keyword
https://read.qxmd.com/read/38647881/progress-of-mitochondrial-function-regulation-in-cardiac-regeneration
#1
REVIEW
Yi-Xi Chen, An-Ran Zhao, Tian-Wen Wei, Hao Wang, Lian-Sheng Wang
Heart failure and myocardial infarction, global health concerns, stem from limited cardiac regeneration post-injury. Myocardial infarction, typically caused by coronary artery blockage, leads to cardiac muscle cell damage, progressing to heart failure. Addressing the adult heart's minimal self-repair capability is crucial, highlighting cardiac regeneration research's importance. Studies reveal a metabolic shift from anaerobic glycolysis to oxidative phosphorylation in neonates as a key factor in impaired cardiac regeneration, with mitochondria being central...
April 22, 2024: Journal of Cardiovascular Translational Research
https://read.qxmd.com/read/38647426/congenital-gastric-teratoma-presenting-with-gastrointestinal-bleeding-case-report-and-review-of-literature
#2
JOURNAL ARTICLE
Khadiga M Ali, Gena Abdel-Azeem, Tarik Barakat, Sherine M Elzeiny, Mohammed Albishbishy, Ahmed Megahed
BACKGROUND: Gastric teratoma is an extremely rare tumor, representing <1% of all pediatric teratomas, and commonly manifests as a palpable abdominal mass. Upper gastrointestinal tract bleeding in newborns and infants is rare and is mostly caused by a benign lesion. CASE REPORT: We present a 3-month-old boy who presented with recurrent attacks of hematemesis, vomiting, and melena which on work up revealed a gastric teratoma. DISCUSSION/CONCLUSION: Owing to the unique characteristics and the extreme rarity of this entity, accurate preoperative diagnosis has remained elusive...
April 22, 2024: Fetal and Pediatric Pathology
https://read.qxmd.com/read/38647361/incidence-and-risk-factors-of-neonatal-hypothermia-a-systematic-review-and-meta-analysis
#3
REVIEW
Jing Ruan, Xuemei Zhong, Lijiao Qin, Jiaxuan Mai, Jiaying Chen, Huiyang Ding
AIM: Hypothermia poses a threat to the health and lives of newborns. Therefore, it is essential to identify the factors that influence neonatal hypothermia and provide targeted intervention suggestions for clinical practice to reduce its occurrence. METHODS: We conducted a literature search to identify factors influencing neonatal hypothermia and performed a meta-analysis to determine the prevalence of neonatal hypothermia and its associated factors. The Newcastle-Ottawa Scale (NOS) was used to assess the quality of cohort and case-control studies, while the Agency for Healthcare Research and Quality (AHRQ) was used to evaluate the quality of cross-sectional studies...
April 22, 2024: Acta Paediatrica
https://read.qxmd.com/read/38646578/dairy-calf-transportation-in-the-united-states-challenges-and-strategies-to-improve-animal-welfare
#4
JOURNAL ARTICLE
M C Cramer, J A Pempek, I N Román-Muñiz, L N Edwards-Callaway
The objectives of this symposium review are to summarize relevant research and key welfare issues relative to calf transportation and identify strategies to mitigate welfare challenges. An important animal welfare concern across the US dairy industry is the transportation of preweaning calves from the source dairy to a calf-raising facility (e.g., calf ranches, heifer raising facilities, veal operations), auction, livestock market, or directly to slaughter. Millions of calves are transported annually in the United States and calf transport has garnered increased attention...
May 2024: JDS Commun
https://read.qxmd.com/read/38646248/serendipitous-discovery-a-case-of-twin-congenital-pseudarthrosis-of-the-clavicle-in-saudi-arabia-and-literature-review
#5
Ammar Abed Alqader Okasha, Areeg Kamal Abbas, Mohamad Alsamal, Idris Sula
Congenital pseudarthrosis of the clavicle (CPC) is a rare disorder with an unknown etiology, which is caused by a failure of the clavicle ossification nuclei union process. This is the first CPC twin instance documented in Saudi Arabia, and the fourth overall. In the 33rd week, a set of twins was born prematurely with respiratory distress syndrome. They were both admitted to the neonatal intensive care unit. X-rays of the chest were taken, and the clavicular deformity was discovered. Because the twins were born via a cesarean section, a traumatic clavicular fracture was ruled out...
March 2024: Curēus
https://read.qxmd.com/read/38645668/travelling-numbers-and-broken-loops-a-qualitative-systematic-review-on-collecting-and-reporting-maternal-and-neonatal-health-data-in-low-and-lower-middle-income-countries
#6
REVIEW
Jil Molenaar, Lenka Beňová, Aliki Christou, Isabelle L Lange, Josefien van Olmen
Data and indicator estimates are considered vital to document persisting challenges in maternal and newborn health and track progress towards global goals. However, prioritization of standardised, comparable quantitative data can preclude the collection of locally relevant information and pose overwhelming burdens in low-resource settings, with negative effects on the provision of quality of care. A growing body of qualitative studies aims to provide a place-based understanding of the complex processes and human experiences behind the generation and use of maternal and neonatal health data...
