Pediatric ED Case Conference Date: 2006/04/25 Presented by R1 劉政忠 Instructor: MA 張玉吉吉 醫師 MA 吳孟書 醫師
General data Name: 張 X 浩 Chart number: Age: 3 week 2 day-old Gender: Male Body weight : 3kg
Vital sign :43 (0hr0min) T:36, P:165, R: 65 E4V5M6, SpO 2 :93% 檢傷分類 : 3 級 病患主訴因食慾差 Chief complaints: SOB for 2 days
Present illness Vomiting for 2 days No cough Poor appetite(+) 看起來很乾 ?
Past history Nil
PAT Appearance: ? Breathing: tachypnea Circulation: ?
Physical examination General appearance: poor activity HEENT: lip cyanosis, dry lip Chest: bil coarse BS, wheezing(+), rales(+), retraction(+) Heart: RHB Abdomen:? Extremity:? Skin:?
ED initial impression r/o GER r/o aspiration pneumonia
Further history taking Dyspnea? Cough? Foreign body? Cyanosis? Vomiting? Content? Projectile? Feeding? Diarrhea? Urine amount? Body weight change? Fever? Activity? Appetite? Drug hx? Birth hx: BBW? IUGR? Preterm baby?CHD? Maternal hx: GDM? PROM?
Further PE Appearance: TICLS HEENT: frontanelle, tears, dry mouth or mucosa, throat, nasal flaring, accessory muscle use Chest: retraction, breathing sound Heart: murmur Abdomen: soft or distension, tenderness, bowel sound, umbilicus, mass Skin: rash, turgor, pallor, cyanosis, CRT
Detail Hx from admission note(1) Birth hx: G1P1 GA:39+weeks, NSD, APGAR score? Born in LMD, BBW: 2850g, BH: 50cm, NB screen:? Drug hx: 八寶粉 topical use? Vaccine: HBV on Maternal hx: 20y/o,G1P1, No maternal fever, no PROM, no chorioamnionitis, no maternal GDM, no PIH, no eclampsia, and no use of drug during pregnancy
Detail Hx from admission note(2) 3 days ago…. Vomiting decreased appetite (80~100cc to 20~30 per meal) progressive tachypnea, cyanosis when feeding BW: 2850 to 2880g (<3rd percentile)
Detail PE from admission note(1) General appearance : ill looking, poor activity and irritable HEENT : grossly normal, no facial dysmorphism, no anterior or posterior frontanel bulging, no icteric sclera, no neck mass, no periorbital edema Heart : regular heart beat, no murmur Chest : coarse breath sound, no wheeze, no rales, tachypnea and obvious subcostal or supraclavicular retraction, mild nasal flaring
Detail PE from admission note(2) Abdomen : soft, flat, no distension, normoactive bowel sound, no abnormal palpable mass, no pus discharge from umbilical area, no hepatosplenomegaly, no perianal redness Genital organ : grossly normal Extremity :no edema, distal four limb : warm and pink, no limb cyanosis, peripheral pulse palpable, capillary refill time < 2 sec Skin: no rash Neurologic examination : muscle power : +5/+5, no hypotonia
How about this baby? Respiratory distress + dehydration + poor activity => ? Infection: pneumonia, UTI, viral infection… Endocrine and metabolism: electrolyte imbalance, Inborn errors of metabolism, Hypoglycemia… GI: pyloric stenosis, AGE, T-E fistula, obstruction…
Initial order 3/29 13:18 (0hr35min) CXR CBC/DC, CRP, AST, ALT, BUN, Cr, Na, K, Cl, Ca, sugar, CRP, B/C*1 IVF: D5S1/4 run 15cc/hr O2 hood A+B inhalation st NPO
Lab—hemogram WBC Hemoglobin 15.5 Hematocrit 43.9 Platelets Segment 48.0 % Band 1.0 % Lymphocyte 41.0 % Monocyte 5.0 % Eosinophil 5.0 %
Lab--biochemistry Sugar 615 !! BUN (B) 17 Creatinine(B) 0.5 AST (GOT) 23 ALT/GPT 22 Calcium 10.4 Na 125 K 5.7 Cl 96 CRP 0.83
3/29 14:45(2hr02min) Admission to NICU
3/29 15:10(2hr27min) IVF 改 half saline run 15cc/hr 補 ketone body(B) => 3+
Admission impression Vomiting and severe dehydration Severe metabolic acidosis Respiratory distress and cyanosis episode, r/o sepsis Leukocytosis and thrombocytopenia
