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Patterns of Seasonality and Subtype-Linked Outcomes of Pediatric Guillain-Barré Syndrome ICU Admissions: A 10-Year Audit from Southern India. 小儿格林-巴勒综合征ICU入院的季节性模式和亚型相关结局:印度南部10年审计
IF 1.5 4区 医学 Q2 PEDIATRICS Pub Date : 2026-01-22 DOI: 10.1007/s13312-025-00251-x
Rohini M Surve, Prachi Sharma, Roshan Nisal, Dhritiman Chakrabarti

Objective: To evaluate the seasonal variation in Guillain-Barré Syndrome (GBS) subtype distribution and its association with clinical outcomes in pediatric patients requiring intensive care unit (ICU) admission.

Methods: An audit of pediatric patients with GBS admitted to the neuro-ICU of a tertiary center in Southern India between 2008 and 2018 was conducted. Seasonal distribution was defined as per meteorological classification: summer (March-May), monsoon (June-September), post-monsoon (October-November), and winter (December-February). Clinical subtypes, treatment, and outcomes, including length of mechanical ventilation (LOMV), ICU stay (LOIS), hospital stay (LOHS), and Hughes disability scores, were analyzed across seasons.

Results: Among 75 patients, the highest admissions occurred during the monsoon (n = 29). Acute motor axonal neuropathy (AMAN) was more frequent in monsoon, while acute inflammatory demyelinating polyneuropathy (AIDP) was common in winter and summer. Across the full cohort, no statistically significant seasonal differences were found in the outcomes. However, within the AMAN subtype, LOHS was significantly longer in summer compared to post-monsoon (P = 0.005). Axonal variants showed higher rates of intubation and severe disability (Hughes disability score > 3), while AIDP had milder outcomes.

Conclusion: Seasonal clustering of GBS subtypes was observed, with axonal variants more common during the monsoon. However, seasonal variation did not significantly impact the overall clinical outcomes in pediatric ICU patients.

目的:探讨儿童重症监护病房(ICU)患者吉兰-巴罗综合征(GBS)亚型分布的季节变化及其与临床结局的关系。方法:对2008年至2018年印度南部某三级中心神经icu收治的小儿GBS患者进行审计。季节分布按气象分类确定:夏季(3 - 5月)、季风(6 - 9月)、季风后(10 - 11月)和冬季(12 - 2月)。临床亚型、治疗和结果,包括机械通气时间(LOMV)、ICU住院时间(LOIS)、住院时间(LOHS)和Hughes残疾评分,在不同季节进行分析。结果:75例患者中,雨季住院率最高(29例)。急性运动轴索神经病(AMAN)多发于季风季节,急性炎性脱髓鞘多神经病变(AIDP)多发于冬夏季节。在整个队列中,在结果中没有发现统计学上显著的季节性差异。然而,在AMAN亚型中,夏季LOHS明显长于季风后(P = 0.005)。轴突变异显示出更高的插管率和严重致残率(Hughes致残评分bb0.3),而AIDP的结果较轻。结论:GBS亚型具有季节性聚集性,轴突变异在季风期间更为常见。然而,季节变化对儿科ICU患者的总体临床结果没有显著影响。
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引用次数: 0
Biallelic IL11RA Variants in Twin Brothers with Complex Craniosynostosis: Identification of a Novel Variant and Postulation of Epigenetic Differences. 复杂颅缝紧闭双胞胎兄弟的双等位基因IL11RA变异:一种新变异的鉴定和表观遗传差异的假设。
IF 1.5 4区 医学 Q2 PEDIATRICS Pub Date : 2026-01-21 DOI: 10.1007/s13312-025-00260-w
Meiling Liu, Birong Gao, Bingxue Liu, Lingzhao Min, Xiaoqiang Wang
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引用次数: 0
Reference range for target oxygen saturation in late preterm neonates delivered by cesarean section following delayed cord clamping: a prospective observational study. 延迟脐带夹紧后剖宫产晚期早产儿靶血氧饱和度参考范围:一项前瞻性观察研究。
IF 1.5 4区 医学 Q2 PEDIATRICS Pub Date : 2026-01-21 DOI: 10.1007/s13312-025-00258-4
Thangaraj Abiramalatha, Balakrishnan Rajaiah, Sanjana Ravi, Rajendran Karupanan, Ashwath Duraiswamy, Sujatha Chinnappan, Manonmani Ganesan, Jeevithan Shanmugam, Srinivas Ramakrishnan

Objective: To develop reference range for target oxygen saturation levels during the first 10 min of life in late preterm neonates born by cesarean delivery.

