Risk Conditions Related to Pregnancy Flashcards
Bleeding during pregnancy
Implantation bleeding: occurs 10 to 14 days after conception. Usually lasts 1 to 2 days and is lighter than the typical menstrual period (often confused). No treatment necessary.
Other causes: abortion, malignancy, polyps, trauma, ectopic pregnancy, idiopathic, infection, molar pregnancy, subchorionic hemorrhage, vaginitis, UTI, cervicitis, postcoital bleeding, placenta previa, and abruptio placentae.
Abortion: definition, risk factors and assessment
- pregnancy that ends before 20 weeks (spontaneous or elective)
- Risk factors: advanced maternal age, previous miscarriage, previous elective abortion, uterine abnormalities, prolonged time to achieve pregnancy, low serum progesterone, celiac disease, polycystic ovarian syndrome, thyroid dysfunction or Cushing’s, lupus, infection, fever, trauma, low BMI, smoking, alcohol, cocaine use, certain meds, high caffeine intake.
- Assessment: spontaneous vaginal bleeding, low uterine cramping or contractions, blood clots or tissue through the vagina, hemorrhage and shock can result if bleeding is excessive.
Abortion: Types and interventions
- Miscarriage: natural causes
- Induced: therapeutic or elective reasons exist for terminating.
- Threatened: spotting and cramping occur without cervical change.
- Inevitable: spotting and cramping occur and cervix begins to dilate and efface.
- Incomplete: loss of some of the products of conception (most often placenta is retained).
- Complete: loss of all products of conception.
- Missed: products are retained in utero after fetal death.
- Habitual: miscarriages occur in 3 or more successive pregnancies.
Interventions: bed rest as prescribed, monitor vital signs, cramping and bleeding. Count perineal pads to evaluate blood loss and save expelled tissues and clots. IV fluids as prescribed. Prepare client for dilation and curettage. Adm RH0 immune globulin as prescribed for Rh-neg woman. Provide psychological support.
Cardiac Disease: description, assessment and interventions
A pregnant client with cardiac disease may be unable physiologically to cope with the added plasma volume and increased cardiac output (blood volume peakes at weeks 32-34)
- Assessment: cough and respiratory congestion, dyspnea and fatigue, palpitations and tachycardia, peripheral edema, chest pain.
- Interventions: monitor vital signs, FHR and condition, cardiac stress and decompensation. Limit physical activities, encourage adequate nutrition (to prevent anemia) and low-sodium diet may be prescribed to prevent fluid retention and heart failure. Avoid excessive weight gain.
- During labor: monitor client and fetal, maintain bed rest, with client lying on her side with her head and shoulders elevated. Adm oxygen as prescribed, manage pain early, and use controlled push efforts.
Chorioamnionitis: description, assessment, and intervention.
- Bacterial infection, of the amniotic cavity, can result from premature or prolonged rupture of the membranes, vaginitis, amniocentesis, or intrauterine procedures. May result in the development of postpartum endometritis and neonatal sepsis.
- Assessment: uterine tenderness and contractions, elevated temperature, maternal or fetal tachycardia, foul odor to amniotic fluid, leucocytosis.
- Interventions: Monitor maternal VS and FHR, results of blood cultures, adm antibiotics and oxytocic meds as prescribed. Prepare to obtain neonatal cultures after birth.
Diabetes Mellitus
- Pregnancy places demands for carbohydrates metabolism and causes insulin requirements to change.
- Insulin resistance and hyperinsulinemia may predispose some women to diabetes.
- Maternal glucose crosses the placenta, but insulin does not. The fetus produces its own and pulls glucose from the mother, which predisposes the mother to hypoglycemic reactions.
- Newborn of a diabetic mother may be large in size and is at risk for hypoglycemia, hyperbilirubinemia, respiratory distress syndrome, hypocalcemia, and congenital anomalies.
- During the first trimester, maternal insulin needs decrease. During second and third trimester, increases in placental hormones cause an insulin-resistant state, requiring an increase in the client’s insulin dose.
