INTRA UTERINE FETAL DEMISE DR SHABNAM NAZ ASSISTANT PROFESSOR CMC,SMBBMU LARKANA
IUFD   Definition  –  IUFD denotes death of fetus in utero or weighing >500gm or >24 weeks, before the onset of labour. Incidence: 4.5/1000
Etiology Unknown in 25 – 60% of cases Identifiable causes can be attributed to Maternal conditions Fetal conditions Placental conditions
Fetal causes -- 25-40% Chromosomal anomalies Birth defects Non immune hydrops Infections TORCH
 
 
 
 
Placental -- 25-35% Abruption Cord accidents Placental insufficiency Intrapartum asphyxia P Praevia Twin-twin transfusion Synd: Chorio-amnionitis
Cord prolapse
Calcification and haemorrhage in placenta
Vasa Previa
Maternal  5-10% Antiphospho-lipid antibody DM HTN Trauma Abnormal labor Sepsis Uterine rupture Post-term pregnancy Drugs
Ruptured uterus
Mom with no prenatal care delivers undiagnosed twins at EGA 34 weeks
 
 
 
Diagnosis to confirm iud history &examination -Absence of fetal movements  -Retrogression of the positive breast changes. Gradual retrogression of the height of the uterus Uterine tone is diminished  Fetal movement are not felt during palpation. Fetal heart sound are not audible
Diagnosis (contd…) Straight- X-ray abdomen Spalding sign:  it usually appears 7 days after I.U.F.D. Hyperflexion of the spine  Crowding of the ribs shadow  ( Robert’s sign ) Appearance of gas shadow in great vessels : 12 hours
cont Sonography :   absent fetal  movements  Oligohydramnios and collapsed cranial bones Spalding sign
Evaluation of iufd to detect the cause I-Maternal medical conditions VTE/ PE DM HPT Thrombophilia SLE Autoimmune disease Severe Anemia Epilepsy Heart disease II-Past OB Hx Gestational HTN with adverse sequele Placental abruption IUFD Recurrent abortions Baby with congenital anomaly / hereditary condition IUGR
Current Pregnancy Hx Maternal age  Gestational age at fetal death HPT DM/ Gestational D Smoking , alcohol, or drug abuse Abdominal trauma Choliestasis Placental abruption PROM or prelabour ROM
FAIMLY HISTORY Recurrent abortions VTE/ PE Congenital anomalies Abnormal karyotype Hereditary conditions Developmental delay
2-Evaluation of still born infants Infant desciption Malformation Skin staining Degree of maceration Color-pale ,plethoric Umbilical cord Prolapse Entanglement-neck, arms, ,legs Hematoma or stricture Number of vessels Length Amniotic fluid Color-meconium, blood Volume
Knots in cord
 
 
EXAMINATION OF PLACENTA Placenta Weight Staining Adherent clots Structural abnormality Velamentous insertion Edema/ hydropic changes Membranes Stained  Thickening
 
Vasa Previa
3. INVESTIGATIONS Maternal investigations: CBC Blood Group & antibody screen HB A1 C Kleihauer Baket test Serological screening for Rubella CMV, Toxoplasmosis, Syphilis, Herpes & Parvovirus Karyotyping of both parents Hb electrophoresis' Antiplatelet antibodies Thrombophilia screening (ant thrombin iii, Protein C & S deficiency , factor IV leiden,Factor II mutation, lupus anticoagulant, anticardolipin antibodies) DIC
cont Fetal investigations Fetal autopsy Karyotype  (specimen taken from cord blood, intracardiac blood, body fluids, skin, spleen, Placental wedge, or amniotic Fluid) Fetography Radiography
cont Placental investigations Chorionicity of placenta in twins  Cord thrombosis or  knots  Infarcts, thrombosis, abruption, Vascular malformations Signs of infection Bacterial culture for E coli,  Listeria, group B strept.
Pregnancy Management Single or multiple gestation Gestational age at death The  parents wish
Management  Explain the problem   to the woman and her family. Discuss with them the options of expectant or active management. If expectant management is planned: Await  spontaneous onset of labour  during the next four weeks Reassure  the woman that in 90% of cases the fetus is spontaneously expelled during the waiting period with no complicatons. If platelets are decreasing ,  four weeks have passed without spontaneous labour, fibrinogen levels are low or the woman request it,consider active management (induction of labour)
Management  (contd…) If induction  of labour is planned, assess the cervix If the cervix is favourable (soft, thin, partly dilated) labour using oxytocin. If the cervix is unfavourable(firm, thick, closed) ripen the cervix. Note: Do not rupture the membranes.  If spontaneous labor does not occur within four weeks, platelets are decreasing and the cervix is unfavourable, ripen the cervix.
Complications  Psychological upset Infection: Once the membranes rupture, infection, especially by gas forming organism like CI. Welchi. Blood coagulation disorders  During labour : Uterine inertia and PPH
Prevention of IUFD: Regular antenatal care  To screen out the at-risk patients to monitor carefully for the assessment of fetal well being and to terminate the pregnancy at the earliest evidences of fetal compromise.
Morbid pathology of IUFD A dead fetus  undergoes an aseptic destructive process called   maceration . The  epiderm  is the  first structure to undergo the process, whereby blistering and peeling off of the skin occur. It appears between 12-24 hours after death.  The foetus becomes swollen and looks dusky red.  Gradually  aseptic autolysis   of the ligamentous structure  and liquefaction of the brain matter and other viscera take place.
Moen Jo Daro Larkana Sindh

