Background: plasma exchange (PE) involves the separation and removal of plasma from corpuscular blood and the replacement of it with various fluids, while plasmapheresis only refers to the removal of plasma. AIM OF STUDY: To study our experience with PE in our 487 patients of different neurological disorders, determined most referring diseases. Materials and Methods: Retrospective study of PE procedures done during a period of 36 months, from January 2013to January 2016 in a neurosciences hospital in Baghdad/Iraq. Data analysis is used SPSS 20. Results: The main indication for PE was CIDP (339 patients; 69.20%). Age of patients ranged from 8-85 (mean = 46.22 years). Up to our knowledge is largeset number of patients used in that period, no mortality found. Conclusion: The analysis of 487 cases of PE done in our department shows that PF is usually well tolerated. Possible adverse reactions mainly relate to vascular access.
Published in | American Journal of Internal Medicine (Volume 4, Issue 6) |
DOI | 10.11648/j.ajim.20160406.16 |
Page(s) | 120-123 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2016. Published by Science Publishing Group |
Chronic Inflammatory Demylinating Polyneuropathy, Plasmapheresis, Therapeutic Plasma Exchange
[1] | Selective Plasma Component Removal: Alternatives to Plasma Exchange. Alvaro A. Pineda and, Howard F. Taswell, Version of Record online: 12 NOV 2008. |
[2] | V. Abdul Gafoor, James Jose, K. Saifudheen. Plasmapheresis in neurological disorders: Experience from a tertiary care hospital in South India. Ann Indian Acad Neurol. 2015 Jan-Mar;18(1):15–19. [PubMed]. |
[3] | Clark WF, Rock GA, Buskard N, Shumak KH, LeBlond P, Anderson D, et al. Therapeutic plasma exchange: An update from the Canadian Apheresis Group. Ann Intern Med. 1999;131:453–62. [PubMed]. |
[4] | The use of therapeutic plasmapheresis for neurological disorders. National Institutes of Consensus Development Conference.Transfus Med Rev. 1998; 2:48–53. [PubMed]. |
[5] | Weinstein R. Therapeutic apheresis in neurological disorders. J ClinApher.2000;15:74–128. [PubMed]. |
[6] | Alexandra Schröder, Ralf A Linker & Ralf Gold. Review Plasmapheresis for neurological disorders. Expert Review of Neurotherapeutics: Volume 9, Issue 9, 2009. |
[7] | Bouget J, Chevret S, Chastang C, Raphael JC. Plasma exchange morbidity in GBS: Results from the French prospective, randomised, multicentre study. French Cooperative Group. Crit Care Med. 1993;21:651–8. [PubMed]. |
[8] | Hartung HP, Willison HJ, Keiseier BC. Acute immuneinflammatory neuropathy: Update on Guillain-Barre syndrome. CurrOpin Neurol. 2002;15:571–7. [PubMed]. |
[9] | Van der Meche FG, Schmitz PI. A randomised trial comparing intravenous immunoglobulin and plasma exchange in Guillain-Barre Syndrome. Dutch Guillain Barre Study Group. N Engl J Med. 1992;326:1123–9. [PubMed]. |
[10] | Cortese I, Chaudhry V, So YT, Cantor F, Cornblath DR, Rae-Grant A. Evidence-based guideline update: Plasmapheresis in neurologic disorders: Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. Neurology.2011; 76: 294–300. [PMC free article][PubMed]. |
[11] | Sharma KR, Cross J, Farronay O, Ayyar DR, Shebert RT, Bradley WG, Demyelinating neuropathy in diabetes mellitus. Arch Neurol. 2002 May; 59(5):758-65. |
[12] | Wong EC, Balogun RA. Therapeutic apheresis in pediatrics: Technique adjustments, indications and nonindications, a plasma exchange focus. J ClinApher. 2012;27:132–7. [PubMed]. |
[13] | Basic-Jukic N, Brunetta B, Kes P. Plasma exchange in elderly patients. TherApher Dial.2010;14:161–5. [PubMed]. |
[14] | Korach JM, Berger P, Giraud C, Le Perff-Desman C, Chillet P. Role of replacement fluids in the immediate complications of plasma exchange. French Registry Cooperative Group. Intensive Care Med. 1998;24:452–8. [PubMed]. |
[15] | Stegmayr B, Ptak J, Wikstrom B, Berlin G, Axelsson CG, Griskevicius A, et al. World apheresis registry 2003-2007 data. TransfusApher Sci. 2008;39:247–54. [PubMed]. |
