Presentation Utk State Meetng ( DR DAUD)

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    Nama Ibu dan No. K/P Nama Anak Alamat Tetap KlinikBerhampiranTarikh /Tempat

    Kematianibu

    MatiDalamPerut

    Umur Semasa Mati

    SebabKematianDan Lain-

    Lain Catitan0 - 6 Hari 7 - 27 hari28 - 1

    Tahun

    1- 4

    tahun

    5 - 6

    Tahun

    MAIZATUL AKMA 821119036081 TG NUR AMALINA BTTG TARMIZI

    KG CHENGALLEMPONG

    KK BALOK

    26/10/13HOSPKOTA

    BHARU

    6 BULANSEPTICEAMIAWITH BILIARY

    ATREASIA

    SENARAI KEMATIAN DIDAWAH UMUR 5 TAHUN PKD KUANTANOKT DEC 2013

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    SECTION 1:

    Patient Details

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    1. Name: TENGKU NUR AMALINA BT TG. M.TARMIZI

    2. MyKid No.: 130507060586 (5 MONTHS 19 DAYS)

    3. Residence: NO.9 KG. PANJANG BANGGU, 16150 KOTA BHARU

    4. Ethnicity: MALAY Nationality: MALAYSIAN

    5. Gender: FEMALE

    6. Date of Birth: 07 TH MAY 2013 @1300

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    SECTION 2:Patient Death Details

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    7. Date & Time of Death: 26/10/ 2013 @ 1800PM

    8. Place of Death: Home Clinic On way to hospital

    / Others, specify: PICU HPSZ II

    9. Person Certifying Death:

    / Medical, specify: M O

    Non-medical, specify:

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    10a. Symptom(s) of current illness leading to death:

    / Not Applicable

    Duration (days OR hours)Fever

    Cough

    Difficult breathing

    Diarrhoea

    Convulsion

    Lethargy

    Unconscious

    Not able to drink/feed

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    10a. Symptom(s) of current illness leading to death: Continue...

    Duration (days OR hours)

    /Others, specify: Yellowish discolouration of skin

    Since day 5 of l ife

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    10b. Treatment(s) received for current illness?

    / Yes, Place of Treatment No. of times:

    /a. Hospital

    /GovernmentUniversity

    Private

    Others, specify:

    b. Clinic Government

    University

    Private

    Others, specify:

    c. Unknown

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    10b. Treatment(s) received for current illness? Continue...

    No, Reason(s):

    /Traditional / complementary treatmentNo transport

    Unaware child is seriously ill

    Others, specify:

    Not Applicable, specify:

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    12. Certified Cause of Death in Death Certificate:

    SEPTI CAEMI C SH OCK WI TH UNDE RLYI NG BI L I ARY ATRESI A

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    13. Cause of Death:

    ase or condition directlying to death

    (a) septicemia

    due to (or as a consequence of)

    e c e d en t c a u s e (b) biliary atresia.

    bid conditions, if any, giving

    to the above cause, stating theerlying condition last

    due to (or as a consequence of)

    (c )

    due to (or as a consequence of)

    (d).

    er significant conditionstributing to the death, but notted to the disease or conditionsing it

    ...

    ...

    .

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    14. ICD Classification of Cause of Death:

    / Infection & Parasitic Disease

    NeoplasmDisease of Blood & Immune System

    Endocrine, Nutritional, Metabolic

    CNS

    Circulatory System

    Respiratory

    Gastro-Intestinal

    Genitourinary Tract

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    14. ICD Classification of Cause of Death: Continue...

    Conditions from Perinatal Period

    / Congenital Malformation

    Injuries & External Causes

    Symptoms, signs & abnormal findings, not elsewhere classified

    Others

    Specify Details:

    Congeni tal bil iary atresia

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    15. Is Death Preventable?

    / Yes

    /Patient & Family FactorPeripheral / Referral Centre

    Transport Problem

    Department / Treatment Problem

    Others

    Specify Details:

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    15. Is Death Preventable? Continue...

