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1

Simonsen, K. A., A. L. Anderson-Berry, S. F. Delair, and H. D. Davies. "Early-Onset Neonatal Sepsis." Clinical Microbiology Reviews 27, no. 1 (2014): 21–47. http://dx.doi.org/10.1128/cmr.00031-13.

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2

Chiesa, Claudio, Lucia Pacifico, John F. Osborn, Enea Bonci, Nora Hofer, and Bernhard Resch. "Early-Onset Neonatal Sepsis." Medicine 94, no. 30 (2015): e1230. http://dx.doi.org/10.1097/md.0000000000001230.

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3

Gohil, Jayendra R. "Early onset neonatal sepsis." Indian Journal of Pediatrics 73, no. 3 (2006): 251. http://dx.doi.org/10.1007/bf02825497.

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4

Flannery, Dustin D., and Karen M. Puopolo. "Neonatal Early-Onset Sepsis." NeoReviews 23, no. 11 (2022): 756–70. http://dx.doi.org/10.1542/neo.23-10-e756.

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Early-onset sepsis (EOS) is a significant cause of morbidity and mortality among newborn infants, particularly among those born premature. The epidemiology of EOS is changing over time. Here, we highlight the most contemporary data informing the epidemiology of neonatal EOS, including incidence, microbiology, risk factors, and associated outcomes, with a focus on infants born in high-income countries during their birth hospitalization. We discuss approaches to risk assessment for EOS, summarizing national guidelines and comparing key differences between approaches for term and preterm infants.
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5

Chandra, Dr Rohitha S. "Early Onset Neonatal Sepsis in a Tertiary Care Centre." Journal of Medical Science And clinical Research 05, no. 02 (2017): 17614–19. http://dx.doi.org/10.18535/jmscr/v5i2.68.

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6

Bhambri, Dr Mohit, Dr Pankaj Bansal, and Dr Gurmeet Kaur. "Neonatal Peripheral Gangrene: An Unusual Presentation of Early Onset Neonatal Sepsis (Eons)." Indian Journal of Applied Research 3, no. 10 (2011): 1. http://dx.doi.org/10.15373/2249555x/oct2013/105.

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7

Jyoti, Ranjan Behera, Ranjan Mallick Manas, Kumar Jena Sanjaya, Prajna Paramita Bhanja Sonali, and Mallick Bijayalaxmi. "Aetiological Profile of Early and Late Onset Neonatal Sepsis." International Journal of Pharmaceutical and Clinical Research 15, no. 10 (2023): 1388–93. https://doi.org/10.5281/zenodo.11303697.

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<strong>Introduction:&nbsp;</strong>Neonatal sepsis is defined as a systemic condition of bacterial, viral, or fungal (yeast) origin in newborn infants less than 28 days old that is associated with hemodynamic changes and other clinical manifestations and results in substantial mortality and morbidity. Sepsis continues to be an important cause of neonatal morbidity and mortality.&nbsp; It is a common problem in the newborn intensive care unit (NICU) population particularly in premature neonates. Sepsis is classified as early onset sepsis (EOS) presents within 72 hrs of life, and late onset sep
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8

Shrestha, Nipun, and Dhruba Shrestha. "Salmonella Sepsis presenting as Early Onset Neonatal Sepsis." Journal of Nepal Paediatric Society 38, no. 1 (2018): 53–55. http://dx.doi.org/10.3126/jnps.v38i1.20052.

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Neonatal sepsis is one of the feared cause of neonatal death in both term and preterm infants, leading up to 30% of neonatal death in developing countries. Salmonella sepsis is one of the uncommon causes of early onset neonatal sepsis. Here we present a case of early onset neonatal sepsis due to Salmonella species. Baby was delivered vaginally with good Apgar score. Within few hours of birth, baby developed respiratory distress and was admitted with empirical antibiotics. The blood culture showed the growth of Salmonella species. Child was treated with IV antibiotics and responded well to it a
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Jarovsky, Daniel, Ivan Cese Marchetti, Mariana Alves da Silva Mori, et al. "Early-onset Neonatal Pneumococcal Sepsis." Pediatric Infectious Disease Journal 37, no. 4 (2018): e111-e112. http://dx.doi.org/10.1097/inf.0000000000001818.

