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Neonatal Candidiasis: Clinical Spectrum and Epidemiology at a Tertiary Care Centre, Bhopal, India 新生儿念珠菌病:印度博帕尔三级保健中心的临床谱和流行病学
Pub Date : 2023-01-01 DOI: 10.7860/ijnmr/2023/57554.2372
Introduction: Neonatal candidiasis is one of the leading causes of sepsis amongst newborns admitted to newborn care unit, especially premature and Low Birth Weight (LBW) babies. It is one of the significant contributors to neonatal morbidity and mortality. Aim: To describe the spectrum and epidemiology of fungal sepsis in Neonatal Intensive Care Unit (NICU) at a tertiary care level. Materials and Methods: A longitudinal study was conducted from January 2018- December 2019 in NICU of Chirayu Medical College and Hospital, a tertiary level hospital in Bhopal, Central India. All neonates, who had positive fungal blood culture were included in the study, their demographic data was analysed (age, birth weight, predisposing factors etc.,), maternal history, their response to the antifungal treatment documented and complications. Statistical analysis was done using the Chi- square test with the help of Statistical Package for Social Sciences (SPSS) software version 2.0. Results: A total of 409 neonates admitted in the NICU during the study period, were suspected clinically to have sepsis and their blood culture was done, of which 110 samples were culture positive. Amongst the 110 neonates, 41(37.2%) were positive for fungal infection {29 showed Candida albicans, 12 Non Albicans Candida (NAC)}. Total 25 neonates were preterm (60.97%). The mean age of admission was 3.02 days, 51.2% (21/41) of the neonates had a history of respiratory distress and related symptoms at birth. There was no significant maternal history. Amongst the risk factors, lower birth weight (<2.5 kg), preterm (<34 weeks), and presence of invasive central lines were statistically associated with morbidity. Urine for candidial hyphae was positive in 12 out of 41 cases (29.27%). Incidence of candidal meningitis was seen in four neonates (13.33%). Thrombocytopenia was the most common laboratory finding amongst these cases (32/41). Among the different regimens used the combination regimen of Lipid based amphotericin B and voriconazole was associated with a better survival. Conclusion: Candida sepsis was found to be the most common cause of septicaemia in the NICU. LBW and preterm babies are especially at greater risk of candida sepsis. Candida albicans still continues to be a dominant aetiology for fungal sepsis, as compared to non candida species.
新生儿念珠菌病是新生儿败血症的主要原因之一,特别是早产儿和低出生体重(LBW)婴儿。它是新生儿发病率和死亡率的重要因素之一。目的:描述三级护理水平新生儿重症监护病房(NICU)真菌脓毒症的频谱和流行病学。材料与方法:2018年1月至2019年12月,在印度中部博帕尔市三级医院Chirayu医学院和医院的NICU进行了一项纵向研究。所有真菌血培养阳性的新生儿都被纳入研究,分析了他们的人口统计学数据(年龄、出生体重、易感因素等)、母亲史、他们对抗真菌治疗的反应和并发症。采用社会科学统计软件包(SPSS) 2.0版软件,采用卡方检验进行统计分析。结果:研究期间NICU共收治临床怀疑脓毒症的新生儿409例,进行血培养,其中培养阳性110例。110例新生儿中真菌感染阳性41例(37.2%),其中白色念珠菌29例,非白色念珠菌12例。早产25例(60.97%)。平均入院年龄为3.02 d, 51.2%(21/41)的新生儿出生时有呼吸窘迫及相关症状。无明显的母系病史。在危险因素中,低出生体重(<2.5 kg)、早产(<34周)和侵入性中央线的存在在统计学上与发病率相关。41例患者尿念珠菌检出阳性12例(29.27%)。4例新生儿出现念珠菌脑膜炎(13.33%)。血小板减少症是这些病例中最常见的实验室发现(32/41)。在使用的不同方案中,脂基两性霉素B和伏立康唑联合方案与更好的生存相关。结论:念珠菌败血症是新生儿重症监护病房最常见的败血症原因。低体重婴儿和早产儿患念珠菌败血症的风险尤其大。与非念珠菌相比,白色念珠菌仍然是真菌败血症的主要病因。
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引用次数: 0
Assessment of Neonates with Extended Sick Neonate Score (ESNS) for Predicting Mortality in a Tertiary Care Center in Dharwad, Karnataka, India: A Prospective Cohort Study 印度卡纳塔克邦Dharwad三级保健中心评估延长患病新生儿评分(ESNS)预测死亡率:一项前瞻性队列研究
Pub Date : 2023-01-01 DOI: 10.7860/ijnmr/2023/65335.2393
Yeruva Ramani Maria, Kavita Shantmalappa Konded, Kulkarni Poornima Prakash, Jasmine Kandagal
Introduction: High neonatal mortality rates may be attributed to the lack of early recognition of severe illness, early and safe referral, and proper care. Therefore, there is a need to develop a simple, cost-effective scoring system that can be quickly applied to newborns referred from peripheral to tertiary care settings in resource-constrained areas. The Extended Sick Neonate Score (ESNS) is one such scoring system used to assess the severity of illness in critically ill neonates and predict their outcomes. Aim: To evaluate the effectiveness of the Extended Sick Newborn Score in predicting outcomes for neonates admitted to the Neonatal Intensive Care Unit (NICU) of a tertiary care centre. Materials and Methods: This prospective cohort study included 122 outborn neonates admitted to the NICU of SDM College of Medical Sciences and Hospital in Dharwad, Karnataka, India, from June 2021 to June 2022. All the required parameters for scoring, such as respiratory effort, heart rate, mean blood pressure, axillary temperature, capillary filling time, random blood sugar, SpO2, Moro reflex, and modified Downe’s score, were assessed and documented in a predesigned proforma. The ESNS was calculated upon admission to predict the outcomes. Statistical analysis included ANOVA test and independent t-test, using SPSS version 17.0 and MS Excel. Results: The study evaluated a total of 122 neonates, including 78 males and 44 females. Of these, 99 were term neonates and 23 were preterm neonates. The mean age for term neonates was 8.5 days ±8.6, and for preterm neonates, it was 4.1 days ±4.3. Term neonates with an ESNS Score ≤11 exhibited higher mortality, while preterm neonates with an ESNS score ≤12 showed higher mortality. The sensitivity and specificity of the ESNS score in predicting death were 78.57% and 99.07%, respectively. The ESNS score at admission was significantly lower in non-survivors compared to survivors, and it demonstrated a positive correlation with the outcome. Conclusion: This study found a significant correlation between the ESNS score at admission and in-hospital mortality. The use of the ESNS score is an acceptable method for risk stratification and prognosis of newborns in the NICU.