[16] | Shemin D, Briggs D, Greenan M. Complications of therapeutic plasma exchange: A prospective study of 1,727 procedures. J ClinApher.2007;22:270–6. [PubMed]. |
[17] | Sharma RR, Saluja K, Jain A, Dhawan HK, Thakral B, Marwaha N. Scope and application of therapeutic apheresis: Experience from a tertiary care hospital in North India. TransfusApher Sci. 2011;45:239–45. [PubMed]. |
[18] | Ward DM. Conventional apheresis therapies: A review. J ClinApher.2011;26:230–8. [PubMed]. |
APA Style
Basim Hanoon Jabar, Bahaa A. Hassan. (2016). Theraputic Plasmapheresis in Neurological Disorders, Baghdad/Iraq. American Journal of Internal Medicine, 4(6), 120-123. https://doi.org/10.11648/j.ajim.20160406.16
ACS Style
Basim Hanoon Jabar; Bahaa A. Hassan. Theraputic Plasmapheresis in Neurological Disorders, Baghdad/Iraq. Am. J. Intern. Med. 2016, 4(6), 120-123. doi: 10.11648/j.ajim.20160406.16
AMA Style
Basim Hanoon Jabar, Bahaa A. Hassan. Theraputic Plasmapheresis in Neurological Disorders, Baghdad/Iraq. Am J Intern Med. 2016;4(6):120-123. doi: 10.11648/j.ajim.20160406.16
@article{10.11648/j.ajim.20160406.16, author = {Basim Hanoon Jabar and Bahaa A. Hassan}, title = {Theraputic Plasmapheresis in Neurological Disorders, Baghdad/Iraq}, journal = {American Journal of Internal Medicine}, volume = {4}, number = {6}, pages = {120-123}, doi = {10.11648/j.ajim.20160406.16}, url = {https://doi.org/10.11648/j.ajim.20160406.16}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajim.20160406.16}, abstract = {Background: plasma exchange (PE) involves the separation and removal of plasma from corpuscular blood and the replacement of it with various fluids, while plasmapheresis only refers to the removal of plasma. AIM OF STUDY: To study our experience with PE in our 487 patients of different neurological disorders, determined most referring diseases. Materials and Methods: Retrospective study of PE procedures done during a period of 36 months, from January 2013to January 2016 in a neurosciences hospital in Baghdad/Iraq. Data analysis is used SPSS 20. Results: The main indication for PE was CIDP (339 patients; 69.20%). Age of patients ranged from 8-85 (mean = 46.22 years). Up to our knowledge is largeset number of patients used in that period, no mortality found. Conclusion: The analysis of 487 cases of PE done in our department shows that PF is usually well tolerated. Possible adverse reactions mainly relate to vascular access.}, year = {2016} }
TY - JOUR T1 - Theraputic Plasmapheresis in Neurological Disorders, Baghdad/Iraq AU - Basim Hanoon Jabar AU - Bahaa A. Hassan Y1 - 2016/12/16 PY - 2016 N1 - https://doi.org/10.11648/j.ajim.20160406.16 DO - 10.11648/j.ajim.20160406.16 T2 - American Journal of Internal Medicine JF - American Journal of Internal Medicine JO - American Journal of Internal Medicine SP - 120 EP - 123 PB - Science Publishing Group SN - 2330-4324 UR - https://doi.org/10.11648/j.ajim.20160406.16 AB - Background: plasma exchange (PE) involves the separation and removal of plasma from corpuscular blood and the replacement of it with various fluids, while plasmapheresis only refers to the removal of plasma. AIM OF STUDY: To study our experience with PE in our 487 patients of different neurological disorders, determined most referring diseases. Materials and Methods: Retrospective study of PE procedures done during a period of 36 months, from January 2013to January 2016 in a neurosciences hospital in Baghdad/Iraq. Data analysis is used SPSS 20. Results: The main indication for PE was CIDP (339 patients; 69.20%). Age of patients ranged from 8-85 (mean = 46.22 years). Up to our knowledge is largeset number of patients used in that period, no mortality found. Conclusion: The analysis of 487 cases of PE done in our department shows that PF is usually well tolerated. Possible adverse reactions mainly relate to vascular access. VL - 4 IS - 6 ER -