img
img
Evaluation of analytical process in clinical laboratories six sigma methodology   
Yazarlar (6)
İren Emekli Dilek
Kenan Güçlü
Esin Avcı
Pamukkale Üniversitesi, Türkiye
Doç. Dr. Bilal İLANBEY Doç. Dr. Bilal İLANBEY
Kırşehir Ahi Evran Üniversitesi, Türkiye
Rukiye Nar
Kırşehir Ahi Evran Üniversitesi, Türkiye
Dr. Öğr. Üyesi Gamze TURNA SALTOĞLU Dr. Öğr. Üyesi Gamze TURNA SALTOĞLU
Kırşehir Ahi Evran Üniversitesi, Türkiye
Devamını Göster
Özet
Objective: Analytical reliability of clinical laboratories may be obtained by internal quality control, external quality control by analyzing the data with statistical methods. In Six Sigma Methodology, which is one of these methods, the analytical performance of the tests is determined by process sigma values. In this study, we aimed to assess the analytical process performances of most frequently used tests in our laboratory according to six sigma methodology.Material and Methods: Internal quality control data between July-October 2014 were obtained from the laboratory information system. Process sigma levels based on formula (% TEa-% Bias)/% CV) were calculated for the analytes. The results were classified in 3 groups according to sigma level as low≤ 4; acceptable between 4–6; good≥ 6.Results: Tests having a process sigma level of≤ 4; in July: level 1; Glucose, Creatinine, level 2; Urea, Glucose, Creatinine …
Anahtar Kelimeler
Bildiri Türü Tebliğ/Bildiri
Bildiri Alt Türü Özet Metin Olarak Yayınlanan Tebliğ (Uluslararası Kongre/Sempozyum)
Bildiri Niteliği Alanında Hakemli Uluslararası Kongre/Sempozyum
Bildiri Dili İngilizce
Kongre Adı EuroMedLab Paris 2015
Kongre Tarihi 21-06-2015 / 25-06-2015
Basıldığı Ülke
Basıldığı Şehir
BM Sürdürülebilir Kalkınma Amaçları
Atıf Sayıları
Google Scholar 2
Evaluation of analytical process in clinical laboratories six sigma methodology

Paylaş