新生儿死亡率高可能是由于缺乏对严重疾病的早期认识、早期和安全的转诊以及适当的护理。因此,有必要开发一种简单、具有成本效益的评分系统,可以快速应用于资源有限地区从外围医疗机构转介到三级医疗机构的新生儿。延长患病新生儿评分(ESNS)是一个这样的评分系统,用于评估疾病的严重程度,危重新生儿和预测他们的结果。目的:评估延长患病新生儿评分在预测三级护理中心新生儿重症监护病房(NICU)新生儿预后方面的有效性。材料与方法:本前瞻性队列研究纳入了2021年6月至2022年6月在印度卡纳塔克邦达瓦德SDM医学科学院和医院NICU收治的122名早产新生儿。所有评分所需的参数,如呼吸努力度、心率、平均血压、腋窝温度、毛细血管充血时间、随机血糖、SpO2、Moro反射和修改的唐氏评分,都被评估并记录在预先设计的表格中。入院时计算ESNS以预测预后。统计分析采用方差分析和独立t检验,使用SPSS 17.0和MS Excel。结果:本研究共对122例新生儿进行了评估,其中男78例,女44例。其中99个是足月新生儿,23个是早产儿。足月新生儿的平均年龄为8.5天±8.6天,早产儿的平均年龄为4.1天±4.3天。ESNS评分≤11的足月新生儿死亡率较高,而ESNS评分≤12的早产儿死亡率较高。ESNS评分预测死亡的敏感性和特异性分别为78.57%和99.07%。入院时,非幸存者的ESNS评分明显低于幸存者,且与预后呈正相关。结论:本研究发现入院时ESNS评分与住院死亡率有显著相关性。ESNS评分是NICU新生儿风险分层和预后的一种可接受的方法。
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引用次数: 0
Risk Factors for Hearing Loss in High-Risk Neonates at a Tertiary Care Centre in Central India: A Prospective Observational Study 印度中部三级保健中心高危新生儿听力损失的危险因素:一项前瞻性观察研究
Pub Date : 2023-01-01 DOI: 10.7860/ijnmr/2023/59711.2392
Leena Dhande, Prerana Ganaboor, Rasika Hattewar, Chetan Jaiswal
Introduction: Hearing impairment and deafness are global issues that affect 5% of the world’s population, with nearly 34 million children requiring rehabilitation to address their hearing loss (HL). An approximately 10-20 fold higher incidence of audiological risk factors has been noted in Neonatal Intensive Care Units (NICUs), which translates that 2-5% of all newborns in NICUs may be affected. Early diagnosis of HL and intervention can be advantageous from the timely fitting of hearing aids or cochlear implants. Aim: The aim of this study was to evaluate the risk factors for HL in NICUs and Special Neonatal Care Units (SNCUs) at a tertiary care hospital in Central India. Materials and Methods: This prospective, observational, single-centre study was conducted from October 2019 to September 2021 in the Department of Paediatrics at Indira Gandhi Government Medical College and Hospital, Nagpur, Maharashtra, India. A total of 319 neonates at high risk for HL, discharged from NICUs and SNCUs, were included in the study. The association between risk factors like prematurity, low birth weight (LBW), Toxoplasmosis, Rubella, Cytomegalovirus, Herpes Simplex (TORCH) infections, neonatal asphyxia, neonatal sepsis, meningitis, exchange transfusion, assisted ventilation, and HL were studied. The chi-square test was used to assess the association between SNHL and risk factors. Results: The incidence of Sensorineural Hearing Loss (SNHL) was 3.76%. Neonatal asphyxia (p-value <0.01), exchange transfusion (p-value <0.001), TORCH infections (p-value < 0.001), meningitis (p-value <0.001), and assisted ventilation (p-value <0.001) were found to be significant risk factors associated with SNHL. Conclusion: Based on the assessment of risk factors, it was concluded that neonates should undergo hearing screening tests within the first month of life, and a diagnosis should be made by three months of age. This allows specialists to initiate treatment and intervention by six months of age, helping children with impaired hearing avoid the harmful consequences of semantic deprivation.