Methods: A prospective observational study conducted at a tertiary hospital in India between April 2022 and September 2024 included 200 late preterm neonates delivered by cesarean section following delayed cord clamping. Preductal peripheral oxygen saturation (SpO2), heart rate, and temperature were recorded every minute at 2-10 min after birth.

Results: The mean (SD) gestational age and birth weight were 35.6 (1.3) weeks and 2260 (496) g, respectively. The median (q1, q3) preductal SpO2 at 2, 5, and 10 min were 77 (70, 84), 88 (82, 92) and 95 (93, 96), respectively. The median (q1, q3) time taken to reach saturations of ≥ 80%, ≥ 85% and ≥ 90% were 4 (3, 5), 5 (3, 6) and 6 (4, 7) minutes, respectively. Only 73.3% late preterm neonates reached the target SpO2 of ≥ 80% at 5 min; 98.8% reached ≥ 85% at 10 min without any intervention.

Conclusion: Nearly one-fourth of healthy late preterm neonates did not reach the thresholds laid by the Neonatal Resuscitation Program (NRP) until 5 min after birth, yet nearly all achieved the ≥ 85% threshold of SpO2 by 10 min without intervention. This suggests a slightly delayed but adequate transition, indicating routine supplemental oxygen may be unnecessary in clinically stable late preterm neonates.

目的:探讨剖宫产晚期早产儿生命前10min血氧饱和度指标的参考范围。方法:一项前瞻性观察研究于2022年4月至2024年9月在印度一家三级医院进行,包括200名延迟脐带夹后剖宫产的晚期早产儿。出生后2-10分钟,每分钟记录一次外周血氧饱和度(SpO2)、心率和体温。结果:平均(SD)胎龄为35.6(1.3)周,出生体重为2260 (496)g。在2、5和10分钟时,产SpO2的中位数(q1, q3)分别为77(70,84)、88(82,92)和95(93,96)。达到≥80%、≥85%和≥90%饱和所需的中位时间(q1、q3)分别为4(3,5)、5(3,6)和6(4,7)分钟。只有73.3%的晚早产儿在5 min达到SpO2≥80%的目标;98.8%在无任何干预的情况下10 min达到≥85%。结论:近四分之一的健康晚期早产儿在出生后5分钟才达到新生儿复苏计划(NRP)设定的阈值,而在不干预的情况下,几乎所有的早产儿在出生后10分钟就达到了SpO2≥85%的阈值。这提示有轻微延迟但充分的过渡,提示对于临床稳定的晚期早产儿,常规补充氧可能是不必要的。
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引用次数: 0
Pediatric Endocrinology. 儿科内分泌学。
IF 1.5 4区 医学 Q2 PEDIATRICS Pub Date : 2026-01-21 DOI: 10.1007/s13312-025-00262-8
Ayesha Ahmad
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引用次数: 0
Polyuria due to central diabetes insipidus in an infant with pseudo-TORCH syndrome. 假性torch综合征婴儿中枢性尿崩症所致多尿。
IF 1.5 4区 医学 Q2 PEDIATRICS Pub Date : 2026-01-20 DOI: 10.1007/s13312-026-00276-w
Anitha Sengottaian, Sriram Krishnamurthy
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引用次数: 0
Chronic Myeloid Leukemia as a Secondary Malignancy in a Child Treated for T Cell Acute Lymphoblastic Leukemia. 慢性髓系白血病作为继发性恶性肿瘤在儿童治疗的T细胞急性淋巴细胞白血病。
IF 1.5 4区 医学 Q2 PEDIATRICS Pub Date : 2026-01-20 DOI: 10.1007/s13312-025-00264-6
Ayush Sopori, Manas Kalra, Jyoti Kotwal, Meena Lall, Anupam Sachdeva
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引用次数: 0
Standard Nasal-Tragus Length Formula Versus Alternate Insertional Length Formula for Optimal Placement of Endotracheal Tube in Neonates: A Randomized Controlled Trial (SNAIL Trial). 标准鼻耳膜长度公式与替代插入长度公式对新生儿气管插管最佳放置的影响:一项随机对照试验(SNAIL试验)。
IF 1.5 4区 医学 Q2 PEDIATRICS Pub Date : 2026-01-19 DOI: 10.1007/s13312-025-00265-5
Sachin Dangi, Anup Thakur, Neelam Kler, Pankaj Garg

