Skip to document

Topics 5 & 6 - Important information for Final Exam highlighted & bolded within material

Important information for Final Exam highlighted & bolded within material
Course

Nursing Care of the Childbearing Family (NSG-432)

77 Documents
Students shared 77 documents in this course
Academic year: 2023/2024
Uploaded by:
Anonymous Student
This document has been uploaded by a student, just like you, who decided to remain anonymous.
Grand Canyon University

Comments

Please sign in or register to post comments.

Related Studylists

nsg 432Maternal Nsgfinal

Preview text

Assessment of High-Risk Pregnancy: - Assessment of Risk Factors: o Biophysical Factors: those that originate within mother/fetus  Genetic: inherited disorders, chromosomal anomalies, multiple gestation, large fetal size, ABO incompatibility  Nutrition: adolescents, three pregnancies in 2 years, tobacco/alcohol/drug use, dietary intake (illness, fads, bariatric surgery), inadequate or excessive weight gain, low hematocrit (<33%)  Medical & Obstetric: Complications (current or previous), pregnancy- related illness, previous loss  Polyhydramnios (fetal GI issues) or oligohydramnios (possible fetal renal issues, PROM, IUGR, maternal hypertension/dehydration, uteroplacental insufficiency)  IUGR- Intrauterine growth restriction o Mother- hx of HTN, diabetes, cardiac or autoimmune issues, pulmonary disease  Chromosomal abnormalities: o Advanced maternal age o Parental chromosomal rearrangements or previous hx of this o Psychosocial factors: behaviors/adverse life events  Smoking, caffeine (recommended no more than 12 oz/day)  Alcohol/drugs  Emotional distress, depression/mental health problems  Psychological status:  History of abuse, social environment, unsafe practice, situational crises o Sociodemographic Factors:  Low income/Social Determinants of Health (SDOH)  Lack of prenatal care  Age: adolescents – anemia, preeclampsia, CPD  Mature mothers (“advanced age” i. over 35) increased risk of genetic issues, chronic disease o Environmental factors:  Infections, chemicals, pollutants (industrial, at home smoking), cat litter, gardening - Antepartum Testing: o Purpose: to identify those at risk for injury due to interrupted acute or chronic oxygenation  Diabetes, hypertension, preeclampsia, renal or heart issue, IUGR, previous stillbirth, poly or oligohydramnios, etc

o Methods:  Biophysical profile (BPP): noninvasive dynamic assessment of a fetus that is based on acute and chronic markers of fetal disease  Usually done late in second trimester or third trimester- reliable predictor of fetal well-being (8-10 = normal)  Lower the number, more the concerns- may need to do an amniocentesis to check on lung development or may need to deliver the baby  Limitation; if fetus is sleepy, may require longer observation  5 components o NST: to determine fetal heart rate reactivity o Fetal breathing movements (FBMs) o Fetal movements: daily fetal movement count (DFMC) “kick count” o Fetal tone o Amniotic fluid  Scoring: normal = 2 in each category o NST: reactive pattern o Fetal breathing movements: ≥1 episode lasting ≥ seconds o Gross body movements: ≥3 discrete body/limb movement o Fetal muscle tone: ≥1 episode of extension (limb or trunk) with return of flexion o Amniotic fluid: ≥1 pocket measuring 2cm in two perpendicular planes  Ultrasound:  Detection of FHR, gestational age, growth, anatomy, genetic disorders, anomalies, position of fetus, position of placenta  Levels of US: o Standard (“basic”)  Diagnostic tool throughout pregnancy o Limited:  To determine a specific piece of info about the pregnancy o Specialized (“detailed”)  May be referred to as “targeted”  Comprehensive exam for abnormal hx or lab findings  Performed by highly trained professionals  Nursing role: counsel and educate about the procedure

 Women with a prior child with a structural birth defect or with a structural fetal defect identified by ultrasound during their current pregnancy  Women with prior child with a chromosomal abnormality  Chronic Villus Sampling: “placental biopsy” o 10-13 weeks o Small specimen from placenta o Allows for earlier diagnosis & rapid genetic results (reflects genetic makeup of fetus)  Percutaneous Umbilical Blood Sampling (PUBS): o Direct access to fetal circulation o 2 nd and 3rd trimesters o Can be used for sampling or transfusion o Insertion of needle into umbilical vessel (vein preferred) o Often used for evaluation of amnio or CVS results:  Determines specific mutation o May also be used to assess for fetal anemia, infection, or thrombocytopenia o Risks:  Transient fetal bradycardia  Bleeding from puncture site; fetomaternal bleeding  Occasional fetal loss  Maternal Assays: o Alpha fetoprotein: (AFP)  Normal values correlate with gestational age and multiple maternal factors  Screen for fetal anomalies  High levels help to confirm neural tube defects such as spina bifida or anencephaly or an abdominal wall defect (omphalocele) o Lung maturity: LS ratio & LBC  2:1 for adequate fetal lung maturity o Multiple marker screen:  Detects chromosomal abnormalities (trisomy 21- Down syndrome)  Available at 11-14 weeks o Coombs test:  Screen for Rh alloisoimmunization (incompatibility)  Screens for other antibodies that may place fetus at risk for incompatibility with maternal antigens  Elevated titer may require amnio to test for fetal hemolytic anemia

