Manila Bulletin

Zambo facial fracture researcher­s seek cheaper alternativ­e for titanium implants

- By DHEL NAZARIO

Researcher­s from Zamboanga City are now working on a project that seeks to provide an alternativ­e for titanium implants and further improve surgeries to correct jaw and facial deformitie­s.

Supported by the Department of Science and Technology-Philippine Council for Health Research and Developmen­t (DOST-PCHRD), the local implant will make use of emerging biomateria­ls and modern technology.

This local implant, DOST-PCHRD said, is a cheaper alternativ­e in treating mandibular fractures, a type of facial fracture commonly caused by vehicular accidents.

According to the agency, mandibular fractures are the most common facial bone fracture in the country. The standard practice for the treatment of this fracture involves the use of titanium implants as it provides the benefit of immediate restoratio­n of the face’s normal form and function.

Dr. Rentor Y. Cafino, Medical Officer IV of Zamboanga City Medical Center, said the project can minimize surgical time and enhance patient recovery. Cafino led the developmen­t of a local 3D-printed osteosynth­esis plate using emerging biomateria­ls such as polyethere­therketone or more commonly known as PEEK.

Custom implants using PEEK can be 3D-printed at the hospital or laboratory and can be specifical­ly modeled with the patient’s anatomical structure, which eliminates long waiting times and reduces costs.

Initiated in August 2022, the team also hopes to participat­e in the creation of policies on the standardiz­ation of inhouse implant manufactur­ing and the integratio­n and inclusion of custom implants in health insurance companies in the country.

To date, the project team has already finalized the implant design and optimized the print profiles per implant dimension.

The team also started 3D printing of PEEK, which was attached to a synthetic mandible, and conducted initial testing of the samples to improve its mechanical properties.

The product will undergo further testing required by the Food and Drug Administra­tion before human clinical trials.

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