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10

Bharad, Dr Rahul V. "Risk Factors and Immediate Outcome of Early Onset Neonatal Sepsis." Journal of Medical Science And clinical Research 05, no. 04 (2017): 21050–56. http://dx.doi.org/10.18535/jmscr/v5i4.207.

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11

Teacoe, Dumitru Alin, Ioana Andrada Radu, and Maria Livia Ognean. "Early-onset neonatal sepsis diagnosis – still a challenge after 30 years - Part 1." Newborn Research & Reviews 2, no. 2 (2024): 83–91. http://dx.doi.org/10.37897/newborn.2024.2.7.

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Despite all the advances in diagnosis and treatment, early-onset neonatal sepsis remains a serious and potentially life-threatening condition, with increased morbidity and mortality. The authors review the persistent controversies and challenges surrounding the definitions of neonatal sepsis, neonatal early- and late-onset sepsis, clinical signs and risk factors, and different approaches for identifying neonates at risk for early-onset sepsis. The impact of neonatal early-onset sepsis on short- and long-term outcomes is also resumed.
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12

Almurabet, Fathia A., and Kheria O. Almamori. "Shewanella Algae Meningitis and Early Onset Neonatal Sepsis." Libyan Journal of Medical Research 14, no. 1 (2020): 84–92. http://dx.doi.org/10.54361/ljmr.v14i1.09.

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Neonatal sepsis still a main leading cause of morbidity and mortality among neonates, especially in the developing countries ,Most cases of Neonatal sepsis in neonatal intensive care unit are attributed to GB streptococcus, klebsiellapneumonia and other members of Enterobacteriaceae family.Shewanella algae (S.algae)is a gram –negative saprophytic bacillus, commonly associated with the marine environment,which has been isolated from humans.Early onset neonatal sepsis caused by S.algae is uncommon.Wereporta first case of Shewanella. Algaemeningitis in newborn with early onset neonatal sepsis whi
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13

Almurabet, Fathia A., and Kheria O. Almamori. "Shewanella algae meningitis and early onset neonatal sepsis." Libyan Journal of Medical Research 14, no. 2 (2020): 61–69. http://dx.doi.org/10.54361/ljmr.v14i2.06.

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Neonatal sepsis still a main leading cause of morbidity and mortality among neonates, especially in the developing countries, Most cases of Neonatal sepsis in neonatal intensive care unit are attributed to GB streptococcus, klebsiella pneumonia and other members of Enterobacteriaceae family. Shewanella algae (S.algae) is a gram –negative saprophytic bacillus, commonly associated with the marine environment ,which has been isolated from humans. Early onset neonatal sepsis caused by S.algae is uncommon. We report a first case of Shewanella. Algae meningitis in newborn with early onset neonatal s
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14

Kumar, Ashwani, Gursharan Singh Narang, Gurmeet Singh, Navneet Virk, and Ashiana Singh. "Clinico-epidemiological spectrum of early onset neonatal sepsis in neonates admitted in NICU of a tertiary care institute." International Journal of Contemporary Pediatrics 6, no. 3 (2019): 1046. http://dx.doi.org/10.18203/2349-3291.ijcp20191071.

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Background: Neonatal sepsis is a clinical syndrome characterized by signs and symptoms of infection with or without accompanying bacteremia in the first month of life. Neonatal sepsis may be classified into two groups : early onset sepsis and late onset sepsis . Early onset neonatal sepsis is generally associated with the acquisition of microorganisms from the mother and usually presents with respiratory distress and pneumonia.Methods: The study included one hundred term neonates with early onset neonatal sepsis. A septic screen including total leukocyte count, absolute neutrophil count, blood
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15

Puopolo, K. M. "Epidemiology of Neonatal Early-onset Sepsis." NeoReviews 9, no. 12 (2008): e571-e579. http://dx.doi.org/10.1542/neo.9-12-e571.

