Research Team Develops Standard for Measuring Facial Palsy

New guideline expected to improve future care

An international team of researchers, including a psychologist at Oregon State University, has developed a standardized measurement for pediatric facial palsy that will improve the care for current and future patients with the condition.

The team, which includes researchers from nine countries, published their findings Thursday in JAMA Facial Plastic Surgery.

“Facial palsy profoundly impacts many aspects of a child’s life, from functional issues like eating and vision, to core psychological issues such as social communication, peer relationships and quality of life,” said Kathleen Bogart, an associate professor of psychology in the College of Liberal Arts at Oregon State and the only psychologist on the research team. “Using a standard set of measurement tools to track these outcomes after treatments will ensure that clinicians understand patient strengths and challenges while enabling them to verify what treatments are effective.”

Historically, there has been a wide range of measurement tools to evaluate treatment plans for patients with the condition, but efforts to create a universal measurement tool have been unsuccessful. Pediatric facial palsy is notoriously difficult to treat, and inconsistent use of outcome measures have hampered understanding of treatment effectiveness. A nonprofit organization called the International Consortium for Health Outcomes Measurement aimed to change that.

The result was the standard measurement tool that allows the recording of outcomes following facial palsy treatment, surgical and non-surgical, for pediatric patients.

The measurement tool takes into account a number of factors: facial appearance and movement; oral continence; speech; facial discomfort; vision and ocular symptoms; health-related quality of life; social health; and major complications from interventions. Each factor is assessed using a scientifically validated tool.

SOURCE: News Medical

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