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dc.contributor.authorGonullu, Guzin
dc.contributor.authorDemircan, Sabri
dc.contributor.authorDemirag, Mustafa Kemal
dc.contributor.authorErdem, Dilek
dc.contributor.authorYucel, Idris
dc.date.accessioned2020-06-21T14:18:53Z
dc.date.available2020-06-21T14:18:53Z
dc.date.issued2012
dc.identifier.issn0941-4355
dc.identifier.issn1433-7339
dc.identifier.urihttps://doi.org/10.1007/s00520-011-1226-5
dc.identifier.urihttps://hdl.handle.net/20.500.12712/16479
dc.descriptionWOS: 000304614200009en_US
dc.descriptionPubMed: 21773677en_US
dc.description.abstractNausea and vomiting are among the major problems occurring during and after the chemotherapy treatments of cancer patients. The recently developed 5-HT3 antagonists have proved much more effective than former agents. Several studies have shown that these agents cause certain ECG changes. We aimed to evaluate the ECG changes caused by palonosetron, one of the new 5-HT3 antagonists. Our study includes a total of 50 patients diagnosed with solid-organ tumors receiving chemotherapy. The patients were applied 12-lead ECG before palonosetron infusion. Afterwards, subsequent ECGs were applied on the 30th, 60th, and 90th minutes following the infusion of palonosetron. Arterial blood pressure was measured before and after the infusion. PR, QRS, QT, QTmax, QTmin, QTd, Pmax, Pmin, Pd, QTc, QTcmax, QTcmin, and QTcd values were evaluated for each ECG. We did not detect significant correlations between the systolic and diastolic blood pressures before and after (30 min) palonosetron infusion (p > 0.05). However, there was a statistically significant decrease in heart rate (p = 0.000). The evaluation of ECG findings revealed that there was a significant prolongation in PR distance, as shown by the comparisons of 0 min with 30, 60, and 90 min. On the other hand, there was no significant difference in QRS, QT, QTmax, QTmin, QTd, Pmax, Pmin, Pd, QTc, QTcmax, QTcmin, and QTcd values (p > 0.05). In this study, we revealed that palonosetron did not cause any severe rhythmic disorders or symptomatic ECG changes. We concluded that it could be safe to administer palonosetron antiemetically.en_US
dc.language.isoengen_US
dc.publisherSpringeren_US
dc.relation.isversionof10.1007/s00520-011-1226-5en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectPalonosetronen_US
dc.subject5-HT3 receptor antagonisten_US
dc.subjectP waveen_US
dc.subjectQT intervalen_US
dc.subjectQRS complexen_US
dc.titleElectrocardiographic findings of palonosetron in cancer patientsen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume20en_US
dc.identifier.issue7en_US
dc.identifier.startpage1435en_US
dc.identifier.endpage1439en_US
dc.relation.journalSupportive Care in Canceren_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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