June 2024: SSM—Population Health
https://read.qxmd.com/read/38645225/characteristic-fetal-brain-mri-abnormalities-in-pyruvate-dehydrogenase-complex-deficiency
#7
Olivier Fortin, Kelsey Christoffel, Abdullah Shoaib, Charu Venkatesan, Kate Cilli, Jason W Schroeder, Cesar Alves, Rebecca D Ganetzky, Jamie L Fraser
Pyruvate dehydrogenase complex deficiency (PDCD) is a disorder of mitochondrial metabolism that is caused by pathogenic variants in multiple genes, including PDHA1 . Typical neonatal brain imaging findings in PDCD have been described, with a focus on malformative features and chronic encephaloclastic changes. However, fetal brain MRI imaging in confirmed PDCD has not been comprehensively described. We sought to demonstrate the prenatal neurological and systemic manifestations of PDCD determined by comprehensive fetal imaging and genomic sequencing...
April 10, 2024: medRxiv
https://read.qxmd.com/read/38644454/efgartigimod-as-a-novel-fcrn-inhibitor-for-autoimmune-disease
#8
REVIEW
Yun Yang, Zhengxuan Shen, Fan Shi, Fei Wang, Ning Wen
Immunoglobulin G (IgG) autoantibodies can lead to the formation of autoimmune diseases through Fab and/or Fc-mediated interactions with host molecules as well as activated T cells. The neonatal Fc receptor (FcRn) binds at acidic pH IgG and albumin, and the mechanism for prolonging serum IgG half-life is making IgG re-entry into circulation by prompting it not to be degraded by lysosomes and back to the cell surface. Given the FcRn receptor's essential role in IgG homeostasis, one of the strategies to promote the quick degradation of endogenous IgG is to suppress the function of FcRn, which is beneficial to the treatment of IgG-driven autoimmune disorders like myasthenia gravis (MG), chronic inflammatory demyelinating polyradiculoneuropathy (CIDP), stiff person syndrome, and immune thrombocytopenia (ITP)...
April 22, 2024: Neurological Sciences
https://read.qxmd.com/read/38644208/-cutting-edge-of-diagnosis-and-treatment-for-chronic-inflammatory-demyelinating-polyradiculoneuropathy-cidp-based-on-the-ean-pns-guideline-2021
#9
JOURNAL ARTICLE
Satoshi Kuwabara
Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) is a most common chronic immune-mediated demyelinating neuropathy, and includes a number of clinical subtypes. The major phenotype is "typical CIDP", which is characterized by symmetric polyneuropathy and "proximal and distal" muscle weakness. During the historical changes in the concept of CIDP, multifocal motor neuropathy, anti-myelin-associated glycoprotein (MAG) neuropathy, and autoimmune nodopathy have been excluded. Currently CIDP is considered as a syndrome including typical CIDP and CIDP variant such as distal CIDP and multifocal CIDP...
April 20, 2024: Rinshō Shinkeigaku, Clinical Neurology
https://read.qxmd.com/read/38642570/global-incidence-prevalence-years-lived-with-disability-ylds-disability-adjusted-life-years-dalys-and-healthy-life-expectancy-hale-for-371-diseases-and-injuries-in-204-countries-and-territories-and-811-subnational-locations-1990-2021-a-systematic-analysis-for
#10
JOURNAL ARTICLE
(no author information available yet)
BACKGROUND: Detailed, comprehensive, and timely reporting on population health by underlying causes of disability and premature death is crucial to understanding and responding to complex patterns of disease and injury burden over time and across age groups, sexes, and locations. The availability of disease burden estimates can promote evidence-based interventions that enable public health researchers, policy makers, and other professionals to implement strategies that can mitigate diseases...
April 15, 2024: Lancet
https://read.qxmd.com/read/38641936/oxygenation-saturation-index-in-neonatal-hypoxemic-respiratory-failure
#11
JOURNAL ARTICLE
Shinichiro Tsurukawa, Masashi Zuiki, Yuki Naito, Kazumasa Kitamura, Utsuki Matsumura, Takuyo Kanayama, Eisuke Ichise, Go Horiguchi, Satoshi Teramukai, Hiroshi Komatsu
BACKGROUND: This study aimed to assess the validity of the oxygenation saturation index (OSI) and the ratio of oxygen saturation to the fraction of inspired oxygen (FI O2 ) (S/F ratio) with percutaneous oxygen saturation (OSISpO2 and the Sp /F ratio) and to evaluate the correlation between these values and the oxygen index (OI). It also determined their cut-off values for predicting OI in accordance with neonatal hypoxic respiratory failure severity. METHODS: We reviewed the data of 77 neonates (gestational age 31...