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16

McAdams, Ryan M., Sanjuanita Garza-Cox, and Bradley A. Yoder. "Early-onset neonatal pneumococcal sepsis syndrome." Pediatric Critical Care Medicine 6, no. 5 (2005): 595–97. http://dx.doi.org/10.1097/01.pcc.0000163677.58249.77.

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17

Ilboudo, C. M., and M. A. Jackson. "Early Onset Neonatal Sepsis and Meningitis." Journal of the Pediatric Infectious Diseases Society 3, no. 4 (2014): 354–57. http://dx.doi.org/10.1093/jpids/piu003.

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18

Divya, Dr Buthu, Dr S. Narasimha Rao, Dr Kundan Gorikapudi, and Dr Manisha Dr. Manisha. "Early Onset Neonatal Sepsis with Premature Rupture of Membranes in Preterm Neonates." Scholars Journal of Applied Medical Sciences 10, no. 12 (2022): 2451–54. http://dx.doi.org/10.36347/sjams.2022.v10i12.063.

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Objectives: To determine the frequency of early onset neonatal sepsis with premature rupture of membranes in preterm babies in a tertiary care hospital. Materials and Methods: Neonates of singleton pregnancies complicated by premature rupture of membranes with delivery occurring between 30 and 36 weeks gestation were included in the study. The frequency of neonatal sepsis was assessed based on clinical and laboratory parameters. Incidence of sepsis in relation to gestational age and duration of rupture of membranes was studied. Results: Out of 60 babies, 38(63%) were female and 22(37%) were ma
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19

Jahan, Nasim, Zabrul SM Haque, Md Abdul Mannan, et al. "Patient characteristics, Bacteriological profile & outcome of Neonatal Sepsis: A Hospital Based Study." Community Based Medical Journal 2, no. 1 (2013): 49–54. http://dx.doi.org/10.3329/cbmj.v2i1.14184.

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Neonatal sepsis is a major cause of mortality and morbidity in newborn. The spectrum of bacteria which causes neonatal sepsis varies in different parts of the world. The organisms responsible for early onset and late onset sepsis are different. The objective of the study was undertaken to determine the pattern of bacterial isolates responsible for early and late onset neonatal sepsis. A prospective descriptive study over the period of one year was conducted at the Department of Neonatal Intensive care unit of Ad-din Women’s Medical College and Hospital, Dhaka, Bangladesh.Organisms were isolate
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20

Yadav, Pratibha, and Shailendra Kumar Yadav. "Progress in Diagnosis and Treatment of Neonatal Sepsis: A Review Article." Journal of Nepal Medical Association 60, no. 247 (2022): 318–24. http://dx.doi.org/10.31729/jnma.7324.

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Neonatal sepsis is a serious condition in which the pathogens infiltrate the bloodstream, multiply and produce toxins causing deleterious effects to the health of neonates. It is divided into two types on the basis of the time of onset. Early onset sepsis occurs within 72 hours of birth and late onset sepsis begins after 72 hours of delivery. Neonatal sepsis continues to be a common and significant health care burden, especially in very low birth weight infants (with birthweight less than 1500 grams). Though intrapartum antibiotic prophylaxis has decreased the incidence of early-onset group B
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21

Qadir, Ehsan, Syed Awais Ul Hassan Shah, Zeeshan Ahmed, Nauman Naseer, Zohaib Akhtar, and Farah Shahid. "Comparison of Derangement of Cerebrospinal Fluid Markers in Neonates with Early and Late-Onset Sepsis." Pakistan Armed Forces Medical Journal 73, no. 5 (2023): 1407–10. http://dx.doi.org/10.51253/pafmj.v73i5.9175.

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Objective: To compare derangement of cerebrospinal fluid markers in neonates with early and late-onset sepsis managed at the Neonatal Intensive Care Unit. Study Design: Comparative cross-sectional study. Setting and Duration of Study: Neonatology Department, Pak Emirates Military Hospital, Rawalpindi Pakistan, from Jul 2021 to Jun 2022. Methodology: This study was conducted on neonates managed at our Neonatal Intensive Care Unit for late or early-onset sepsis. A consultant neonatologist diagnosed neonatal sepsis based on clinical and laboratory findings. The cerebrospinal fluid routine examina
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22

Deaneva, Almira Muthia, Rustam Siregar, and Sri Martuti. "Delta Neutrophil Index and C-Reactive Protein as Predictors of Mortality in Early Onset Neonatal Sepsis at Dr. Moewardi Hospital." Journal of Maternal and Child Health 9, no. 2 (2024): 217–27. http://dx.doi.org/10.26911/thejmch.2024.09.02.08.

