Please use this identifier to cite or link to this item: https://hdl.handle.net/11499/8108
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dc.contributor.authorKorkmaz, S.-
dc.contributor.authorKeklik, M.-
dc.contributor.authorSivgin, S.-
dc.contributor.authorYildirim, R.-
dc.contributor.authorTombak, A.-
dc.contributor.authorKaya, M.E.-
dc.contributor.authorAcik, D.Y.-
dc.date.accessioned2019-08-16T12:35:34Z
dc.date.available2019-08-16T12:35:34Z
dc.date.issued2013-
dc.identifier.issn1473-0502-
dc.identifier.urihttps://hdl.handle.net/11499/8108-
dc.identifier.urihttps://doi.org/10.1016/j.transci.2013.04.016-
dc.description.abstractThrombotic thrombocytopenic purpura (TTP) is a particular form of thrombotic microangiopathy typically characterized by thrombocytopenia, microangiopathic hemolytic anemia, fever, neurological abnormalities, and renal dysfunction. TTP requires a rapid diagnosis and an adapted management in emergency. Daily sessions of therapeutic plasma exchange (TPE) remain the basis of management of TTP. Also, TTP is a rare disease that is fatal if it is not treated. TPE has resulted in excellent remission and survival rates in TTP patients. Aim: We aimed to present our experience in 163 patients with TTP treated with TPE during the past 5. years from 10 centers of Turkey. Patients and methods: One hundered and sixty-three patients with TTP treated with TPE during the past 5years from 10 centers of Turkey were retrospectively evaluated. TPE was carried out 1-1.5times plasma volume. Fresh frozen plasma (FFP) was used as the replacement fluid. TPE was performed daily until normalization of serum lactate dehydrogenase (LDH) and recovery of the platelet count to 150×109/dL. TPE was then slowly tapered. Clinical data, the number of TPE, other given therapy modalities, treatment outcomes, and TPE complications were recorded. Results: Fifty-eight percent (95/163) of the patients were females. The median age of the patients was 42. years (range; 16-82). The median age of male patients was significantly higher than female (53 vs. 34. years; p<. 0.001). All patients had thrombocytopenia and microangiopathic hemolytic anemia. At the same time, 82.8% (135/163) of patients had neurological abnormalities, 78.5% (128/163) of patients had renal dysfunction, and 89% (145/163) of patients had fever. Also, 10.4% (17/163) of patients had three of the five criteria, 10.4% (17/163) of patients had four of the five criteria, and 6.1% (10/163) of patients had all of the five criteria. Primary TTP comprised of 85.9% (140/163) of the patients and secondary TTP comprised of 14.1% (23/163) of the patients. Malignancy was the most common cause in secondary TTP. The median number of TPE was 13 (range; 1-80). The number of TPE was significantly higher in complete response (CR) patients (median 15.0 vs. 3.5; p<. 0.001). CR was achieved in 85.3% (139/163) of the patients. Similar results were achieved with TPE in both primary and secondary TTP (85% vs. 87%, respectively; p=. 0.806). There was no advantage of TPE. +. prednisolone compared to TPE alone in terms of CR rates (82.1% vs. 76.7%; p=. 0.746). CR was not achieved in 14.7% (24/163) of the patients and these patients died of TTP related causes. There were no statistical differences in terms of mortality rate between patients with secondary and primary TTP [15% (21/140) vs. 13% (3/23); p=. 0.806]. But, we obtained significant statistical differences in terms of mortality rate between patients on TPE alone and TPE. +. prednisolone [14% (12/86) vs. 3% (2/67), p<. 0.001]. Conclusions: TPE is an effective treatment for TTP and is associated with high CR rate in both primary and secondary TTP. Thrombocytopenia together with microangiopathic hemolytic anemia is mandatory for the diagnosis of TTP and if these two criteria met in a patient, TPE should be performed immediately. © 2013 .en_US
dc.language.isoenen_US
dc.relation.ispartofTransfusion and Apheresis Scienceen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectComplete responseen_US
dc.subjectFresh frozen plasmaen_US
dc.subjectTherapeutic plasma exchangeen_US
dc.subjectThrombotic thrombocytopenic purpuraen_US
dc.subjectfresh frozen plasmaen_US
dc.subjectlactate dehydrogenaseen_US
dc.subjectprednisoloneen_US
dc.subjectadolescenten_US
dc.subjectadulten_US
dc.subjectageden_US
dc.subjectallergic reactionen_US
dc.subjectarticleen_US
dc.subjectcatheter complicationen_US
dc.subjectfemaleen_US
dc.subjectfeveren_US
dc.subjecthemolysisen_US
dc.subjecthumanen_US
dc.subjecthuman cellen_US
dc.subjecthuman tissueen_US
dc.subjecthypocalcemiaen_US
dc.subjecthypotensionen_US
dc.subjectlactate dehydrogenase blood levelen_US
dc.subjectmajor clinical studyen_US
dc.subjectmaleen_US
dc.subjectmortalityen_US
dc.subjectoutcome assessmenten_US
dc.subjectplasma volumeen_US
dc.subjectplasmapheresisen_US
dc.subjectretrospective studyen_US
dc.subjecttachycardiaen_US
dc.subjectthrombocyte counten_US
dc.subjectthrombocytopeniaen_US
dc.subjectthrombotic thrombocytopenic purpuraen_US
dc.subjecttreatment responseen_US
dc.subjectTurkey (republic)en_US
dc.subjectAdolescenten_US
dc.subjectAdulten_US
dc.subjectAgeden_US
dc.subjectAged, 80 and overen_US
dc.subjectFemaleen_US
dc.subjectHumansen_US
dc.subjectL-Lactate Dehydrogenaseen_US
dc.subjectMaleen_US
dc.subjectMiddle Ageden_US
dc.subjectPlasmaen_US
dc.subjectPlasma Exchangeen_US
dc.subjectPlatelet Counten_US
dc.subjectPurpura, Thrombotic Thrombocytopenicen_US
dc.subjectRemission Inductionen_US
dc.subjectRetrospective Studiesen_US
dc.subjectTreatment Outcomeen_US
dc.subjectYoung Adulten_US
dc.titleTherapeutic plasma exchange in patients with thrombotic thrombocytopenic purpura: A retrospective multicenter studyen_US
dc.typeArticleen_US
dc.identifier.volume48en_US
dc.identifier.issue3en_US
dc.identifier.startpage353
dc.identifier.startpage353en_US
dc.identifier.endpage358en_US
dc.identifier.doi10.1016/j.transci.2013.04.016-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.pmid23602056en_US
dc.identifier.scopus2-s2.0-84878855493en_US
dc.identifier.wosWOS:000321403400017en_US
dc.identifier.scopusqualityQ3-
dc.ownerPamukkale University-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
Appears in Collections:PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Tıp Fakültesi Koleksiyonu
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection
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