Peds Flashcards
What is the appropriate technique for fluid resuscitation in a 7kg 5MO?
In states of acidosis, the excess hydrogen ions displace calcium bound by albumin and thus ionized levels of calcium increase. This process is reversed in the setting of alkalosis and should be considered before administering sodium bicarbonate to a patient with pre-existing hypocalcemia.
When should dextrose containing fluids be given?
Child <3months, Surgery >3 hours, or other comorbidities
PONV risks for Peds?
1) Duration of surgery > 30 minutes 2) Age > 3 years 3) History of PONV in the patient, parent, or sibling 4) Strabismus surgery
Frequent blood transfusions for patients with beta-thalassemia would result in what possibly? what anesthetic concerns do you have?
Cardiomyopathy from repeated transfusions 2/2 iron overload and hemosiderosis Thalassemias are a hemolytic anemia Anesthetic considerations for these patients include: Preoperative hemoglobin levels Provision of leukocyte-reduced blood transfusions Cardiac, endocrine, hepatic assessments Bony deformities that may render the airway more difficult Fragile demineralized extremities that may render positioning challenging Post-splenectomy hypertension Thromboembolism prophylaxis and treatment
fetal vascular accident affecting the first and second branchial arches. As such, it is a unilateral or asymmetric condition affecting the facial bones and muscles (micrognathia, cleft palate, abnormal tongue, hemivertebrae), eyes (microphthalmia, coloboma, etc), and ears (microtia, hearing loss). Anomalies of other systems are possible (e.g., tracheoesophageal fistula, renal agenesis, ventricular septal defect, hydrocephalus). Laryngoscopy is difficult but supraglottic airways have been repeatedly proven successful.
Goldenhar Syndrome
consists of craniosynostosis (premature cranial suture ossification), hypertelorism (increased distance between the orbits), shallow orbits causing ocular proptosis, maxillary hypoplasia, and parrot-like beaked nose. Depending on the specific mutation, patients may or may not have acanthosis nigricans. Unlike Goldenhar/Pierre Robin/Treacher Collins patients, …. patients do not have mandibular hypoplasia/micrognathia. In fact, the maxillary hypoplasia with normal size mandible creates a relative prognathism. The main airway difficulties are difficult mask fitting and upper airway obstruction, whereas intubation is not as difficult unless neck mobility is decreased (cervical spine fusion may coexist).
Crouzon Syndrome
tosomal recessive disorder due to an abnormality in alpha-L-iduronidase, which leads to intellectual disability, short stature, and multiorgan involvement secondary to mucopolysaccharide deposition. Treatment with recombinant human alpha-L-iduronidase or bone marrow transplantation can ameliorate the course of the disease. Anesthetic considerations are mostly those of airway management, complicated by abnormal facies, abundant secretions, large tongue, and short neck. The epiglottis may be higher in the neck and potentially displaced downward by insertion of an oral airway.
Hurler Syndrome
micrognathia, glossoptosis, and cleft palate. Often an isolated finding, it can also occur in the context of multiple malformations. Unlike Goldenhar syndrome, … sequence is bilateral, and typically does not involve the eyes and ears. Patients with this sequence may require prone positioning or a tongue-lip stitch for spontaneous ventilation.
Pierre Robin
syndrome consists of malar hypoplasia, downslanting palpebral fissures, colobomas of the lower eyelid, external ear abnormalities often involving hearing loss, and mandibular and pharyngeal hypoplasia. These patients are considerably more dysmorphic than Robin or Goldenhar patients, but their intelligence is normal, so they should be addressed as appropriate for age (other than speaking louder if they are hard of hearing).
Treacher Collins
What are the 5 congenital abnormalities that I need to know for difficult airway in the pediatric patients?
Five congenital anomalies are specifically mentioned in the ABA Content Outline in relation to the difficult airway. Four of these can be grouped together as having mandibular (Goldenhar, Robin, Treacher Collins) or maxillary (Crouzon) hypoplasia with normal intelligence. The other is Hurler, which for airway purposes can be remembered because it shares certain traits with the much more common Down syndrome, namely short neck, large tongue, large adenoids, obstructive sleep apnea, small trachea, and potential atlantoaxial instability. All 5 anomalies are associated with obstructive sleep apnea, and supraglottic airway devices (e.g., laryngeal mask airway) have been reported to be useful in all of them. Robin sequence is the only anomaly that becomes easier to intubate with age, whereas Treacher Collins, Goldenhar, and Hurler reportedly become progressively more difficult. Crouzon syndrome becomes more difficult to intubate as a consequence of maxillary advancement surgery (distraction osteotomy is commonly performed in these patients).
when does separation anxiety begin? How would you dose preoperative midazolam orally?
6-8 months. 0.5-0.75mg/kg
what opioid is contraindicated post tonsillectomy?
Codeine because it is metabolized into morphine (active form) via cyto 2D6. Rapid metabolizers can have respiratory depression
What is the estimated allowable blood loss equation?
MABL = EBV x (patient’s starting HCT – minimum acceptable HCT) /patient’s starting HCT
what neurologic abnormalities are associated with myelomenigocele? what toxins are associated with its formation?
Myelomeningocele is the most severe of the spina bifida defects. It is associated with Arnold-Chiari malformations and the patient may require VPS placement later in life for hydrocephalus Even after repair, no neuraxial anesthesia MMC occurs in the 3rd week of development Toxins associated with MMC formation include: Calcium-channel blockers Carbamazepine Cytochalasins Hyperthermia Valproic acid
Infant has hypothermia..what is the worst thing that happens to him/her? how does this happen?
Metabolic acidosis -nonshivering thermogenesis of brown fat (4-10% of fat stores in neonate and is high in mitochondria) (disappears around 3-6months after birth)…hypothermia causes norepinephrine release which binds to brown fat via CAMP causing breakdown of triglycerides by using O2 and glucose causing heat production. Ketones and water are byproducts.
what should be the initial bolus be for a kid that needs resucitation? 12kg kid?
20ml/kg up to 30ml/kg of 0.9% NS. NO additives
what are the common side effects of PRIS?
metabolic acidosis, rhabdomyolysis, hyperkalemia, hepatomegaly, renal failure, hyperlipidemia, arrhythmia, and cardiac failure maximum dose of propofol is 4mg/kg/hr
The evaporative water loss per kg is _____ proportional to age
inversely 2/2 increased ratio of body surface area to Total body weight kids have a higher total body water content for size compared to adults
is myelinization of the nerves in children advanced or delayed?
delayed. Means easier blocking but shorter duration.
what causes gastroschisis ?
Occlusion of the omphalomesenteric artery (this is not associated without omphaloceles)
explain the difference between adult and pediatric larynx?
relatively larger tongue of an infant, a more cephalad larynx, angled vocal cords and an omega shaped epiglottis. The infant’s epiglottis is narrower, omega-shaped, and angled away from the axis of the trachea.