and those with history of prematurity. It presents with severe symptoms. The results of the study highlight the importance of considering atypical bacteria in under-5s with the symptoms of pneumonia.</p>","PeriodicalId":19731,"journal":{"name":"Paediatrics and International Child Health","volume":null,"pages":null},"PeriodicalIF":1.8,"publicationDate":"2021-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791631/pdf/nihms-1741896.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39596458","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Neurodevelopmental outcome in neonates with hypoxic-ischaemic encephalopathy managed with therapeutic hypothermia in a tertiary-level public hospital outside an intensive care unit setting. 低氧缺血性脑病患儿在三级公立医院重症监护病房外接受低温治疗的神经发育结局
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2021-08-01 Epub Date: 2021-09-08 DOI: 10.1080/20469047.2021.1967625
S Mbatha, F L Nakwa, K Thandrayen, S Velaphi

Background: Management of hypoxic-ischaemic encephalopathy (HIE) by therapeutic hypothermia (TH) is a major challenge in low- and middle-income countries (LMIC) because of the limited resources. Clinicians in LMIC offer this intervention outside neonatal intensive care units (NICU). The effect of this practice on neurodevelopmental outcome is not well known.

Aim: To determine neurodevelopmental outcome in neonates with HIE managed with TH outside NICU settings.

Methods: : This was a retrospective descriptive study of neonates with HIE managed with TH and followed up for neurodevelopmental assessment at 12 and 18-24 months postnatal age. Patients were reviewed over a 24-month period. Outcome at 12 and 18-24 months was compared.

Results: Of 178 neonates with HIE attending the clinic, there was information on TH for 155 (87.1%), 113 of whom (72.9%) received TH. HIE was moderate in 88% and severe in 10%. Twenty-seven (23.9%) and 16 (14.1%) were assessed at one time-point at 12 or 18-24 months, respectively, 40 (35.3%) at both time-points, and 30 (26.6%) were not assessed. At 18-24 months, 32% had moderate-to-severe disability compared with 6% at 12 months, with the sensitivity and specificity of assessment at 12 months being 50% and 100%, respectively. The disability attrition rate at 18-24 months was 50%.

Conclusions: The relatively low prevalence of disability (32%) at 18-24 months suggests that use of TH in a Level 2 nursery is feasible and possibly beneficial. More studies are needed to confirm these findings.

Abbreviations: aEEG: amplitude electroencephalogram; CP: cerebral palsy; GMDS: Griffiths mental developmental scales; GQ: general quotient; HIC: high-income countries; HIE: hypoxic-ischaemic encephalopathy; LMIC: low- and middle-income countries; LTFU: loss to follow-up; NICU: neonatal intensive care unit; TH: therapeutic hypothermia; TOBY: total body hypothermia.

