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Changes in Serum Osmolality and the Clinical Manifestations of the Dialysis Disequilibrium SyndromeYoung, Donna L. 01 January 1978 (has links)
The purpose of this study was to determine if a relationship existed between the change in serum osmolality in the chronic renal failure patient on hemodialysis and the number of clinical symptoms of the dialysis disequilibrium syndrome experienced during hemodialysis. The study was conducted at the Renal Dialysis Unit of an urban medical center located in a southeastern city. Data were collected from May 25, 1978 to June 30, 1978. Data were obtained during 28 hemodialysis procedures performed on 11 subjects. Serum osmolality measurements were collected prior to initiation of the dialysis procedure, at half-hour intervals during dialysis, and prior to termination of dialysis. Clinical symptoms which occurred during dialysis were recorded by the patients and nursing personnel. The hypothesis was that the number of clinical symptoms of the dialysis disequilibrium syndrome experienced by the chronic renal failure patient during hemodialysis will increase as the serum osmolality decreases.
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Analysis and interpretation of Iron studies and Vitamin C levels in paediatric patients with chronic renal failureLutz, Tracey Leigh 24 August 2010 (has links)
MMed (Paediatrics), Faculty of Health Sciences, University of the Witwatersrand / This prospective observational study analysed iron studies and vitamin C levels in patients
with chronic kidney disease attending Johannesburg Hospital Paediatric Nephrology Clinic.
The rationale behind this study was to determine the extent of iron deficiency among patients
in chronic renal failure. Vitamin C deficiency is common among dialysis patients, it is easy
to test for and easy to prevent. This study may assist in guiding future management with
regards to vitamin C supplementation in patients with chronic renal insufficiency on dialysis.
The study contained 45 patients of which 27 (60 %) were male and 18 (40 %) were female.
The ages of the children varied from 2 years 1 month to 19 years and 7 months. The study
included patients from all ethnic groups; 9 were Caucasian, 33 African, 2 Indian and 1
Coloured. Two male patients did not have Vitamin C levels analyzed.
The patients were divided into 3 distinct groups; firstly those patients on haemodialysis (12
patients), those on peritoneal dialysis (22 patients) and those not yet dialysed (11 patients).
In all patients who were not yet on dialysis the GFR ranged between 18.1 and 45
ml/min/1.73m2.
There were no statistically significant differences between the three groups when the results
of the iron studies were analysed. However, despite iron treatment 26.6 % of patients were
iron deficient as indicated by their transferrin saturation which was less than 20 %.
Vitamin C levels were also analysed in this study. Forty one percent of children in chronic
renal failure were vitamin C deficient. There was no statistically significant variability among the three groups. Two patients (4.6%) were noted to be Vitamin C toxic. One of
these patients was haemodialysed; the other was not yet on dialysis.
Vitamin C deficiency in chronic renal insufficient patients on dialysis is easily correctable
when identified. Vitamin C in specific well documented doses is safe to administer to this
group of patients. It will also enhance the absorption of iron and thereby have an indirect
effect on anaemia.
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The experiences of patients receiving haemodialysis treatment in an open setting environment at an academic hospital in JohannesburgKhomba, Mayamiko Munthali 26 August 2014 (has links)
BACKGROUND: Patients receiving haemodialysis (HD) treatment experience a significant
symptom burden and their needs are multifaceted. In HD unit, patients receive treatment in a
diverse cultural and open ward setting. However, patients‟ experiences of receiving HD
treatment in an open ward setting are not known.
OBJECTIVES: The central aim of this study was to explore and describe the experiences of
patients receiving HD treatment in an open setting environment at an academic hospital in
Johannesburg.
DESIGN: A qualitative, exploratory and descriptive study was conducted at a public, tertiary
level academic hospital in Johannesburg after obtaining ethical approval from Wits University
and relevant authorities.
SETTING: The research setting for this study was an adult Chronic Renal Dialysis Unit.
POPULATION: Sixteen adult (age 18 and above) patients receiving chronic HD treatment
were recruited purposively in this study.
INTERVENTIONS: An in-depth semi-structured interview was conducted either before or
after receiving HD treatment, which was audio-recorded, transcribed then analysed by using
Giorgi Phenomenological method.
