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https://read.qxmd.com/read/33418166/seizures-in-the-neonate-a-review-of-etiologies-and-outcomes
#21
REVIEW
Francesco Pisani, Carlotta Spagnoli, Raffaele Falsaperla, Lakshmi Nagarajan, Georgia Ramantani
Neonatal seizures occur in their majority in close temporal relation to an acute brain injury or systemic insult, and are accordingly defined as acute symptomatic or provoked seizures. However less frequently, unprovoked seizures may also present in the neonatal period as secondary to structural brain abnormalities, thus corresponding to structural epilepsies, or to genetic conditions, thus corresponding to genetic epilepsies. Unprovoked neonatal seizures should be thus considered as the clinical manifestation of early onset structural or genetic epilepsies that often have the characteristics of early onset epileptic encephalopathies...
February 2021: Seizure: the Journal of the British Epilepsy Association
https://read.qxmd.com/read/32818434/covid-19-and-multisystem-inflammatory-syndrome-in-children-and-adolescents
#22
REVIEW
Li Jiang, Kun Tang, Mike Levin, Omar Irfan, Shaun K Morris, Karen Wilson, Jonathan D Klein, Zulfiqar A Bhutta
As severe acute respiratory syndrome coronavirus 2 continues to spread worldwide, there have been increasing reports from Europe, North America, Asia, and Latin America describing children and adolescents with COVID-19-associated multisystem inflammatory conditions. However, the association between multisystem inflammatory syndrome in children and COVID-19 is still unknown. We review the epidemiology, causes, clinical features, and current treatment protocols for multisystem inflammatory syndrome in children and adolescents associated with COVID-19...
November 2020: Lancet Infectious Diseases
https://read.qxmd.com/read/33194923/hypertensive-crisis-in-pediatric-patients-an-overview
#23
REVIEW
Rupesh Raina, Zubin Mahajan, Aditya Sharma, Ronith Chakraborty, Sarisha Mahajan, Sidharth K Sethi, Gaurav Kapur, David Kaelber
Hypertensive crisis can be a source of morbidity and mortality in the pediatric population. While the epidemiology has been difficult to pinpoint, it is well-known that secondary causes of pediatric hypertension contribute to a greater incidence of hypertensive crisis in pediatrics. Hypertensive crisis may manifest with non-specific symptoms as well as distinct and acute symptoms in the presence of end-organ damage. Hypertensive emergency, the form of hypertensive crisis with end-organ damage, may present with more severe symptoms and lead to permanent organ damage...
2020: Frontiers in Pediatrics
https://read.qxmd.com/read/33250515/practical-approaches-to-sedation-and-analgesia-in-the-newborn
#24
REVIEW
Christopher McPherson, Cynthia M Ortinau, Zachary Vesoulis
The prevention, assessment, and treatment of neonatal pain and agitation continues to challenge clinicians and researchers. Substantial progress has been made in the past three decades, but numerous outstanding questions remain. In this setting, clinicians must establish safe and compassionate standardized practices that consider available efficacy data, long-term outcomes, and research gaps. Novel approaches with limited data must be carefully considered against historic standards of care with robust data suggesting limited benefit and clear adverse effects...
March 2021: Journal of Perinatology: Official Journal of the California Perinatal Association
https://read.qxmd.com/read/33386343/identification-and-management-of-eating-disorders-in-children-and-adolescents
#25
REVIEW
Laurie L Hornberger, Margo A Lane
Eating disorders are serious, potentially life-threatening illnesses afflicting individuals through the life span, with a particular impact on both the physical and psychological development of children and adolescents. Because care for children and adolescents with eating disorders can be complex and resources for the treatment of eating disorders are often limited, pediatricians may be called on to not only provide medical supervision for their patients with diagnosed eating disorders but also coordinate care and advocate for appropriate services...