2024: Pediatrics International: Official Journal of the Japan Pediatric Society
https://read.qxmd.com/read/38641832/nr1h4-disease-rapidly-progressing-neonatal-intrahepatic-cholestasis-and-early-death
#12
JOURNAL ARTICLE
Zhong-Die Li, Yu-Chuan Li, Jing-Zhao, Jian-She Wang, Xin-Bao Xie
BACKGROUND: Clinical studies on progressive familial intrahepatic cholestasis (PFIC) type 5 caused by mutations in NR1H4 are limited. METHODS: New patients with biallelic NR1H4 variants from our center and all patients from literature were retrospectively analyzed. RESULTS: Three new patients were identified to be carrying five new variants. Liver phenotypes of our patients manifests as low-γ-glutamyl transferase cholestasis, liver failure and related complications...
April 19, 2024: Orphanet Journal of Rare Diseases
https://read.qxmd.com/read/38641597/comparison-of-safety-and-effectiveness-of-antiretroviral-therapy-regimens-among-pregnant-women-living%C3%A2-with-hiv-at-preconception-or-during-pregnancy-a-systematic-review-and-network-meta-analysis-of-randomized-trials
#13
Fatemeh Mehrabi, Mohammad Karamouzian, Behnam Farhoudi, Shahryar Moradi Falah Langeroodi, Soheil Mehmandoost, Samaneh Abbaszadeh, Shahrzad Motaghi, Ali Mirzazadeh, Behnam Sadeghirad, Hamid Sharifi
BACKGROUND: Mother-to-child transmission is the primary cause of HIV cases among children. Antiretroviral therapy (ART) plays a critical role in preventing mother-to-child transmission and reducing HIV progression, morbidity, and mortality among mothers. However, after more than two decades of ART during pregnancy, the comparative effectiveness and safety of ART medications during pregnancy are unclear, and existing evidence is contradictory. This study aimed to assess the effectiveness and safety of different ART regimens among pregnant women living with HIV at preconception or during pregnancy...
April 19, 2024: BMC Infectious Diseases
https://read.qxmd.com/read/38641466/adolescent-onset-epilepsy-and-deterioration-associated-with-cad-deficiency-a-case-report
#14
Sebastián Silva, Mónica Rosas, Benjamín Guerra, Marión Muñoz, Atsushi Fujita, Masamune Sakamoto, Naomichi Matsumoto
INTRODUCTION: CAD (MIM*114010) encodes a large multifunctional protein with the enzymatic activity of the first three enzymes initiating and controlling the de novo pyrimidine biosynthesis pathway. Biallelic pathogenic variants in CAD cause the autosomal recessive developmental and epileptic encephalopathy 50 (MIM #616457) or CAD deficiency presenting with epilepsy, status epilepticus (SE), neurological deterioration and anemia with anisopoikilocytosis. Mortality is around 9% of patients, mainly related to the no use of its specific treatment with uridine...
April 18, 2024: Brain & Development
https://read.qxmd.com/read/38640988/exposure-to-organophosphate-esters-and-maternal-child-health
#15
REVIEW
Sarvenaz Shahin, Eleanor A Medley, Mrudula Naidu, Leonardo Trasande, Akhgar Ghassabian
Organophosphate esters (OPEs) are a class of chemicals now widely used as flame retardants and plasticizers after the phase-out of polybrominated diphenyl ethers (PBDEs). However, OPEs carry their own risk of developmental toxicity, which poses concern for recent birth cohorts as they have become ubiquitous in the environment. In this review, we summarize the literature evaluating the association between OPE exposure and maternal, perinatal, and child health outcomes. We included original articles investigating associations of OPE exposure with any health outcome on pregnant women, newborns, children, and adolescents...
April 17, 2024: Environmental Research
https://read.qxmd.com/read/38640129/diagnosis-and-management-of-macrosomia-and-shoulder-dystocia-a-comprehensive-review-of-major-guidelines
#16
JOURNAL ARTICLE
Sonia Giouleka, Ioannis Tsakiridis, Elpida Ralli, Apostolos Mamopoulos, Ioannis Kalogiannidis, Apostolos Athanasiadis, Themistoklis Dagklis
IMPORTANCE: Macrosomia represents the most significant risk factor of shoulder dystocia (SD), which is a severe and emergent complication of vaginal delivery. They are both associated with adverse pregnancy outcomes. OBJECTIVE: The aim of this study was to review and compare the most recently published influential guidelines on the diagnosis and management of fetal macrosomia and SD. EVIDENCE ACQUISITION: A comparative review of guidelines from the American College of Obstetricians and Gynecologists (ACOG), the Royal College of Obstetricians and Gynaecologists, the National Institute for Health and Care Excellence, the Royal Australian and New Zealand College of Obstetricians and Gynaecologists (RANZCOG), and the Department for Health and Wellbeing of the Government of South Australia on macrosomia and SD was conducted...
