Literature DB >> 10973038

Cystic fibrosis patients with and without central nervous system complications following lung transplantation.

A B Goldstein1, L S Goldstein, M K Perl, M T Haug, A C Arroliga, P C Stillwell.   

Abstract

Central nervous system (CNS) complications occur more frequently in cystic fibrosis (CF) patients than other lung transplant recipients. The purpose of this study was to compare CF patients with and without CNS complications following lung transplantation, to identify risk factors for CNS events. Records of 21 patients with CF who underwent lung transplant between 1991-1996 were reviewed. Data were collected on multiple variables, including: age at transplant; gender; cytomegalovirus (CMV) status; cholesterol and triglyceride levels; sinusitis; percent ideal body weight (IBW); body mass index (BMI); augmented immunosuppression, acute lung rejection episodes (ALR); cyclosporine doses; electrolytes; magnesium, blood urea nitrogen (BUN), and creatinine levels; and 6-month survival. CNS complications identified were seizures, severe headaches (HA), strokes, or confusional episodes. Eleven of 21 patients (52%) with CF had CNS events: eight had seizures, five HA, three strokes, and one confusional episode. There was no difference in age at transplant, pretransplant percent IBW or BMI, cholesterol and triglyceride levels, or number of ALR. CMV mismatch and clinical sinusitis had no effect. Cyclosporine doses did not differ between groups at 30 days, or 3 or 6 months posttransplant. Both BUN and creatinine concentrations showed a rise over time that did not differ between groups. Potassium levels were within normal limits for both groups. While sodium levels did not differ between groups pretransplant, or at 30 days or 6 months posttransplant, a decrease in sodium values was seen at the time of CNS events. There was no difference in 6-month survival. We could not identify any pre- or posttransplant risk factors that predicted CNS events. It is likely that cyclosporine toxicity is the major cause of CNS complications. Despite the high rate of CNS events, the overall prognosis was good, and 6-month survival was not affected. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10973038     DOI: 10.1002/1099-0496(200009)30:3<203::aid-ppul4>3.0.co;2-5

Source DB:  PubMed          Journal:  Pediatr Pulmonol        ISSN: 1099-0496


  6 in total

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2.  Synergistic post-transcriptional regulation of the Cystic Fibrosis Transmembrane conductance Regulator (CFTR) by miR-101 and miR-494 specific binding.

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3.  Influence of early neurological complications on clinical outcome following lung transplant.

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Journal:  PLoS One       Date:  2017-03-16       Impact factor: 3.240

4.  CNS imaging studies in cystic fibrosis patients presenting with sudden neurological events.

Authors:  Samantha Ellis; Catherine Rang; Tom Kotsimbos; Dominic Keating; Felicity Finlayson; Richard Stark; Dominic Thyagarajan; John Wilson
Journal:  BMJ Open Respir Res       Date:  2019-08-09

5.  Expression and distribution of cystic fibrosis transmembrane conductance regulator in neurons of the spinal cord.

Authors:  Yong Guo; Min Su; Meng Su; Michael A McNutt; Jiang Gu
Journal:  J Neurosci Res       Date:  2009-12       Impact factor: 4.164

6.  Drug development in targeting ion channels for brain edema.

Authors:  Zheng-Wei Luo; Andrea Ovcjak; Raymond Wong; Bao-Xue Yang; Zhong-Ping Feng; Hong-Shuo Sun
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  6 in total

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