نمایش مختصر رکورد

dc.contributor.authorTavakoli Ardakani, Mariaen_US
dc.contributor.authorTafazoli, Alien_US
dc.contributor.authormehdizadeh, mahshiden_US
dc.contributor.authorhajifathali, abbasen_US
dc.contributor.authorDadashzadeh, Siminen_US
dc.date.accessioned1399-07-09T06:55:14Zfa_IR
dc.date.accessioned2020-09-30T06:55:14Z
dc.date.available1399-07-09T06:55:14Zfa_IR
dc.date.available2020-09-30T06:55:14Z
dc.date.issued2016-02-01en_US
dc.date.issued1394-11-12fa_IR
dc.date.submitted2014-10-07en_US
dc.date.submitted1393-07-15fa_IR
dc.identifier.citationTavakoli Ardakani, Maria, Tafazoli, Ali, mehdizadeh, mahshid, hajifathali, abbas, Dadashzadeh, Simin. (2016). A 16 Month Survey of Cyclosporine Utilization Evaluation in Allogeneic Hematopoietic Stem Cell Transplant Recipients. Iranian Journal of Pharmaceutical Research, 15(1), 331-339. doi: 10.22037/ijpr.2016.1788en_US
dc.identifier.issn1735-0328
dc.identifier.issn1726-6890
dc.identifier.urihttps://dx.doi.org/10.22037/ijpr.2016.1788
dc.identifier.urihttp://ijpr.sbmu.ac.ir/article_1788.html
dc.identifier.urihttps://iranjournals.nlai.ir/handle/123456789/312031
dc.description.abstractObjectives: Graft versus host disease (GVHD) is a life threatening reaction in the stem cell transplantation process. Nowadays Cyclosporine is the most commonly utilized agent for GVHD prophylaxis and it has a major role in successful transplantation. Cyclosporine has been applied for many years in this field but it could be stated that currently no general consensus is available for its optimal method of administration. Conditions related to cyclosporine administration and possible related adverse reactions observed closely in our patients with the aim of constructing a comprehensive practice guideline in the future. Patients and Methods: Allogeneic stem cell transplant recipients who have been taking cyclosporine were monitored during and after their hospitalization while recording all observations on predefined questionnaires on the basis of periodic clinical and laboratory examinations for a 16 month period. Results: Mean recorded duration of infusions was 1.44 ± 0.68 h and by twice daily administration, means intravenous and oral dose was 101.85 ± 22.03 mg and 219.28 ± 63.9 mg, respectively. A mean CsA trough level after about 12 h of specified unique doses was 223 ± 65 ng/mL. We found hypertension, nephrotoxicity, neurotoxicity, hypertension, and dyslipidemia in about 14, 20, 48, and 94 percent of patients. Conclusions: This study proposed that permanent guidance of healthcare team according to a fixed and standard method of cyclosporine administration routine with using efficient facilities and protocols would be helpful considerably for an optimal pharmacotherapy.en_US
dc.format.extent967
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoen_US
dc.publisherSchool of Pharmacy, Shahid Beheshti University of Medical Sciencesen_US
dc.relation.ispartofIranian Journal of Pharmaceutical Researchen_US
dc.relation.isversionofhttps://dx.doi.org/10.22037/ijpr.2016.1788
dc.subjectAdministrationen_US
dc.subjectadverse effectsen_US
dc.subjectcyclosporineen_US
dc.subjectDrug utilization evaluationen_US
dc.subjectgraft versus host diseaseen_US
dc.subjecthematopoietic stem cell transplantationen_US
dc.subjectPharmacotherapy (Clinical Pharmacy)en_US
dc.titleA 16 Month Survey of Cyclosporine Utilization Evaluation in Allogeneic Hematopoietic Stem Cell Transplant Recipientsen_US
dc.typeTexten_US
dc.typeResearch articleen_US
dc.contributor.departmentDepartment of Clinical Pharmacy, Shahid Beheshti University of Medical Sciences School of Pharmacy, Tehran, Iranen_US
dc.contributor.departmentDepartment of Bone Marrow Transplant, Taleghani Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.en_US
dc.contributor.departmentDepartment of Bone Marrow Transplant, Taleghani Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran.en_US
dc.contributor.departmentDepartment of Pharmaceutics, School of Pharmacy, Shahid Beheshti Medical University, Tehran, Iranen_US
dc.citation.volume15
dc.citation.issue1
dc.citation.spage331
dc.citation.epage339


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