听力障碍和耳聋是影响世界5%人口的全球性问题,近3400万儿童需要康复来解决听力损失问题。在新生儿重症监护病房(NICUs)中,听力危险因素的发生率大约高出10-20倍,这意味着新生儿重症监护病房中2-5%的新生儿可能受到影响。HL的早期诊断和干预可以从及时配戴助听器或人工耳蜗中获益。目的:本研究的目的是评估印度中部一家三级医院新生儿重症监护病房和特殊新生儿护理病房(sncu)发生HL的危险因素。材料和方法:这项前瞻性、观察性、单中心研究于2019年10月至2021年9月在印度马哈拉施特拉邦那格浦尔英迪拉·甘地政府医学院和医院儿科进行。本研究共纳入319名从nicu和sncu出院的HL高危新生儿。研究了早产、低出生体重(LBW)、弓形虫病、风疹、巨细胞病毒、单纯疱疹(TORCH)感染、新生儿窒息、新生儿败血症、脑膜炎、换血、辅助通气和HL等危险因素之间的关系。采用卡方检验评估SNHL与危险因素的相关性。结果:感音神经性听力损失(SNHL)发生率为3.76%。新生儿窒息(p值<0.01)、换血(p值<0.001)、TORCH感染(p值<0.001)、脑膜炎(p值<0.001)和辅助通气(p值<0.001)被发现是SNHL相关的重要危险因素。结论:根据危险因素的评估,新生儿应在出生后1个月内进行听力筛查,并在3个月大时做出诊断。这使得专家可以在六个月大的时候开始治疗和干预,帮助听力受损的儿童避免语义剥夺的有害后果。
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引用次数: 0
Transcranial Ultrasonography Doppler in Detecting Clinical Outcome of Term Neonates with Perinatal Asphyxia: A Longitudinal Study 经颅超声多普勒检测足月新生儿围产期窒息的临床预后:一项纵向研究
Pub Date : 2023-01-01 DOI: 10.7860/ijnmr/2023/58192.2381
Jayesh R Solanki, Janakiram .
Introducton: Perinatal asphyxia is one of the most important causes of mortality and morbidity in full-term neonates, where due to the hypoxic insult, mortality and various morbidities happens. So, it is important to predict both the outcomes to aid in patient management, as well as to counsel the caregivers regarding the outcome of the patient, especially the neurological outcome. Aim: To determine the usefulness of abnormal Resistive Index (RI) values on transcranial USG doppler and its association with clinical outcomes in term neonates with perinatal asphyxia. Materials and Methods: This prospective longitudinal study was conducted in the extramural Neonatal Intensive Care Unit (NICU) and Rukmani Chainani NICU of Sir Sayaji General (SSG) Hospital, Vadodara, Gujarat, India, from June 2020 to November 2021. Study was conducted among a cohort of 174 term newborns with perinatal asphyxia admitted in both intramural and extramural NICU of SSG Hospital Vadodara. Neurodevelopmental assessment was done by Amiel-tison scoring system, done at birth, at the time of discharge, at three and six months of age with simultaneous RI value monitoring by a trained radiology resident. The clinical association was done in terms of mortality at birth, morbidities encountered during the NICU stay and neurological outcome at six months of age. Development assessment was done by history taking and clinical examination, patients with delay in two or more domains were classified as global developmental delay, patients with delay in less than two domains were classified as mild developmental delay. Continuable variables were analysed using one-way Analysis of Variance (ANOVA). Categorical data were analysed with Pearson’s Chi-square test. Significance was defined by p-values less than 0.05 using a two-tailed test. Results: Out of 174 newborns enrolled, 97 patients had normal RI values at birth, and 77 patients had abnormal RI values. Forty-eight patients expired after birth, with 27% mortality, and among which 43 patients had abnormal RI values at birth, which was statistically significant (p-value <0.0001). The majority of the newborns with abnormal RI required invasive mechanical ventilation (n=62) and had persistent pulmonary hypertension of newborn (n=40), ventricular dysfunction (n=33), feed intolerance (n=17), acute kidney injury (n=19) and sepsis (n=27). Conclusion: Transcranial Ultrasonography (USG) doppler in the calculation of RI at birth is a useful non invasive point of care method to determine immediate short-term outcomes in the form of mortality and short-term morbidities encountered during NICU stay.
