Urinary tract infection
1. What is a urinary tract infection (UTI)? UTI is the presence of microorganisms in the urine or tissues of the normally sterile genitourinary tract. Infection may be localized to…
1. What is a urinary tract infection (UTI)? UTI is the presence of microorganisms in the urine or tissues of the normally sterile genitourinary tract. Infection may be localized to…
Technical aspects of hemodialysis 1. What are the components used during a hemodialysis procedure? The components needed to conduct dialysis include a dialysis machine, a method to access the patient’s…
1. What is the incidence of end-stage kidney disease (ESKD) in african americans? African Americans represent about 13% of the United States population but account for more than one-third of…
1. What is the prevalence of chronic kidney disease in the elderly? Approximately 11% of patients older than age 65 years are noted to have chronic kidney disease (CKD) as…
1. What is the pathophysiology of sickle cell disease (SCD)? Hemolysis, vasoocclusion, and ischemia reperfusion are the clinical hallmarks of SCD. The substitution of glutamate for valine at position 6…
1. What changes take place in the kidney during pregnancy? The kidney undergoes anatomic and physiologic changes during normal pregnancy. The length of the kidney increases by 1 to 1.5…
1. What are cystic diseases of the kidneys? Cystic diseases of the kidney are a heterogeneous group of disorders that can be inherited, developmental, or acquired ( Box 43.1 )….
Acute tubulointerstitial nephritis 1. What is acute tubulointerstitial nephritis? Acute tubulointerstitial nephritis (ATIN) is characterized by inflammation and edema in the kidney tubulointerstitium and can cause acute kidney injury (AKI)….
1. What is familial or inherited hematuria? Familial (inherited) hematuria is defined as a group of genetic kidney disorders that are clinically characterized by the onset of persistent microscopic hematuria…
1. What is Fabry disease? Fabry disease is a systemic, X-linked, lysosomal storage disorder that results from the deficient activity of the enzyme α-galactosidase A (α-Gal A) and the lysosomal…