背景:低氧缺血性脑病(HIE)的治疗性低温(TH)管理是低收入和中等收入国家(LMIC)的主要挑战,因为资源有限。LMIC的临床医生在新生儿重症监护病房(NICU)外提供这种干预。这种做法对神经发育结果的影响尚不清楚。目的:确定新生儿缺氧缺血性脑病在NICU外接受TH治疗的神经发育结局。方法:本研究是一项回顾性描述性研究,对新生儿HIE进行TH治疗,并在出生后12个月和18-24个月随访神经发育评估。对患者进行为期24个月的评估。比较12个月和18-24个月的结果。结果178例新生儿HIE患者中,155例(87.1%)接受过TH治疗,其中113例(72.9%)接受过TH治疗。中度HIE占88%,重度HIE占10%。27例(23.9%)和16例(14.1%)分别在12个月或18-24个月的一个时间点进行评估,40例(35.3%)在两个时间点进行评估,30例(26.6%)未进行评估。在18-24个月时,32%的患者有中度至重度残疾,而12个月时为6%,12个月时评估的敏感性和特异性分别为50%和100%。18-24月龄残疾损失率为50%。结论:18-24月龄儿童的致残率相对较低(32%),这表明在二级托儿所使用TH是可行的,可能是有益的。需要更多的研究来证实这些发现。缩写:aEEG:振幅脑电图;CP:脑瘫;格里菲斯心理发展量表;GQ:通商;高收入国家:高收入国家;HIE:缺氧缺血性脑病;中低收入国家:低收入和中等收入国家;LTFU:随访损失;NICU:新生儿重症监护病房;TH:治疗性低温;托比:全身体温降低。
{"title":"Neurodevelopmental outcome in neonates with hypoxic-ischaemic encephalopathy managed with therapeutic hypothermia in a tertiary-level public hospital outside an intensive care unit setting.","authors":"S Mbatha,&nbsp;F L Nakwa,&nbsp;K Thandrayen,&nbsp;S Velaphi","doi":"10.1080/20469047.2021.1967625","DOIUrl":"https://doi.org/10.1080/20469047.2021.1967625","url":null,"abstract":"<p><strong>Background: </strong>Management of hypoxic-ischaemic encephalopathy (HIE) by therapeutic hypothermia (TH) is a major challenge in low- and middle-income countries (LMIC) because of the limited resources. Clinicians in LMIC offer this intervention outside neonatal intensive care units (NICU). The effect of this practice on neurodevelopmental outcome is not well known.</p><p><strong>Aim: </strong>To determine neurodevelopmental outcome in neonates with HIE managed with TH outside NICU settings.</p><p><strong>Methods: </strong>: This was a retrospective descriptive study of neonates with HIE managed with TH and followed up for neurodevelopmental assessment at 12 and 18-24 months postnatal age. Patients were reviewed over a 24-month period. Outcome at 12 and 18-24 months was compared.</p><p><strong>Results: </strong>Of 178 neonates with HIE attending the clinic, there was information on TH for 155 (87.1%), 113 of whom (72.9%) received TH. HIE was moderate in 88% and severe in 10%. Twenty-seven (23.9%) and 16 (14.1%) were assessed at one time-point at 12 or 18-24 months, respectively, 40 (35.3%) at both time-points, and 30 (26.6%) were not assessed. At 18-24 months, 32% had moderate-to-severe disability compared with 6% at 12 months, with the sensitivity and specificity of assessment at 12 months being 50% and 100%, respectively. The disability attrition rate at 18-24 months was 50%.</p><p><strong>Conclusions: </strong>The relatively low prevalence of disability (32%) at 18-24 months suggests that use of TH in a Level 2 nursery is feasible and possibly beneficial. More studies are needed to confirm these findings.</p><p><strong>Abbreviations: </strong>aEEG: amplitude electroencephalogram; CP: cerebral palsy; GMDS: Griffiths mental developmental scales; GQ: general quotient; HIC: high-income countries; HIE: hypoxic-ischaemic encephalopathy; LMIC: low- and middle-income countries; LTFU: loss to follow-up; NICU: neonatal intensive care unit; TH: therapeutic hypothermia; TOBY: total body hypothermia.</p>","PeriodicalId":19731,"journal":{"name":"Paediatrics and International Child Health","volume":null,"pages":null},"PeriodicalIF":1.8,"publicationDate":"2021-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39410975","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Peritoneal dialysis in children with sepsis-associated AKI (SA-AKI): an experience in a low- to middle-income country. 腹膜透析治疗败血症相关性AKI (SA-AKI)儿童:中低收入国家的经验
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2021-05-01 Epub Date: 2021-01-17 DOI: 10.1080/20469047.2021.1874201
Apurva Tomar, Virendra Kumar, Abhijeet Saha