简介:围产期窒息是导致足月新生儿死亡和发病的重要原因之一,由于缺氧损伤,围产期窒息可导致死亡和各种疾病的发生。因此,重要的是预测结果,以帮助患者管理,以及咨询护理人员关于患者的结果,特别是神经系统的结果。目的:探讨经颅USG多普勒电阻指数(RI)异常值与围产期窒息足月新生儿临床预后的关系。材料和方法:本前瞻性纵向研究于2020年6月至2021年11月在印度古吉拉特邦瓦多达拉市Sir Sayaji General (SSG)医院的新生儿重症监护室(NICU)和Rukmani Chainani NICU进行。研究对象为174名在瓦多达拉SSG医院内、外NICU住院的围产期窒息足月新生儿。神经发育评估采用Amiel-tison评分系统,在出生时、出院时、3个月和6个月时进行,同时由训练有素的放射科住院医师进行RI值监测。临床关联是根据出生时的死亡率,在新生儿重症监护病房逗留期间遇到的发病率和6个月大时的神经预后来进行的。通过病史记录和临床检查进行发育评估,两项及两项以上发育迟缓者为全面发育迟缓,两项以下发育迟缓者为轻度发育迟缓。可持续性变量采用单因素方差分析(ANOVA)进行分析。分类资料采用Pearson卡方检验进行分析。采用双尾检验,p值小于0.05定义显著性。结果:入组的174例新生儿中,97例新生儿出生时RI值正常,77例新生儿出生时RI值异常。48例患者出生后死亡,死亡率27%,其中43例患者出生时RI值异常,差异有统计学意义(p值<0.0001)。大多数RI异常新生儿需要有创机械通气(n=62),并伴有新生儿持续性肺动脉高压(n=40)、心室功能障碍(n=33)、饲料不耐受(n=17)、急性肾损伤(n=19)和脓毒症(n=27)。结论:经颅超声(USG)多普勒计算出生时的RI是一种有用的无创护理点方法,可以确定新生儿在新生儿重症监护病房期间的短期死亡率和短期发病率。
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引用次数: 0
Efficacy of Enhanced Dose of Expressed Breast Milk in Neonatal Procedural Pain Relief: A Randomised Placebo-controlled Study 提高母乳表达量对新生儿程序性疼痛缓解的疗效:一项随机安慰剂对照研究
Pub Date : 2023-01-01 DOI: 10.7860/ijnmr/2023/59294.2377
L. Jha, Vasanth Kumar, Subho Sankar Banerjee, Chandreyi Bandhopadhyay
Introduction: Procedural pain remedies in neonates is an area of active research due to better understanding of short and long-term outcomes of neonatal painful exposures. Non pharmacological interventions are especially attractive as it avoids unnecessary drug exposure. While dextrose is known to be effective, results with small volumes (2 mL) of Expressed Breast Milk (EBM) are equivocal. There is recent theoretical evidence to show that larger doses of EBM may be more efficacious. Aim: To compare the efficacy of a larger volume of EBM 5 mL and 2 mL of 25% Dextrose (25D) in relief of procedural pain from venipuncture in term and preterm neonates. Materials and Methods: A single center randomised placebo- controlled study was conducted at Bokaro General Hospital, Bokaro Steel City, Jharkhand, India, between March 2014 and February 2016. Neonates ≥34 week gestation, requiring venipuncture in a neonatal care unit were randomly allocated into 3 equal groups using a random number table- Sterile Water (SW), 2mL 25D, 5 mL EBM was given two minutes prior to venipuncture. Video of facial response, cry times, Maximal Heart Rate (MHR), and minimum Oxygen Saturation (SpO2) were recorded till five minutes after venipuncture. The Premature Infant Pain Profile (PIPP) score was used to assess the effect of the interventions on procedural pain. Subgroup analysis was done in term and preterm neonates. Continuous variables were presented as mean±SD or median. Categorical variables were expressed as frequencies and percentages. The comparison of normally distributed continuous variables between the groups was performed using Analysis of Variance (ANOVA). Results: The PIPP score in the 25D group (2.94±1.41) was significantly lower than the EBM (7.42±1.69) and SW (10.56±1.69) groups (p-value<0.001). MHR was significantly lower in the 25D group, but no difference was found between the EBM and SW groups (p-value=0.23). SpO2 was significantly higher in the 25D group but for the initial 2.5 minutes only. Cry times were significantly lower in the intervention groups. There was no difference in outcomes in term vs. preterm infants. Conclusion: The use of 2 mL 25D was more effective in reducing procedural pain from venipuncture compared to 5 mL EBM. The return of physiological markers (MHR and SpO2) to baseline were faster and more complete in the 25D group.
由于对新生儿疼痛暴露的短期和长期结果有了更好的了解,新生儿的程序性疼痛补救措施是一个积极研究的领域。非药物干预特别有吸引力,因为它避免了不必要的药物暴露。虽然葡萄糖已知是有效的,但小体积(2ml)的母乳(EBM)的结果是模棱两可的。最近有理论证据表明,大剂量的EBM可能更有效。目的:比较大体积EBM 5ml和2ml 25%葡萄糖(25D)对足月儿和早产儿静脉穿刺术后疼痛的缓解效果。材料和方法:2014年3月至2016年2月,在印度贾坎德邦Bokaro Steel City Bokaro总医院进行了一项单中心随机安慰剂对照研究。采用随机数字表法,将妊娠≥34周、在新生儿监护室需要静脉穿刺的新生儿随机分为3组——静脉穿刺前2分钟给予无菌水(SW) 2mL 25D, 5ml EBM。静脉穿刺后5分钟,记录患者面部反应、哭泣次数、最大心率(MHR)、最低血氧饱和度(SpO2)。采用早产儿疼痛概况(PIPP)评分来评估干预措施对程序性疼痛的影响。对足月和早产儿进行亚组分析。连续变量以均数±标准差或中位数表示。分类变量用频率和百分比表示。组间正态分布连续变量的比较采用方差分析(ANOVA)。结果:25D组PIPP评分(2.94±1.41)明显低于EBM组(7.42±1.69)和SW组(10.56±1.69)(p值<0.001)。25D组MHR明显降低,但EBM组与SW组间无差异(p值=0.23)。25D组的SpO2明显升高,但仅在最初的2.5分钟内。干预组的哭泣次数明显较低。足月婴儿和早产儿的结果没有差异。结论:与5ml EBM相比,2ml 25D能更有效地减轻静脉穿刺的程序性疼痛。生理指标(MHR和SpO2)在25D组恢复到基线更快,更完整。
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引用次数: 0
Early Cranial Ultrasound Changes as Predictors of Outcome during First Year of Life in Infants with Perinatal Asphyxia- A Prospective Cohort Study 早期颅超声变化作为围产儿窒息婴儿第一年预后的预测因子——一项前瞻性队列研究
Pub Date : 2023-01-01 DOI: 10.7860/ijnmr/2023/60764.2373
S. Agrawal, .. Ravanagomagan, Sethi Rohith Shamsher, Chaurasiya Rachna