Iufd by dr shabnam

  • 1.
    INTRA UTERINE FETALDEMISE DR SHABNAM NAZ ASSISTANT PROFESSOR CMC,SMBBMU LARKANA
  • 2.
    IUFD Definition – IUFD denotes death of fetus in utero or weighing >500gm or >24 weeks, before the onset of labour. Incidence: 4.5/1000
  • 3.
    Etiology Unknown in25 – 60% of cases Identifiable causes can be attributed to Maternal conditions Fetal conditions Placental conditions
  • 4.
    Fetal causes --25-40% Chromosomal anomalies Birth defects Non immune hydrops Infections TORCH
  • 5.
  • 6.
  • 7.
  • 8.
  • 9.
    Placental -- 25-35%Abruption Cord accidents Placental insufficiency Intrapartum asphyxia P Praevia Twin-twin transfusion Synd: Chorio-amnionitis
  • 10.
  • 11.
  • 12.
  • 13.
    Maternal 5-10%Antiphospho-lipid antibody DM HTN Trauma Abnormal labor Sepsis Uterine rupture Post-term pregnancy Drugs
  • 14.
  • 15.
    Mom with noprenatal care delivers undiagnosed twins at EGA 34 weeks
  • 16.
  • 17.
  • 18.
  • 19.
    Diagnosis to confirmiud history &examination -Absence of fetal movements -Retrogression of the positive breast changes. Gradual retrogression of the height of the uterus Uterine tone is diminished Fetal movement are not felt during palpation. Fetal heart sound are not audible
  • 20.
    Diagnosis (contd…) Straight-X-ray abdomen Spalding sign: it usually appears 7 days after I.U.F.D. Hyperflexion of the spine Crowding of the ribs shadow ( Robert’s sign ) Appearance of gas shadow in great vessels : 12 hours
  • 21.
    cont Sonography : absent fetal movements Oligohydramnios and collapsed cranial bones Spalding sign
  • 22.
    Evaluation of iufdto detect the cause I-Maternal medical conditions VTE/ PE DM HPT Thrombophilia SLE Autoimmune disease Severe Anemia Epilepsy Heart disease II-Past OB Hx Gestational HTN with adverse sequele Placental abruption IUFD Recurrent abortions Baby with congenital anomaly / hereditary condition IUGR
  • 23.
    Current Pregnancy HxMaternal age Gestational age at fetal death HPT DM/ Gestational D Smoking , alcohol, or drug abuse Abdominal trauma Choliestasis Placental abruption PROM or prelabour ROM
  • 24.
    FAIMLY HISTORY Recurrentabortions VTE/ PE Congenital anomalies Abnormal karyotype Hereditary conditions Developmental delay
  • 25.
    2-Evaluation of stillborn infants Infant desciption Malformation Skin staining Degree of maceration Color-pale ,plethoric Umbilical cord Prolapse Entanglement-neck, arms, ,legs Hematoma or stricture Number of vessels Length Amniotic fluid Color-meconium, blood Volume
  • 26.
  • 27.
  • 28.
  • 29.
    EXAMINATION OF PLACENTAPlacenta Weight Staining Adherent clots Structural abnormality Velamentous insertion Edema/ hydropic changes Membranes Stained Thickening
  • 30.
  • 31.
  • 32.
    3. INVESTIGATIONS Maternalinvestigations: CBC Blood Group & antibody screen HB A1 C Kleihauer Baket test Serological screening for Rubella CMV, Toxoplasmosis, Syphilis, Herpes & Parvovirus Karyotyping of both parents Hb electrophoresis' Antiplatelet antibodies Thrombophilia screening (ant thrombin iii, Protein C & S deficiency , factor IV leiden,Factor II mutation, lupus anticoagulant, anticardolipin antibodies) DIC
  • 33.
    cont Fetal investigationsFetal autopsy Karyotype (specimen taken from cord blood, intracardiac blood, body fluids, skin, spleen, Placental wedge, or amniotic Fluid) Fetography Radiography
  • 34.
    cont Placental investigationsChorionicity of placenta in twins Cord thrombosis or knots Infarcts, thrombosis, abruption, Vascular malformations Signs of infection Bacterial culture for E coli, Listeria, group B strept.
  • 35.
    Pregnancy Management Singleor multiple gestation Gestational age at death The parents wish
  • 36.
    Management Explainthe problem to the woman and her family. Discuss with them the options of expectant or active management. If expectant management is planned: Await spontaneous onset of labour during the next four weeks Reassure the woman that in 90% of cases the fetus is spontaneously expelled during the waiting period with no complicatons. If platelets are decreasing , four weeks have passed without spontaneous labour, fibrinogen levels are low or the woman request it,consider active management (induction of labour)
  • 37.
    Management (contd…)If induction of labour is planned, assess the cervix If the cervix is favourable (soft, thin, partly dilated) labour using oxytocin. If the cervix is unfavourable(firm, thick, closed) ripen the cervix. Note: Do not rupture the membranes. If spontaneous labor does not occur within four weeks, platelets are decreasing and the cervix is unfavourable, ripen the cervix.
  • 38.
    Complications Psychologicalupset Infection: Once the membranes rupture, infection, especially by gas forming organism like CI. Welchi. Blood coagulation disorders During labour : Uterine inertia and PPH
  • 39.
    Prevention of IUFD:Regular antenatal care To screen out the at-risk patients to monitor carefully for the assessment of fetal well being and to terminate the pregnancy at the earliest evidences of fetal compromise.
  • 40.
    Morbid pathology ofIUFD A dead fetus undergoes an aseptic destructive process called maceration . The epiderm is the first structure to undergo the process, whereby blistering and peeling off of the skin occur. It appears between 12-24 hours after death. The foetus becomes swollen and looks dusky red. Gradually aseptic autolysis of the ligamentous structure and liquefaction of the brain matter and other viscera take place.
  • 41.
    Moen Jo DaroLarkana Sindh

Editor's Notes