Antepartum care, preterm labour, and postpartum hemorrhage Flashcards

1
Q

UTIs in Pregnancy

A
  • UTIs are common in pregnancy. Can be either lower tract (acute cystitis) or upper tract (acute pyelonephritis)
  • Although the incidence of UTIs in the same in pregnant and non-pregnant women there is a high rate of recurrent bacteriuria and pyelonephritis.
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2
Q

Incidence of UTIs in Pregnancy

A
  • 2-7% of pregnant women develop amsyptomatic bacteriura.
    • Risk factors include: prior UTI, pre-existing diabetes, increased parity, low SES.
    • Without treatment 30-40% of pregnant women will go on to develop symptomatic UTI
  • Acute cystitis occurs in 1-2% or pregnant women
  • Pyelonephritis occurs in 0.5-2% of pregnant women
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3
Q

Pregnancy outcomes with UTI

A
  • Untreated bacteriruia is associated with increase risk of preterm birth, low birth weight, and perinatal mortality.
  • There seems to be no major adverse effects to acute cystitis. This is likely because these women receive treatment.
  • Pyelonephritis is associated with adverse pregnancy outcomes, such as preterm birth, anemia, sepsis, and respiratory distress.
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4
Q

Pathogenesis UTIs in pregnancy

A
  • The same organisms that cause bacteriuria and UTI in non-pregnant women cause them in pregnant women (E. Coli)
  • However, certain physical changes in pregnancy may facilitate bacteria entery and increase risk of pyelonephritis.
    • Specificially, in pregnancy women experience smooth muscle relaxation and ureteral dilation that can make it easier for bacteria to move up the kidney. Furthermore, pressure on the bladder from enlarging uterus and immunosuppression of pregnancy may contribute
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5
Q

Asymptomatic Bacteriuria in Pregnancy

A
  • Finding of a high-level of bacterial growth on urine culture in absence of symptoms consistent with UTI.
  • Screening - recommended to screen pregnant women for this at least once early on (12-16 weeks gestation) with a urine culture. Generally, there is no need to retest women unless they have certain risk factors (history of UTI, diabetes, etc).
  • Diagnostic criteria - 2 consective voided urine specimens with isolation of the same bacterial strain in quantitative counts ≥ 105cfu
    • If bacteria strain is group B streptococcus diagnosis can be made at >104cfu
    • Rapid screening like dipstick should not be used
  • Management - antibotic therapy tailored to culture results. Important to do a follow-up culture to test for clearance.
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6
Q

Acute cystitis Pregnancy

A
  • Symptomatic infection of the bladder
    • Symptoms = urinary urgency, urinary frequency, and dysuria
  • Acute cystitis should be suspected in women who complain of dysuria (urgency and frequency are common in all pregnant women). Urinalysis and urine culture should be preformed. Cultures as low as 102cfu are indicative of UTI in symptomatic patients
  • Management - empiric antiboitic therapy that is tailored once cultures are available. Follow up cultures should be done afterwards to confirm treatment success.
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7
Q

Acute Pyelonephritis Pregnancy

A
  • Manfestation of infection of the upper urinary tract and kindeys.
  • Most cases occur during second or third trimester.
  • Symptoms - fever, flank pain, nausa, vomiting, and/or costovertebral angle tenderness
  • Severe complications are assoicated with pyelonephritis in pregnancy - septic shock, respiratory distess, anemia, bacteremia, and renal dysfunction.
  • Management - hospital admission for perenterla antibotics. Can be converted to oral following clinical improvement. These women can be given prophylatic antiboitics for remainder of the pregnancy.
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8
Q

Preconception Care

A
  • Set of interventions that aim to identify and modify biomedical, behavioural, and social risks to a women’s health or pregnancy outcome through prevention and management
  • Ex. Smoking cessation, health weight, infections and immunizations, genetic screening, family history, nutritinal assessment, substance abuse, psychosocial concerns, etc.
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9
Q

Basics of Prenatal Care

A
  • Early and continuing risk assessment - history and physical exam, lab tests, assessment of fetal growth and well-being
  • Health and promotion - providing information on care, increase knowledge on pregnancy and parenting, promoting healthful behaviours
  • Medical and psychosocial interventions and follow up treatment of existing illness, provision of social and financial resources, referral to consultation with other specialized providers
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10
Q