Admission order 3/29 16:06(day1) IVF: D2.5S1/2 IV+ PO 140cc/q8h (150cc/kg/day) NPO Check F/S stat and q8h On OG tube U/C, U/A, urine GBS Ag Sugar, NA, K, Ca, Cl, ABG Ampicillin 70mg q6h iv + GM 7mg q8h ivf
U/A Color Yellow Turbidity Clear SP.Gravity pH 5.0 Leukocyte Negative Nitrite Negative Protein Negative Glucose Ketone 2+ Urobilinogen 0.1 Bilirubin Negative Blood 2+ RBC 6 WBC 0 Epith-Cell 0
ABG and biochemistry TEMP 37°C PH PCO2 7.0 PO HCO3 2.4 SBE SAT 97.9% Sugar 715 Calcium 10.3 Na 128 K 4.8 Cl 96 AG: 29.6 Osmo(C): 301.7
Hospital course 3/29 (day 1) 16:20 on nasal CPAP 16:45 NS challenge 40cc, jusomine 8mL ivf 21:00 F/S:524 N/S challenge 30cc IVF 改 HS run 40cc/hr RI 10U in N/S 500 rum 3mL/hr 21:25 on endo
Hospital course 3/30 (day 2) 01:00 F/S:266, RI line 改 run 2mL/hr 07:00 jusomin 8mL ivf IVF 改 D mL KCl run 140/q8h consult endocrine check Osmo(B): 301 => OG: normal 23:00 F/S:216 RI line 改 run 0.5mL/hr
Hospital course 3/31(day 3): extubation DC RI line 改 NPH 0.5U SC q8h 4/1(day 4): try feeding 4/4(day 7): DC anti 4/6(day 9): NPH 1U SC q8h 4/12(day 15): 轉 5L 4/17(day 20): 轉 7L, NPH1.25U SC q8h 4/18(day 21): MBD and OPD F/U
Other study during hospitalization Abdominal echo=> negative findings Serum amylase and lipase=> normal C peptite=> 0.34(low 0.47~3.15) Insulin antibody=> P11.0(>10) HbA1C=> 9.6.% Urine GBS Ag, U/C and B/C=> negative
Final diagnosis 1. Neonatal DM (type 1 DM) under NPH control, complicated with DKA and severe dehydration 2. Thrombocytopenia post blood transfusion 3. Respiratroy distress due to severe metabolic acidosis with respiratory compensation
Discussion DDx of hyperglycemia in infant DKA in childhood Management of DKA Neonatal DM
The ill-appearing infant:DDx(1) Infectious: Bacterial sepsis, Meningitis, Urinary tract infection, Viral infections… Cardiac: CHD, SVT, MI, Pericarditis, Myocarditis, Kawasaki disease Endocrine: CAH Metabolic: Hyponatremia, hypernatremia, Cystic fibrosis, Inborn errors of metabolism, hypoglycemia Textbook of Pediatric Emergency Medicine, 5th edition
The ill-appearing infant:DDx(2) Drugs/toxins—aspirin, carbon monoxide Hematologic: Severe anemia, Methemoglobinemia Gastrointestinal: Gastroenteritis with dehydration, Pyloric stenosis, Intussusception, Necrotizing enterocolitis, Appendicitis, Volvulus Neurologic: Infant botulism, Child abuse=> ICH Textbook of Pediatric Emergency Medicine, 5th edition
Hyperglycemia in infant: DDx More often in premature infant Excess glucose administration IVF, feeding Inability to metabolize glucose Premature, sepsis, stress Neonatal DM Rare, 2 days ~ 6 weeks, C-peptide may be normal or transiently low Medications Caffine, theophylline, steroid, phenytoin Type 1 DM Vary rare, low to absent C-peptide level LANGE clinical manual, Neonatology: management, principle, on-call problems, disease and drugs. 5 th edition(2004)
DKA in childhood Type 1 diabetes: the most common pediatric endocrine disorder Prevalence: 1/400 Islet-cell autoantibody, insulin antibody, glutamic acid decarboxylase antibody 27 ~ 40% of new-onset diabetics present in DKA The leading cause of mortality in diabetics < 24 y/o cerebral edema: the leading cause of mortality
Definition metabolic acidosis (pH <7.25 to 7.30 or serum bicarbonate <15 mEq/L) hyperglycemia (serum glucose >300 mg/dL) ketonemia
Clinical feature Polyuria, polydipsia, dehydration, ketotic breath, hyperpnea, nausea, vomiting, abdominal pain, general malaise, coma The most common cause: poor compliance Viral illness and focal infections such as urinary tract infection or gastroenteritis