Background: In critically ill children, sepsis-associated acute kidney injury (SA-AKI) has significant morbidity and mortality.Aim: To estimate whether early initiation of peritoneal dialysis (PD) has a better short-term outcome than standard PD.Methods: Early PD (n = 25) was defined as a need for PD in Kidney Disease: Improving Global Outcomes (KDIGO) stage 2 AKI, while those fulfilling the criteria for stage 3 KDIGO were categorised as a standard PD group (n = 25). The primary outcome measure was the estimated glomerular filtration rate (eGFR) at discharge or at 4 weeks after initiation of PD, whichever occurred earlier.Results: A prospective cohort of 50 children (32 boys) aged 2 months to 16 years with SA-AKI who underwent PD were recruited. The most frequent indication for PD was fluid overload (40%), followed by persistent metabolic acidosis (36%). Children in the early PD group had lower creatinine and higher eGFR at discharge/4-week follow-up (p < 0.001). The duration of PD was less if it was commenced early (p < 0.04); 24 of 25 (96%) children in the early PD group were off PD within 6 days of initiation compared with 13 of 25 (52%) in the standard PD group (p < 0.001).Conclusions: Compared with standard PD, early PD in SA-AKI resulted in a favourable renal outcome, decreased duration of PD and early discontinuation of dialysis.Abbreviations : AKI: acute kidney injury; CRRT: continuous renal replacement therapy; CS-AKI: cardiac surgery-associated acute kidney injury; eGFR: estimated glomerular filtration rate; ELAIN: early versus late initiation of renal replacement therapy in critically ill patients with acute kidney injury; ESCAPE: effect of strict blood pressure control and ACE inhibition on the progression of chronic kidney disease in paediatric patients; HIC: high-income countries; ISN: international society of nephrology; KDIGO: Kidney Disease: Improving Global Outcomes; LMIC: low- to middle-income countries; PD: peritoneal dialysis; PICU: paediatric intensive care unit; RRT: renal replacement therapy; SA-AKI: sepsis-associated acute kidney injury; SYL: Saving Young Lives; SOFA: sequential (sepsis-related) organ failure assessment score; STARRT-AKI: standard versus accelerated initiation of renal replacement therapy in acute kidney injury.

背景:在危重儿童中,败血症相关急性肾损伤(SA-AKI)具有显著的发病率和死亡率。目的:评估早期开始腹膜透析(PD)是否比标准PD有更好的短期预后。方法:早期PD (n = 25)被定义为需要PD治疗肾脏疾病:改善总体结局(KDIGO) 2期AKI,而满足KDIGO 3期标准的患者被归类为标准PD组(n = 25)。主要结局指标是出院时或PD开始后4周估计的肾小球滤过率(eGFR),以较早者为准。结果:招募了50名2个月至16岁的SA-AKI儿童(32名男孩),他们接受了PD治疗。PD最常见的适应症是体液超载(40%),其次是持续性代谢性酸中毒(36%)。早期PD组患儿出院时肌酐较低,eGFR较高(p p p) /4周随访(p p p p)结论:与标准PD相比,SA-AKI早期PD患者的肾脏预后良好,PD持续时间缩短,且早期停止透析。AKI:急性肾损伤;CRRT:持续肾替代治疗;CS-AKI:心脏手术相关急性肾损伤;eGFR:估计肾小球滤过率;ELAIN:急性肾损伤危重患者早期与晚期肾替代治疗的比较ESCAPE:严格控制血压和抑制ACE对儿科慢性肾病进展的影响高收入国家:高收入国家;ISN:国际肾脏病学会;KDIGO:肾病:改善全球预后;中低收入国家:中低收入国家;PD:腹膜透析;PICU:儿科重症监护病房;RRT:肾脏替代疗法;SA-AKI:脓毒症相关急性肾损伤;SYL:拯救年轻生命;SOFA:序贯(败血症相关)器官衰竭评估评分;start - aki:急性肾损伤的标准与加速启动肾脏替代治疗。
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引用次数: 10
Comparison of adverse birth outcomes among HIV-infected and HIV-uninfected women delivering in high and low risk settings in the era of universal ART in Malawi: a registry study. 马拉维普遍抗逆转录病毒治疗时代在高风险环境和低风险环境中分娩的艾滋病毒感染妇女和未感染妇女不良分娩结局的比较:一项登记研究
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2021-05-01 Epub Date: 2021-04-21 DOI: 10.1080/20469047.2021.1874200
Rachel Chamanga, Chaplain Katumbi, Luis Gadama, Rachel Kawalazira, Dingase Dula, Bonus Makanani, Sufia Dadabhai, Taha E Taha

