Chapter 24: Cleft Lip and Palate (Children) Flashcards
Cleft lip (CL), Cleft palate (CP)
multi-factorial congenital defect that has genetic and environmental predispositions
-Cleft lip and cleft palate are openings or splits in the upper lip, the roof of the mouth (palate) or both.
What happens during intrauterine fetal life for this to occur?
-the primary palate does not fully fuse, and and one of the several variations of clefts can occur depending on the timing of the insult
Signs and Symptoms
- unilaterally or bilaterally cleft lip
- can occur with or without a cleft of the hard and/or soft palate
- both or either of the palates can have a cleft without the lip
- uvula can also contain a cleft
Diagnosis
-CL is obvious, but CP calls for examination of the mouth with a light source
Nursing Care
- maintain adequate nutrition
- can be successfully breastfed; breastfeeding can be interrupted for a period of time based on the need for surgical repair
- bottle feeding is initiated with a special nipple that is longer than a regular nipple to help prevent aspiration
- Haberman feeder (longer and has a reservoir to regulate the flow of formula
- newborns with clefts are fed in an upright position to decrease the incidence of regurgitation and aspiration
- no sucking until lip is healed, use syringe or dropper
Haberman Feeder
- longer
- has a reservoir to regulate flow of formula
What position do we feed a newborn with clefts?
upright position to decrease the incidence of regurgitation an aspiration
Surgical repair
surgical repair of Cleft lip is done at 3 months of age
- Cleft palate repaired before 18 months
- some clefts require more than one surgical repair
Education/ Discharge
- parents supported by having all the treatments, feeding methods, and care measures explained
- emotional support needed to assist in grieving process of dealing with the reality of a “non-perfect” child with possible on-going surgical needs and feeding problems
- later in life may experience psychosocial problems b/c of facial deformity