Objective: To compare the performance of an alternate nasal-tragus length (NTL) formula for the calculation of insertional length (IL) during endotracheal intubation with the standard NTL formula (NTL + 1 cm) for optimal placement of endotracheal tube.

Methods: A randomized controlled trial was conducted in a level IIIB neonatal intensive care unit between June 2022 and December 2023. Neonates who required endotracheal intubation were randomized to either standard NTL group or alternate NTL group. In standard NTL group, the IL of ETT was calculated as NTL + 1 cm and in the alternate NTL group, IL was calculated as IL = NTL + 0.5 cm for a measured NTL ≤ 5.5 cm and IL = NTL for a measured NTL > 5.5 cm.

Results: A total of 158 neonates were randomized, 79 per group. Baseline maternal and neonatal characteristics were similar. Optimal placement of endotracheal tube was more frequent in alternate NTL group than in the standard NTL group [48 (65%) and 30 (39%), respectively, P = 0.002]. Low placement of endotracheal tube was observed more frequently in standard NTL group versus alternate NTL group [41 (54%) vs 14 (19%); P < 0.001]. There was no difference in other secondary outcomes such as rate of reintubation within 1 h, need for mechanical ventilation for > 72 h, pneumothorax or other air-leak syndromes, lung atelectasis and mortality.

Conclusion: Use of alternate NTL formula in neonates requiring endotracheal intubation leads to a higher rate of optimal placement of endotracheal tube compared to standard NTL formula.

Trial registry: CTRI/2022/09/045209.

目的:比较鼻耳膜置换长度(NTL)公式与标准NTL公式(NTL + 1 cm)计算气管插管插入长度(IL)的性能。方法:于2022年6月至2023年12月在某IIIB级新生儿重症监护病房进行随机对照试验。需要气管插管的新生儿随机分为标准NTL组或替代NTL组。标准NTL组ETT的IL计算为NTL + 1 cm,交替NTL组测量NTL≤5.5 cm计算IL = NTL + 0.5 cm,测量NTL bb0 5.5 cm计算IL = NTL。结果:158例新生儿随机分组,每组79例。基线产妇和新生儿特征相似。替代NTL组气管插管最佳放置次数高于标准NTL组[分别为48例(65%)和30例(39%),P = 0.002]。标准NTL组与替代NTL组相比,气管内插管低置的发生率更高[41例(54%)vs 14例(19%);p72小时,气胸或其他漏气综合征,肺不张和死亡。结论:与标准NTL配方相比,在需要气管插管的新生儿中使用替代NTL配方可获得更高的气管插管最佳放置率。试验注册:CTRI/2022/09/045209。
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引用次数: 0
Development and Formative Assessment of an Innovative Blended Educational Course for Care of Small and Sick Neonates in India and SEARO Countries. 印度和东南亚国家照顾小病新生儿的创新混合教育课程的发展和形成性评估。
IF 1.5 4区 医学 Q2 PEDIATRICS Pub Date : 2026-01-19 DOI: 10.1007/s13312-025-00244-w
Praveen Kumar, Ashok Deorari, Pratima Anand, Srinivas Murki, Era Dayal, Surender Singh Bisht, Amit Upadhyay, Anitha M Balachandran, Ankita Raj

Objectives: To develop and disseminate an innovative blended educational programme comprising of evidence-based neonatal healthcare practices across India and to identify and empower local champions who could sustain and scale quality improvement (QI) efforts regionally.

