ABSTRACT
BACKGROUND: Although tuberculosis (TB) is associated with significant mortality and morbidity, its impact on kidney function is not well understood and is often attributed to anti-TB drugs. We aimed to assess the incidence of acute kidney injury (AKI) in the immediate post-TB diagnosis period in Uganda, a TB/HIV-endemic country in sub-Saharan Africa. METHODS: We included patients enrolled in an observational cohort study of adults diagnosed with drug-susceptible TB followed longitudinally. Adults (≥ 18years) without known kidney disease were enrolled between 8/2022-7/2023 at three regional hospitals serving 12.5% of the Ugandan population. Our primary outcome was incidence of KDIGO-defined AKI within two weeks of TB diagnosis. Other outcomes included predictors of AKI and its association with 30-day survival. RESULTS: A total of 156 adults were included. The median (IQR) age was 39 (28-53) years, most were male (68.6%) and 49.4% had HIV. People with HIV had shorter time to TB diagnosis from symptom onset (21[7-30] days) compared to HIV-negative participants (60[23-90] days), p<0.001. The incidence of AKI was 33.3% (52/156), and was similar between people with and without HIV. Proteinuria or hematuria at enrollment was associated with higher odds of AKI (OR-2.68, 95%CI 1.09-6.70, pâ¼0.033). AKI was associated with significant risk of mortality (aHR-8.22, 95% CI, 1.94-34.72, p â¼0.004) independent of HIV status. CONCLUSION: The overall incidence of AKI in the immediate post-TB diagnosis period is high and associated with increased mortality risk. Our findings suggest monitoring kidney function should be routine for patients with TB, including prior to treatment initiation.
Subject(s)
Kidney Diseases , Humans , Pregnancy , Female , Kidney Diseases/diagnosis , Kidney/pathology , BiopsyABSTRACT
Women pursue pregnancy with comorbidities such as hypertension and kidney disease, necessitating primary care physicians to remain up to date with current clinical practice. Hypertensive disorders of pregnancy pose risks to the pregnancy and to the woman in the short and long term. These risks and their management are detailed in this review. Normally, pregnancy is associated with hemodynamic and kidney-specific changes. Here the authors discuss these changes and review the impact and management of pregnancy-related acute kidney injury, chronic kidney disease, and dialysis in pregnant patients. Kidney transplant recipients may experience return of fertility and require counseling to improve outcomes.
Subject(s)
Acute Kidney Injury , Pregnancy Complications , Renal Insufficiency, Chronic , Pregnancy , Female , Humans , Pregnant Women , Renal Insufficiency, Chronic/complications , Renal Insufficiency, Chronic/epidemiology , Renal Insufficiency, Chronic/therapy , Pregnancy Complications/therapy , Acute Kidney Injury/diagnosis , Acute Kidney Injury/etiology , Acute Kidney Injury/therapySubject(s)
Nephrology , Nephrology/education , Fellowships and Scholarships , Biopsy , Nephrectomy , Kidney/pathologySubject(s)
Delivery of Health Care , Renal Dialysis , Global Health , Health Care Costs , Uganda/epidemiologySubject(s)
Strongyloides stercoralis , Strongyloidiasis , Animals , Feces , Humans , Microscopy , Strongyloidiasis/diagnosis , Strongyloidiasis/drug therapy , UrinalysisABSTRACT
Pigmented urine in a hospitalized patient has a broad differential diagnosis including urinary tract infection or bacterial colonization, hemolysis, rhabdomyolysis, and drugs. We present a case of purple urine in a patient who received methylene blue and hydroxocobalamin for catecholamine-refractory vasodilatory shock. The patient's purple urinary discoloration is presumed to have resulted from a combination of the blue and red pigments of methylene blue and hydroxocobalamin, respectively. As these drugs are increasingly being used to treat vasoplegia in cardiopulmonary bypass, it is important for clinicians to be aware of this benign cause of urine discoloration.
Subject(s)
Hydroxocobalamin/chemistry , Methylene Blue/chemistry , Pigmentation , Urine , Vasoplegia/drug therapy , Cardiopulmonary Bypass/adverse effects , Humans , Hydroxocobalamin/therapeutic use , Male , Methylene Blue/therapeutic use , Middle Aged , Vasoplegia/etiologySubject(s)
Copper/deficiency , Deficiency Diseases/diagnosis , Gait Disorders, Neurologic/etiology , Zinc Sulfate/adverse effects , Zinc/pharmacology , Copper/metabolism , Copper/therapeutic use , Deficiency Diseases/chemically induced , Deficiency Diseases/complications , Humans , Kidney Failure, Chronic/complications , Kidney Failure, Chronic/therapy , Magnetic Resonance Imaging , Middle Aged , Peritoneal Dialysis , Spinal Cord/diagnostic imaging , Zinc Sulfate/therapeutic useABSTRACT
BACKGROUND: Collapsing Glomerulopathy (CG), also known as the collapsing variant of Focal Segmental Glomerulosclerosis (FSGS), is distinct in both its clinical severity and its pathophysiologic characteristics from other forms of FSGS. This lesion occurs disproportionally in patients carrying two APOL1 risk alleles, and is the classic histologic lesion resulting from Human Immunodeficiency Virus (HIV) infection of podocytes. Other viral infections, including parvovirus B19, and drugs such as interferon that perturb the immune system, have also been associated with CG. Despite significant advances, explaining such genetic and immune/infectious associations with causative mechanisms and supporting evidence has proven challenging. CASE PRESENTATION: We report the case of a healthy (HIV-negative) pregnant 36 year-old Caribbean-American woman who presented with nephrotic syndrome and fetal demise in the setting of acute parvovirus B19 infection. A series of three renal biopsies and rapid clinical course showed progression from significant podocyte injury with mild light microscopy findings to classic viral-associated CG to ESRD in less than 3 months. Genetic analysis revealed two APOL1 G1 risk alleles. CONCLUSIONS: This is the first published case report of CG in the setting of acute parvovirus infection in a patient with two APOL1 risk allelles, and parvoviral proteins identified in renal epithelium on kidney biopsy. These findings support the causative role of parvovirus B19 infection in the development of CG on the background of APOL1 genetic risk.
