Cleft palate
PEMBIMBING :
AKBP HENRY SETIAWAN,DRG, M.KES, SP.BM
DENNY HERIAWAN
(2014-16-064)
GIOVANI TRIXIE NIRAHUA (2014-16-079)
Cleft Palate or Palatoschizis
Palatoschisis or cleft palate congenital abnormality
that occurs because there is no unification (fusion) is
normally of the soft palate at the embryonic process
where there is a failure processus closure
frontonasal, maxillary and mandibular either of
partially or completely. The normal position of the
canal nasopalatinis palate split into two parts, namely
primary and secondary palate palate.
Etiology
Classification
Cleft Palates Effect
FOOD INTAKE
TOOTH
OCCLUSAL PLANE
SKELETAL
HEARING
SPEECH
AIRWAY MAINTENANCE
Therapy for cleft palate (Palatoplasty)
Surgical procedure used to correct or reconstruct cleft palate
Usually done at six to eighteen months of age.
Although the child may look normal from the outside, the
cleft palate can be seen by looking for a separation in the roof
of the child's mouth.
A cleft palate should be repaired for several reasons, namely
to improve speech and to reestablish the barrier between the
mouth and the nasal cavity.
Rarely, more than one operation may be needed to close the
cleft palate.
Von Lagenbeck Palatoplasty
Veau-Wardill-Kilner / VY Pushback Palatoplasty
Two Flap Palatoplasty
Furlow double Z-palatoplasty
Post Operation Treatment
Open the obturator after 5-7 days postoperatively
soft diet
Clean the suture line with caution
Apply antibiotic ointment on the suture line
Avoid inserting objects into the child's mouth after feeding to prevent
aspiration
Monitor for signs of infection at the surgical site and systemic
Monitor the level of pain in infants and the need for pain medication
Note hemorrhage, edema, drainage
Monitor the integrity of the skin tissue
Note the position of the seam, avoid contact network with unsterilized tools
Complication
Airway obstruction
Bleeding
Palatal fistule
Midface anomalies
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