Background: Recent studies show that ART is associated with an adverse birth outcome in HIV-infected women.Aim: To compare rates of low birthweight (LBW) and preterm birth (PTB) between HIV-infected women receiving lifelong ART and HIV-uninfected women giving birth in low- and high-risk settings in Malawi.Methods: This observational, registry study was conducted from January 2016 to August 2017 in one large, tertiary referral hospital and four primary healthcare (PHC) facilities in Blantyre, Malawi. Women who delivered singleton live births or stillbirths of ≥20 weeks gestation were included in the analysis. Descriptive and stratified analyses were conducted using χ2 tests and multivariable logistic models to control for maternal age, gravidity and health facility.Results: A total of 14,233 births were included in the analysis (7715 from the tertiary hospital and 6518 from PHC facilities). In the univariable analysis, there were no differences in rates of LBW (6.7% vs 6.4%) and PTB (42.5% vs 42.0%) between HIV-infected and -uninfected women delivering in PHC facilities. However, differences in LBW were significantly higher in HIV-infected women in multivariable analysis (LBW aOR 1.40, 95% CI 1.01-1.95). Rates of LBW and PTB were significantly higher in HIV-infected women than in uninfected women delivering at the tertiary hospital (LBW 17.6% vs 13.2%, aOR 1.53, 95% CI 1.27-1.85; PTB 28.2% vs 24.9%, aOR 1.37, 95% CI 1.17-1.60)Conclusion: Rates of adverse birth outcomes are significantly higher in HIV-infected women than in HIV-uninfected women, and this is more apparent in high-risk hospital settings than in low-risk PHC settings.

背景:最近的研究表明,抗逆转录病毒治疗与艾滋病毒感染妇女的不良分娩结果有关。目的:比较马拉维低高风险环境中接受终身抗逆转录病毒治疗的艾滋病毒感染妇女和未感染艾滋病毒的妇女的低出生体重(LBW)和早产(PTB)率。方法:这项观察性登记研究于2016年1月至2017年8月在马拉维布兰太尔的一家大型三级转诊医院和四家初级卫生保健(PHC)机构进行。分析包括单胎活产或妊娠≥20周死产的妇女。采用χ2检验和多变量logistic模型进行描述性和分层分析,以控制产妇年龄、妊娠和卫生设施。结果:共有14233例分娩被纳入分析(7715例来自三级医院,6518例来自初级保健机构)。在单变量分析中,在初级保健机构分娩的hiv感染妇女和未感染妇女的LBW (6.7% vs 6.4%)和PTB (42.5% vs 42.0%)发生率没有差异。然而,在多变量分析中,艾滋病毒感染妇女的LBW差异明显更高(LBW aOR 1.40, 95% CI 1.01-1.95)。在三级医院分娩的hiv感染妇女中,LBW和PTB的发生率显著高于未感染妇女(LBW 17.6% vs 13.2%,比值比1.53,95% CI 1.27-1.85;结论:艾滋病毒感染妇女的不良分娩结局率明显高于未感染艾滋病毒的妇女,这在高风险医院环境中比在低风险初级保健环境中更为明显。
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引用次数: 0
Caregiver experiences and healthcare worker perspectives of accessing healthcare for low-birthweight. 照顾者经验和卫生保健工作者对低出生体重儿童获得卫生保健的看法。
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2021-05-01 Epub Date: 2021-02-28 DOI: 10.1080/20469047.2021.1881269
Sarah Unsworth, Hellen C Barsosio, Florence Achieng, Daniel Juma, Linda Tindi, Fred Omiti, Simon Kariuki, Helen M Nabwera

Background: Low-birthweight (LBW) infants (<2500 g) are at greatest risk of mortality in the neonatal period, particularly in low- and middle-income countries. Timely access to quality healthcare averts adverse outcomes.

Aim: To explore caregiver experiences and healthcare provider perspectives of accessing healthcare for LBW infants in rural Kenya.

Methods: This qualitative study was undertaken in Homa Bay County of in rural western Kenya in June 2019. In-depth interviews with eleven caregivers and four healthcare providers were conducted by a trained research assistant. All interviews were transcribed verbatim, and transcripts in the local languages were translated into English. A thematic framework was used to analyse the data.