Methods: The study was conducted in two phases and engaged healthcare professionals mentored by trained facilitators (1:8 ratio). A structured methodology was adopted comprising of: (i) assessment of learning needs, (ii) identification of the target audience and local facilitators, (iii) development of content and blended learning strategy, (iv) alignment with measurable QI objectives, (v) documentation of outcomes and (vi) implementation through the support of the National Neonatology Forum. Participant and facilitator feedback guided course evaluation.

Results: The course engaged 1073 healthcare professionals (590 doctors, 483 nurses) with 2-10 years of neonatal experience mentored by 132 facilitators. Phase 1 included 250 participants from five Indian states, and 823 participants from 18 Indian states and four South-East Asia Regional Organization (SEARO) countries-Bangladesh, Bhutan, Maldives and Nepal-were enrolled in Phase 2. Overall, 57% participants completed weekly online quizzes, and the average attendance for live webinars was 50%. 43 hands-on skill workshops were held training 685 professionals.

Conclusion: This flipped-classroom, blended model promoted exploratory and self-directed learning. Its adaptability and emphasis on faculty development and QI projects offer a replicable framework for future neonatal training initiatives.

目标:制定和传播一项创新的混合教育方案,包括全印度以证据为基础的新生儿保健实践,并确定和授权能够在区域内维持和扩大质量改进(QI)工作的地方冠军。方法:本研究分两阶段进行,由训练有素的辅导员(1:8比例)指导卫生保健专业人员。采用了一种结构化的方法,包括:(i)评估学习需求,(ii)确定目标受众和当地协调员,(iii)开发内容和混合学习策略,(iv)与可衡量的QI目标保持一致,(v)记录结果,以及(vi)通过国家新生儿学论坛的支持实施。参与者和推动者的反馈指导课程评估。结果:该课程共有1073名医护人员参加,其中590名医生,483名护士,具有2-10年的新生儿经验,由132名辅导员指导。第一阶段包括来自印度5个邦的250名参与者,第二阶段招募了来自印度18个邦和四个东南亚区域组织国家(孟加拉国、不丹、马尔代夫和尼泊尔)的823名参与者。总体而言,57%的参与者完成了每周在线测验,现场网络研讨会的平均出勤率为50%。举办实践技能培训班43期,培训专业人员685人。结论:这种翻转课堂、混合模式促进了探索性和自主学习。它的适应性和对教师发展和QI项目的重视为未来的新生儿培训计划提供了一个可复制的框架。
{"title":"Development and Formative Assessment of an Innovative Blended Educational Course for Care of Small and Sick Neonates in India and SEARO Countries.","authors":"Praveen Kumar, Ashok Deorari, Pratima Anand, Srinivas Murki, Era Dayal, Surender Singh Bisht, Amit Upadhyay, Anitha M Balachandran, Ankita Raj","doi":"10.1007/s13312-025-00244-w","DOIUrl":"https://doi.org/10.1007/s13312-025-00244-w","url":null,"abstract":"<p><strong>Objectives: </strong>To develop and disseminate an innovative blended educational programme comprising of evidence-based neonatal healthcare practices across India and to identify and empower local champions who could sustain and scale quality improvement (QI) efforts regionally.</p><p><strong>Methods: </strong>The study was conducted in two phases and engaged healthcare professionals mentored by trained facilitators (1:8 ratio). A structured methodology was adopted comprising of: (i) assessment of learning needs, (ii) identification of the target audience and local facilitators, (iii) development of content and blended learning strategy, (iv) alignment with measurable QI objectives, (v) documentation of outcomes and (vi) implementation through the support of the National Neonatology Forum. Participant and facilitator feedback guided course evaluation.</p><p><strong>Results: </strong>The course engaged 1073 healthcare professionals (590 doctors, 483 nurses) with 2-10 years of neonatal experience mentored by 132 facilitators. Phase 1 included 250 participants from five Indian states, and 823 participants from 18 Indian states and four South-East Asia Regional Organization (SEARO) countries-Bangladesh, Bhutan, Maldives and Nepal-were enrolled in Phase 2. Overall, 57% participants completed weekly online quizzes, and the average attendance for live webinars was 50%. 43 hands-on skill workshops were held training 685 professionals.</p><p><strong>Conclusion: </strong>This flipped-classroom, blended model promoted exploratory and self-directed learning. Its adaptability and emphasis on faculty development and QI projects offer a replicable framework for future neonatal training initiatives.</p>","PeriodicalId":13291,"journal":{"name":"Indian pediatrics","volume":" ","pages":""},"PeriodicalIF":1.5,"publicationDate":"2026-01-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145998053","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: 0
A Prospective Study on the Effect of Antiseizure Medications on the Bone Mineral Density of Children with Drug-Naïve Epilepsy. 抗癫痫药物对Drug-Naïve癫痫患儿骨密度影响的前瞻性研究。
IF 1.5 4区 医学 Q2 PEDIATRICS Pub Date : 2026-01-14 DOI: 10.1007/s13312-025-00253-9
Aleesha Kanakuzhi Aliyar, Ramachandran Rameshkumar, Tamil Selvan, Jayaprakash Sahoo, Ananthanarayanan Kasinathan