April 2024: Obstetrical & Gynecological Survey
https://read.qxmd.com/read/38639514/effect-of-nutrition-and-behavior-modification-program-nbmp-on-maternal-and-neonatal-outcomes-among-hyperglycemic-mothers
#17
JOURNAL ARTICLE
P Premalatha, H M A Maha, H A Shadia, V Krishnaraju, K Prabahar, N T Mathar Mohideen, V Vinoth Prabhu, B Prema, R M Mashat, E L Sampayan, A E Hala, A A Z Marwa, G Kandasamy, R Ahmed, M A Mervat
OBJECTIVE: Hyperglycemic mothers and their offspring are at increased risk of various maternal and neonatal complications such as macrosomia, future type 2 diabetes, and metabolic abnormalities. Early diagnosis and individualized dietary management, exercise, and emotional well-being are expected to reduce these risks. The study aims to identify the effect of the Nutrition and Behavior Modification Program (NBMP) on maternal and neonatal outcomes of hyperglycemic mothers. PATIENTS AND METHODS: A pre-experimental study was performed among 89 hyperglycemic mothers...
April 2024: European Review for Medical and Pharmacological Sciences
https://read.qxmd.com/read/38639099/cerebral-rsco2-measured-by-near-infrared-spectroscopy-nirs-during-therapeutic-hypothermia-in-neonates-with-hypoxic-ischemic-encephalopathy-a-systematic-review
#18
REVIEW
Sergio Agudelo-Pérez, Gloria Troncoso, Alejandra Roa, Ana Gabriela Ariza, Georgina Doumat, Natalia M Reinoso, Daniel Botero-Rosas
INTRODUCTION: Perinatal asphyxia, a leading cause of neonatal mortality and neurological sequelae, necessitates early detection of pathophysiological neurologic changes during hypoxic-ischaemic encephalopathy (HIE). This study aimed to review published data on rScO2 monitoring during hypothermia treatment in neonates with perinatal asphyxia to predict short- and long-term neurological injury. METHODS: A systematic review was performed using the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) guidelines...
February 1, 2024: Journal of mother and child
https://read.qxmd.com/read/38638590/impact-of-pharmaceutical-validation-on-prescribing-errors-in-a-neonatal-intensive-care-unit-randomised-and-controlled-study
#19
JOURNAL ARTICLE
M D Canales-Siguero, C García-Muñoz, J M Caro-Teller, S Piris-Borregas, S Martín-Aragón, J M Ferrari-Piquero, M T Moral-Pumarega, C R Pallás-Alonso
PURPOSE: To compare the frequency of electronic prescription errors when the prescription was validated by the clinical pharmacist vs. when it was not. METHODS: This prospective randomised controlled study was conducted in three phases. A randomised phase, in which patients were divided into control and intervention groups, and a pre- and post-intervention phase were consecutively performed to analyse the impact of pharmaceutical validation of prescriptions in a neonatal intensive care unit (NICU)...
2024: Frontiers in Pediatrics
https://read.qxmd.com/read/38638587/partnering-early-to-provide-for-infants-at-risk-of-cerebral-palsy-p%C3%A4-pi-arc-protocol-for-a-feasibility-study-of-a-regional-hub-for-early-detection-of-cerebral-palsy-in-aotearoa-new-zealand
#20
JOURNAL ARTICLE
Angelica Allermo Fletcher, Gaela Kilgour, Meghan Sandle, Sally Kidd, Alison Sheppard, Stephanie Swallow, Ngaire Susan Stott, Malcolm Battin, Wyllis Korent, Sian A Williams
INTRODUCTION: Cerebral palsy (CP) can now be diagnosed in infants with identified CP risk factors as early as three months of age; however, many barriers prevent equitable access to early detection pathways. The "Partnering Early to Provide for Infants At Risk of Cerebral Palsy" feasibility study (PĒPI ARC) seeks to trial a new approach to decrease inequitable health service in Aotearoa New Zealand for high-risk infants and their families. PĒPI ARC incorporates face-to-face clinics, an in-person and virtual Hub, and the use of telehealth to enable flexible access to CP assessments and support for health professionals in early CP detection...
2024: Frontiers in Pediatrics
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