First Prenatal Visit (8-12weeks)

A
  • Review medical, reproductive, family, genetic, nutritional, and psychosocial histories
  • Reproductive history - preterm birth, low birth weight, preeclampsia, stillbirth, congenital abnormalities, and gestational diabetes (Important to know about these because of high risk of reoccurance).
  • Type of delivery in previous pregnancy
  • A complete physical exam - certain physical finding are normal during pregnancy (systolic murmurs, exaggerated splitting, S3, spider angioma, palmar erythemia, linear nigra, striae). A pelivc exam should be done and Pap status determined.
  • Lab - screening and treatment for asymptomatic bacteriruia, syphilis testing, hepatitis B surface antigen, HIV testing, STI testing, TB screen if high risk
  • Rh - women should recieve Rho(D) immune globulin at 28 weeks gestation and postpartum if needed.
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11
Q

Alleviating unpleasant symptoms during pregnancy

A
  • Nausea and vomiting - affects up to 70% of pregnances. Eating small, frequent meals, and avoiding greasy or spicy foods may help. If medication is necessdary antihistamines are recommended.
  • Heartburn - affects 2/3rds of pregnant women due to progesterone induced relaxaion of esophageal spincter. patients should be tuaght about the behavioural factors that can help eliminate symptoms - not lying down imediately after a meal, elevating head of bed. If these dont work patient can take an antacid.
  • Constipation - increase fiber and water intake. Stool softeners can be used with bulking agents
  • Hemorrhoids - Caused by increase venous pressure in the rectum. To avoid this, patients should be encouraged to rest with legs elevated. Constipation should also be avoided.
  • Leg cramps - affects 50% of pregnant women- especially at night and later months of pregnancy. Massage and stretching may help. Calcium and sodium chloride may also reduce cramps.
  • Backaches - common in pregnancy. Can be avoided by preventing excessive wieght gain, exercising, wearing comfortable shoes, and having special pillows.
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12
Q

Prenatal Nutitional Counselling

A
  • Women should eat a balanced diet and avoid harmful and unsafe foods
  • Recommended rates of weight gain in 2nd and 3rd trimester per week is 1.1, 0.9, and 0.66 pounds in underweight, normal weight, and overweight women respectively.
    • Excessive weight gain is associated with fetal macrosomia and maternal obesity
    • Inadequate weight gain is associated with low birth weight
  • Women should avoid fasting (>13hrs) or skipping meals - increase risk of ketosis and preterm delivery
  • pregnant women should eat 5 times per day - breakfast, lunch, afternoon snack, dinner, and bedtime snack
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13
Q

Follow up prenatal visits

A
  • First prenatal visit - 8-12 weeks
  • Additional prenatal visits tend to be scheduled every 4 weeks until 30 weeks gestation, every 2 weeks until 36 weeks gestation, and then weekly until delivery
    • Visits should be regular enough to monitor progession, provide education and recommended screening, assess well-being of fetus and mother, reassure the mother, and detect and treat medical and psychosocial complications
  • Physician should evaluate BP, weight, urine protein and glucose, uterine size for progressive growth, and fetal heart rate.
  • Mother should have first sensatation of fetal movement ~20 weeks and should be asked about fetal movements at subsequent visits
  • At 24-34 weels women should be taught the warning symptoms of preterm labour - uterine contractions, leakage of fluids, vaginal bleeding, low pelvic pain, and low back pain.
  • Screening for gestation diabetes should be preformed between 24-28 weeks
  • Starting at 28 weeks systemic examination of the abdomen is done to identify lie, presentation, and position of the fetus
  • Mother can be retested for STIs are 32-36 weeks if women has risk factors.
  • Recommended for women to have universal screening for Group B Streptococcous at 35-37 weeks
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14
Q

Preterm Labour

A
  • Regular contractions of the uterus resulting in changes in the cervix that start before 37 weeks (but after 20 weeks).
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15
Q

Pathogenesis of Preterm Labour

A
  • Involved at least 4 primary pathogenic processes that ultimately result in a final common pathway ending in spontaneous preterm labour and delivery
    • Activation of maternal or fetal HPA axis associated with either maternal anxiety and depression or fetal stress
    • Inflammation and infection
    • Decidual hemorrhage
    • Pathological uterine distension
  • Clinical findings of true labour are the same whether labour occurs preterm or at term
    • Cramping; mild irregular contractions; low back ache; pressure sensation in vagina or pelvic; bloody show; spotting
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16
Q