Gestational Diabetes Mellitus
- occurs during the second or third trimester when the pancreas cannot respond to the demand for more insulin.
- should be screened between 24 and 28 weeks.
- frequently can be treated by diet alone, however some clients may need insulin.
- most women return to a euglycemic state after birth, but there is a increased risk for developing DM in their lifetimes.
- the need for a cesarean section is more likely, and neonatal hypoglycemia and macrosomia may be evident.
- Overt diabetes occurs in the first trimester.
Gestational Diabetes Mellitus: Risk Factors
- older than 35, obesity (BMI > 30), nonwhite race, previous unexplained perinatal loss, previous child born with congenital anomalies, polycystic ovarian syndrome, multiple gestation, first degree relative with DM or GDM, previous delivery of a fetur weighing greater than 9lb, maternal birth weight less than 6lb or greater than 9lb, previous pregnancy with GDM, glycosuria, essential or pregnancy-related hypertension, use of glucocorticoids.
Gestational Diabetes Mellitus: Assessment
- Excessive thirst, hunger, weight loss, frequent urination, blurred vision, recurrent urinary tract infections and vaginal yeast infections, glycosuria and ketonuria, signs of gestational hypertension and preeclampsia, polyhydramnios, large for gestational age fetus.
Gestational Diabetes Mellitus: Interventions
- Employ diet, meds, exercise, and blood glucose determination 4 times daily to maintain <95 (fasting), <130-140 (1h post-prandial), < 120 (2h post-prandial)
- Observe for signs of infection, hyperglycemia, glycosuria, ketonuria and hypoglycemia.
- Monitor weight and calorie intake.
- Assess for complications such as preeclampsia, fetal status.
- Schedule visits every 2 weeks until 36 weeks and then every week from 36 weeks and up.
- During birth: monitor for signs of fetal distress and prepare for c-section. Regulate insulin and provide glucose IV as prescribed because labor depletes glycogen.
- After birth: Observe for hypoglycemic reaction of the mother because a decline in insulin normally occurs. Reregulate insulin needs as prescribed. Assess dietary needs based on blood glucose. Monitor for signs of infection or postpartum hemorrhage.
Disseminated intravascular Coagulation (DIC)
- A maternal condition in which the clotting cascade is activated, resulting in the formation of clots in the microcirculation.
- Predisposing conditions: abruptio placentae, amniotic fluid embolism, gestational hypertension, HELLP syndrome, intrauterine fetal death, liver disease, sepsis, severe postpartum hemorrhage and blood loss.
- Assessment: uncontrolled bleeding, bruising, purpura, petechiae, and ecchymosis, presence of occult blood in excretions, hematuria, hematemesis, signs of shock, decreased fibrinogen level, platelet count, and hematocrit level. Increased prothrombin time, clotting time, and fibrin degradation products.
- Interventions: remove underlying cause, monitor VS, assess for bleeding and shock. Prepare for oxygen therapy, volume replacement, and possibly heparin therapy. Monitor for complications, urine output (maintain at least 30ml/h).
Ectopic Pregnancy
- Implantation of the fertilized ovum outside of the uterine cavity.
- Sites: Ampullar, Fimbrial, Isthmic, Intertitial
- Assessment: missed menstrual period, abdominal pain, vaginal spotting to bleeding that is dark red or brown. If rupture > increased pain, referred shoulder pain, signs of shock.
- Intervention: obtain assessment data and VS, monitor bleeding and initiate measures to prevent rupture and shock. Methotrexate, a folic acid antagonist, may be prescribed to inhibit cell division in the developing embryo. Prepare for laparotomy. Adm Rh0 if Rh- women.
Fetal death in utero
- refers to the death of a fetus after the 20th week and before birth.
- Can develop DIC if the fetus is retained for more than 3 weeks.
- Assessment: absence of fetal movement, heart tones, maternal weight loss, lack of fetal growth, decrease in fundal height.