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Background: Neonatal sepsis is an infection disease in newborns that still be a major problem in developing countries such as Indonesia. Early onset sepsis has higher mortality and morbidity. A simple and applicable biomarkers are needed to predict mortality in early onset neonatal sepsis. This study aimed to investigate whether Delta Neutrophil Index (DNI) and C-Reactive Protein (CRP) can be used as predictors of mortality in early onset neonatal sepsis. Subjects and Method: A cohort study that was conducted at neonatal HCU and NICU at Dr. Moewardi Hospital from March to June 2023. Total of 3
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23

Meliton-Ruiz, Anne Melva, and Robert Dennis Garcia. "Outcome of Current Antibiotic Regimens used for Neonatal Sepsis in a Tertiary Hospital." Pediatric Infectious Disease Society of the Philippines Journal 19, no. 2 (2018): 51–59. http://dx.doi.org/10.56964/pidspj20181902007.

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Objective: This paper looked into the outcome of currently used antibiotic regimens for neonatal sepsis in a tertiary hospital. Methods: This retrospective study reviewed all cases of culture positive neonatal sepsis delivered in a tertiary hospital between January 1, 2000 to December 31, 2015. Demographic profile, stratification as to early-onset and late-onset sepsis, clinical manifestations, culture and antimicrobial susceptibility results, and outcomes were analyzed. Results: There were 28 cases of culture positive neonatal sepsis reported during the study period, and prematurity and low b
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24

Rompis, Johnny Lambert, Rocky Wilar, Johnny Lambert Rompis, Gregory Joey, Raynald Octavianus Takumansang, and Hesti Lestari. "Platelet-to-lymphocyte ratio in early onset neonatal." Paediatrica Indonesiana 63, no. 3 (2023): 202–7. http://dx.doi.org/10.14238/pi63.3.2023.202-7.

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Objectives Neonatal sepsis is a major contributor to morbidity and mortality worldwide. Although blood culture is the gold standard of sepsis diagnosis, it often lacks sensitivity and diagnostic speed. Platelet-to-lymphocyte ratio (PLR) is a widely available, effective, simple, and affordable marker that can predict early onset neonatal sepsis (EONS).&#x0D; Objective To assess the correlation between PLR and EONS as well as the diagnostic value of PLR for predicting EONS.&#x0D; Methods This study included all inpatient neonates with suspected early-onset neonatal sepsis at Dr. R. D. Kandou Hos
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25

Edwin, Dias*1 Sandhra Nair2. "A Comprehensive Review of Diagnosis and Management of Neonatal Sepsis: Focus on Newer Antibiotic Drugs." International Journal of Pharmaceutical Sciences 3, no. 1 (2025): 859–80. https://doi.org/10.5281/zenodo.14632344.

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Sepsis is a leading cause of mortality in neonatal foals, and recent advancements have been achieved in comprehending the underlying pathophysiology. Early diagnosis and treatment aimed at supporting vital functions and neutralizing the effects of the causative organisms are crucial for achieving a successful outcome. Newborns infected with multi-drug-resistant (MDR) pathogens, which have restricted treatment alternatives, may get advantages from innovative antimicrobials. This review offers a comprehensive examination of the incidence, diagnosis, treatments, and management utilizing novel ant
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26

Priti, Chowdhary, Ranjan Ritesh, and Pandey Anita. "Diagnostic role of interleukin-6 and quantitative C-reactive protein in suspected early onset neonatal sepsis." World Journal of Advanced Research and Reviews 8, no. 1 (2020): 263–70. https://doi.org/10.5281/zenodo.4318115.