Introduction: Perinatal Asphyxia (PA) causes impaired exchange of ventilatory gases, or ischemia that leads to persistent decrease in oxygen levels (hypoxemia) and increase in carbon dioxide levels (hypercarbia). It occurs during the peripartum period can contribute to early neonatal mortality and morbidity. Aim: To assess the role of early changes in cranial ultrasound a predictor of outcome in babes with PA. Materials and Methods: This prospective cohort study was conducted in a tertiary care neonatal unit in Maharani Laxmi Bai Medical College, Jhansi, Uttar Pradesh, India, from July 2018 to October 2019. A total of 50 neonates with PA were studied. Cranial ultrasound was performed at or after seven days of life. Neurodevelopment assessment of the subjects were done at 3, 6, 9 and 12 months of life using Development Quotient (DQ). Variables were analysed by student’s t-test and categorical variables were analysed by Fisher’s-exact probability test using graph pad software. Results: Out of 50 infants of PA, 29 had an abnormal ultrasound scan and 21 had normal ultrasound scan. A 16/29 patients had abnormal outcome along with abnormal ultrasound scan while rest of the 13 had normal outcome. The mean DQ of the neonates having abnormal ultra sonographic examination was significantly lower as compared to those with normal examination. A 6 out of 21 neonates had abnormal outcome inspite of having normal ultrasound scan. Cranial ultrasound has a specificity=55%, sensitivity=73%, Positive Predictive Value (PPV)=58% and Negative Predictive Value (NPV)=71% in predicting neurodevelopment outcome of patients with birth asphyxia. Conclusion: Cranial Utrasonography (USG) findings in PA babies reveal a strong association with the development severity.
围产期窒息(PA)导致通气气体交换受损,或缺血导致氧水平持续下降(低氧血症)和二氧化碳水平增加(高碳血症)。它发生在围产期期间,可导致早期新生儿死亡和发病率。目的:评估早期颅脑超声变化对PA患儿预后的预测作用。材料和方法:本前瞻性队列研究于2018年7月至2019年10月在印度北方邦贾西马哈拉尼拉克西米白医学院的三级护理新生儿病房进行。对50例PA新生儿进行了研究。在出生后7天或7天后进行颅脑超声检查。分别在3、6、9和12个月时使用发育商数(DQ)对受试者进行神经发育评估。变量分析采用学生t检验,分类变量分析采用Fisher精确概率检验,采用图形pad软件。结果:50例PA患儿超声扫描异常29例,正常21例。29例患者中有16例超声检查结果异常,其余13例结果正常。超声检查异常新生儿的平均DQ明显低于正常新生儿。21例新生儿中有6例在超声检查正常的情况下出现异常。颅超声预测新生儿窒息患者神经发育结局的特异性为55%,敏感性为73%,阳性预测值(Positive Predictive Value, PPV)为58%,阴性预测值(Negative Predictive Value)为71%。结论:PA婴儿的颅超声(USG)结果显示与发育严重程度密切相关。
{"title":"Early Cranial Ultrasound Changes as Predictors of Outcome during First Year of Life in Infants with Perinatal Asphyxia- A Prospective Cohort Study","authors":"S. Agrawal, .. Ravanagomagan, Sethi Rohith Shamsher, Chaurasiya Rachna","doi":"10.7860/ijnmr/2023/60764.2373","DOIUrl":"https://doi.org/10.7860/ijnmr/2023/60764.2373","url":null,"abstract":"Introduction: Perinatal Asphyxia (PA) causes impaired exchange of ventilatory gases, or ischemia that leads to persistent decrease in oxygen levels (hypoxemia) and increase in carbon dioxide levels (hypercarbia). It occurs during the peripartum period can contribute to early neonatal mortality and morbidity. Aim: To assess the role of early changes in cranial ultrasound a predictor of outcome in babes with PA. Materials and Methods: This prospective cohort study was conducted in a tertiary care neonatal unit in Maharani Laxmi Bai Medical College, Jhansi, Uttar Pradesh, India, from July 2018 to October 2019. A total of 50 neonates with PA were studied. Cranial ultrasound was performed at or after seven days of life. Neurodevelopment assessment of the subjects were done at 3, 6, 9 and 12 months of life using Development Quotient (DQ). Variables were analysed by student’s t-test and categorical variables were analysed by Fisher’s-exact probability test using graph pad software. Results: Out of 50 infants of PA, 29 had an abnormal ultrasound scan and 21 had normal ultrasound scan. A 16/29 patients had abnormal outcome along with abnormal ultrasound scan while rest of the 13 had normal outcome. The mean DQ of the neonates having abnormal ultra sonographic examination was significantly lower as compared to those with normal examination. A 6 out of 21 neonates had abnormal outcome inspite of having normal ultrasound scan. Cranial ultrasound has a specificity=55%, sensitivity=73%, Positive Predictive Value (PPV)=58% and Negative Predictive Value (NPV)=71% in predicting neurodevelopment outcome of patients with birth asphyxia. Conclusion: Cranial Utrasonography (USG) findings in PA babies reveal a strong association with the development severity.","PeriodicalId":31116,"journal":{"name":"Indian Journal of Neonatal Medicine and Research","volume":"843 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"71267438","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: 0