    No

    Not Sure16. Comments:

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    CASERN :

    Name : TENGKU NUR AMALINA BT TG. M.TARMIZIMy Kid : 130507060586 (F)Address : NO.9 KG. PANJANG BANGGU,

    16150 KOTA BHARUAge : 5 MONTHS 19 DAYSDate of birth : 07/05/2013 @1300Date of Admission: 11/09/2013

    Date of death : 26/10/2013 @ 1800hDeath classification : SEPTICAEMIC SHOCK WITH UNDERLYINGBILIARY ATRESIA

    Birth weight : 2.45 kg

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    ANTENATAL CARE

    Mother 30 years old, married, G4 P3 Booking at KK BALOK on 5/11/2012, SOD, POG 11 weeks, B/P:

    120/70 mmHg, Wt : 64.2kg, Urine Alb/Sug : Neg/ Neg, Hb:

    13gm%

    Clinic visited : 12 times (antenatally uneventful)

    HIV : Non- reactive Hep B : Non- reactive

    VDRL : Non-reactive Hep C : Non-reactive

    Previous antenatal history : uneventful

    LMP : 20/8/2012 EDD : 27/5/2013, REDD 14/5/2013( early

    scan at 14w)

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    Cont

    Associated condition Yes No Unknown

    Hypertensive Disorders of Pregnancy

    Diabetes Mellitus

    Vaginal Bleeding

    Anemia in Pregnancy

    Prolonged Rupture of Membrane

    Preterm Labor

    Heart Disease (Mild MVP)

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    DELIVERY Delivery in HTAA on 7/5/2013 @ 1300H, 39W, via SVD

    Baby Girl Birth weight : 2.45kg

    Length: 48cm

    COH : 31cm

    A/Score : 8/9

    G6PD : Normal, cord blood TSH 8.71

    Face : normal

    Other examinations : Normal

    IMP: Asymmetrical SGA

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    Homevisit at day 14 noted jaundice, referred to KK, pt refused

    At day 15 of life, noted still jaundice at face and chest, still had

    rashes.advised to go to KK for prolonged jaundice work up but

    husband didnt allow to go to clinic for blood taking.

    At day 20 of life, baby well, still had rashes, no jaundice noted

    ,otherwise child breast feeding well.

    Baby gaining weight throughout follow up. Pt attended clinic visit for RME 1 month. Seen by MO, no fever/URTI

    sx/vomiting/loose stool/feeding well, grossly normal baby. Wt : 3.4 kg

    (gain 1kg of BW)

    At 2 month old, seen by SN for immunisation and nil of complaint and

    no jaundice noted. (wt 4.0kg)

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    CHRONOLOGY ON ADMISSION TO HRPZ II, KB

    Problem list: Biliary atresia Type III Portal Hypertension secondary to chronic liver disease ARDS secondary to stenotrophomonas sepsis with multiple

    episode of pulmonary hemorrhage Candidiasis sepsis CMV reactive Klebsiella sepsis

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    1. Biliary Atresia Type III

    History of jaundice since day 5 of life notedupon home visit, advice for proper check up atKK Balok , parents refused. Never beenadmitted for phototherapy before.

    Parents migrated to Kelantan, referred fromKK Kedai Lalat for prolonged jaundice. Upon

    admission , noted the child having pale colorstool, tea colored urine and deep jaundice.

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    Underwent Kasai Prosedure on 19.9.2013 (failed)

    Intraop finding: gall bladder atretic, liver enlarged withcirrhosis, fibrosed tissue Developed periportal hypertension and ascites Persistent jaundice, with distended abdomen, and dilated

    veins, hepatomegaly Episodes of RT aspirate with blood, possible varices? Increased total bilirubin, impaired liver enzymes Regular IV vit K 1mg OD On IV lasix and syp spironolactone

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    2. ARDS secondary toStenotrophomonas sepsis

    Ventilated for 21 days (conventional + HFOV) Blood C&S on 26.0.2013- Stenotrophomonas Maltophilia (MRO) TA C&S on 8.10.2013:- Sternotophomonas Maltophilia Antibiotics:- IV Levofloxacin 50mg BD x 10d- IV Vancomycin 50mg QID x 10 d- IV Imipinem 105mg TDS x 10d- IV Bactrim 20mg BD x 14d

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    Repeated blood C&S on 30.9.2013 and 17.10.2013: No growth Multiple episodes of pulmonary hemorrhage-blood stain

    during suctions Required multiple FFP transfusion Extubated on 20.10.2013 T/O to Anggerik on 21.10.2013 Under nasal prong 2L/min, baseline RR : 40-50 breath/min,

    oxygenation maintain >95%

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    3. Candidiasis sepsis

    Urine C&S on 1.10.2013 : Candida albicans Fungal C&S on17.10.2013 : no growth

    On IV amphotericin for 19 days Repeated urine C&S on 10.10.2013 : no

    growth

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    4. Cytomegalovirus infections

    CMV reactive No antiviral

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    Upon review in Anggerik on22.10.2013

    Fairly stable, afebrile Mildly tachypnoeic with recessions Tolerating infusion feeding and was on TPN

    Plan:- To isolate patients had risk to spread infection to other

    patients and to other patients other nosocomial infections- Cont. surgical managements (started IV EES)