Risk factors for preterm labour

A
  • Demorgraphic characteristics - nonwhite, extremes of maternal age (<17 or >35), low SES, low prepregnancy weight
  • Behavioural factors - stressful life situations, domestic violence, insecurity over food or home
  • Obstetic history - previous preterm birth
  • Incompentent cervix - rare condition where cervix dilates early
  • Fibroids in uterus
  • Vaginal, cervical, kidney, or bladder infections
  • Mother is underweight
  • Placenta previa
  • PROM
  • Gestational hypertension
  • Chronic illness in the mother
17
Q

Post-Partum Hemorrhage (PPH)

A
  • PPH is considered an obstetric emergency
    • Occurring in first 24hrs after delivery = primary or early PPH
    • Occuring from 24hrs to 12 weeks after delivery = secondary or late PPH
18
Q

Why is potential of hemorrage high after delivery?

A
  • Potential for massive hemorrhage after delivery is high becuase in late pregnancy uterine artery blood flow is 500-700mL/min and accounts for 15% of CO.
  • Normally, hemostasis occurs upon placental separation because uterine bleeding is controlled by
    • Contraction of myometrium - compresses blood vessels
    • Local decidual hemostatic factors (platetes, clotting factors) that cause clotting.
      • Hemorrage occurs when one of these processes is disturbed.
19
Q

Pathogenesis PPH

A
  • Focal or diffuse atony - lack of effective contraction of the uterus after delivery. Diagnosis of atony can be made when uterus does not become firm after management of placental delivery (oxytocin).
  • Trauma - trauma related bleeding due to lacerations (including uterine rupture) or surgical incision
  • Coagulopathy - cause of PPH in women with inherited or acquired bleeding disorders, or when there is a reduction of clotting factors due to persistent heavy bleeding and hemodilution of remaning clotting factors.
    • Can be caused by amniotic fluid embolism, placental abruption, severe preeclampsia, or HELLP syndrome
20
Q

Risk factors for PPH

A
  • Retained placental membranes
  • Failure to progess during second stage
  • Lacerations
  • Instrumental delivery
  • Large for gestational age newborn
  • Hypertensive disorders
  • Induction of labour
  • Prolonged first or second stage of labour
21
Q

Treatment for PPH

A
  • Traumatic, hemorrhaging lacerations - need srugical control, either transvaginally or tansabdominally
  • Coagulopathy - treated medically, with transfusion of blood and blood products
  • Atony - treatment depends on route of delivery and bleeding severity
    • Vaginal - start with uterotonic drugs and minimally invasive procedure (intrauterine ballon tamponade) and progress to mvoe invasive (uterine artery embolization)
    • C-section - uterotonic drugs can be used. However, sine abdomen is already open, surgical procedure requiring laparotomy are employed sooner
  • Hemodynamically unstable - management with blood and blood products. In extreme cases you may need to restort to hysterectomy
  • Hemodynamically stable - arterial embolization tends to be effective treatment for persistent bleeding
22
Q

Risk from PPH

A
  • Sheehan Syndrome - Postpartum hypopituitarism due to infaraction from hypovolemic shock
  • Abdominal compartment syndrome - abdomen experience increase in pressure, which reduces blood flow in abdominal organs and impairs pulmonary, cardiovascular, renal, and GI function
  • Asherman syndrome - development of intrauterine adhersions - can lead to menstrual abnormalities and infertility
  • Severe postpartum anemia - may require red cell transfusion, depending on the severity
23
Q

Explain the third stage of labour

A
  • Delivery of the placenta
  • Myometria thickening after delivery reduces uterine surface area, creating a shearing force at placental attachment site resulting in plaental separation
  • Starts at lower portion of placental margine and moves up, so that top of placenta detaches last
  • Signs of placenta separation (Do not place traction on cord before seeing these signs)
    • Gush of blood
    • Lengthening of umbilical cord
    • Upward movement of uterine fundus
    • Uterus becomes firmer of globular
  • Should give patient prophylatic administration of uterotonic agent (ex. oxytocin) before placenta delivery + controlled cord traction after clamping to reduce risk of hemorrhage.