The recent progress in cardiac pacing increased the usefulness of artificial pacemakers. The initial purpose of avoiding Stokes-Adams attacks, was changed by a complex way to completely give back the physiologic response of cardiac rate and atrioventricular synchronism. However, this process forced the patients to take care of their pacemakers, and to spend more time in follow-up procedures. Additionally, the pacemakers became more vulnerable to environmental and hospital interferences. Basic rules, for all patients, are described in this paper, in order to improve their quality of life. Follow-up procedures are related in detail. It is described how programmed electronic evaluations can contribute to avoid complications, to detect subclinic problems and to improve the patient's haemodynamics and physical capacity. It shows also how to use complementary examinations, like thoracic X-rays, exercise testing and Holter monitoring to optimize the cardiac pacing system. Interferences in pacemakers are focused with special attention to myo-potentials, environmental electromagnetic fields, and damage to system owing to medical procedures, like therapeutic radiation, defibrillation and electrocauterization. The approach to infective processes in pacemakers gives special emphasis to prevention of direct surgical contamination, erosion of the skin, and haematogenic dissemination of distant infective focus.
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Cureus
December 2024
Medical Affairs, Zydus Lifesciences, Ahmedabad, IND.
Background Human epidermal growth factor receptor 2 (HER2)-positive breast cancer is a highly aggressive subtype characterized by a high recurrence rate. Trastuzumab emtansine (T-DM1), an antibody-drug conjugate targeting HER2, has shown improved outcomes; however, its effectiveness in cases with brain metastases remains unclear. The T-DM1 biosimilar has emerged as a cost-effective treatment option.
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December 2024
Internal Medicine, Centro Hospitalar de Trás-os-Montes e Alto Douro, Vila Real, PRT.
Autoimmune polyglandular syndromes (APS) are characterized by associations of two or more autoimmune diseases (AID). APS type 3 is characterized by the presence of autoimmune thyroid disease associated with other AID, excluding adrenal gland involvement. Here we report a case of a 64-year-old male, with history of type 1 diabetes mellitus (T1DM), diagnosed at the age of 32, who was referred to a Diabetes consultation in 2014 due to poor metabolic control.
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December 2024
General Practice, Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo, São Paulo, BRA.
Felty's syndrome (FS) is a rare and complex condition most commonly seen as a complication of longstanding rheumatoid arthritis (RA), characterized by a triad of RA, splenomegaly, and neutropenia. Diagnosing FS can be challenging due to its diverse clinical presentations and overlap with other hematologic and autoimmune conditions. We report a 47-year-old male with a history of severe anemia, recurrent blood transfusions, and a chronic leg ulcer.
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December 2024
General Surgery, Florida State University College of Medicine, Pensacola, USA.
Glucagon-like peptide-1 (GLP-1) receptor agonists, including tirzepatide (Mounjaro), are widely used to manage type 2 diabetes mellitus (T2DM) and obesity. While gastrointestinal side effects are common, acute pancreatitis remains a rare but significant complication. Limited evidence exists on the risks associated with switching between GLP-1 agonists, emphasizing the need for clinical awareness.
View Article and Find Full Text PDFClin Kidney J
January 2025
Department of Nephrology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Peking Union Medical College and Chinese Academy, Beijing, China.
Nucleoporins, as major components of nuclear pore complex, have been recently discovered to participate in organ development. Here, we report a young female patient with nephrotic proteinuria resistant to immune suppressant treatment and congenital ovarian insufficiency. Renal pathology confirmed focal segmental glomerulosclerosis and whole-exome sequencing revealed compound heterozygous mutations in Nucleoporin 160 (), NM_015231.
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