A Study on Incidence, Pattern of Clinical Features, Laboratory Abnormalities and Outcome of Neonatal Polycythaemia in a Tertiary Care Hospital, Odisha, India 印度奥里萨邦一家三级医院新生儿红细胞增多症的发病率、临床特征、实验室异常和结局的研究
Pub Date : 2023-01-01 DOI: 10.7860/ijnmr/2023/58137.2367
S. Panda, Simanta Das, D. Behera, Sanaga Meghna, Suchismit Mahapatra, Nibedita Pradhan
Introduction: Neonatal polycythaemia is a commonly encountered morbidity and mortality among neonates admitted to neonatal care units and sick newborn care units. Most affected infants have no clinical symptoms and signs, but neonates may present with lethargy, poor feeding, plethora, cyanosis and jaundice within 12-72 hrs. Aim: To find out the incidence and clinical manifestations of neonatal polycythaemia along with detection of disease by laboratory abnormalities. Materials and Methods: This was a hospital-based, prospective, observational study conducted in the Neonatal Care Unit of Sriram Chandra Bhanja Medical College, Eastern Odisha, India, in 1760 neonates, from October 2018 to September 2020. All neonates admitted through Outdoor and Emergency were included in this study irrespective of gestation, birth weight, maturity and mode of delivery with haematocrit >65% at 12 hours of life. These polycythaemic babies were further categorised on the basis of maturity, gestational age, birth weight, gender and the clinical features, laboratory abnormalities were noted, Partial Exchange Transfusion (PET) when required was done through central route, the umbilical venous catheter was used for withdrawing blood while same amount of normal saline was replaced through a peripheral vein, and in asymptomatic cases additional fluid of 20 mL/kg was added to the daily fluid requirements either through enteral or parenteral route and outcomes were noted. Short-term outcome at 48 hours was measured by decreasing haematocrit with improvement of signs and symptoms. Chi-square test was employed to analyse the collected data using Statistical Package for the Social Sciences (SPSS) software version 20.0. The p-value <0.05 was considered statistically significant. Results: Out of 1760 newborns enrolled, (n=75) were polycythaemic. The Incidence of polycythaemia was 4.26%), which was significantly higher among Small for Gestational Age (SGA) compared to Large for Gestational Age (LGA) neonates (p-value=0.0214). Clinical features in decreasing order were lethargy (66.6%), poor feeding (66.6%), Plethora (53.3%), cyanosis (40%) and jaundice (33.3%). Main laboratory abnormalities were hypoglycaemia (36%), hyperbilirubinaemia (28%), thrombocytopenia (22.66%) and hypocalcaemia (13.3%). Out of 75 polycythemic neonates, n=17 (22.67%) underwent PET and rest 58 (77.33%) neonates were treated with extra fluid of 20 mL/kg/day. Conclusion: Study showed that lethargy and poor feeding were the main presentation and hypoglycaemia as the major laboratory abnormality. The incidence of polycythaemia was high among SGA neonates and the response to partial exchange transfusion as well as extra fluid was good which was characterised by decreasing haematocrit values with improvement of signs and symptoms.
新生儿红细胞增多症是一种常见的发病率和死亡率的新生儿入院新生儿护理单位和生病的新生儿护理单位。大多数受影响的婴儿没有临床症状和体征,但新生儿可在12-72小时内出现嗜睡、喂养不良、过多、发绀和黄疸。目的:了解新生儿红细胞增多症的发病率、临床表现及实验室检查结果。材料和方法:这是一项以医院为基础的前瞻性观察性研究,于2018年10月至2020年9月在印度东奥里萨邦Sriram Chandra Bhanja医学院新生儿监护室进行,研究对象为1760名新生儿。所有通过户外和急诊入院的新生儿都被纳入本研究,无论其妊娠、出生体重、成熟度和分娩方式如何,12小时时红细胞压积为65%。这些红细胞增多症患儿根据成熟度、胎龄、出生体重、性别和临床特征进一步分类,注意实验室异常,必要时通过中心路径进行部分交换输血(PET),使用脐静脉导管抽血,同时通过外周静脉更换等量生理盐水。在无症状的病例中,通过肠内或肠外途径在每日所需液体中添加20毫升/公斤的液体,并记录结果。48小时的短期结果是通过降低红细胞压积和改善体征和症状来衡量的。采用社会科学统计软件包(SPSS) 20.0版软件对收集到的数据进行卡方检验。p值<0.05认为有统计学意义。结果:入组的1760例新生儿中,有75例出现红细胞增多症。多红细胞血症的发生率为4.26%,小胎龄儿(SGA)明显高于大胎龄儿(LGA) (p值=0.0214)。临床表现由大到小依次为嗜睡(66.6%)、进食不良(66.6%)、过多(53.3%)、发绀(40%)、黄疸(33.3%)。主要实验室异常为低血糖(36%)、高胆红素血症(28%)、血小板减少症(22.66%)和低钙血症(13.3%)。在75例红细胞增多症新生儿中,17例(22.67%)接受了PET治疗,其余58例(77.33%)接受了20 mL/kg/天的额外液体治疗。结论:嗜睡和摄食不良是主要表现,低血糖是主要的实验室异常。多红细胞血症在SGA新生儿中发病率很高,对部分交换输血和额外液体的反应良好,其特征是红细胞压积值降低,体征和症状改善。
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引用次数: 0
Effect of Haemoglobin and Iron Status of the Antenatal Mothers on their Newborns at Birth: A Cross-sectional Study 产前母亲血红蛋白和铁状态对新生儿出生时的影响:一项横断面研究
Pub Date : 2022-01-01 DOI: 10.7860/ijnmr/2022/57853.2360
Hemachitra Jagannathan, Arunkumar Ramachandran, V. Subramanian, Aravind Shanmugam, K. Rajendran