FINDINGS: A mood enhancer appeared a major theme as participants positively valued the
open setting environment for their overall and psychological well-being. Participants
expressed by being with others and sharing experiences, a sense of community likened to a
family developed. Common to all participants‟ language was the use of the “we” in relation to
being in the open setting environment. This expression of the “we” by participants was
interpreted as a community concept. The use of “we” associated with the concept of
community described as a space to which every patient receiving HD belonged. They
described their experiences in a collective manner. This was evident in repetitive reference to
their common space, being together, sharing experiences, and finding identity from one
another, being understood and a sense of being protected with personal relations that extend
beyond 10 years for some.
This open space contributed to shaping their perception of body image and illness. The nurse‟s
role in timeously providing HD care was appreciated by many.
However, being exposed to multiple situations of chronic illness and treatment a sense of fear
developed. Any negative event experienced, watched, observed, or heard in the HD unit
triggered fear in the patients. Two common fears were of HD complications and the constant
threat of death. Complications such as clotting, muscle cramps and collapsing because of
hypotension as well as watching somebody dying on the machine were all reported in this
study and so psychological counselling was felt to be very important.
CONCLUSION
The recommendations proposed in this study hopefully will assist HD staff to intervene and
make adjustments to support patients‟ holistic needs. Further studies into patients receiving
HD in open settings and mixed-gender space are required for diversity of experiences and
knowledge from different settings.
Keywords: Haemodialysis, hospital environment, open setting, patient experiences
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Measurement of plasma and urine carnitine in patients with cardiomyopathy, renal failure and metabolic abnormalities.January 1994 (has links)
by Leung Cheuk Wa. / Thesis (M.Sc.)--Chinese University of Hong Kong, 1994. / Includes bibliographical references (leaves 97-106). / ACKNOWLEDGEMENTS --- p.i / LIST OF FIGURES --- p.v / LIST OF TABLES --- p.vi / SUMMARY --- p.1 / Chapter 1. --- INTRODUCTION --- p.3 / Chapter 2. --- BASIC ASPECTS OF CARNITINE / Chapter 2.1 --- BIOSYNTHESIS OF CARNITINE --- p.5 / Chapter 2.2 --- CARNITINE TRANSPORT --- p.8 / Chapter 2.3 --- THE ROLE OF CARNITINE IN INTRACELLULAR METABOLISM --- p.10 / Chapter 2.4 --- THE ROLE OF KIDNEY IN CARNITINE METABOLISM --- p.16 / Chapter 3. --- CARNITINE DEFICIENCY --- p.18 / Chapter 3.1 --- PRIMARY CARNITINE DEFICIENCY --- p.20 / Chapter 3.1.1 --- MYOPATHIC CARNITINE DEFICIENCY --- p.21 / Chapter 3.1.2 --- SYSTEMIC CARNITINE DEFICIENCY --- p.21 / Chapter 3.2 --- SECONDARY CARNITINE DEFICIENCY --- p.22 / Chapter 4. --- CARNITINE METABOLISM IN SELECTED DISEASES / Chapter 4.1 --- CARDIOMYOPATHY --- p.23 / Chapter 4.2 --- ORGANIC ACIDURIAS --- p.24 / Chapter 4.3 --- VALPROIC ACID THERAPY --- p.26 / Chapter 4.4 --- RENAL DIALYSIS ANDTRANSPLANTATION --- p.28 / Chapter 5. --- ANALYTICAL METHODS FOR CARNITINE ASSAYS --- p.30 / Chapter 6. --- DETERMINATION OF TOTAL AND FREE CARNITINE / Chapter 6.1 --- PRINCIPLE OF THE ASSAYS --- p.32 / Chapter 6.1.1 --- FREE CARNITINE DETERMINATION --- p.32 / Chapter 6.1.2 --- TOTAL CARNITINE DETERMINATION --- p.33 / Chapter 6.2 --- INSTRUMENTATION --- p.34 / Chapter 6.3 --- PREPARATION OF REAGENTS AND STANDARDS --- p.36 / Chapter 6.4 --- SPECIMEN COLLECTION --- p.42 / Chapter 6.5 --- SAMPLE PREPARATION --- p.43 / Chapter 6.6 --- ASSAY PROTOCOL FOR FREE CARNITINE --- p.44 / Chapter 6.7 --- ASSAY PROTOCOL FOR TOTAL CARNITINE --- p.46 / Chapter 6.8 --- FACTORS AFFECTING THE PERFORMANCE OF ASSAYS --- p.48 / Chapter 6.9 --- EVALUATION OF FREE AND TOTAL CARNITINE ASSAYS --- p.50 / Chapter 7. --- RESULTS OF EVALUATION OF TOTAL AND FREE CARNITINE ASSAYS / Chapter 7.1 --- CALIBRATION --- p.52 / Chapter 7.2 --- PRECISION --- p.55 / Chapter 7.3 --- LINEARITY RANGE --- p.56 / Chapter 7.4 --- RECOVERY --- p.58 / Chapter 7.5 --- INTERFERENCE OF ACETYLCARNITINE ON FREE CARNITINE ASSAY --- p.59 / Chapter 7.6 --- DISCUSSION --- p.59 / Chapter 8. --- STUDY IN NORMAL SUBJECTS / Chapter 8.1 --- SUBJECTS --- p.61 / Chapter 8.2 --- RESULTS OF THE NORMAL SUBJECTS --- p.61 / Chapter 8.3 --- DISCUSSION --- p.63 / Chapter 9. --- PATIENTS STUDY / Chapter 9.1 --- PATIENTS WITH CARDIOMYOPATHY / Chapter 9.1.1 --- SUBJECTS --- p.66 / Chapter 9.1.2 --- RESULTS OF THE STUDY --- p.66 / Chapter 9.1.3 --- DISCUSSION --- p.69 / Chapter 9.2 --- PATIENTS WITH METABOLIC DISEASES / Chapter 9.2.1 --- SUBJECTS --- p.71 / Chapter 9.2.2 --- RESULTS OF THE STUDY --- p.71 / Chapter 9.2.3 --- DISCUSSION --- p.74 / Chapter 9.3 --- PATIENTS ON VALPROIC ACID THERAPY / Chapter 9.3.1 --- SUBJECTS --- p.75 / Chapter 9.3.2 --- RESULTS OF THE STUDY --- p.75 / Chapter 9.3.3 --- DISCUSSION --- p.77 / Chapter 9.4 --- PATIENTS ON RENAL DIALYSIS AND AFTER TRANSPLANTATION / Chapter 9.4.1 --- SUBJECTS --- p.79 / Chapter 9.4.2 --- RESULTS OF THE STUDY --- p.79 / Chapter 9.4.3 --- DISCUSSION --- p.81 / Chapter 10. --- GENERAL DISCUSSION --- p.84 / Chapter 11. --- REFERENCES --- p.97
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Artificial cell live yeast microcapsule formulation for use in renal failure uremiaCoussa, Razek. January 2008 (has links)
Renal failure uremia occurs when the kidneys fail to function properly. Despite being the main treatment, dialysis and other therapeutic approaches are not only associated with numerous long-term adverse complications often leading to morbidity and mortality events, but are also not affordable. Orally administrating Alginate-Poly-L-Lysine-Alginate microcapsules entrapping live yeast cells to treat renal failure uremia has not yet been investigated. In this thesis, the growth and microencapsulation of yeast were optimized. The efficacy of these microcapsules in removing unwanted electrolytes was tested in vitro in simulated gastro-intestinal media, in vitro in a column bioreactor and in vivo in an uremic rat model. Results showed that these novel microcapsules can not only maintain morphological stability and membrane integrity under gastro-intestinal environments and mechanical stresses, but also, preserve the viability of yeast. These microcapsules were successful in reducing urea concentrations while not harming the human GI tract's microbial flora.
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Studies on pathophysiological mechanisms in experimental models of acute renal failure /Nitescu, Nicoletta, January 2007 (has links)
Diss. (sammanfattning) Göteborg : Göteborgs universitet , 2007. / Härtill 5 uppsatser.
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Intracellular free amino acids and nutritional status in children with chronic renal failure on different treatments /Canepa, Alberto, January 1900 (has links)
Diss. (sammanfattning) Stockholm : Karol. inst., 2001. / Härtill 5 uppsatser.
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Renal manifestations of septic patients with scrub typhus at Maharaj Nakhon Ratchasima Hospital /Maung, Myo Nyunt Naing, Weerapong Phumratanaprapin, January 2003 (has links) (PDF)
Thesis (M.C.T.M. (Clinical Tropical Medicine))--Mahidol University, 2002.
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Examination of end-stage renal disease services at Henry Ford Hospital submitted to the Program in Hospital Administration ... in partial fulfillment ... for the degree of Master of Health Services Administration /Ford, W. Raymond C. January 1976 (has links)
Thesis (M.H.S.A.)--University of Michigan, 1976.
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Examination of end-stage renal disease services at Henry Ford Hospital submitted to the Program in Hospital Administration ... in partial fulfillment ... for the degree of Master of Health Services Administration /Ford, W. Raymond C. January 1976 (has links)
Thesis (M.H.S.A.)--University of Michigan, 1976.
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