    ** at 8pm : patients has transfer to ward 1 as condition moretachypnoeic, less active, vital sign stable

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    Progression in ward 1 (22.10.2013 25.10.2013)

    Had intermittent low grade fever especially inthe afternoon (37.5-37.9C)

    Tachypnoeic, RR : 40-50 No desaturation, SPO2 > 95% Tolerating infusion feeding

    More active upon handling Altered sleep pattern, more active at night

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    Examination:- Vital sign stable

    - Good urine output, glucometer stable- Jaundice, cachexic, alert, responsive to

    surrounding- Lung: transmitted sound- CVS: dual rhythm, no murmur- Abd: soft, distended, multiple dilated veins,

    hepatomegaly about 6cm, firm, nodularsurface.splenomegaly about 3c m

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    Investigations:- hyponatremia, septic parameters improving Management:- Na supplement in infusion feeding and TPN

    - Antibiotics off on 23.10.2013

    - Physiotherapy- Step up infusion feeding- Plan to restart antibiotic if condition worsening, persistent

    spiking of fever

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    26.10.2013 at 7.20am (morningreview by passive on call MO)

    - Tolerating feeding well- No vomiting, no feverExaminations:

    Alert, mild tachypnoiec, dry, jaundiceBP: 101/53 HR: 131 RR: 36r/minT: 37CLung: transmitted soundPer abdomen: soft, distended, liver and spleen palpablePlan:To increase feedingRepated FBC/BUSE and to inform result

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    26.10.2013 at 2.30pm Patient cough out blood, blood streak secretions from nostril More tachypnoeic, laboured breathing Temperature spike to 38.2C Spo2 desturated 80% under NP 2L/min Manual bagging, Spo2 85-95%. Intubated due to respiratory

    distress IV NS bolus 10ml/kg Noted few episodes of bradycardia then started IV dopamine

    infusion 5mcg/kg/min Transfer out to PICU

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    Upon arrival to PICU Connect to ventilator, unable to maintain saturations (80-85%) Manual bagging commented Developed massive pulmonary hemorrhage, suctions blood

    continuosly from ETT x2 Poor perfusions: given IV NS bolus upto 40ml/kg Transfused PC 10ml/kg Started IV dopamin infusion 20mcg/kg/min Increased IV Dobutamin 20mcg/kg/min Noted patient bradycardia, HR 55 CPR commenced for 30 min

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    Resuscitated with- IV adrenalin 1:10000 x 5- IV sodium Bicarbonate 5:5 x 1- IV Calcium gluconate 5:5 x 1 Unable to revived pt Pronouced death at 6.00pm COD: Septicemic shock with underlying biliary

    atresia

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    DATE 17.10.2013 21.10.2013 24.10.2013 26.10.2013

    ALB/GLOB 24/23 27/25

    TP 66 52 53

    BIL 390 213 377

    ALP 255 213 259

    ALT 166 147 128

    AST 355 201 356

    PH 7.45 6.56

    PCO2 40 60

    PO2 96 30

    HCO3 27 9.1

    BE 3.9 -28

    LACTATE 15

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    C&S DATE RESULTBlood 17.9.2013 Coagulase neg staph

    Blood 20.9.2013 NG

    Blood 26.9.2013 StanotrophomonasmatrophiliaSensitivity:Levofloxacin,bactrim,monocyclineResistence: Imipinem,

    tetracyclinBlood 30.9.2013 NG

    Blood 17.10.2013 NG

    Blood for fungal 17.10.2013 NG

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    C&S Date Result

    Urine 26.9.2013 NG

    Urine 1.10.2013 Candida albican

    Urine 4.10.2013 Candida albican

    TA 8.10.2013 StanotrophomonasmaltophiliaS: BatrimR: imipinem, tetracycline,minocycline

    TA 20.10.2013 Acinobacter spS: unasyn,ceftazidime,ciprofloxacin,gentamycinIntermdediate: pepracilin

    Klebsiella pneumonia:S; augmentin,cefotaxime, gentamycin,bactrimR: ampicillin

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    Investigations Date Result

    BLOOD C&S 26.10.2013 Klebsiella ozaneeS: augmentin, ceforoximeBactrim, gentamycin

    Intermediate: ampicillinIntracardiac blood 26.10.2013 NG

    LP 26.10.2013 Appearance: clear andcolourlessNo cell countGram stain: no organismseenC&S: NGIndian ink: NEGProtein : Normal

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    Death: preventable

    - Early detection of biliary atresia, early surgical

    procedure may improve prognosis- Sepsis maybe improved if early intervention upon

    septic parameter and clinical symptomsworsening, and appropriate antibiotics should bestarted accordingly

    Issues:- Isolate pt

    - Infectious control to prevent nosocomial infection

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