January 2021: Pediatrics
https://read.qxmd.com/read/33139410/hair-loss
#26
JOURNAL ARTICLE
Reese L Imhof, Dawn Marie R Davis, Megha M Tollefson
No abstract text is available yet for this article.
November 2020: Pediatrics in Review
https://read.qxmd.com/read/32382828/ipna-clinical-practice-recommendations-for-the-diagnosis-and-management-of-children-with-steroid-resistant-nephrotic-syndrome
#27
REVIEW
Agnes Trautmann, Marina Vivarelli, Susan Samuel, Debbie Gipson, Aditi Sinha, Franz Schaefer, Ng Kar Hui, Olivia Boyer, Moin A Saleem, Luciana Feltran, Janina Müller-Deile, Jan Ulrich Becker, Francisco Cano, Hong Xu, Yam Ngo Lim, William Smoyer, Ifeoma Anochie, Koichi Nakanishi, Elisabeth Hodson, Dieter Haffner
Idiopathic nephrotic syndrome newly affects 1-3 per 100,000 children per year. Approximately 85% of cases show complete remission of proteinuria following glucocorticoid treatment. Patients who do not achieve complete remission within 4-6 weeks of glucocorticoid treatment have steroid-resistant nephrotic syndrome (SRNS). In 10-30% of steroid-resistant patients, mutations in podocyte-associated genes can be detected, whereas an undefined circulating factor of immune origin is assumed in the remaining ones...
August 2020: Pediatric Nephrology
https://read.qxmd.com/read/33194904/overgrowth-syndromes-evaluation-diagnosis-and-management
#28
REVIEW
Joshua Manor, Seema R Lalani
Abnormally excessive growth results from perturbation of a complex interplay of genetic, epigenetic, and hormonal factors that orchestrate human growth. Overgrowth syndromes generally present with inherent health concerns and, in some instances, an increased risk of tumor predisposition that necessitate prompt diagnosis and appropriate referral. In this review, we introduce some of the more common overgrowth syndromes, along with their molecular mechanisms, diagnostics, and medical complications for improved recognition and management of patients affected with these disorders...
2020: Frontiers in Pediatrics
https://read.qxmd.com/read/33160639/clinical-management-of-hyperkalemia
#29
REVIEW
Biff F Palmer, Juan Jesus Carrero, Deborah J Clegg, Gates B Colbert, Michael Emmett, Steven Fishbane, Debra J Hain, Edgar Lerma, Macaulay Onuigbo, Anjay Rastogi, Simon D Roger, Bruce S Spinowitz, Matthew R Weir
Hyperkalemia is an electrolyte abnormality with potentially life-threatening consequences. Despite various guidelines, no universally accepted consensus exists on best practices for hyperkalemia monitoring, with variations in precise potassium (K+ ) concentration thresholds or for the management of acute or chronic hyperkalemia. Based on the available evidence, this review identifies several critical issues and unmet needs with regard to the management of hyperkalemia. Real-world studies are needed for a better understanding of the prevalence of hyperkalemia outside the clinical trial setting...
November 4, 2020: Mayo Clinic Proceedings
https://read.qxmd.com/read/33262177/why-is-covid-19-less-severe-in-children-a-review-of-the-proposed-mechanisms-underlying-the-age-related-difference-in-severity-of-sars-cov-2-infections
#30
REVIEW
Petra Zimmermann, Nigel Curtis
In contrast to other respiratory viruses, children have less severe symptoms when infected with the novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). In this review, we discuss proposed hypotheses for the age-related difference in severity of coronavirus disease 2019 (COVID-19).Factors proposed to explain the difference in severity of COVID-19 in children and adults include those that put adults at higher risk and those that protect children. The former include: (1) age-related increase in endothelial damage and changes in clotting function; (2) higher density, increased affinity and different distribution of angiotensin converting enzyme 2 receptors and transmembrane serine protease 2; (3) pre-existing coronavirus antibodies (including antibody-dependent enhancement) and T cells; (4) immunosenescence and inflammaging, including the effects of chronic cytomegalovirus infection; (5) a higher prevalence of comorbidities associated with severe COVID-19 and (6) lower levels of vitamin D...
