155 results match your criteria: "Clinical Emergency Hospital for Children "Louis Turcanu" Timisoara[Affiliation]"

Background: The plasma level of antipsychotics and their metabolites depends on the activity of the cytochrome P450 (CYP) system in the liver. This research aims to test the individual response variability to atypical antipsychotic drugs, depending on the activity of the CYP2D6 enzyme.

Methods: In a prospective, noninterventional study, we included 56 adolescents, 51.

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Genetic Characterization of Dilated Cardiomyopathy in Romanian Adult Patients.

Int J Mol Sci

February 2024

Department of Microscopic Morphology, Genetics Discipline, Center of Genomic Medicine, University of Medicine and Pharmacy "Victor Babeș" Timișoara, 2 Piaţa Eftimie Murgu Street, 300041 Timişoara, Romania.

Article Synopsis
  • Dilated cardiomyopathy (DCM) is a serious heart condition linked to genetic factors, increasing the risk of heart failure and sudden cardiac death; genetic testing plays a crucial role in managing and understanding the disease.
  • A study of 122 Romanian patients with DCM revealed that over half (50.8%) had identifiable genetic variants that could cause the disease, along with 31 new variants that had not been reported before.
  • The findings indicate that more than half of the patients had a family history of DCM or sudden cardiac death, underscoring the importance of genetic testing for better risk assessment and treatment strategies in this population.
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Background: There is limited data on the organisation of paediatric echocardiography laboratories in Europe.

Methods: A structured and approved questionnaire was circulated across all 95 Association for European Paediatric and Congenital Cardiology affiliated centres. The aims were to evaluate: (1) facilities in paediatric echocardiography laboratories across Europe, (2) accredited laboratories, (3) medical/paramedical staff employed, (4) time for echocardiographic studies and reporting, and (5) training, teaching, quality improvement, and research programs.

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Cystic echinococcosis (CE) is a cosmopolitan parasitic disease caused by We aimed to assess the epidemiological aspects of the disease in hospitalized children from Western Romania, a well-known endemic area for CE. We retrospectively investigated the medical records of children hospitalized between 1998 and 2022. A total of 144 patients were included, and 58.

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Hypertrophic cardiomyopathy (HCM) is a heterogeneous genetic disorder, most often caused by sarcomeric gene mutations, with a small proportion due to variants in non-sarcomeric loci. Phospholamban (PLN) is a phosphoprotein associated with the cardiac sarcoplasmic reticulum, a major determinant of cardiac contractility and relaxation. We conducted a retrospective study to determine the prevalence, phenotypical spectrum and clinical course of patients carrying the p.

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Pediatric chronic kidney disease (CKD) has a substantial global impact because is associated with notable morbidity. Secondary hyperparathyroidism (SPHT) frequently emerges as a complication in the early stages of renal insufficiency, it is an adaptive response to uphold mineral balance. It is a component of the chronic kidney disease-mineral and bone disorder (CKD-MBD).

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Objectives: This study aimed to determine the status of training of adult congenital heart disease (ACHD) cardiologists in Europe.

Methods: A questionnaire was sent to ACHD cardiologists from 34 European countries.

Results: Representatives from 31 of 34 countries (91%) responded.

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Neonatal diffuse cutaneous mastocytosis (NDCM) is defined as the infiltration of the epidermis by a clonal proliferation of mast cells, observed at birth, without initial signs of systemic involvement. The typical driver mutation is in the gene. We report a rare case of a boy, born at term, already presenting at birth with generalized subcutaneous nodules on the face, scalp, trunk, back, hands, and feet.

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Diabetic ketoacidosis (DKA), a common onset modality of type 1 diabetes mellitus (T1DM), can lead, in rare instances, to the development of cerebral edema, which is the leading cause of mortality in T1DM. Aside from the identification of several demographic and clinical risk factors for cerebral edema, attention has also been drawn to the possible link between systemic inflammation and neuroinflammation. This single-center retrospective study of 98 children with severe DKA aimed to investigate the possible relationship between neutrophil-to-lymphocyte ratio NLR) levels and the presence of cerebral edema.

