Diseases in the newborn child Flashcards
(40 cards)
How common is it for a child to become jaundiced within the first week of life?
50-60 % of children become jaundiced within the first week of life.
What is kernicterus?
Kernicterus is a bilirubin-induced brain dysfunction. Unconjugated bilirubin crosses the blood-/brain
barrier and acts neurotoxic (mainly in the basal ganglia).
What should be suspected if jaundice within first day of life or there is rapidly increasing bilirubin levels?
Suspect hemolysis due to immunization.
True or false: ABO-immunization is common in pregnancies, but rarely cause any prenantal symptoms.
True. It occurs 15-20% of pregnancies, but rarely causes prenatal symptoms.
What are fetal consequences of serious Rh-immunization?
Erythroblastosis foetalis: Serious anemia → heart failure in the fetus.
Hepatoslenomegaly: Extramedullary hematopoiesis. Liver failure lead to low albumin.
Hydrops foetalis: Heart failure and low albumin leads to edema. Ascites, pericardial effusion, pleural effusion, subcutanous edema.
What are the causes of physiologic jaundice?
Degradation of fetal hemoglobin. Immature liver (low activity of conjugating enzymes).
When does physiologic jaundice usually disappear?
In 4-7 days.
What is the treatment for breastfeeding jaundice?
Breastfeeding jaundice is a benign condition and resolves itself within 12 weeks of life. (Photo-therapy is indicated in cases of “not enough breastfeeding” jaundice.)
In what ways can pathological jaundice in newborn be treated?
Oral hydration – breast milk.
Phototherapy.
Immunoglobuline.
Exchange transfusion.
What are indications for exchange transfusion as treatment against jaundice in newborns? Is this type of therapy common?
Indications include serious anemia and hydrops fetalis - like in Rh-immunization.
It is seldom used as therapy in Norway (about 9-10 cases per year need exchange transfusion).
Besides exchange transfusion, what treatment is used when managing antibody mediated jaundice in newborns?
Intravenous immunoglobulin.
What are causes of conjugated jaundice > 2 weeks in newborns?
Conjugated jaundice: Bile duct atresia. Neonatal hepatitis. Prolonged total parenteral nutrition.
What are the main types of newborn infections based on when and how it is acquired?
Transplacental infections.
Ascending infection.
Intrapartum infections.
Postnatal infections.
What is a congenital infection?
Maternal infection with transplacental hematogen transmission in utero.
When should a congenital infection be suspected?
Fetal growth restriction (FGR) Enlarged liver and spleen CNS symptoms/signs Microcephaly, hydrocephalus, intracerebral calcifications, cataract, chorioretinitis, deafness Trombocytopenia and anemia Skin hemorrhages Jaundice/neonatal hepatitis (conjugated)
What are some viral agents that may cause congenital infections?
Rubella Cytomegalovirus Parvovirus Varicella Herpes Enterovirus Hepatitis B and C (Syphilis is caused by a bacterial agent and toxoplasmosis by a parasite, but may cause congenital infections.)
What are risk factors of congenital herpes?
Premature rupture of membranes, prematurity and traumatic lesions.
True or false: Neonatal herpes simplex is a common disease in Norway.
False. Incidence of 1-3 per year.
What is characteristic of neonatal herpes infection skin-eye-mouth disease?
Vesicles in skin, mouth and/or conjunctiva.
Age of onset 5-11 days.
All cases have vesicles at onset of disease.
The mortality and disability are 0 %.
What is characteristic of congenital herpes infection?
Vesicles. Scarring of skin. Brain damage. Microcephaly.
Disability is 100 %, mortality is unknown.
How is neonatal herpes infection diagnosed and treated?
Diagnosis: PCR from vesicles or spinal fluid. Serology.
Treatment: At first intravenous acyclovir, followed by 6 months of treatment with oral acyclovir to reduce the risk of recurrence.
Are congenital CMV infection most commonly symptomatic or asymptomatic?
Asymptomatic infections are most common - but may cause deafness.
What is the most important non-genetic cause of deafness?
Congenital CMV infections in newborn children.
How are CMV infections in newborn children diagnosed?
PCR based on saliva, urine or blood. Serology of maternal blood. Liver and hematological blood tests. Eye examination. Ultrasound or MRI. Auditory test. Lumbar puncture can by considered.