Significant Operational Improvements with Implementation of Next Generation Laboratory Automation

被引:4
作者
Tanasijevic, Milenko J. [1 ,3 ]
Melanson, Stacy E. F. [1 ,3 ]
Tolan, Nicole, V [1 ,3 ]
Ransohoff, Jaime R. [1 ,2 ]
Conrad, Michael J. [1 ]
Paik, Hyun-il [1 ]
Petrides, Athena K. [1 ,3 ]
机构
[1] Brigham & Womens Hosp, Dept Pathol, 75 Francis St, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Dept Med, 75 Francis St, Boston, MA 02115 USA
关键词
automation; preanalytical line; turnaround time; add-on testing; clinical chemistry; chemistry systems; TURNAROUND TIME; SYSTEM;
D O I
10.1093/labmed/lmaa108
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objectives: To investigate the benefits and challenges of introducing next generation chemistry and coagulation automation. Methods: We replaced the Roche modular preanalytic system attached to Roche Cobas 6000 analyzers with the Roche 8100 preanalytical line attached to the Roche Cobas 8000 and Stago STA R Max analyzers. The system included 2 add-on buffers (AOBs) for automated specimen archival and retrieval and primary-tube specimen processing. We measured turnaround time (TAT) from specimen receipt to result for chemistry and coagulation tests before, during, and after system implementation. TAT for add-on tests was also measured. Results: We completed the system implementation during a 17-month period using existing laboratory space. The TAT for chemistry, coagulation, and add-on tests decreased significantly (P <.005, P <.001, and P <.005, respectively). We encountered several challenges, including barcode-label errors, mechanical problems, and workflow issues due to lack of bidirectional track for coagulation testing. Conclusions: Next generation laboratory automation yielded significantly shortened and less-variable TAT, particularly for add-on testing. Our approach could help other laboratories in the process of implementing and configuring automated systems.
引用
收藏
页码:329 / 337
页数:9
相关论文
共 21 条
[1]   Reducing the time between inoculation and first-read of urine cultures using total lab automation significantly reduces turn-around-time of positive culture results with minimal loss of first-read sensitivity [J].
Bailey, Adam L. ;
Burnham, Carey-Ann D. .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2019, 38 (06) :1135-1141
[2]   Pre-analytical workstations: A tool for reducing laboratory errors [J].
Da Rin, Giorgio .
CLINICA CHIMICA ACTA, 2009, 404 (01) :68-74
[3]   Total laboratory automation: Do stat tests still matter? [J].
Dolci, Alberto ;
Giavarina, Davide ;
Pasqualetti, Sara ;
Szoke, Dominika ;
Panteghini, Mauro .
CLINICAL BIOCHEMISTRY, 2017, 50 (10-11) :605-611
[4]   Implementation of total laboratory automation at a tertiary care hospital in Saudi Arabia: effect on turnaround time and cost efficiency [J].
Ellison, Tracy Louise ;
Alharbi, Maha ;
Alkaf, Morad ;
Elimam, Shamad ;
Alfaries, Mariam ;
Al Nounou, Randa ;
Nasr, Rasheed ;
Owaidah, Tarek .
ANNALS OF SAUDI MEDICINE, 2018, 38 (05) :352-357
[5]   Nonanalytic Laboratory Automation: A Quarter Century of Progress [J].
Hawker, Charles D. .
CLINICAL CHEMISTRY, 2017, 63 (06) :1074-1082
[6]   Total Automation for the Core Laboratory: Improving the Turnaround Time Helps to Reduce the Volume of Ordered STAT Tests [J].
Ialongo, Cristiano ;
Porzio, Ottavia ;
Giambini, Ilio ;
Bernardini, Sergio .
JALA, 2016, 21 (03) :451-458
[7]  
La Porta Anthony D, 2004, Lab Hematol, V10, P95, DOI 10.1532/LH96.04022
[8]  
Leung KYE., TRIALS IMPLEMENTING
[9]   Evaluation of the impact of a total automation system in a large core laboratory on turnaround time [J].
Lou, Amy H. ;
Elnenaei, Manal O. ;
Sadek, Irene ;
Thompson, Shauna ;
Crocker, Bryan D. ;
Nassar, Bassam .
CLINICAL BIOCHEMISTRY, 2016, 49 (16-17) :1254-1258
[10]   Key Performance Indicators to Measure Improvement After Implementation of Total Laboratory Automation Abbott Accelerator a3600 [J].
Miler, Marijana ;
Gabaj, Nora Nikolac ;
Dukic, Lora ;
Simundic, Ana-Maria .
JOURNAL OF MEDICAL SYSTEMS, 2018, 42 (02)