Functional oral intake and time to reach unrestricted dieting for patients with traumatic brain injury

Hansen TS, Engberg AW, Larsen K. Functional oral intake and time to reach unrestricted dieting for patients with traumatic brain injury.

Objectives

To investigate the status of functional oral intake for patients with severe traumatic brain injury (TBI) and time to return to unrestricted dieting; and to investigate whether severity of brain injury is a predictor for unrestricted dieting.

Design

Observational retrospective cohort study.

Setting

Subacute rehabilitation department, university hospital.

Participants

Patients age 16 to 65 years (N=173) with severe TBI (posttraumatic amnesia from 7d to >6mo) admitted over a 5-year period. Patients are transferred to the brain injury unit as soon as they ventilate spontaneously.

Intervention

Facial oral tract therapy.

Main Outcome Measure

Unrestricted dieting assessed by the Functional Oral Intake Scale (FOIS).

Results

We found that 93% of all patients had problems with functional oral intake at admission. Within 126 days of rehabilitation, 64% recovered to unrestricted dieting before discharge. The chance of returning to total oral diet depends on the severity of the brain injury and can be predicted by Glasgow Coma Scale (GCS; measured the day after cessation of sedation; Wald χ²=42.78, P<.01), Rancho Los Amigos Scale (RLAS) level (Wald χ²=11.84, P=.01), FIM instrument (Wald χ²=44.40, P<.01), and FOIS score at admission (Wald χ²=82.93, P<.01).

Conclusions

Impairment in functional oral intake was found to be very common for patients with severe TBI admitted to a subacute rehabilitation department. For those who recovered during hospital rehabilitation, return to unrestricted dieting happened within 126 days of rehabilitation. The chance of returning to unrestricted dieting depends on the severity of the brain injury and can be predicted by GCS score, RLAS level, FIM score, and functional oral intake at admission. These results are important when planning rehabilitation, giving information to patients and relatives, and designing efficacy studies of facial oral tract therapy, which are highly recommended.