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http://dx.doi.org/10.1056/nejm198309293091318 | DOI Listing |
Ren Fail
December 2024
Department of Cardiology, Rambam Health Care Campus and the Rappaport Faculty of Medicine, Technion - Israel Institute of Technology, Haifa, Israel.
Hemodialysis patients are susceptible to excess volume accumulation, particularly over the 2-day interval (long interdialytic gap), resulting in higher interdialytic weight gain (IDWG). We thought to determine whether a novel device designed to enhance fluid and salt loss by activating the eccrine sweat glands can mitigate IDWG. Patients eligible for the study were undergoing regular hemodialysis for ≥3 months, without residual renal function, and with IDWG (as a percentage of IDWG/dry body weight) ≥2.
View Article and Find Full Text PDFJ Am Assoc Nurse Pract
September 2024
Cystic Fibrosis Foundation, Bethesda, Maryland, Bethesda, MD.
Cystic fibrosis (CF) is a complex life-limiting genetic condition that affects the respiratory, digestive, reproductive system, and sweat glands. Advances in treatment have led to improved survival and quality of life. Today, most persons with CF live to adulthood but require highly specialized care at accredited CF Care Centers.
View Article and Find Full Text PDFArch Pathol Lab Med
September 2024
From the the Departments of Dermatopathology (de Almeida Verdolin, Pantaleão), Dermatology (El Kadi, Reis Gavazzoni Dias), and Statistics (Raggio Luiz), Fluminense Federal University, Rio de Janeiro, Brazil.
Context.—: Clinical, dermoscopic, and histologic diagnostic criteria may overlap in cases with scarring and nonscarring alopecia, making diagnosis difficult for clinicians and pathologists. New histopathologic discoveries indicate that the cutaneous adnexal structural and homeostatic unit made up of the pilosebaceous unit, eccrine sweat gland coils (ESGCs), and dermal white adipose tissue may have a role in hair follicle renewal.
View Article and Find Full Text PDFCureus
September 2023
Pediatric Department, Barzilai University Medical Center, Ashqelon, ISR.
Cystic fibrosis (CF) is a multiorgan disease, caused by autosomal recessive (AR) mutations in the cystic fibrosis transmembrane regulator (CFTR) acting primarily as a chloride channel. CF is most commonly diagnosed in Caucasian populations. Common clinical presentations in pediatric patients include chronic cough, respiratory tract infections such as pneumonia, digestive symptoms, and stunted growth, and malnutrition due to gastrointestinal malabsorption and pancreatic insufficiency.
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