Auditory Brain-Stem Responses in Neonatal Hyperbilirubinemia and effect of therapy
Sanaa Mohamed Tantawy;
Abstract
SUMMARY
T
his prospective case control study was designed to determine the effect of neonatal hyperbilirubinemia on auditory brainstem response (ABR) and evaluate the effect of treatment of hyperbilirubinemia on ABR findings.
Patients and Methods: This study was performed on newborns with pathologic hyperbilirubinemia. The inclusion criteria were healthy term and near term (35 - 37 weeks) newborns with pathologic hyperbilirubinemia with serum bilirubin values of >13 mg/dL.
Inclusion criteria:
1. Fetomaternal blood group incompatibility.
2. Rh incompatibility.
3. History of previous sibling with significant hyperbilirubinemia.
4. Onset of jaundice before 24 hours of age.
5. A rise in serum bilirubin levels of over 0.5 mg/dl/hour.
6. Infant of diabetic mother.
Exclusion criteria:
1. Syndromes associated with hearing loss as: Waardenberg Syndrome, Pendred Syndrome, and Usher Syndrome...etc.
2. Family history of hereditary childhood sensorineural hearing loss.
3. Craniofacial abnormalities.
4. Congenital infections such as cytomegalovirus, rubella, syphilis, herpes simplex and toxoplasmosis.
5. Bacterial meningitis.
6. Birth weight less than 1500 grams.
7. Ototoxic medications use like amino glycosides, loop diuretics etc.
8. Low Apgar scores of 0–4 at 1 min or 0–6 at 5 min.
9. Mechanical ventilation lasting ≥5 days.
A total of 30 newborns with hyperbilirubinemia met the enrolment criteria as the case group and 20 healthy newborns as the control group, who werechosen from Neonatal Intensive Care unit and Maternity department of AL Zahraa Hospital of Al-Azhar University respectively. ABR was performed on both groups. The evaluated variable factors were latency time, inter peak intervals time, and loss of waves.
T
his prospective case control study was designed to determine the effect of neonatal hyperbilirubinemia on auditory brainstem response (ABR) and evaluate the effect of treatment of hyperbilirubinemia on ABR findings.
Patients and Methods: This study was performed on newborns with pathologic hyperbilirubinemia. The inclusion criteria were healthy term and near term (35 - 37 weeks) newborns with pathologic hyperbilirubinemia with serum bilirubin values of >13 mg/dL.
Inclusion criteria:
1. Fetomaternal blood group incompatibility.
2. Rh incompatibility.
3. History of previous sibling with significant hyperbilirubinemia.
4. Onset of jaundice before 24 hours of age.
5. A rise in serum bilirubin levels of over 0.5 mg/dl/hour.
6. Infant of diabetic mother.
Exclusion criteria:
1. Syndromes associated with hearing loss as: Waardenberg Syndrome, Pendred Syndrome, and Usher Syndrome...etc.
2. Family history of hereditary childhood sensorineural hearing loss.
3. Craniofacial abnormalities.
4. Congenital infections such as cytomegalovirus, rubella, syphilis, herpes simplex and toxoplasmosis.
5. Bacterial meningitis.
6. Birth weight less than 1500 grams.
7. Ototoxic medications use like amino glycosides, loop diuretics etc.
8. Low Apgar scores of 0–4 at 1 min or 0–6 at 5 min.
9. Mechanical ventilation lasting ≥5 days.
A total of 30 newborns with hyperbilirubinemia met the enrolment criteria as the case group and 20 healthy newborns as the control group, who werechosen from Neonatal Intensive Care unit and Maternity department of AL Zahraa Hospital of Al-Azhar University respectively. ABR was performed on both groups. The evaluated variable factors were latency time, inter peak intervals time, and loss of waves.
Other data
| Title | Auditory Brain-Stem Responses in Neonatal Hyperbilirubinemia and effect of therapy | Other Titles | دراسة استجابة جذع المخ فى حالات ارتفاع نسبة الصفراء فى الاطفال حديثى الولادة و تأثير العلاج | Authors | Sanaa Mohamed Tantawy | Issue Date | 2016 |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| G11957.pdf | 240.48 kB | Adobe PDF | View/Open |
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