Real-world considerations for the rapid prototyping and manufacture of a ventilator for the COVID-19 pandemic

被引:0
作者
Wong, Judith Ju Ming [1 ,2 ,9 ]
Loke, Fiona Wei Ling [3 ]
Tan, Herng Lee [1 ]
Quah, Jessica Lishan [4 ]
Cheong, Wai Chye [3 ]
Khan, Shariq Ali [5 ]
Thomas, Biju [2 ,6 ]
Phua, Ghee Chee [7 ]
Chan, Derrick Wei Shih [2 ,8 ]
机构
[1] KK Womens & Childrens Hosp, Childrens Intens Care Unit, Singapore, Singapore
[2] SingHealth Duke NUS Acad Med Ctr, Singapore, Singapore
[3] SingHealth, Med Technol Off, Singapore, Singapore
[4] Changi Gen Hosp, Resp & Crit Care Med, Singapore, Singapore
[5] Sengkang Gen Hosp, Anaesthesiol, Singapore, Singapore
[6] KK Womens & Childrens Hosp, Pediat Resp Med Serv, Singapore, Singapore
[7] Singapore Gen Hosp, Resp & Crit Care Med, Singapore, Singapore
[8] KK Womens & Childrens Hosp, Pediat Neurol, Singapore, Singapore
[9] KK Womens & Childrens Hosp, Childrens Intens Care Unit, 100 Bukit Timah Rd, Singapore 229899, Singapore
关键词
artificial respiration; mechanical ventilator; innovative therapies; medical device design; SARS-CoV-2;
D O I
10.1177/20101058231182004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundIn the COVID-19 pandemic, ventilators vital to keeping infected patients alive, were in short supply globally. Our aim was to rapidly prototype and implement production of basic ventilators to serve the local and regional needs in this emergency situation.MethodsWe adopted a supply-to-design approach, estimating the potential demand for ventilator units and sourcing for common off-the-shelf components available in the estimated quantities, to assemble ventilator units which met the essential requirements for clinical use. We determined the minimum requirements of a basic ventilator based on published specifications and clinician input. Building the ventilator involved interdisciplinary collaboration (between clinicians, industry, hospital innovation engineers and government partners), prototyping and repeated iterations, bench testing, animal testing, regulatory processes, ISO13485 quality management processes, licensing and user acceptability testing.ResultsWe prototyped a limited feature ventilator to supplement hospital ventilators which could be manufactured in sufficient numbers within a short span of time from easily available component parts. Developed with close attention to clinician user input with compliance to ISO standards and quality management processes where possible, this ventilator system was composed of coupled resuscitation bags, motor systems, and pressure and flow sensors capable of delivering ventilator breaths within safe and clinically important targets. This system is functional on ambient air with or without low pressure oxygen supplementation. User feedback cited size, alarms and intuitiveness of controls as potential areas for improvement.ConclusionsFurther modification based on user acceptability testing results are needed to refine the usability of this limited feature ventilator.
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页数:8
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  • [11] Yock P., 2009, BIODESIGN PROCESS IN, V2nd Edition ed.