Objective: The study aimed to evaluate the effect of antiseizure medications (ASMs) on bone health in children with drug-naive epilepsy and its associated risk factors over a one-year follow-up period.

Methods: A prospective study enrolled children aged 5-15 years with drug-naïve epilepsy. At baseline and after one year of treatment with ASMs, bone mineral density (BMD) was measured by Dual energy X-ray absorptiometry (DXA), and bone metabolism markers (calcium, phosphorus, alkaline phosphatase, vitamin D, intact parathyroid hormone (i-PTH)). The primary outcome was the change in BMD after one year of treatment; secondary outcomes included BMD change in mono- and polytherapy, and changes in bone metabolism markers and risk factors for reduced BMD.

Results: Sixty-five patients (40 boys) with mean (SD) age 8.6 (2.8) years completed one-year follow-up; 50 (77%) had generalized epilepsy, and 42 (65%) had an unknown etiology. 30 (46%) and 35 (54%) children received monotherapy and polytherapy, respectively. At one-year follow-up, the median (Q1, Q3) BMD was significantly lower compared to baseline [0.623, (0.540, 0.714) vs. 0.656 (0.582, 0.745); P < 0.001]. Likewise, the median (Q1, Q3) DXA Z-score was significantly lower compared to the baseline [0.20, (- 0.50, 0.60) vs. 0.50, (0.20, 0.80); P < 0.001]. At one-year, median (Q1, Q3) serum 25-OH vitamin D levels [20, (17, 27) vs. 26, (23, 33.5); P < 0.001] and i-PTH [34, (24, 56) vs. 31, (20.50, 44); P = 0.008] had significantly reduced and increased, respectively. Both mono- and polytherapy subgroups showed significant reduction in BMD, DXA z-score, and serum 25-OH vitamin D levels. Multivariate analysis identified male gender as an independent risk factor for low BMD [adjusted odds ratio 4.46, (95% CI 1.16-17.21); P = 0.030).

Conclusion: Antiseizure medications affect the bone health adversely in children with drug-naïve epilepsy, leading to significant reductions in BMD and altered bone metabolism markers.