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Introduction: Neonatal sepsis is a major cause of morbidity and mortality most remarkable in the third world nations. Early diagnosis and subsequent therapy for the infected infants may play a vital role in lowering such mortality and morbidity rates. Aim: To study the clinical profile of neonatal sepsis in a tertiary care hospital and to correlate the findings with quantitative C-reactive protein (CRP) and Interleukin-6 (IL-6). Settings and Design: A total of 296 neonates admitted in neonatal intensive care unit (NICU) with clinical signs and symptoms suggestive of sepsis were studied. Based
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27

Ogundare, Ezra, Akinyemi Akintayo, Theophilus Aladekomo, Lateef Adeyemi, Tinuade Ogunlesi, and Oyeku Oyelami. "Presentation and outcomes of early and late onset neonatal sepsis in a Nigerian Hospital." African Health Sciences 19, no. 3 (2019): 2390–99. http://dx.doi.org/10.4314/ahs.v19i3.12.

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Background: Neonatal Sepsis remains a major cause of morbidity and mortality in neonates despite great advances in antimicrobial therapy and life support measures.Objectives: To compare the aetiology, risk factors, presentation and outcomes of care between early onset neonatal sepsis (EOS) and late onset neonatal sepsis (LOS).Methods: Bacterial isolates were identified using blood cultures and antibiotic susceptibility testing was done using disc diffusion method. The risk factors, clinical presentation, laboratory findings and neonatal outcomes of the babies with EOS were compared with LOS. S
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28

Ashraf, Muhammad Nadeem, Muhammad Zia ul Haq, Muhammad Waseem Ashraf, Rabia Sajjad, and Farooq Ahmed. "EARLY ONSET NEONATAL SEPSIS IN PRETERM PREMATURE RUPTURE OF MEMBRANES." Pakistan Armed Forces Medical Journal 65, no. 2 (2015): 226–30. http://dx.doi.org/10.51253/pafmj.v65i2.821.

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Objective: To determine the frequency of early onset neonatal sepsis in newborn with various duration of preterm premature rupture of membranes (PPROM).&#x0D; Study Design: Cross sectional study.&#x0D; Place and Duration of Study: Neonatal Intensive Care Unit Combined Military Hospital, Lahore from November 2009 to November 2010.&#x0D; Material and Methods: Neonates of singleton pregnancies complicated by preterm premature rupture of the membranes (PPROM) with delivery between 30 and 36 weeks gestation were included in the study. The overall frequency of neonatal sepsis was calculated on clini
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29

Ozdemir, Abdurrahman, and Yusuf Elgormus. "Value of Resistin in Early Onset Neonatal Sepsis." Journal of Child Science 07, no. 01 (2017): e146-e150. http://dx.doi.org/10.1055/s-0037-1608713.

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AbstractThe diagnosis of neonatal sepsis is usually difficult because the sign and symptoms are nonspecific. Although C-reactive protein (CRP) and procalcitonin (PCT) are the most commonly used auxiliary tests, they are not reliable enough markers to be used for diagnosis of neonatal sepsis. This study aimed to evaluate the efficacy of resistin in diagnosing early onset neonatal sepsis and to compare its effectiveness to CRP and PCT. This prospective study was performed in the neonatal intensive care unit of Medicine Hospital between June and September 2016. Twenty-nine infants in the sepsis g
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30

Om, Shankar Chaurasiya, Ahmad Tauseef, Chhabra Kawalpreet, Nath D, and J. Shobhne Hema. "Procalcitonin Level in Neonatal Sepsis." PJSR 10, no. 1 (2017): 29–32. https://doi.org/10.5281/zenodo.8242513.

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A prospective study was conducted in a tertiary care centre from June 2015 to October 2016 to evaluate role of serum procalcitonin (PCT) level in predicting neonatal sepsis and comparison with CRP as a marker of neonatal sepsis. 100 neonates admitted in newborn intensive care unit (NICU) from the study group. These newborns were categorized into proven sepsis, suspected sepsis and control group based on symptoms and signs of infection and blood culture findings. Procalcitonin and CRP level were done for all these newborns. These levels were then statistically compared for all the groups. Out o
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31

HABIB, M. "PROPORTION OF EARLY ONSET SEPSIS IN LOCAL NICU AND IDENTIFICATION OF MATERNAL RISK FACTORS." Biological and Clinical Sciences Research Journal 2024, no. 1 (2024): 1127. http://dx.doi.org/10.54112/bcsrj.v2024i1.1127.