December 1, 2020: Archives of Disease in Childhood
https://read.qxmd.com/read/33150968/diagnostic-approach-to-paediatric-movement-disorders-a-clinical-practice-guide
#31
JOURNAL ARTICLE
Rick Brandsma, Martje E van Egmond, Marina A J Tijssen
Paediatric movement disorders (PMDs) comprise a large group of disorders (tics, myoclonus, tremor, dystonia, chorea, Parkinsonism, ataxia), often with mixed phenotypes. Determination of the underlying aetiology can be difficult given the broad differential diagnosis and the complexity of the genotype-phenotype relationships. This can make the diagnostic process time-consuming and difficult. In this overview, we present a diagnostic approach for PMDs, with emphasis on genetic causes. This approach can serve as a framework to lead the clinician through the diagnostic process in eight consecutive steps, including recognition of the different movement disorders, identification of a clinical syndrome, consideration of acquired causes, genetic testing including next-generation sequencing, post-sequencing phenotyping, and interpretation of test results...
March 2021: Developmental Medicine and Child Neurology
https://read.qxmd.com/read/33016981/acute-respiratory-distress-syndrome
#32
REVIEW
George W Williams, Nathaniel K Berg, Alexander Reskallah, Xiaoyi Yuan, Holger K Eltzschig
Acute Respiratory Distress Syndrome (ARDS) is defined as the rapid onset of non-cardiogenic pulmonary edema resulting in respiratory failure and hypoxemia. Efforts over the past 25 years, such as those of the ARDS and Prevention and Early Treatment of Acute Lung Injury (PETAL) Networks, have demonstrated a praiseworthy collaboration to further optimize the management of ARDS. However, improvements have been only moderate and ARDS remains a leading cause of mortality in the perioperative and critical care setting...
February 1, 2021: Anesthesiology
https://read.qxmd.com/read/33017828/treatment-of-metabolic-syndrome-in-children
#33
REVIEW
Veronica Maria Tagi, Sona Samvelyan, Francesco Chiarelli
Although metabolic syndrome (MetS) in children and adolescents is a frequently discussed topic in the literature, uniform guidelines on its definition and treatment are still lacking. Insulin resistance, central obesity, dyslipidaemia, and hypertension are commonly considered the main components of MetS. The first recommended approach to all these pathological conditions in children and adolescents is lifestyle intervention (diet and physical exercise); however, in some selected cases, a pharmacological or surgical treatment might prove useful for the prevention of metabolic and cardiovascular complications...
2020: Hormone Research in Pædiatrics
https://read.qxmd.com/read/32788269/a-16-year-old-boy-with-cough-and-fever-in-the-era-of-covid-19
#34
JOURNAL ARTICLE
Kelsey R Anderson, Natalie Villafranco, Lindsay Hatzenbuehler Cameron, Erica K Schallert, Ashley Joshi-Patel, Amy Arrington, Andrea Dean
A 16-year-old white boy with a history of chronic lung disease of prematurity, cough-variant asthma, and incidental lung nodules presented to the emergency center in spring 2020 with acute onset dry cough, shortness of breath, and fever. An initial history, gathered from his mother because of the patient's respiratory distress, revealed no recent travel. However, his mother is a health care worker at a hospital, and sick contacts included ongoing contact with a friend with cold-like symptoms. He had a variety of animals at home, including a dog, cats, fish, rodents, and reptiles...