目的:本研究旨在评价抗癫痫药物(asm)对药源性癫痫患儿骨骼健康的影响及其相关危险因素。方法:前瞻性研究纳入5-15岁drug-naïve癫痫患儿。在基线和治疗一年后,采用双能x线骨密度仪(DXA)测量骨密度(BMD)和骨代谢指标(钙、磷、碱性磷酸酶、维生素D、完整甲状旁腺激素(i-PTH))。主要结局是治疗一年后骨密度的变化;次要结局包括单一和多种治疗的骨密度变化,骨代谢标志物的变化和骨密度降低的危险因素。结果:65例患者(40例男性)完成1年随访,平均(SD)年龄8.6(2.8)岁;50例(77%)患有全身性癫痫,42例(65%)病因不明。分别有30例(46%)和35例(54%)儿童接受单一治疗和多种治疗。在一年的随访中,中位BMD (Q1, Q3)与基线相比显著降低[0.623,(0.540,0.714)比0.656 (0.582,0.745);结论:抗癫痫药物对drug-naïve癫痫患儿的骨骼健康有不利影响,导致骨密度显著降低和骨代谢指标改变。
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引用次数: 0
Lactobacillus rhamnosus GG to Reduce Necrotising Enterocolitis, Sepsis, and Mortality in Very Low Birth Weight Infants: A Randomized Controlled Trial. 鼠李糖乳杆菌GG减少极低出生体重婴儿坏死性小肠结肠炎、败血症和死亡率:一项随机对照试验。
IF 1.5 4区 医学 Q2 PEDIATRICS Pub Date : 2026-01-14 DOI: 10.1007/s13312-025-00252-w
Sachin Shah, Amita Kaul, Prerna Pandey, Surabhi Wattal, Rajesh Nare

Objectives: To evaluate the efficacy of oral Lactobacillus rhamnosus GG (LGG) in reducing neonatal enterocolitis (NEC), sepsis and mortality in very low birth weight (VLBW) infants.

Methods: This open-label randomized controlled trial included enterally-fed VLBW infants with gestational age ≤ 32 weeks; those with gastrointestinal anomalies, severe birth asphyxia (APGAR score < 3 at 5 min), cyanotic congenital heart disease, and those not started on feeds by 14 days of life were excluded. Participants were randomized to receive either no probiotic (control) group, or probiotic (LGG; intervention) group. The intervention group received the first dose of LGG (probiotic) at feed initiation and was continued till 35 weeks of corrected gestational age. The control group received only breast milk. Clinical outcomes (mortality, NEC, sepsis) were compared in both groups during hospital stay.

Results: A total of 236 infants were enrolled. The primary composite outcome of sepsis, NEC or mortality was seen in 35 (30.4%) and 33 (27.2%) infants, respectively in the LGG and control groups (RR 0.85; 95%CI 0.48-1.50, P = 0.592). The mean (SD) time to reach full feeds was 11.9 (4.2) and 12.0 (5.5) days in the LGG and control groups, respectively; P = 0.561. The mean (SD) time to regain birth weight was 13.5 (3.9) and 13.6 (3.9) days in the LGG and control groups, respectively (P = 0.982). There was no significant difference in duration of hospital stay, duration of mechanical ventilation, or duration of antimicrobial therapy between the two groups (P > 0.05).

Conclusions: Use of LGG as single component probiotic in VLBW infants did not confer any significant benefit on the composite outcome of mortality, sepsis or NEC.

Trial registry: Clinical Trial Registry of India; Ref. No. CTRI/2021/03/031724 dated Mar 03, 2021.

目的:评价口服鼠李糖乳杆菌GG (LGG)降低极低出生体重儿(VLBW)新生儿小肠结肠炎(NEC)、败血症和死亡率的疗效。方法:该开放标签随机对照试验纳入胎龄≤32周的肠内喂养VLBW婴儿;结果:共纳入236例婴儿。在LGG组和对照组中,败血症、NEC或死亡的主要复合结局分别为35例(30.4%)和33例(27.2%)(RR 0.85; 95%CI 0.48-1.50, P = 0.592)。LGG组和对照组达到完全饲料的平均(SD)时间分别为11.9(4.2)天和12.0 (5.5)d;p = 0.561。LGG组和对照组恢复出生体重的平均(SD)时间分别为13.5(3.9)天和13.6(3.9)天(P = 0.982)。两组患者住院时间、机械通气时间、抗菌药物治疗时间差异无统计学意义(P < 0.05)。结论:在VLBW婴儿中使用LGG作为单组分益生菌对死亡率、败血症或NEC的综合结果没有任何显著的益处。试验注册:印度临床试验注册中心;Ref。不。CTRI/2021/03/031724日期为2021年3月3日。
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引用次数: 0
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Indian pediatrics
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