Cleft lip __palate

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Cleft lip __palate

  1. 1. Cleft Lip & PalatePRESENTED BY:A.PRIYADHARSHINI M.Sc (N)LECTURER,JAI INSTITUTE OF NURSING ANDRESEARCH, GWALIOR
  2. 2. INTRODUCTION: Cleft lip (cheiloschisis) and cleft palate (palatoschisis), which can also occur together as cleft lip and palate, are variations of a type of clefting congenital deformity caused by abnormal facial development during gestation. A cleft is a fissure or opening—a gap. It is the non-fusion of the bodys natural structures that form before birth.
  3. 3. CLEFT LIP- DEFINITION: Cleft lip is formed in the top of the lip as either a small gap or an indentation in the lip (partial or incomplete cleft) or it continues into the nose (complete cleft). Lip cleft can occur as a one sided (unilateral) or two sided (bilateral). It is due to the failure of fusion of the maxillary and medial nasal processes(formation of the primary palate).
  4. 4. INCIDENCE: Approximately 1 in 700 children born have a cleft lip and/or a cleft palate. Left side unilateral cleft is the most common.
  5. 5. Unilateral incomplete Unilateral complete Bilateral complete
  6. 6. CLEFT PALATE: Cleft palate is a condition in which the two plates of the skull that form the hard palate (roof of the mouth) are not completely joined. In most cases, cleft lip is also present. Cleft palate occurs in about one in 700 live births worldwide. Palate cleft can occur as complete or incomplete
  7. 7. CONTD… When cleft palate occurs, the uvula is usually split. It occurs due to the failure of fusion of the lateral palatine processes, the nasal septum, and/or the median palatine processes (formation of the secondary palate). The hole in the roof of the mouth caused by a cleft connects the mouth directly to the  nasal cavity.
  8. 8. Incomplete cleft palate Unilateral complete lip and palate Bilateral complete
  9. 9. Etiology Genetic Environmental agents-seasonal causes (such as pesticide exposure); Maternal diet and vitamin intake; parental exposure to lead Medications- phenytoin, sodium valporate and methotrexate Cigarette smoking during pregnancy Alcohol during pregnancy Folate deficiency
  10. 10. SIGNS AND SYMPTOMS: Split in lip or palate Symptoms related to location of cleft: ◦ Hard & soft palate: Facial defect ◦ Soft palate: leaking of ingested liquids from the nose ◦ Hard palate: weak, dysfunctional suck, trouble swallowing, gagging, choking
  11. 11. Prenatal Diagnosis Diagnosed until the soft tissues of the fetal face can be clearly visualized sonographically (13 to 14 weeks). The majority of infants with cleft lip also have palatal involvement:
  12. 12. Prenatal Diagnosis
  13. 13. CLEFT LIP- TREATMENT: Within the first 2–3 months after birth, surgery is performed to close the cleft lip. While surgery to repair a cleft lip can be performed soon after birth, often the preferred age is at approximately 10 weeks of age, following the "rule of 10s" (the child is at least 10 weeks of age; weighs at least 10 pounds, and has at least 10g hemoglobin). 
  14. 14. CONTD… If the cleft is bilateral and extensive, two surgeries may be required to close the cleft, one side first, and the second side a few weeks later. The most common procedure to repair a cleft lip is the Millard procedure .
  15. 15. Cleft lip repair. The edges of the cleft between the lip and nose are cut (A andB). The bottom of the nostril is formed with suture (C). The upper part of the lip tissue is closed (D), and the stitches are extended down to close the opening entirely (E).
  16. 16. CLEFT PALATE-TREATMENT Often a cleft palate is temporarily covered by a palatal obturator (a prosthetic device made to fit the roof of the mouth covering the gap). Cleft palate can also be corrected by surgery, usually performed between 6 and 12 months.
  17. 17. CONTD.. One of the new innovations of cleft lip and cleft palate repair is the Latham appliance.  The Latham is surgically inserted by use of pins during the childs 4th or 5th month. After it is in place, the doctor, or parents, turn a screw daily to bring the cleft together to assist with future lip and/or palate repair.
  18. 18. Speech and hearing: A tympanostomy tube is often inserted into the eardrum to aerate the middle ear. This is often beneficial for the hearing ability of the child. Children with cleft palate typically have a variety of speech problems. Difficulty in pronouncing /p/, /b/, /t/, /d/, /s/, /z/, etc.This type of errors typically resolve after palate repair.
  19. 19. Feedings Infants with CL/P have few feeding problems. If the cleft involves the hard palate, the infant is usually not able to suck efficiently. The infant should be held in a nearly sitting position during feeding  Prevents flowing to the back into the nose. Should be burped frequently, (q 3-4min).
  20. 20. Feedings It is important to keep the cleft clean Breastfeeding is extremely challenging.
  21. 21. Special Needs Feeder / Haberman Feeder
  22. 22. PIGEON FEEDER:
  23. 23. NURSING DIAGNOSIS: Risk for aspiration related to opening of the palate. Imbalanced nutrition less than body requirement related to poor food intake. Impaired communication related to problem with the production of sound. Deficient knowledge (mother)regarding proper feeding techniques.
  24. 24. THANK YOU

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