This study in analytical study set as prospective cohort, comparing several
parameters before and after the intervention, to the patients on regular hemodialysis in
Haji Adam Malik Hospital Medan and Rasyida Clinic of Kidney and Hypertension Medan,
North Sumatra. The test was conducted from December 2013 to March 2014. A total of
20 regular HD patients participated in this study with the inclusion criteria for men and
women aged 17 years, has been undergoing hemodialysis > 3 month with a frequency
of 2 times a week, notable complaints of itching and pain in the body which does not
respond to medication. Not included in the study are patients suffering from tumors,
thrombocytopenia, leukopenia and irregular HD. The consent and willingness from
subjects of the study to be included in the study were sought in writing (informed
consent). Data collection were done on name, age, gender and other personal data, as
well as phase angle examination by single frequency BIA (SF-BIA) and assessment of
quality of life using modified SF-36 form. SF-36 questionnaire were done by patients
themselves. Beta-2 microglobulin concentration test were done twice. Initial test was
done 1 hour before the first HD + HP treatment. Follow-up test was done between the
6th and 7th HD + HP treatment. HD + HP treatment was done once every 2 weeks for 6 times.
This study in analytical study set as prospective cohort, comparing several
parameters before and after the intervention, to the patients on regular hemodialysis in
Haji Adam Malik Hospital Medan and Rasyida Clinic of Kidney and Hypertension Medan,
North Sumatra. The test was conducted from December 2013 to March 2014. A total of
20 regular HD patients participated in this study with the inclusion criteria for men and
women aged 17 years, has been undergoing hemodialysis > 3 month with a frequency
of 2 times a week, notable complaints of itching and pain in the body which does not
respond to medication. Not included in the study are patients suffering from tumors,
thrombocytopenia, leukopenia and irregular HD. The consent and willingness from
subjects of the study to be included in the study were sought in writing (informed
consent). Data collection were done on name, age, gender and other personal data, as
well as phase angle examination by single frequency BIA (SF-BIA) and assessment of
quality of life using modified SF-36 form. SF-36 questionnaire were done by patients
themselves. Beta-2 microglobulin concentration test were done twice. Initial test was
done 1 hour before the first HD + HP treatment. Follow-up test was done between the
6th and 7th HD + HP treatment. HD + HP treatment was done once every 2 weeks for 6 times.
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