Subject(s)
Apolipoprotein L1/genetics , Glomerulosclerosis, Focal Segmental/etiology , Kidney Failure, Chronic/etiology , Parvoviridae Infections/complications , Parvovirus B19, Human , Pregnancy Complications, Infectious/virology , Acute Disease , Adult , Alleles , Female , Glomerulosclerosis, Focal Segmental/pathology , Humans , PregnancyABSTRACT
A thrombosed dialysis access can be declotted either through an open surgical procedure or a percutaneous one. In choosing how the access should be managed, a nephrologist should balance the experience and outcomes of local providers to ensure the efficient and safe salvage of the vascular access. Percutaneous procedures often offer less disruption to the schedule of the patient and dialysis clinic, give more information about the central vasculature, are less invasive, and ultimately are preferred. Nephrologist should encourage local vascular surgeons and interventional radiologists to become proficient in these procedures to avoid unnecessary open cases.
Subject(s)
Arteriovenous Shunt, Surgical , Kidney Failure, Chronic/therapy , Nephrology/methods , Renal Dialysis , Thrombosis/surgery , Humans , Operating RoomsABSTRACT
A 63-year-old man with HIV (human immunodeficiency virus) infection and end-stage renal disease, treated with lanthanum carbonate phosphate binder for 4 years, presented with anemia and an upper gastrointestinal bleed. Upper endoscopy revealed a nodular hyperplastic epithelium, with an endoscopic ultrasound confirming hyperechoic material within the nodules. Light microscopy showed collections of histiocytes and multinucleated giant cells containing brown granular cytoplasmic material and extracellular crystalline material, a finding confirmed by electron microscopy. Similar pathologic findings associated with lanthanum exposure have been described recently. In our patient, lanthanum carbonate treatment was withdrawn and gastrointestinal bleeding has since ceased. The patient was exposed to a high amount of lanthanum over a long period, which may explain his adverse reaction. However, other contributing factors, such as competing medications or comorbid conditions, also may have increased his sensitivity to the drug.
Subject(s)
Foreign-Body Reaction/chemically induced , Lanthanum/adverse effects , Renal Dialysis , Humans , Male , Middle Aged , Time FactorsABSTRACT
Hyponatremia is the most commonly encountered electrolyte abnormality. Severe hyponatremia in pregnancy poses diagnostic and therapeutic challenges. Pregnancy involves changes in physiology that affect water and sodium homeostasis. Knowledge of these complex physiologic alterations during pregnancy is critical to managing dysnatremias in pregnancy. This teaching case describes a woman with chronic hyponatremia who presented during pregnancy with worsening hyponatremia. She had an activating vasopressin receptor mutation, which was passed on to her child, and her diagnostic workup is described.
Subject(s)
Hyponatremia/diagnosis , Hyponatremia/therapy , Pregnancy Complications/diagnosis , Pregnancy Complications/therapy , Adult , Female , Fluid Therapy , Homeostasis/physiology , Humans , Hyponatremia/genetics , Mutation/genetics , Pregnancy , Pregnancy Complications/genetics , Receptors, Vasopressin/genetics , Sodium/metabolism , Treatment OutcomeABSTRACT
Leukemia and lymphoma are hematologic malignancies that can affect any age group. Disease can be aggressive or indolent, often with multiorgan system involvement. Kidney involvement in leukemia and lymphoma can be quite extensive. Acute kidney injury (AKI) is quite prevalent in these patients, with prerenal and acute tubular necrosis being the most common etiologies. However other prerenal, intrinsic, and obstructive etiologies are possible. AKI can be a direct effect of the malignancy, a complication of the malignancy, or the consequence or side effect of chemotherapy. Nephrotic syndrome and glomerulonephritis, often presenting without overt kidney failure, have also been seen in all forms of leukemia and lymphoma. Lastly, the direct effects of the malignancy and complications from the tumor often result in numerous electrolyte disturbances and acid-base disorders, with life-threatening consequences if left untreated.