January 2021: Pediatrics
https://read.qxmd.com/read/33037123/rhabdomyolysis-as-the-initial-presentation-of-sars-cov-2-in-an-adolescent
#35
JOURNAL ARTICLE
Shawnese Gilpin, Michael Byers, Allison Byrd, Jennifer Cull, Danielle Peterson, Bettina Thomas, Phillip Jacobson
The novel coronavirus disease 2019, caused by severe acute respiratory syndrome coronavirus 2, has created a global pandemic, with many cases affecting the elderly. However, children have been affected as well, with ∼2.4% to 3.7% of cases reported. This case is the first published case of an adolescent presenting with rhabdomyolysis as the first sign of novel coronavirus disease 2019, with extremely elevated creatinine kinase levels, approaching almost 400 000 U/L. This case adds to the growing body of literature of a variety of life-threatening manifestations associated with severe acute respiratory syndrome coronavirus 2 infection and highlights the importance of how prompt recognition of these unique presentations of the disease is important to mitigate complications...
March 2021: Pediatrics
https://read.qxmd.com/read/33001296/hepatorenal-syndrome-in-children-a-review
#36
REVIEW
Priscila Menezes Ferri Liu, Sarah Tayná de Carvalho, Pollyanna Faria Fradico, Maria Luiza Barreto Cazumbá, Ramon Gustavo Bernardino Campos, Ana Cristina Simões E Silva
Hepatorenal syndrome (HRS) occurs in patients with cirrhosis or fulminant hepatic failure and is a kind of pre-renal failure due to intense reduction of kidney perfusion induced by severe hepatic injury. While other causes of pre-renal acute kidney injury (AKI) respond to fluid infusion, HRS does not. HRS incidence is 5% in children with chronic liver conditions before liver transplantation. Type 1 HRS is an acute and rapidly progressive form that often develops after a precipitating factor, including gastrointestinal bleeding or spontaneous bacterial peritonitis, while type 2 is considered a slowly progressive form of kidney failure that often occurs spontaneously in chronic ascites settings...
August 2021: Pediatric Nephrology
https://read.qxmd.com/read/32647755/an-overview-of-rickets-in-children
#37
REVIEW
Rahul Chanchlani, Paul Nemer, Rajiv Sinha, Lena Nemer, Vinod Krishnappa, Etienne Sochett, Fayez Safadi, Rupesh Raina
Rickets is a common bone disease worldwide that is associated with disturbances in calcium and phosphate homeostasis and can lead to short stature and joint deformities. Rickets can be diagnosed based on history and physical examination, radiological features, and biochemical tests. It can be classified into 2 major groups based on phosphate or calcium levels: phosphopenic and calcipenic. Knowledge of categorization of the type of rickets is essential for prompt diagnosis and proper management. Nutritional rickets is a preventable disease through adequate intake of vitamin D through both dietary and sunlight exposure...
July 2020: KI Reports
https://read.qxmd.com/read/32847796/fluid-management-during-diabetic-ketoacidosis-in-children-guidelines-consensus-recommendations-and-clinical-judgement
#38
EDITORIAL
Robert Charles Tasker
No abstract text is available yet for this article.
October 2020: Archives of Disease in Childhood
https://read.qxmd.com/read/32660309/covid-19-a-review-for-the-pediatric-neurologist
#39
REVIEW
Alison Christy
Children are susceptible to infection with the novel coronavirus SARS-CoV-2. In this time of uncertainty, this review attempts to compile information that may be helpful to pediatric neurologists. This review consolidates current data on the disease associated with SARS-CoV-2, called COVID-19, and information from past coronavirus epidemics, to discuss diseases of pediatric neurology including Guillain-Barre syndrome (acute inflammatory demyelinating polyradiculoneuropathy); central demyelinating diseases like multiple sclerosis and acute disseminated encephalomyelitis; infantile spasms; febrile seizures; and maternal-fetal transmission of virus...
November 2020: Journal of Child Neurology
https://read.qxmd.com/read/31043448/pediatric-osteoporosis
#40
EDITORIAL
Coral L Steffey
No abstract text is available yet for this article.
May 2019: Pediatrics in Review
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