Life-threatening complications Cerebral edema Cardiovascular collapse Profound metabolic acidosis Hyperkalemia Hypokalemia Hypophosphatemia
Risk Factors for Cerebral Edema in DKA Elevated BUN Low PCO2 Treatment with bicarbonate Failure of measured serum [Na] to rise steadily with correction of hyperglycemia Age <3 y New-onset diabetes
Initial lab evaluation CBC Glucose Electrolyte (Na, K, Ca, P, Cl) blood gas Serum osmolality ketones Urinary ketones Lactate
Management(1) 10–20 mL/kg NS bolus until hemodynamically stable Then begin 0.45% NS(or 0.9%NS) at 1.5 times maintainance K (if patient is urinating ) add 30 mEq/L. 2.5–3.5 mEq/L=> add 40 mEq/L consider adding more
Management(2) RI at 0.1 units/kg/hr after intravenous fluid bolus. Adjust dose to maintain glucose decline at 50–100 mg/dL/hr. Add dextrose to intravenous fluids when BS is <200–250 mg/dL.
Management(3) Avoid bicarbonate therapy in DKA. Only consider arterial pH<6.9 impaired cardiac contractility and vascular tone life-threatening hyperkalemia. Follow serum electrolytes q2h. Follow serum glucose every hour
Neonatal DM, NDM(1) Hyperglycemia that occurs during the first one month of life Require insulin tx and last more than 2 weeks A rare dx with incidence:1/ neonates IUGR, SGA, hyperglycemia, dehydration, glucosuria, acidosis with or without ketouria Permanent neonatal diabetes mellitus manifesting as diabetic ketoacidosis. Journal of the Formosan Medical Association. 102(12):883-6, 2003 Dec.
NDM(2) Transient NDM Insulin can be discontinued after several weeks or months Maturational delay of the adenyl cyclase-cAMP system of islet cells Permanent NDM pancreatic agenesis or hypoplasia or absent beta cells Gene mutations: ATP-sensitive potassium channel subunit Kir6.2 Type 1 DM Autoimmune dx Manifests later in life Permanent neonatal diabetes mellitus manifesting as diabetic ketoacidosis. Journal of the Formosan Medical Association. 102(12):883-6, 2003 Dec.
NDM(3) In a series of 57 infants with NDM 18=> Transient 13=> Transient with recurrence between 7~20 y/o 26=> Permanent Long-term course of neonatal diabetes. N Engl J Med 1995; 333:704.
Case report of TNDM Age of onsetBBW(gw)Duration of Insulin tx Case 133 days32005 months Case 249 days months Case 349 days months Case 460 days13002 weeks Different faces of non-autoimmune diabetes of infancy. Acta Paediatrica. 87(1):95-7, 1998 Jan
Case report of PNDM A case of PNDM in a 3-day-old female infant. This full-term neonate was born small for gestational age. Respiratory distress, poor activity, hypothermia, poor feeding, dehydration, and ketoacidosis. After insulin therapy and fluid replacement, her condition became stable. Serum C-peptide level to be low for her age. During the first year of life she had catch-up growth, but insulin therapy was still required. Permanent neonatal diabetes mellitus manifesting as diabetic ketoacidosis. Journal of the Formosan Medical Association. 102(12):883-6, 2003 Dec.
PNDM in Oman(1) All children(5) diagnosed as having PNDM between 1991 and 1995 in Oman were included in the study The mean incidence: 2.2 per live births/year IUGR was noted in all (mean BBW 1.86 kg) DKA in 80% Circulating islet cell antibody: (-) Permanent neonatal diabetes mellitus: clinical presentation and epidemiology in Oman Archives of Disease in Childhood Fetal & Neonatal Volume 80(3), May 1999, pp 209F-212F
PNDM in Oman(2)
Thanks for your attention!!