Results: At the community and individual level,community misconceptions about LBW infants, inadequate infant care practices after discharge, lack of maternal support networks, long distances from healthcare facilities and lack of financial support were key challenges. In addition, long hospital waiting times, healthcare worker strikes and the apparent inadequate knowledge and skills of healthcare providers were disincentives among caregivers. Among healthcare providers, health system deficiencies (staff shortages and inadequate resources for optimal assessment and treatment of LBW infants) and maternal illiteracy were key challenges. Education by staff during antenatal visits and community support groups were enablers.

Conclusion: Accessing healthcare for LBW infants in this community is fraught with challenges which have implications for their post-discharge outcome. There is an urgent need to develop and test strategies to address the barriers at the community and health system level to optimise outcome..

背景:低出生体重(LBW)婴儿(目的:探讨护理经验和医疗保健提供者的观点在肯尼亚农村的LBW婴儿获得医疗保健。方法:本定性研究于2019年6月在肯尼亚西部农村的Homa Bay县进行。由一名训练有素的研究助理对11名护理人员和4名医疗保健提供者进行了深入访谈。所有采访都逐字记录下来,并将当地语文的笔录翻译成英文。使用了一个专题框架来分析数据。结果:在社区和个人层面,社区对低出生体重婴儿的误解、出院后婴儿护理实践不足、缺乏孕产妇支持网络、距离医疗机构很远以及缺乏财政支持是主要挑战。此外,医院候诊时间过长、医护人员罢工以及医护人员的知识和技能明显不足,也阻碍了护理人员的积极性。在医疗保健提供者中,卫生系统缺陷(人员短缺和资源不足,无法对低体重婴儿进行最佳评估和治疗)和孕产妇文盲是主要挑战。工作人员在产前检查和社区支持小组期间进行的教育是促成因素。结论:该社区的低体重婴儿获得医疗保健充满了挑战,这对他们的出院后预后有影响。迫切需要制定和测试战略,以解决社区和卫生系统层面的障碍,以优化结果。
{"title":"Caregiver experiences and healthcare worker perspectives of accessing healthcare for low-birthweight.","authors":"Sarah Unsworth,&nbsp;Hellen C Barsosio,&nbsp;Florence Achieng,&nbsp;Daniel Juma,&nbsp;Linda Tindi,&nbsp;Fred Omiti,&nbsp;Simon Kariuki,&nbsp;Helen M Nabwera","doi":"10.1080/20469047.2021.1881269","DOIUrl":"https://doi.org/10.1080/20469047.2021.1881269","url":null,"abstract":"<p><strong>Background: </strong>Low-birthweight (LBW) infants (<2500 g) are at greatest risk of mortality in the neonatal period, particularly in low- and middle-income countries. Timely access to quality healthcare averts adverse outcomes.</p><p><strong>Aim: </strong>To explore caregiver experiences and healthcare provider perspectives of accessing healthcare for LBW infants in rural Kenya.</p><p><strong>Methods: </strong>This qualitative study was undertaken in Homa Bay County of in rural western Kenya in June 2019. In-depth interviews with eleven caregivers and four healthcare providers were conducted by a trained research assistant. All interviews were transcribed verbatim, and transcripts in the local languages were translated into English. A thematic framework was used to analyse the data.</p><p><strong>Results: </strong>At the community and individual level,community misconceptions about LBW infants, inadequate infant care practices after discharge, lack of maternal support networks, long distances from healthcare facilities and lack of financial support were key challenges. In addition, long hospital waiting times, healthcare worker strikes and the apparent inadequate knowledge and skills of healthcare providers were disincentives among caregivers. Among healthcare providers, health system deficiencies (staff shortages and inadequate resources for optimal assessment and treatment of LBW infants) and maternal illiteracy were key challenges. Education by staff during antenatal visits and community support groups were enablers.</p><p><strong>Conclusion: </strong>Accessing healthcare for LBW infants in this community is fraught with challenges which have implications for their post-discharge outcome. There is an urgent need to develop and test strategies to address the barriers at the community and health system level to optimise outcome..</p>","PeriodicalId":19731,"journal":{"name":"Paediatrics and International Child Health","volume":null,"pages":null},"PeriodicalIF":1.8,"publicationDate":"2021-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/20469047.2021.1881269","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"25417118","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 4
Paediatric scurvy: frequently misdiagnosed. 小儿坏血病:常误诊。
IF 1.8 4区 医学 Q2 Medicine Pub Date : 2021-05-01 Epub Date: 2020-09-16 DOI: 10.1080/20469047.2020.1816285
Husna Musa, Imma Isniza Ismail, Nurul Hazwani Abdul Rashid

