Time-motion analysis of 6 cystic fibrosis mutation detection systems

Clin Chem. 2005 Jul;51(7):1116-22. doi: 10.1373/clinchem.2004.047423. Epub 2005 Apr 28.

Abstract

Background: A dramatic increase in requests for routine cystic fibrosis (CF) carrier screening prompted us to conduct a time-motion analysis comparing commercially available CF testing platforms. Questions addressed in the study included: (a) How much time is required to perform each step involved in carrying out the assay procedure? (b) Which system requires the minimum number of manual manipulations to complete a typical run? (c) What workflow benefits can be achieved by automation?

Methods: We used a 96-sample run for comparisons and analyzed each of the 6 methods to determine the number of pipetting steps and manual manipulations, the labor and instrument time, and the total time required to perform the assay. The survey participants included a staff of 4 technologists who perform complex molecular assays regularly. Time required for each procedure was determined by direct observation and from work logs completed by the technologists.

Results: The total number of pipetting motions varied from 78 to 344. Labor time ranged from 2.6 to 8.4 h, and total assay time from 7.6 to 13.7 h.

Conclusion: Time-motion analysis allowed identification of a method that minimized pipetting motions and thus reduced the risk of repetitive stress injury.

Publication types

  • Comparative Study

MeSH terms

  • Clinical Laboratory Techniques*
  • Cystic Fibrosis / genetics*
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics*
  • Humans
  • Mutation
  • Time and Motion Studies*

Substances

  • CFTR protein, human
  • Cystic Fibrosis Transmembrane Conductance Regulator