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Early onset neonatal sepsis (EOS) remains a significant cause of morbidity and mortality in neonatal intensive care units (NICUs). Identifying maternal risk factors associated with EOS is crucial for early diagnosis and prevention. Objective: To evaluate the prevalence of early onset sepsis in neonates admitted to the local neonatal intensive care unit (NICU) and identify maternal risk factors associated with neonatal sepsis. Methods: A comparative cross-sectional study was conducted at the Pediatrics Department, Combined Military Hospital Peshawar, from January 2021 to May 2022. One thousand
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32

Tetiana, Klymenko, Tsodikova Olha, and Serdceva. "Modern approaches to diagnosis and treatment of early-onset neonatal sepsis." ScienceRise: Medical Science, no. 4(37) (July 31, 2020): 49–52. https://doi.org/10.15587/2519-4798.2020.209137.

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Early-onset neonatal sepsis (EOS) remains the leading cause of morbidity and mortality, especially among premature babies. Therefore, accurate diagnosis, prompt monitoring of the course of the disease and an effective therapeutic strategy are a guarantee of improving the quality of medical care for newborns, as well as an important reserve for reducing perinatal losses. <strong>The aim of the work</strong>&nbsp;to summarize modern views on the diagnosis and treatment of early-onset neonatal sepsis in newborns with perinatal pathology. <strong>Results and their discussion.</strong>&nbsp;An anal
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WASEEM, RIZWAN, MUHAMMAD KHAN, TAHIRA S. IZHAR, and Abdul Waheed Qureshi. "NEONATAL SEPSIS." Professional Medical Journal 12, no. 04 (2005): 451–56. http://dx.doi.org/10.29309/tpmj/2005.12.04.5099.

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Objective: To find out the bacterial pathogens in neonatal sepsis and todetermine antimicrobial sensitivity patterns of these pathogens. Place and Duration: At the Neonatal Unit of GhurkiTrust Teaching Hospital Lahore, from February 2003 to December 2004. Design: It was an analytical comparativestudy, done in prospective fashion. Subjects and Methods: A total of 100 culture proven neonates of sepsis wereincluded. Clinical data including neonatal and maternal history, physical examination and laboratory data includingblood counts and cultures were recorded. The cases that have already been give
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Agudelo-Pérez, Sergio, A. Melissa Moreno, Juliana Martínez-Garro, et al. "16S rDNA Sequencing for Bacterial Identification in Preterm Infants with Suspected Early-Onset Neonatal Sepsis." Tropical Medicine and Infectious Disease 9, no. 7 (2024): 152. http://dx.doi.org/10.3390/tropicalmed9070152.

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Background: The high prevalence of suspected early-onset neonatal sepsis among preterm infants leads to immediate antibiotic administration upon admission. Notably, most blood cultures for suspected early-onset neonatal sepsis do not yield a causative pathogen. This study aimed to assess polymerase chain reaction (PCR) targeting the variable region V4 of the 16S ribosomal gene (16S rDNA) and Sanger sequencing for bacterial identification in preterm infants with suspected early-onset neonatal sepsis. Methods: Therefore, this prospective study was conducted. Preterm infants with suspected early-
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Mohsan Nadeem Sheikh, M. Sohail Shahzad, Arshad Rafique, et al. "Neonatal sepsis – etiological study at the Central Park teaching Hospital, Lahore." Professional Medical Journal 31, no. 12 (2024): 1657–63. https://doi.org/10.29309/tpmj/2024.31.12.8310.