Paediatric scurvy is uncommon in the modern age but cases have been reported in children with neurodevelopmental issues and restricted dietary habits. The broad clinical picture is frequently overlooked as primarily other systemic diseases are considered first leading to extensive investigations and delay in diagnosis. A 4-year-old boy with autism and bilateral lower limb pain and refusal to walk is reported. His restricted diet and radiographic findings were highly suggestive of scurvy which was confirmed by the extremely low levels of ascorbic acid. Treatment with ascorbic acid replenishment and maintenance resulted in remarkable improvement. This case highlights the importance of a high index of suspicion in at-risk children so as to avoid unnecessary invasive investigations and procedures.

儿科坏血病在现代并不常见,但在有神经发育问题和饮食习惯受限的儿童中也有报道。广泛的临床情况经常被忽视,因为主要是其他全身性疾病首先被认为导致广泛的调查和延误诊断。一个4岁的男孩自闭症和双侧下肢疼痛和拒绝行走的报告。他的限制饮食和x线检查结果高度提示坏血病,这由极低的抗坏血酸水平证实。补充和维持抗坏血酸治疗效果显著。这一案例强调了高风险儿童高度怀疑指数的重要性,以避免不必要的侵入性调查和程序。
{"title":"Paediatric scurvy: frequently misdiagnosed.","authors":"Husna Musa,&nbsp;Imma Isniza Ismail,&nbsp;Nurul Hazwani Abdul Rashid","doi":"10.1080/20469047.2020.1816285","DOIUrl":"https://doi.org/10.1080/20469047.2020.1816285","url":null,"abstract":"<p><p>Paediatric scurvy is uncommon in the modern age but cases have been reported in children with neurodevelopmental issues and restricted dietary habits. The broad clinical picture is frequently overlooked as primarily other systemic diseases are considered first leading to extensive investigations and delay in diagnosis. A 4-year-old boy with autism and bilateral lower limb pain and refusal to walk is reported. His restricted diet and radiographic findings were highly suggestive of scurvy which was confirmed by the extremely low levels of ascorbic acid. Treatment with ascorbic acid replenishment and maintenance resulted in remarkable improvement. This case highlights the importance of a high index of suspicion in at-risk children so as to avoid unnecessary invasive investigations and procedures.</p>","PeriodicalId":19731,"journal":{"name":"Paediatrics and International Child Health","volume":null,"pages":null},"PeriodicalIF":1.8,"publicationDate":"2021-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1080/20469047.2020.1816285","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38483413","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 2
Blood transfusion and mortality in children with severe anaemia in a malaria-endemic region. 疟疾流行地区严重贫血儿童的输血和死亡率。
IF 1.4 4区 医学 Q3 PEDIATRICS Pub Date : 2021-05-01 Epub Date: 2021-04-19 DOI: 10.1080/20469047.2021.1881270
Elizabeth M Keating, Msandeni Chiume, Elizabeth Fitzgerald, Yamikani Mgusha, Tisungane Mvalo, Nora Fino, Heather L Crouse, Michelle Eckerle, Kathleen Gorman, Emily J Ciccone, Gladstone Airewele, Jeff A Robison

Background: In children in sub-Saharan Africa, severe anaemia (SA) is an important cause of mortality, and malaria is a primary cause. The World Health Organization (WHO) recommends blood transfusion for all children with haemoglobin (Hb) <4 g/dL and for those with Hb 4-6 g/dL with signs of instability. In sub-Saharan Africa, evidence of the effect on mortality of transfusion in children with SA with and without malaria is mixed.

Aim: To determine in children with and without malaria whether receipt of transfusion was associated with lower mortality at WHO transfusion thresholds.

Methods: This was a retrospective cohort study of 1761 children with SA (Hb ≤6 g/dL) admitted to Kamuzu Central Hospital in Malawi. In those whose Hb was 4-6 g/dL, mortality was compared by transfusion, stratified by haemoglobin, malaria status and signs of instability.

