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MORTALITY
• Live, preterm, baby boy• Delivered via stat cesarean section due to
previous CS in labor• 40 yo G3P3 (2-1-0-3)• LMP 31 5/7 weeks; MT 33weeks AGA• APGAR score 9,9
BABY M
• 33 weeks• Appropriate for
gestational age• Birthweight: 1630 g• Birthlength: 41 cm• Head Circ: 28cm • Chest Circ: 25 cm• Abd Circ: 21 cm
MATERNAL HISTORY
• Regular prenatal check-up• (+) Chronic hypertension for 7 years maintained on
Methyldopamine 500mg every 6 hours during pregnancy• (+) Gestational diabetes at 20 weeks AOG advised diet modification• (+) UTI during the third trimester, took Cefalexin for 7 days
UPON ADMISSION
• CBC:
• UA: RBC 6 WBC 6 EC 11 Cast 0 Bacteria 38
Hgb Hct WBC Band Neut Lym Mon Plt
108 32 12 72 18 8 2 278
• Penicillin allergy• No asthma• No previous hospitalization except during past
pregnancies
PAST MEDICAL HISTORY
• Hypertension – maternal side• DM – maternal side
FAMILY HISTORY
• Nonsmoker• Non alcoholic beverage drinker
PERSONAL & SOCIAL HISTORY
• G1- 2006, PCS for failed indution in labor, fullterm, F, 6.5 lbs (GDM, HPN)
• G2- 2010, repeat CS, full term , M, 7.3lbs (GDM, HPN)
• G3-2013-PP
OB HISTORY
• Clear amniotic fluid• HR 150s
APGAR SCORE : 9,9
Upon delivery
ASSESSMENT:Live preterm baby boyDelivered via stat CS for repeat CS in labor at 31 5/7 weeks AOGApgar Score 9,9
ADMISSION
Management• Routine newborn care done• Admitted to NICU Level 3• NPO• O2 support via nasal canula• IVF started• Calcium gluconate started• Septic workup:
Blood CS: No growth in 72 hoursAmpicillin, Amikacin started
Hgb Hct WBC Band Neut Lym Mon Plt
188 56 13.6 35 57 06 02 186
Course in the NICU
1st Day of LifePROBLEMS
• Prematurity
• Probable sepsis
• Patient was placed in an isolette
• NPO• IV fluid continued• Hgt monitoring done
• Ampicillin, Amikacin continued
2nd Day of LifePROBLEMS
• Jaundice
• Apnea– O2 sat 86%– HR 100
• Nutritional buildup
• Phototherapy started
• Aminophylline started• Continue O2 support until
weaning
• Kept on NPO• Aminosteril started
3rd Day of LifePROBLEMS
• Vomiting of coffee ground material after feeding
• Kept on NPO• Vitamin K given
4th Day of LifePROBLEMS
• Nutritional buildup • Feeding with expressed breast milk was started
• Intralipid was started
6th Day of LifePROBLEMS
• Apnea– Less than 10 seconds– Improved by stimulation
• Cyanosis with hemodynamic compromise– HR <60, O2 sat 91%, RR 52,
SBP 32mmHg– Thready and variable pulses– Violaceous lower
extremities
• O2 support via nasal canula
• Resuscitation– Chest compression– Intubation – 2 doses of epinephrine– Fluid resuscitation– NaHCO3 given
• Septic Shock
– Blood CS• Gram (-) cocobacilli
after 9.12 hours• Acinetobacter
baumannii• Sensitive to: Amikacin,
Ceftazidime, Gentamycin, Ciprofloxcin, Levofloxacin, Pip-Taz, TMP-SMX
• Antibiotics shifted to Meropenem, Oxacillin and Metronidazole
• Dopamine drip started
Hgb Hct WBC Band Neut Lym Mon Plt
143 43 6 41 53 01 05 40
VBG Metabolic acidosis
pH 7.05
pCO2 42.5
pO2 37
HCO3 11.8
BE -19
SO2 48
• NaHCO3 given
VBG Metabolic acidosis
Metabolic acidosis
Metabolic acidosis
Metabolic acidosis
Metabolic &
Respiratory acidosis
pH 7.05 6.94 7.18 7.12 6.97
pCO2 42.5 47.1 21.5 43.30 61.4
pO2 37 29 43 24 26
