Technical considerations for medical device manufacturers when designing gastrostomy tubes (G-tubes) using the new ISO 80369-3 connector

• Published in: PloS one Vol. 15; no. 7; p. e0236644
• Main Authors: Guha, Suvajyoti, Herman, Alexander, Herbertson, Luke, Antonino, Mark J., Silverstein, Joshua S., Cooper, Jeffrey, Myers, Matthew R.
• Format: Journal Article
• Language: English
• Published: San Francisco Public Library of Science 30.07.2020; Public Library of Science (PLoS)
• Subjects: Biology and Life Sciences; Bore; Boring tools; Design; Devices; Engineering and Technology; Flow rates; Flow velocity; Health care; Laboratories; Medical equipment; Medicine and Health Sciences; Nutrition; Physical Sciences; Standardization; Syringes; Three dimensional printing; Tidal bores; Tubes; United States > US; Maryland
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0236644

Background Gastrostomy tubes (G-tubes) are typically used when people cannot eat food by mouth. The connector section that allows G-tubes to connect to other devices, such as feeding sets or syringes, has been modified on some of the devices to reduce misconnections in hospital settings. The narrow internal diameter of the new connector, standardized under ISO 80369–3, has caused some users to express concern about a reduced flow rate. Previous studies performed on commercial devices determined that it was not conclusive how much the ISO 80369–3 connector contributed towards the reduced flow rate, because when manufacturers designed these new connector-based devices, they often changed other geometric variables (such as distal tube diameter, or length) at the same time. Thus, it became difficult isolating the effect of the connector from other geometric variables. Method The key objective of this study was to investigate how different design variables impacted the flow rate through the G-tubes. 3D-printed devices were used to assess the geometric parameters in a systematic manner. Commercial diets and Newtonian analog fluids with matched viscosities were used for testing. Results The flow path length of the “transition section” encompassing the standardized ISO 80369–3 connector in the new devices was found to cause reduced flow. Additionally, results showed that a shortened (≤ 10 mm) transition section, along with a 10% increase in the distal inner diameter of large bore devices (e.g., 24 Fr), can restore flow rates to levels consistent with the previous devices prior to the connector standardization. Conclusions The strategy for restoring flow rates to previous levels may help alleviate concerns raised by multiple stakeholders such as health care professionals, patients, caregivers and device manufacturers. In addition, the approach proposed here can be used as a tool for designing future G-tube devices.