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1.
Atherosclerosis ; 323: 30-36, 2021 04.
Article in English | MEDLINE | ID: mdl-33773162

ABSTRACT

BACKGROUNDS AND AIMS: The geriatric nutritional risk index (GNRI), which is calculated using the serum albumin level and body mass index, is a nutritional marker associated with an increased risk of cardiovascular events in patients who are receiving hemodialysis. However, no studies have examined the association between the GNRI level and the incidence of stroke in this population. METHODS: Three thousand forty-five patients were registered in the Q-Cohort Study, which is a multicenter, observational cohort of hemodialysis patients. The main outcomes were brain infarction and brain hemorrhage. The main exposure was GNRI levels at baseline. Patients were divided into quartiles on the basis of baseline GNRI levels: Q1, <90.7; Q2, 90.7-95.5; Q3, 95.6-99.8; Q4, >99.8. The risk of brain infarction or hemorrhage was estimated using the multivariable-adjusted Cox proportional hazard risk models and restricted cubic spline analyses. RESULTS: During the 10-year follow-up period, 326 patients developed brain infarction and 149 patients developed brain hemorrhage. Cox proportional hazard risk models showed that the risk of brain infarction and hemorrhage in Q1 was significantly higher than that in Q4 group. The hazard ratios [95% confidence intervals] were 1.49 [1.05-2.12] and 1.89 [1.11-3.20], respectively. Restricted cubic spline curves showed that a lower GNRI was incrementally associated with an increased risk for both brain infarction and brain hemorrhage. CONCLUSIONS: Our results suggest that a lower GNRI is an independent risk factor for both brain infarction and hemorrhage in patients who are receiving maintenance hemodialysis.


Subject(s)
Nutrition Assessment , Stroke , Aged , Cohort Studies , Geriatric Assessment , Humans , Nutritional Status , Renal Dialysis/adverse effects , Risk Assessment , Risk Factors , Stroke/diagnosis , Stroke/epidemiology
2.
Clin Case Rep ; 8(6): 995-998, 2020 Jun.
Article in English | MEDLINE | ID: mdl-32577250

ABSTRACT

The pharmacokinetics of amikacin makes it difficult to predict the appropriate dosing to avoid harmful side effects in patients undergoing continuous ambulatory peritoneal dialysis (CAPD). The implementation of therapeutic drug monitoring may be useful in controlling amikacin serum concentrations in patients receiving CAPD.

3.
CEN Case Rep ; 9(3): 278-284, 2020 08.
Article in English | MEDLINE | ID: mdl-32277358

ABSTRACT

A 71-year-old woman was hospitalized for the treatment of fatigue, fever, and cough. On admission, she showed increased serum inflammation markers, severe anemia, pulmonary hemorrhage, and advanced acute kidney injury requiring hemodialysis. Her serum anti-glomerular basement membrane (GBM) antibody titer was found to be extremely high on the 7th hospital day. She was eventually diagnosed with anti-GBM disease. She was treated with a combination of corticosteroid pulse therapy, oral prednisolone and cyclophosphamide, and plasma exchange, but continued to require maintenance hemodialysis for end-stage kidney disease. During her treatment, she suddenly developed headache, blindness, seizure, and consciousness disturbance. She was diagnosed by magnetic resonance imaging with posterior reversible encephalopathy syndrome (PRES) with subcortical cerebral hemorrhage. Both the PRES and cerebral hemorrhage subsided soon after control of her hypertension and reinforcement of immunosuppressive treatment. PRES, particularly when accompanied by cerebral hemorrhage, may cause irreversible and lethal neurological abnormalities, and nephrologists should, therefore, be aware of the potential risk of PRES in patients with anti-GBM disease. We discuss the current case in the light of the previous literature.


Subject(s)
Acute Kidney Injury/therapy , Anti-Glomerular Basement Membrane Disease/diagnosis , Cerebral Hemorrhage/diagnosis , Posterior Leukoencephalopathy Syndrome/diagnosis , Renal Dialysis/methods , Acute Kidney Injury/diagnosis , Acute Kidney Injury/etiology , Adrenal Cortex Hormones/administration & dosage , Adrenal Cortex Hormones/therapeutic use , Adult , Aged , Anemia/diagnosis , Anemia/etiology , Anti-Glomerular Basement Membrane Disease/complications , Anti-Glomerular Basement Membrane Disease/drug therapy , Anti-Glomerular Basement Membrane Disease/immunology , Cerebral Hemorrhage/etiology , Combined Modality Therapy , Cyclophosphamide/administration & dosage , Cyclophosphamide/therapeutic use , Female , Hemorrhage/diagnosis , Hemorrhage/etiology , Hospitalization , Humans , Hypertension/complications , Hypertension/drug therapy , Immunosuppressive Agents/administration & dosage , Immunosuppressive Agents/therapeutic use , Lung Diseases/pathology , Magnetic Resonance Imaging/methods , Male , Plasma Exchange/methods , Posterior Leukoencephalopathy Syndrome/etiology , Treatment Outcome , Young Adult
4.
Ther Apher Dial ; 24(1): 72-80, 2020 Feb.
Article in English | MEDLINE | ID: mdl-31125508

ABSTRACT

Preserving residual kidney function (RKF) is important in the management of patients on peritoneal dialysis. However, few studies have examined the association between serum albumin level and the risk of RKF loss. We prospectively recruited 104 patients who began peritoneal dialysis treatment at our hospital between 2006 and 2016. The primary outcome was complete RKF loss, defined as urine volume < 100 mL/day. Serum albumin level at baseline was the main exposure. During a median observation period of 24 months, 33 patients developed RKF loss. A Cox proportional hazards model showed that hypoalbuminemia was associated with an increased risk of RKF, even after adjustments for potential confounding factors. Multivariable-adjusted linear regression analysis also showed that hypoalbuminemia was associated with greater rates of decline in 24-h urine volume and in renal Kt/V urea. Our findings suggest that hypoalbuminemia is associated with an increased risk of RKF loss in patients with peritoneal dialysis.


Subject(s)
Hypoalbuminemia/epidemiology , Peritoneal Dialysis , Renal Insufficiency, Chronic/therapy , Serum Albumin, Human/metabolism , Adult , Aged , Female , Humans , Hypoalbuminemia/complications , Kidney Function Tests , Male , Middle Aged , Prospective Studies , Renal Insufficiency, Chronic/physiopathology
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