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Objective: To identify the causative bacteria responsible for early and late onset neonatal sepsis and to determine their antibiotic susceptibilities at Central Park Teaching Hospital. Study Design: Cross-sectional study. Setting: Neonatal Intensive Care Unit (NICU) of Central Park Teaching Hospital, Lahore. Study Period: Jan to June 2024. Methods: Neonates up to 28 days old with clinical features of sepsis were randomly sampled and included in the study. Key maternal and neonatal risk factors were evaluated. Blood cultures were analyzed to identify microbial isolates and assess resistance pat
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Alam, Didarul, Shanjana Islam, Tarun Kumar Roy, Mahmudur Rahman, Md Shahid, and Shahanaj Sharmin. "Study of Bacteriological Profile and Antibiotic Sensitivity of Neonatal Sepsis in a Tertiary Care Hospital." Journal of Chittagong Medical College Teachers' Association 28, no. 2 (2018): 53–58. http://dx.doi.org/10.3329/jcmcta.v28i2.62422.

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Background: Neonatal sepsis is a major cause of mortality and morbidity in newborn. The spectrum of organisms causing sepsis is different in developing countries. Data on the recent trends of organisms causing sepsis are limited. There are many factors that contribute to neonatal sepsis. The organisms responsible for early and late onset sepsis are different. This study was conducted to analyze the organisms responsible for early and late onset neonatal sepsis and to see the sensitivity of drugs. Materials and methods: A prospective hospital based study over the period of one year (January 201
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Younis, Doaa H., Eglal H. Algohary, Eman A. Ahmed, and Hala M. A. Elaal. "A study of leukocyte surface antigen CD64, as a marker of early-onset and late-onset sepsis in preterm and full-term neonates." Scientific Journal of Al-Azhar Medical Faculty, Girls 5, no. 2 (2021): 292–98. http://dx.doi.org/10.4103/sjamf.sjamf_30_21.

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Background Neonatal sepsis is an important cause of morbidity and mortality among newborns. Its diagnosis depends mainly on blood culture that takes at least 48 h to give results. Therefore, searching for biomarkers for early diagnosis is of value. We aimed to assess neutrophil CD64 as an early diagnostic biomarker in early-onset and late-onset neonatal sepsis in full-term and preterm neonates and to compare it with other diagnostic markers, blood culture, and neonatal scores of sepsis. Patients and methods A case–control study was conducted on 60 neonates with clinical sepsis and 30 neonates
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38

Hudon, Rebecca, Vivian Leung, Vivian Leung, Susan Petit, and David Banach. "1167. Hospital Readmissions among Infants Diagnosed with Early-Onset Neonatal Sepsis in Connecticut." Open Forum Infectious Diseases 8, Supplement_1 (2021): S675. http://dx.doi.org/10.1093/ofid/ofab466.1360.

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Abstract Background Early-onset neonatal sepsis, defined as sepsis within 72 hours of birth, results in significant infant morbidity and mortality. Readmissions associated with neonatal sepsis have not previously been well-described. Early-onset neonatal sepsis is a mandatory reportable condition in Connecticut, allowing for expanded data collection through public health surveillance to evaluate readmissions. Methods Infants with early-onset neonatal sepsis born in Connecticut during 2007–2016 were identified from statewide surveillance data and matched with a statewide hospital discharge data
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Raha, Biplob Kumar, Md Abdul Baki, Tahmina Begum, Nazmun Nahar, Nasim Jahan, and Marium Begum. "Clinical, Bacteriological Profile & Outcome of Neonatal Sepsis in a Tertiary Care Hospital." Medicine Today 26, no. 1 (2014): 18–21. http://dx.doi.org/10.3329/medtoday.v26i1.21306.

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Neonatal sepsis is a major cause of mortality and morbidity in newborn, particularly in developing countries. The spectrum of bacteria which causes neonatal sepsis varies in different parts of the world. The organisms responsible for early onset and late onset sepsis are different. The objective of the study was undertaken to determine the pattern of bacterial isolates responsible for early and late onset neonatal sepsis based on the presence of one or more clinical signs, and its outcome. A cross- sectional prospective study was carried out in the special care baby unit (SCABU) from November
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40

Rukmono, Prambudi, Nani Dharmasetiawani, Warsono Warsono, Yan Wirasti, and Eryati Darwin. "Tumor necrosis factor-alpha and interleukin-6 in early-onset neonatal sepsis." Paediatrica Indonesiana 56, no. 1 (2016): 15. http://dx.doi.org/10.14238/pi56.1.2016.15-8.