Introduction: Iron deficiency (ID) anaemia in pregnant mothers can affect the iron reserves of their newborns and lead to anaemia later. The haematological indices and iron status of pregnant women and its correlation with their neonates is still unclear. Aim: To assess the correlation between maternal and cord blood Hb and iron status. Materials and Methods: The present cross-sectional study included 134 antenatal mothers, at term gestation without any significant antenatal complications. Complete haemogram, serum iron, ferritin, and iron binding capacity were assessed for these mothers before delivery and also from the cord blood samples of their newborns at birth. Statistical difference and correlation were observed using Chi-square test and Pearson’s correlation coefficient. Results: Maternal anaemia Hb <11 gm/dL) was observed in 62 (46.3%). The mean Hb and ferritin of the mothers were 11.06±1.02 gm/dL and 113.3±7.1 μg/L, respectively. The mean Hb and ferritin levels of the cord blood samples were 12.24±0.17 gm/dL and 214.3±20.1 μg/L, respectively. In univariate analysis, maternal Hb showed a significant correlation with cord blood Hb with Odds Ratio (OR) 0.508 and 95% Confidence Interval (CI): 0.428-0.603. The Pearson’s correlation showed a moderate correlation between mother and cord blood Packed Cell Volume (PCV) (r=0.344, p<0.001) and weak correlation between other maternal and cord blood iron indices and serum ferritin (r=0.191, p=0.027 and r=0.203, p=0.019). Conclusion: There is a significant correlation between maternal and cord blood Hb in term neonates. The study indicates that the haematological indices of pregnant women determine the neonatal Hb in term babies.
孕妇缺铁性贫血会影响其新生儿的铁储备,并导致后来的贫血。孕妇血液学指标和铁状态及其与新生儿的相关性尚不清楚。目的:探讨母血和脐带血Hb与铁状态的相关性。材料与方法:本横断面研究包括134名未发生明显产前并发症的足月孕妇。在分娩前对这些母亲的全血图、血清铁、铁蛋白和铁结合能力进行了评估,并对新生儿出生时的脐带血样本进行了评估。采用卡方检验和Pearson相关系数进行统计学差异和相关性分析。结果:产妇贫血Hb <11 gm/dL 62例(46.3%)。母鼠Hb和铁蛋白的平均值分别为11.06±1.02 gm/dL和113.3±7.1 μg/L。脐带血Hb和铁蛋白的平均水平分别为12.24±0.17 gm/dL和214.3±20.1 μg/L。在单因素分析中,母体Hb与脐带血Hb显著相关,优势比(OR)为0.508,95%可信区间(CI)为0.428-0.603。Pearson相关分析显示,母体与脐带血包膜细胞体积(PCV)呈正相关(r=0.344, p<0.001),其他母体与脐带血铁指标与血清铁蛋白呈弱相关(r=0.191, p=0.027, r=0.203, p=0.019)。结论:足月新生儿母血Hb与脐带血Hb有显著相关性。研究表明,孕妇的血液学指标决定了足月儿的新生儿Hb。
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引用次数: 0
Spectrum of Congenital Malformations and Associated Factors: A Cross-sectional Study from Eastern India 先天性畸形谱系及其相关因素:来自印度东部的横断面研究
Pub Date : 2022-01-01 DOI: 10.7860/ijnmr/2022/56379.2343
Tarapada. Ghosh, Sumanta Das, M. P. Mohanta, B. K. Khuntdar
Introduction: Congenital malformations are important contributors for neonatal and infant mortality after prematurity, intrapartum complications and infections. Aim: To find out the prevalence and pattern of congenital malformations among the live born neonates in study area as well as to identify the associated risk factors. Materials and Methods: This descriptive hospital based cross- sectional study was carried out in 305 cases at Midnapore Medical College, Medinipur, West Bengal, from July 2016 to June 2017. All live inborn neonates were assessed for the presence of any malformation(s). The still born or out born babies were excluded. Congenital malformations were diagnosed by clinical examination as well as imaging studies. Data regarding risk factors were collected from the history and the case records. Chi-square test was done to find out the significance of the risk factors. Results: During the study period, there were 14240 live births, out of which 305 cases of congenital malformations were noted. Prevalence of congenital malformations was 214.1 per 10,000 live births or 2.14%. Out of 305 cases, 165 (54.10%) were males, 137 (44.92%) were females, and 3 (0.98%) had ambiguous genitalia. Prevalence of malformations was not significantly different between primi and multipara mothers, and for the different socio-economic backgrounds. A higher prevalence of congenital malformations in mothers above 30 years, consanguinity, low birth weight and prematurity were observed. History of abortion and still birth were associated with higher prevalence. Polyhydramnios, pregnancy induced hypertension and previous abortion and still birth were also associated with higher prevalence of malformations. Musculoskeletal system was majorly involved in 92 (30.16%) cases, followed by central nervous system 48 (15.74%). Conclusion: Prevalence of congenital malformations was found to be 214.1 per 10,000 live births or 2.14%. Maternal age >30, consanguinity, prematurity and low birth weight were associated with increased prevalence of congenital malformations. Musculoskeletal system was the most commonly involved system.
