Evidence map›Paper›PMID 39304678›Full record

ArticleScientific reports2024

Design and validation of a method for evaluating medical device cleanliness by recovering and quantifying residual proteins on stainless plates.

Miyuki Uematsu, Yuko Miyamoto, Masatake Shimizu, Tsuyoshi Kajiura, Atsushi Saito, Masaki Takashina, Satoshi Fujita, Yuko Nakano, Toshiaki Shimizu, Yuki Nagahara and 16 more

Abstract readValidation Study
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

26 authors.

Miyuki UematsuDivision of Medical Devices, National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki-ku, Kawasaki-shi, Kanagawa, 210-9501, Japan. uematsu@nihs.go.jp.
Yuko MiyamotoDivision of Medical Devices, National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki-ku, Kawasaki-shi, Kanagawa, 210-9501, Japan.
Masatake ShimizuDevelopment Laboratory, Inui Medics Co., Ltd., 2-1-4 Honjo, Higashiosaka-shi, Osaka, 578-0953, Japan.
Tsuyoshi KajiuraDevelopment Laboratory, Inui Medics Co., Ltd., 2-1-4 Honjo, Higashiosaka-shi, Osaka, 578-0953, Japan.
Atsushi SaitoCentral Sterile Supply Department, Osaka University Hospital, 2-15 Yamadaoka, Suita-shi, Osaka, 565-0871, Japan.
Masaki TakashinaCentral Sterile Supply Department, Osaka University Hospital, 2-15 Yamadaoka, Suita-shi, Osaka, 565-0871, Japan.
Satoshi FujitaEngineering Department, Clean Chemical Co., Ltd., 4-28-9 Shima, Ibaraki-shi, Osaka, 567-0854, Japan.
Yuko NakanoEngineering Department, Clean Chemical Co., Ltd., 4-28-9 Shima, Ibaraki-shi, Osaka, 567-0854, Japan.
Toshiaki ShimizuInfection Control Business Unit, Sakura Seiki Co., Ltd., 1122-8 Yawata, Chikuma-shi, Nagano, 387-0023, Japan.
Yuki NagaharaInfection Control Business Unit, Sakura Seiki Co., Ltd., 1122-8 Yawata, Chikuma-shi, Nagano, 387-0023, Japan.
Hayato KosakaInfection Control Business Unit, Sakura Seiki Co., Ltd., 1122-8 Yawata, Chikuma-shi, Nagano, 387-0023, Japan.
Hiroki MuramatsuSUD Re-manufacturing Business Preparation Office, Suzuyo & Co., Ltd., 1-2-12 Shibakoen, Minato-ku, Tokyo, 105-0011, Japan.
Masafumi MoriSUD Re-manufacturing Business Preparation Office, Suzuyo & Co., Ltd., 1-2-12 Shibakoen, Minato-ku, Tokyo, 105-0011, Japan.
Takamasa SuzukiSUD Re-manufacturing Business Preparation Office, Suzuyo & Co., Ltd., 1-2-12 Shibakoen, Minato-ku, Tokyo, 105-0011, Japan.
Takayoshi NakamuraInstitute of Surface Science and Technology, Nicca Chemical Co., Ltd., 4-23-1 Bunkyo, Fukui-shi, Fukui, 910-8670, Japan.
Atsushi TanemuraInstitute of Surface Science and Technology, Nicca Chemical Co., Ltd., 4-23-1 Bunkyo, Fukui-shi, Fukui, 910-8670, Japan.
Junki HosakaLaboratory and Speciality Chemicals Division, FUJIFILM Wako Pure Chemical Corp., 6-1 Takata-cho, Amagasaki-shi, Hyogo, 661-0963, Japan.
Takahide MoriLaboratory and Speciality Chemicals Division, FUJIFILM Wako Pure Chemical Corp., 6-1 Takata-cho, Amagasaki-shi, Hyogo, 661-0963, Japan.
Seiichi KatoResearch and Development Division, Hogy Medical Co., Ltd., 1873-1 Fusa, Miho-mura, Inashiki-gun, Ibaraki, 300-0427, Japan.
Ayaka ItagakiResearch and Development Division, Hogy Medical Co., Ltd., 1873-1 Fusa, Miho-mura, Inashiki-gun, Ibaraki, 300-0427, Japan.
Toshiki InoueResearch and Development Division, Hogy Medical Co., Ltd., 1873-1 Fusa, Miho-mura, Inashiki-gun, Ibaraki, 300-0427, Japan.
Shinichi MatsumotoSystem Sales Department, Muranaka Medical Instruments Co., Ltd., Funakoshi-cho, Chuo-ku, Osaka, 540-0036, Japan.
Tomoko NaitoR&D Division, Miura Co., Ltd., 7 Horie-cho, Matsuyama-shi, Ehime, 799-2696, Japan.
Shinji FujiiR&D Division, Miura Co., Ltd., 7 Horie-cho, Matsuyama-shi, Ehime, 799-2696, Japan.
Ryusuke NakaokaDivision of Medical Devices, National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki-ku, Kawasaki-shi, Kanagawa, 210-9501, Japan.
Eiichi YamamotoDivision of Medical Devices, National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki-ku, Kawasaki-shi, Kanagawa, 210-9501, Japan.

Funding

Japan Agency for Medical Research and Development 22mk0102174
6 · The paper itself

Abstract

We recently reported a method for recovering and quantifying residual proteins bound to surfaces of various medical instruments via thermal coagulation under neutral pH and room temperature. The method effectively recovered and solubilised coagulated proteins at high temperatures in dry and humid conditions, with a protein recovery rate of > 90%. This study validated the previous method by comparing residual protein recovery from test samples using a conventional extraction solution (1% SDS, [pH 11.0]) and proposed solution (1% SDS, 10 mM TCEP, and 10 mM HEPES [pH 7.0]). To mimic soiled medical equipment, pseudo-blood-contaminated stainless steel plates were prepared. Residual protein was recovered using conventional and proposed solutions under varying temperature and humidity conditions. Quantitative protein recovery limits were determined at nine facilities. Compared with the conventional solution, the proposed solution recovered proteins more effectively from samples processed at temperatures > 60 °C. However, low recovery rates were observed for samples processed at 95 °C, possibly owing to differences in protein adhesion due to sample and plate-surface properties. Our findings present a method for quantifying residual proteins on medical instruments exposed to high temperatures during use or disinfection. Further studies should standardise test soiling conditions, materials, and solutions to evaluate cleaning methods.

Indexed as

ProteinsStainless SteelEquipment and SuppliesEquipment ContaminationTemperatureProteinsStainless Steel

Identifiers

PMID39304678
PMCPMC11415368

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.