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Background Neonatal sepsis remains a major cause of mortality and morbidity in newborns. Early-onset neonatal sepsis occurs in infants under the age of 72 hours, while late-onset neonatal sepsis occurs in infants over the age of 72 hours and may be due to nosocomial infection. Diagnosing neonatal sepsis is a challenge, as its clinical symptoms are not clear. Corroborating tests include routine blood, C-reactive protein (CRP), serology, tumor necrosis factor-alpha (TNF-α), and interleukin-6 (IL-6) examinations.Objective To compare the TNF-α and IL-6 levels in patients with proven and unproven e
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41

Aguirre-Quiñonero, Amaia, FelicitasElena Calvo Muro, BlancaLodoso Torrecilla, and AndrésCanut Blasco. "Early-Onset Neonatal Pneumococcal Sepsis and Meningitis." Journal of Clinical Neonatology 8, no. 3 (2019): 183. http://dx.doi.org/10.4103/jcn.jcn_43_19.

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42

Moffett, Sarah M., Hollins L. Kitts, and Stephen J. Henderson. "Medication Therapy for Early-Onset Neonatal Sepsis." AACN Advanced Critical Care 27, no. 3 (2016): 253–58. http://dx.doi.org/10.4037/aacnacc2016503.

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43

Mukhopadhyay, Sagori, and Karen M. Puopolo. "Risk Assessment in Neonatal Early Onset Sepsis." Seminars in Perinatology 36, no. 6 (2012): 408–15. http://dx.doi.org/10.1053/j.semperi.2012.06.002.

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44

Khasawneh, Wasim, and Dawood Yusef. "Ochrobactrum anthropi Fulminant Early-onset Neonatal Sepsis." Pediatric Infectious Disease Journal 36, no. 12 (2017): 1167–68. http://dx.doi.org/10.1097/inf.0000000000001660.

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45

Oh, William. "Early Onset Neonatal Group B Streptococcal Sepsis." American Journal of Perinatology 30, no. 02 (2013): 143–48. http://dx.doi.org/10.1055/s-0032-1332804.

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46

Wright, E. D., J. E. Lortan, and R. M. Perinpanayagam. "Early-onset neonatal pneumococcal sepsis in siblings." Journal of Infection 20, no. 1 (1990): 59–63. http://dx.doi.org/10.1016/s0163-4453(90)92368-u.

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47

Díaz Martín, Cristina, Carmen Luz Marrero Pérez, Lorenzo Martín Fumero, Alejandro Torres Moreno, and Iván de Quirós. "Early-onset Streptococcus pneumoniae-induced neonatal sepsis." Archivos de Bronconeumología (English Edition) 56, no. 10 (2020): 671–72. http://dx.doi.org/10.1016/j.arbr.2020.05.006.

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48

Ganatra, Hammad A., Barbara J. Stoll, and Anita K. M. Zaidi. "International Perspective on Early-Onset Neonatal Sepsis." Clinics in Perinatology 37, no. 2 (2010): 501–23. http://dx.doi.org/10.1016/j.clp.2010.02.004.

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49

El Barbary, Mohammed, Mostafa Mostafa, Walaa Kabiel, and Hebatallah Shaaban. "Serum Melatonin in Early Onset Neonatal Sepsis." Egyptian Journal of Medical Microbiology 32, no. 4 (2023): 77–83. http://dx.doi.org/10.21608/ejmm.2023.321198.

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50

Blatt, S., and M. Schroth. "Neonatal Sepsis: Clinical Considerations." Journal of Child Science 07, no. 01 (2017): e54-e59. http://dx.doi.org/10.1055/s-0037-1603802.

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AbstractUnspecific symptoms and rapid development of sepsis up to septic shock from systemic inflammatory response syndrome (SIRS) are well-known, important issues in neonatology. A common cause is the infection by Streptococcus agalactiae (Group B Streptococcus [GBS]) or Escherichia coli, which contributes significantly to neonatal morbidity and mortality. Whereas early-onset sepsis is normally derived from mother during birth, late-onset sepsis can be transmitted by the environment. Management of neonatal sepsis includes the maintenance of cardiovascular and pulmonary function besides antibi
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