简介:先天性畸形是早产、产时并发症和感染后新生儿和婴儿死亡的重要原因。目的:了解研究区活产新生儿先天性畸形的患病率、类型及相关危险因素。材料与方法:本描述性医院横断面研究于2016年7月至2017年6月在西孟加拉邦梅迪尼普尔米德纳波尔医学院进行。所有活产新生儿均被评估是否存在任何畸形。死胎和外胎的婴儿被排除在外。通过临床检查和影像学检查诊断先天性畸形。从病史和病例记录中收集有关危险因素的数据。进行卡方检验,分析危险因素的显著性。结果:研究期间共出生14240例,其中先天性畸形305例。先天性畸形患病率为214.1 / 10,000活产,占2.14%。305例患者中,男性165例(54.10%),女性137例(44.92%),生殖器模糊3例(0.98%)。在不同的社会经济背景下,一胎母亲和多胎母亲的畸形发生率无显著差异。在30岁以上的母亲中,先天性畸形、近亲、低出生体重和早产的发生率较高。流产和死产史与较高的患病率相关。羊水过多、妊高征、流产和死产也与畸形发生率较高有关。以肌肉骨骼系统为主92例(30.16%),其次为中枢神经系统48例(15.74%)。结论:先天性畸形患病率为214.1 / 10000,占2.14%。产妇年龄在30岁至30岁之间、近亲、早产和低出生体重与先天性畸形的患病率增加有关。肌肉骨骼系统是最常见的系统。
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引用次数: 1
Diagnostic Accuracy of Platelet Indices as a Marker for Sepsis in Neonates: A Case-control Study 血小板指标作为新生儿脓毒症标志物的诊断准确性:一项病例对照研究
Pub Date : 2022-01-01 DOI: 10.7860/ijnmr/2022/53542.2341
Daasara Gururaju, Navya N. Parameshwarappa, A. H. Rao, Manjunath Rangappa
Introduction: Diagnosis of sepsis in neonates is challenging due to overlapping of signs and symptoms. Currently blood culture and sepsis screen are used for diagnosis. Blood culture is the gold standard but its usefulness is limited due to low positivity, delay in reporting. Sepsis screen has variable sensitivity and specificity. To overcome these limitations, platelet indices can be used in diagnosis. Aim: To assess platelet indices as a marker to diagnose neonatal sepsis and to calculate sensitivity and specificity of platelet indices in comparison to clinical symptoms, sepsis screen and blood culture. Materials and Methods: This case-control study was conducted from June 2021 to November 2021 in Neonatal Intensive Care Unit (NICU) of tertiary care centre, Karnataka, India. Total of 198 neonates with signs and symptoms of sepsis and/or risk factors of sepsis were included. Weight and gestational age matched 198 healthy neonates served as control. Investigations include blood culture, sepsis screen and platelet indices were sent. Platelet indices were compared between cases and controls. Sensitivity and specificity of platelet indices were calculated in culture positive, screen positive and both negative groups. Data of both the groups were compared using Independent t-test and Chi-square test. Results: Demographic profile was homogenous between both study groups. Out of 198 cases, 145 (73.2%) had platelet count <1.5 lakhs, 132 (66.7%) had Mean Platelet Volume (MPV) >10.8 fl and 109 (55.05%) had Platelet Distribution Width (PDW) >19.1 fl. These values were statistically significant (p-value<0.001) when compared with controls. Statistically significant (p-value <0.001) difference was seen in mean of platelet count (1.3±0.7 lakhs/ cumm), MPV (10.7±0.8 fl), PDW (19.1±2.3 fl) and Plateletcrit (PCT) (0.1±0.1) between cases and controls. Platelet count was more sensitive (73.2%) and specific (81.3%) marker when compared between cases and controls. Conclusion: Platelet indices are cheaper and widely available markers in diagnosing neonatal sepsis. Thrombocytopenia, high MPV and high PDW were associated with neonatal sepsis.
新生儿败血症的诊断是具有挑战性的,由于重叠的体征和症状。目前诊断主要采用血培养和脓毒症筛查。血培养是金标准,但由于阳性率低,报告延迟,其用途有限。脓毒症筛查具有不同的敏感性和特异性。为了克服这些局限性,血小板指数可用于诊断。目的:探讨血小板指标对新生儿脓毒症的诊断价值,并比较血小板指标与临床症状、脓毒症筛查及血培养指标的敏感性和特异性。材料和方法:本病例对照研究于2021年6月至2021年11月在印度卡纳塔克邦三级保健中心的新生儿重症监护病房(NICU)进行。共纳入198例有脓毒症症状和/或脓毒症危险因素的新生儿。体重和胎龄匹配198例健康新生儿作为对照。调查包括血培养、脓毒症筛查和血小板指数。比较两组患者的血小板指数。计算培养阳性组、筛选阳性组和双阴性组血小板指标的敏感性和特异性。两组资料比较采用独立t检验和卡方检验。结果:两个研究组的人口统计学特征是相同的。198例患者中,145例(73.2%)血小板计数10.8 fl, 109例(55.05%)血小板分布宽度(PDW) bb0 19.1 fl,与对照组比较,差异均有统计学意义(p值<0.001)。两组患者血小板计数(1.3±0.7 lakhs/ cumm)、MPV(10.7±0.8 fl)、PDW(19.1±2.3 fl)、血小板电积(PCT)(0.1±0.1)差异有统计学意义(p值<0.001)。与对照组相比,血小板计数更敏感(73.2%)和特异性(81.3%)。结论:血小板指标是诊断新生儿脓毒症的一种较为廉价、应用广泛的指标。血小板减少症、高MPV和高PDW与新生儿脓毒症有关。
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Indian Journal of Neonatal Medicine and Research
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