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Background: Endobronchial squamous cell carcinoma is one of the most common types of tumors located inside the tracheobronchial tree. Patients often present in advanced stages of the disease, which most often leads to a targeted therapeutic attitude of pneumonectomy. Practicing lung parenchyma-preserving surgery led us to undertake this review.

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Chronic Diarrhea Caused by Vasoactive Intestinal Peptide-Secreting Tumor.

Life (Basel)

September 2023

First Pediatric Clinic, Disturbances of Growth and Development on Children Research Center, "Victor Babeș" University of Medicine and Pharmacy, 300041 Timișoara, Romania.

Article Synopsis
  • * In children, VIPomas are less common and often linked to neurogenic tumors located in the retroperitoneum or mediastinum, rather than the pancreas.
  • * A case study of an infant with chronic diarrhea revealed a VIPoma in the retroperitoneum, diagnosed through imaging, leading to successful tumor removal and normalization of both diarrhea and electrolyte levels, confirming the tumor as ganglioneuroblastoma through further tests.
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Large Intron Inversions in Romanian Patients with Hemophilia A-First Report.

Medicina (Kaunas)

October 2023

Department of Hematology and Bone Marrow Transplant, Fundeni Clinical Institute, 022328 Bucharest, Romania.

Article Synopsis
  • Large intron inversions are a major genetic cause of severe hemophilia A, accounting for nearly 50% of cases worldwide, particularly in Romanian patients.
  • In a study of 156 Romanian patients, intron 22 inversions were found in 41.7%, while intron 1 inversions were found in 3.2%, leading to a total of 44.9% with large intron inversions as the genetic defect.
  • The research also indicates that patients with intron 1 inversion have a higher risk of developing inhibitors compared to those without any detected inversions.
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Phenotype of Idiopathic Infantile Hypercalcemia Associated with the Heterozygous Pathogenic Variant of and .

Children (Basel)

October 2023

Department XI of Pediatrics-1st Pediatric Discipline, Center for Research on Growth and Developmental Disorders in Children, 'Victor Babeș' University of Medicine and Pharmacy Timișoara, Eftimie Murgu Sq. No. 2, 300041 Timișoara, Romania.

Idiopathic infantile hypercalcemia (IIH) is a rare genetic disease, also called hypersensitivity to vitamin D3. The molecular heterogeneity allows for the differentiation between the two forms; IIH type 1 caused by genetic variants and IIH type 2 associated with mutations. The affected individuals express a variety of symptoms: hypercalcemia, hypercalciuria, suppressed intact parathormone levels (PTH), nephrocalcinosis, elevated levels of serum 1,25 (OH)2-vitamin D3 or inappropriately normal levels, and kidney phosphate wasting.

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Sepsis represents one of the leading causes of death in newborns and infants, and prompt diagnosis is essential for achieving favorable outcomes. Regarding malnourished children with concurrent infection, most studies have focused, besides blood culture, on C-reactive protein and procalcitonin. Because malnutrition has a deleterious effect on cellular immune competence, the present study characterized the acute-phase response, including hematological indices, in response to sepsis.

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The impact of theory of mind, stress and professional experience on empathy in Romanian community nurses-a cross-sectional study.

BMC Nurs

October 2023

Department of Microscopic Morphology Genetics Discipline, Center of Genomic Medicine, Regional Center of Medical Genetics Timis, "Victor Babes" University of Medicine and Pharmacy Timisoara, 2 Eftimie Murgu Sqr, 300041, Timisoara, Romania.

Background: High empathy levels in health professionals represent an important factor in patient satisfaction and compliance, reducing patient anxiety and pain, enhancing diagnostic and clinical results and strengthening patient empowerment. Our purpose was to determine empathy level and to identify which of the socioeconomic status (SES) and psychological factors were able to predict highest empathy levels in a Romanian sample of community nurses.

Methods: Community nurses were invited in January-February 2023 to provide an answer to an online survey, using an advertisement in a professional network.

