- Biopharma News
Overall benefits of ready-to-administer systems outweigh the initial cost disadvantages, says BD expertGareth Carpenter — 19 May 2021
Pre-fillable syringes for intravenous drugs can replace traditional glass vials and ampoules, particularly in the time-sensitive and fast-paced world of emergency care
Ready-to-administer-systems such as pre-fillable syringes can provide benefits to numerous stakeholders including reduction in medication errors, risk of contamination and nurse saving time.
“The only disadvantage is that the cost of a drug-pre-fillable device combination are much higher than that of a drug in a vial or ampoule,” said Sagar Bejalwar, Senior Manager, Global Acute and Specialty Portfolio Marketing at BD Medical - Pharmaceutical Systems.
“There are quite a few benefits that have been documented: the primary benefits are a reduction in medication errors, the reduced risk of contamination, as well as nurse time saving and a reduction in wastage,” he said.
He pinpointed savings in labour time and accurate dosing as critical factors, given that the coronavirus pandemic has reinforced the need for healthcare systems – particularly critical care -- to be much more efficient.
“Ready-to-administer systems do play a part in bringing about that efficiency at least on the point of care,” Bejalwar said, adding that they have the most impact in systems of critical care, which are relatively fast-paced and where there is very little room for error during the medication process.
He said only around 70% of injectable biologic chronic treatments of 50mL or less are packaged in ready-to-administer formats, with only 50% of vaccines available in this format. However, for acute liquid injectable small molecule drugs, the penetration was much less with only 2% are in ready-to-administer format, he added.
As well as the efficiency and time saving benefits to hospital administrator, Bejalwar said prefilled syringes also presented benefits to pharmaceutical players.
“Pharma companies having a generic drug launched in a ready-to-administer system or a prefilled syringe does provide a competitive edge and an opportunity to differentiate in the market that may be dominated by vials and ampoules,” he said.
Bejalwar said BD had recently launched its BD Hylok glass pre-fillable syringe for intravenous drugs primarily in response to malfunction issues with certain types of pin-activated needleless access devices which essentially led to breakage of the tip of the syringes and ultimately disruption to workflows.
“This really did highlight the aspect of incompatibility of pre-fillable syringes with certain designs of needleless access devices and this was specifically highlighted in emergency care settings,” he said.
Bejalwar said that BD’s objective is to position BD Hylok as a solution that meets market needs: “Many pharma companies conduct steam sterilization prior to launching their drug-device combination, and therefore we’ve tested BD Hylok for steam sterilization with water-for-injection to ensure that the pharma companies have that data at hand and are sufficiently equipped to conduct their respective testing processes.”
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