دورية أكاديمية

False positive results of Bowie and Dick type test used for hospital steam sterilizer with slower come-up ramps: A case study.

التفاصيل البيبلوغرافية
العنوان: False positive results of Bowie and Dick type test used for hospital steam sterilizer with slower come-up ramps: A case study.
المؤلفون: Laranjeira PR; Cardinal Health, Miami Lakes, FL, United States of America., Bronzatti JAG; Nursing School São Paulo, Universidade de São Paulo, São Paulo, SP, Brazil., Bruna CQM; Nursing School São Paulo, Universidade de São Paulo, São Paulo, SP, Brazil., de Souza RQ; Nursing School São Paulo, Universidade de São Paulo, São Paulo, SP, Brazil., Graziano KU; Nursing School São Paulo, Universidade de São Paulo, São Paulo, SP, Brazil., Lusignan V; Research and Development Technician, Getinge, Englewood, CO, United States of America.
المصدر: PloS one [PLoS One] 2020 Jan 27; Vol. 15 (1), pp. e0227943. Date of Electronic Publication: 2020 Jan 27 (Print Publication: 2020).
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
أسماء مطبوعة: Original Publication: San Francisco, CA : Public Library of Science
مواضيع طبية MeSH: Quality Control* , Steam*, Equipment and Supplies, Hospital/*microbiology , Sterilization/*instrumentation, Equipment Contamination/prevention & control ; Gases ; Humans ; Sterilization/methods
مستخلص: Objective: To determine if the standardized B&D type test for hospital steam sterilizer is correctly indicating cycle failures in slower come-up ramps cycles.
Methods: Two commercially available B&D type test were challenged in a quality control sterilizer. A common failure was simulated in triplicate cycles, using a standardized cycle configuration, and then compared to triplicate cycles of a common cycle configuration. Tests procedures were conducted according to B&D manufacturer test standard and results were compared to standardized endpoint specifications.
Results: We found that B&D type tests are only capable of detecting the presence of non-condensable gases if the sterilization equipment is adjusted to meet all the cycle requirements of the test. False positive results were obtained with come-up ramp time of 3 min. Correct results were only obtained with come-up ramp of 1.7-1.9 min.
Conclusions: Until the ISO 17665 and AAMI ST-79 standards are revised, equipment qualification experts should observe come-up time duration criterion for B&D type test cycles according to ISO 11140-4. Sterile Processing Department professionals must add the come-up ramp criterion to cycle evaluation before clearing the equipment for routine use. This will allow B&D correct performance, reducing the infection risk from unsterilized medical device.
Competing Interests: P.R.L. has been a conference speaker for 3M, Getinge, and AMCOR and shareholder in Orion CE (São Paulo, Brazil). V.L. is currently employed by Getinge. R.Q.S. is a key-opinion-leader for the 3M. J.A.G.B. has been a conference speaker for FAMI, B. Braun and 3M. K.U.G. has been a conference speaker for Steris, Radar Hospitalar and 3M. This does not alter our adherence to PLOS ONE policies on sharing data and materials.
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Am J Infect Control. 2008 Mar;36(2):86-92. (PMID: 18313509)
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المشرفين على المادة: 0 (Gases)
0 (Steam)
تواريخ الأحداث: Date Created: 20200128 Date Completed: 20200414 Latest Revision: 20200414
رمز التحديث: 20221213
مُعرف محوري في PubMed: PMC6984693
DOI: 10.1371/journal.pone.0227943
PMID: 31986177
قاعدة البيانات: MEDLINE
الوصف
تدمد:1932-6203
DOI:10.1371/journal.pone.0227943