“Purpose of review

Two diseases


“Purpose of review

Two diseases SNX-5422 clinical trial associated with chronic kidney disease (CKD) have benefited from advances in the past year which are of great importance for rheumatologists: renal osteodystrophy, which is now clearly

associated with vascular calcification and cardiovascular death, and nephogenic systemic fibrosis, which appears presently as a new iatrogenic disorder, and therefore can be prevented.

Recent findings

Vascular calcification is a feature of renal osteodystrophy, which has received much recent attention. Hyperphosphatemia has been shown to play an important role by inducing a transcription factor, osterix, which promotes the transformation of vascular smooth muscle cells into osteoblats-like cells and matrix calcification. The effect of calcium load on vascular calcification is modulated by bone turnover. Calcium has been found to promote more vascular calcification in adynamic bone disease in which bone cannot act anymore as a buffer for absorbed calcium.

Summary

Management of renal osteodystrophy is progressing relentlessly, in particular, since the discovery of new phosphate binders, vitamin D derivates and calcium agonist. The need to maintain serum parathyroid hormone to levels higher than the normal range has been emphasized in CKD patients, who early develop skeletal resistance to the hormone. However, bone turnover has been found

excessively CP-868596 cost suppressed in dialysis patients whose serum parathyroid hormone levels met the recommended values, reflecting imperfections in the assays presently

used in clinical practice.

Nephrogenic systemic fibrosis has been linked to exposition of CKD patients to gadolinium-based contrast agents, by epidemiological and experimental data. Avoidance of gadolinium – in particular gadodiamide – enhanced MRI in CKD patients, now appears as an efficient way to prevent this very serious disease.”
“Purpose: To evaluate the safety and efficacy of spinal anesthesia compared with general anesthesia in patients who underwent percutaneous nephrolithotomy GW786034 nmr (PCNL).

Patients and Methods: One hundred patients with American Society of Anesthesiologists (ASA) score <3 were randomly divided into two groups according to the type of anesthesia. Spinal anesthesia was performed using an injection of 0.25 mg/kg bupivacaine 0.5% in the intrathecal space; no opium (fentanyl) agent was used. All procedures were performed with the patient in the prone position. Stone access was made by using fluoroscopic guidance, and the tract was dilated using a single-stage technique. All patients received a solution including 1 mg/kg morphine in every 100 mL physiologic saline through the volumetric pump during the 3-hour post-PCNL period in the recovery room. Afterward, morphine (0.05 mg/kg) was injected only according to the verbal rating scale greater than 3 after discharge from the recovery room until 24 hours after surgery.

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