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Kinetic estimation of glomerular filtration rate (KeGFR) has proved its utility in predicting acute kidney injury (AKI) in both adults and children. Our objective is to assess the clinical utility of KeGFR in predicting AKI severity and progression to acute kidney disease (AKD) in patients already diagnosed with AKI and to examine major adverse kidney events at 30 days (MAKE30). We retrospectively calculated the KeGFR within the first 24 h of identified AKI (KeGFR) and in the 24 h prior to AKD (KeGFR) in all admitted children under 18 years old.

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We conducted a retrospective multicentre study to investigate the association between acute pancreatitis, COVID-19, and pleural effusion. The study involved a total of 433 patients. Among them, 405 patients did not have COVID-19 infection, while 28 patients had both acute pancreatitis and COVID-19.

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COVID-19 has significantly impacted the whole world, and Romania was no exception. Biomarkers play a crucial role in understanding and managing the disease. However, research regarding laboratory analyses for patients with COVID-19 is fairly limited.

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Speckle tracking-echocardiography (STE) is a novel non-invasive imaging tool capable of quantifying myocardial deformation, and thus holds promise in detecting early subclinical myocardial injury. This study aimed to evaluate the correlation of STE with traditional biomarkers in predicting anthracycline-induced cardiotoxicity in the context of varying dosages and treatment protocols in pediatric hemato-oncology patients. We conducted a retrospective study involving pediatric hemato-oncology patients undergoing anthracycline-based chemotherapy.

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Article Synopsis
  • Pediatric patients receiving anthracycline therapy for cancer are at risk for heart damage, with the study investigating how cancer type and treatment impact cardiac function.
  • Advanced echocardiographic techniques like STE, GLS, and MPI may reveal early signs of heart issues that traditional methods miss.
  • Results showed significant differences in heart function measurements between patients and controls, indicating poorer cardiac health in patients, with the combination of GLS, SMOD, and MPI being particularly effective in predicting cardiotoxicity risk.
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Article Synopsis
  • The study investigates primary nonresponse status (PNRS) and secondary nonresponse status (SNRS) in rheumatoid arthritis (RA) patients across different age and sex groups, highlighting the challenges in defining these conditions and their effects on patient quality of life.
  • 115 RA patients were analyzed, focusing on factors like age, body mass index (BMI), and the type and duration of therapy to understand their association with PNRS and SNRS.
  • Results showed that age, sex, and BMI significantly impact the development of PNRS and SNRS, with specific therapies affecting different demographics in distinct ways.
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The aim of this study is to evaluate the test results of neonates delivered by COVID-19-positive mothers during pregnancy with those of neonates born to unvaccinated mothers who are COVID-19-free. A cohort study was conducted on 367 pregnant women who gave birth at Premiere Hospital, Timisoara, Romania, between May 2021 and February 2022. Two groups were established: Group 1, with 167 pregnant women infected with COVID-19, and Group 2, with 200 pregnant women who were not affected by COVID-19 during pregnancy.

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Childhood respiratory tract infections (RTIs) pose a significant health burden, especially in children under six years old. The main objective of this systematic review was to assess the effectiveness of vitamin D supplementation in the prevention of RTI in this population while also exploring potential effect modifiers such as age, baseline vitamin D status, and type of respiratory infection. A systematic review of the literature published up to February 2023 was conducted according to PRISMA guidelines, searching PubMed, Web of Science, Cochrane, and Scopus databases.

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Background: Breast cancer (BC) stroma has CD34- and αSMA-positive cancer-associated fibroblasts (CAFs) differently distributed. During malignant transformation, CD34-positive fibroblasts decrease while αSMA-positive CAFs increase. The prevalence of αSMA-positive CAFs in BC stroma makes microscopic examination difficult without digital image analysis processing (DIA).

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Background: While communication plays an important role in medicine, it also often represents a challenge when the topic at hand is the prognosis of a high-risk condition. When it comes to pediatric oncology, the challenge becomes even greater for physicians who have to adapt their discourse to both the child and their family.

Methods: Following the PRISMA guidelines, an advanced search on PubMed, Scopus and the Cochrane Library was performed, from 1 January 2017 to 31 October 2022.

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