- Interventions: prepare for birth of fetus, provide support, accept behaviors, refer to support group.
Hepatitis B
- Risk of prematurity, low birth weight, and neonatal death. Transmitted through blood, saliva, vaginal secretions, semen, breast milk, and across the placental barrier.
- Interventions: limit the number of vaginal examinations, suction fluids and remove maternal blood immediately after birth. Bathe before any invasive procedure, clean and dry the face before instilling eye prophylaxis. Adm HepB immune globulin and vaccine soon after birth, after bath.
Hematoma
- Occurs following the escape of blood into the maternal tissue after birth. Predisposing condition include operative delivery with forceps or injury to a blood vessel.
- Assessment: abnormal, severe pain. Pressure in the perineal area, palpable sensitive swelling with discolored skin. Inability to void, decreased hemoglobin and hematocrit levels. Signs of shock.
- Interventions: Monitor VS, apply ice, adm analgesics, monitor intake and output, encourage fluids and voiding (prepare for catheterization if necessary). Adm blood and antibiotics as prescribed, monitor for signs of infection. Prepare for incision and evacuation of the hematoma.
HIV and AIDS
- Women infected with HIV may first show signs and symptoms at the time of pregnancy or possibly develop life-threatening infections because normal pregnancy involves some suppression of the maternal immune system.
- 3-drug combination HAART treatment is recommended to reduce mother-to-child transmission. Zidovudine is recommended and adm based on the following:
= antepartum: orally beginning after 12 weeks of gestation, maternal HAART is given to reduce the viral load to undetectable.
= intrapartum: IV during labor, zidovudine is given 1h before vaginal birth and 3h before c-section if the HIV RNA is greater than 400 copies/ml or unknown, if less may not be required. Vaginal birth is acceptable if less than 1000 copies/ml.
= postpartum: in the form of syrup to the newborn 2h after birth and every 12h for 6 weeks. May be placed in ICU. Avoid adm of oxytocin and place pads under the hips to absorb blood and fluids. Minimize neonate’s exposure. - Prenatal exposure of an infant to infected secretions through birth or breast feeding is a form of transmission.
- A mother with HIV is considered high risk because she is vulnerable to infections.
Hydatidiform Mole: Description
- is a form of gestational trophoblastic disease that occurs when the trophoblasts, which are the peripheral cells that attach the fertilized ovum to the uterine wall, develop abnormally.
- the mole manifests as an edematous grape-like cluster that may be nonmalignant or may develop into choriocarcinoma.
Hydatidiform Mole: Assessment
- fetal heart rate not detectable.
- vaginal bleeding, which may occur by the fourth week or not until the second trimester; may be bright red or dark brown and may be slight, profuse, or intermittent.
- signs of preeclampsia before the 20th week.
- fundal height greater than expected.
- elevated human chorionic gonadotropin levels.
- characteristic snowstorm pattern shown on US.
Hydatidiform Mole: Interventions
- diagnostic tests are done to detect metastatic disease.
- prepare the client for uterine evacuation, which is done by vacuum aspiration and oxytocin may be adm after to contract the uterus.
- monitor for post-procedure hemorrhage and infection.
- tissue is sent to lab for evaluation.
- human chorionic gonadotropin levels are monitored every 1 to 2 weeks until normal levels are attained. Levels are checked every 1 to 2 months for 1 year.
- Instruct client and partner to prevent pregnancy during 1 year.
Hyperemesis Gravidarum
- Intractable nausea and vomiting during the first trimester that causes disturbances in nutrition and fluid and electrolyte balance.
- assessment: nausea, persistent vomiting, weight loss, signs of dehydration, fluid and electrolyte imbalances.
- interventions: medication therapy and if unsuccessful, IV adm fluid and electrolyte imbalances or parental nutrition. Monitor VS, intake and output, weight, calorie count, lab data, urine for ketones, FHR, activity, and growth. Encourage intake of small portions, liquids between meals, and sit upright after meals.