HCO3 11.8 10.10 8.1 13.9 14
BE -19 -22 -20 -16 -18
SO2 48 27 68 26 24
• CXR
• Fine reticulonodular opacities seen throughout both lungs, predominantly in the inner lung zones
Impression: Consider bilateral pneumonia
• t/c DIC– Bleeding at the puncture
sites– Fresh blood draining at
the OGT– Purpura fulminans– Platelet count of 40,000
• Vitamin K• Famotidine• IVIG• Blood transfusion– Platelet concentrate – Fresh frozen plasma– Packed RBC (not given)
Hgb 122 112 82 75 61
Hct 36 33 24 22 18
• Acute renal failure– No urine output x 12
hours
• Fluid resuscitation• Furosemide
• Electrolyte imbalance • Calcium gluconate given
Na 144 148 149 147 144K 3.9 4 6.2 8 >9iCa 1.13 1 0.82 0.73 0.71
• Seizure (t/c Intraventricular Hemorrhage)
• Phenobarbital
7th Day of Life
• Desaturation despite bag tube ventilation• Bradycardia (HR 40s), Hypotension
(Undetectable)• Resuscitation with chest compression and
epinephrine • After 45 minutes of resuscitation, patient was
pronounced dead.• Postmortem care done.
FINAL DIAGNOSIS
• Prematurity• Septic shock secondary to Acinetobacter
baumannii• Disseminated Intravascular Coagulation• r/o Intraventricular Hemorrhage• Neonatal Pneumonia• Acute renal failure
Acinetobacter baumanniiThe most resistant of the genospecies and has the greatest clinical importance
• Naturally inhabits water and soil• Isolated from foods and arthropods • In humans, can colonize:– Skin, wounds– Respiratory– GI
• Can survive environmental dessication for weeks promotes transmission through fomite contamination in hospital
RISK FACTORS AMONG NEONATES
• Low birth weight• Total parenteral nutrition• Central venous catheters
Mittal N, Nair D, Gupta N, et al. Outbreak of Acinetobacter spp septicemia in a neonatal ICU. Southeast Asian J Trop Med Public Health 2003; 34:365.Huang YC, Su LH, Wu TL, et al. Outbreak of Acinetobacter baumannii bacteremia in a neonatal intensive care unit: clinical implications and genotyping analysis. Pediatr Infect Dis J 2002; 21:1105.
Health Care Associated Infection
• Acinetobacter outbreaks have been traced to: 1. common-source contamination (particularly
contaminated respiratory and ventilator equipment)
2. cross-infection by the hands of health care workers caring for colonized or infected patients
Hartstein AI, Rashad AL, Liebler JM, et al. Multiple intensive care unit outbreak of Acinetobacter calcoaceticus subspecies anitratus respiratory infection and colonization associated with contaminated, reusable ventilator circuits and resuscitation bags. Am J Med 1988; 85:624.Maragakis LL, Cosgrove SE, Song X, et al. An outbreak of multidrug-resistant Acinetobacter baumannii associated with pulsatile lavage wound treatment. JAMA 2004; 292:3006.
Bloodstream Infection
• Acinetobacter accounts for 1.5 to 2.4 percent of nosocomial bloodstream infections
• Most frequent source: vascular catheter , respiratory tract
• Less common: Wounds, urinary tract• Septic shock develops in up to one-third of
patients.
• Data regarding the prognosis of patients: limited• Patients usually have longer ICU stay, higher rate of
organ failure and higher mortality rates • Risk factors for mortality:– Imipinem resistence– ICU stay– Female gender– Old age– Pneumonia– Diabetes– Septic shock