Results: Children with profound anaemia (Hb <4 g/dL) and malaria were the only subgroup who had a significant decrease in the odds of in-hospital death if they received a transfusion (OR 0.43, p = 0.01). Although children with Hb 4-6 g/dL and at least one sign of instability had higher mortality than children with none, there was no difference in the odds of mortality between those who received a transfusion and those who did not (OR 1.16, p = 0.62).

Conclusions: This study suggests that transfusion of children with profound anaemia and malaria may confer increased in-hospital survival. An understanding of the factors associated with mortality from SA will allow for interventions to prioritise the provision of limited blood.

背景:在撒哈拉以南非洲地区的儿童中,严重贫血(SA)是导致死亡的一个重要原因,而疟疾则是主要原因。世界卫生组织(WHO)建议为所有有血红蛋白(Hb)的儿童输血。 目的:在患有和未患有疟疾的儿童中,确定接受输血是否与WHO输血阈值下的较低死亡率相关:这是一项回顾性队列研究,研究对象是马拉维卡穆祖中心医院收治的1761名患有SA(血红蛋白≤6 g/dL)的儿童。在血红蛋白为 4-6 g/dL 的儿童中,根据血红蛋白、疟疾状况和不稳定迹象对输血死亡率进行了比较:严重贫血的儿童(血红蛋白 p = 0.01)。虽然血红蛋白为 4-6 g/dL 且至少有一种不稳定迹象的儿童的死亡率高于无不稳定迹象的儿童,但接受输血和未接受输血的儿童的死亡几率没有差异(OR 1.16,p = 0.62):这项研究表明,为患有严重贫血和疟疾的儿童输血可提高他们的院内存活率。了解与严重贫血死亡率相关的因素将有助于采取干预措施,优先提供有限的血液。
{"title":"Blood transfusion and mortality in children with severe anaemia in a malaria-endemic region.","authors":"Elizabeth M Keating, Msandeni Chiume, Elizabeth Fitzgerald, Yamikani Mgusha, Tisungane Mvalo, Nora Fino, Heather L Crouse, Michelle Eckerle, Kathleen Gorman, Emily J Ciccone, Gladstone Airewele, Jeff A Robison","doi":"10.1080/20469047.2021.1881270","DOIUrl":"10.1080/20469047.2021.1881270","url":null,"abstract":"<p><strong>Background: </strong>In children in sub-Saharan Africa, severe anaemia (SA) is an important cause of mortality, and malaria is a primary cause. The World Health Organization (WHO) recommends blood transfusion for all children with haemoglobin (Hb) <4 g/dL and for those with Hb 4-6 g/dL with signs of instability. In sub-Saharan Africa, evidence of the effect on mortality of transfusion in children with SA with and without malaria is mixed.</p><p><strong>Aim: </strong>To determine in children with and without malaria whether receipt of transfusion was associated with lower mortality at WHO transfusion thresholds.</p><p><strong>Methods: </strong>This was a retrospective cohort study of 1761 children with SA (Hb ≤6 g/dL) admitted to Kamuzu Central Hospital in Malawi. In those whose Hb was 4-6 g/dL, mortality was compared by transfusion, stratified by haemoglobin, malaria status and signs of instability.</p><p><strong>Results: </strong>Children with profound anaemia (Hb <4 g/dL) and malaria were the only subgroup who had a significant decrease in the odds of in-hospital death if they received a transfusion (OR 0.43, <i>p</i> = 0.01). Although children with Hb 4-6 g/dL and at least one sign of instability had higher mortality than children with none, there was no difference in the odds of mortality between those who received a transfusion and those who did not (OR 1.16, <i>p</i> = 0.62).</p><p><strong>Conclusions: </strong>This study suggests that transfusion of children with profound anaemia and malaria may confer increased in-hospital survival. An understanding of the factors associated with mortality from SA will allow for interventions to prioritise the provision of limited blood.</p>","PeriodicalId":19731,"journal":{"name":"Paediatrics and International Child Health","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2021-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8523581/pdf/nihms-1667283.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"38895635","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","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
Paediatrics and International Child Health
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