 (>1:8 to 1:32) o Cell-free DNA screening:  Looks for chromosomal anomalies (trisomy 13, 18, & 21)- extra/missing chromosomes  Uses maternal blood  Also provides a definitive diagnosis noninvasively for fetal Rh status, sex, and certain paternally transmitted single gene disorders  Nonstress Test: a reliable screening of fetal well-being  Done to determine whether the intrauterine environment continues to support the fetus  Procedure: o Placed on a monitor- given a button to press when movement is felt o May have to stimulate/wake up the baby- vibracoustic tool  Sound & vibration stimulation o Repeated 1-2x weekly for remainder of pregnancy  Interpretation: o “reaction” is positive = NORMAL o Two accelerations in a 20 min period, each lasting at least 15 secs and peaking at least 15 bpm above baseline o RELIABLE SCREENING OF FETAL WELL-BEING o “non reactive” is negative  Does not demonstrate at least two qualifying accelerations w/in a 20 min period  Doesn’t always mean baby is compromised  Will do further testing- monitor mom and baby  Contraction Stress test:  Provides an earlier warning of fetal compromise than the NST and produces fewer false-positive results  Procedure: o Nipple stimulation- stimulation of nipples with warm washcloths or through clothes for 5-10 mins to start contractions o Oxytocin- three uterine contractions of moderate intensity, each lasting 40-60 secs, observed w/in a 10-minute period  Interpretation: o Negative is GOOD- no signs of fetal issues o Positive is NOT GOOD- appear to be issues with fetal well- being (late decels w/ contraction = fetal hypoxia)

 Preconception counseling: for pregestational (preexisting)  1 st trimester: requires less insulin- may need to reduce dose to prevent hypoglycemia o Nausea, vomiting, and cravings may cause dietary fluctuations in glucose o Hyperglycemia in first trimester may cause congenital anomalies  2 nd & 3rd trimester: Insulin needs may increase  Maternal risks:  Recommend reliable contraception until glycemic control is optimal  Poor blood glucose control: o Increased risk of macrosomia- LGA (100-4500g or more than 90th percentile) o Increased risk for should dystocia:  Related to disproportionate increase in shoulder, trunk, and chest size  Increased risk for preeclampsia, polyhydramnios, DKA (especially during stress, infection, or illness) o Can occur with blood glucose levels barely exceeding 200, compared with 300-350 in nonpregnant state  Fetal & Neonatal Risk:  Hyperglycemia in 1st trimester o Main cause of diabetes related anomalies  CV system, CNS  Breastfeeding should not have significant impact on insulin levels o Gold hour very important because baby is at risk for hypoglycemia  Assessment:  Acute and chronic complications: o Retinopathy, nephropathy, cardiac involvement  Antepartum:  Diet: adjustment of insulin needs  Exercise: encouraged with careful monitoring of blood glucose  Insulin Therapy: may need adjustment  Self-monitoring of blood glucose  Urine testing: specifically for ketones  Complications requiring hospitalization: o Dehydration & infection may lead to hyperglycemia and DKA  Fetal surveillance: o Baseline EDB o Nonstress testing: 1-2x/week after 32 weeks

 Determination of birthday and mode of birth o Optimal time 39 weeks  May be earlier delivery with maternal or fetal complications  Intrapartum:  Compilations r/t dehydration, hypoglycemia, hyperglycemia  Care: o 1 st stage:  IV fluids, monitoring of blood glucose, continuous fetal monitoring o 2 nd stage: risks for should dystocia and other CPD risks (cephalopelvic dystocia)  Postpartum:  Insulin requirements: decrease substantially after birth and placenta delivered o Gestational Diabetes mellitus:  Increased incidence r/t overweight/obesity  Likely to reoccur for future pregnancies  Maternal risks:  Less risk than pregestational diabetes  Preeclampsia & cesarean birth  Development of type II diabetes later in life  Fetal risks:  Less risk that pregestational diabetes o Critical development period is prior to development of GDM  Greater risk of macrosomia and birth trauma  Risk for neonatal hypoglycemia  Screening for gestational diabetes mellitus:  Early pregnancy screening: o Screened with history, risk factors, blood glucose  Screening at 24-28 weeks of gestation o 50g oral glucose & 1 hour measurement o 130-140 or above = positive o If positive; 3 hours 100g oral glucose tolerance test (OGTT)  Antepartum:  Similar modification as with pregestational DM o Strict blood glucose control  Diet: standard diabetic diet (usually 2000-2500 kcal/day)  Exercise: moderate exercise o Build lean muscle mass (improves sensitivity to insulin)  Self-monitoring of blood glucose o Usually done at home, reviewed at prenatal visits

 Avoid triggers, use prophylactic medications, management of acute episodes  Poorly controlled asthma may need additional monitoring and testing o Cystic Fibrosis:  Common autosomal recessive genetic disorder  Production of excessive viscous secretions  Pregnancy generally well-tolerated  May need closely followed pulmonary function testing  Fetal assessment essential  During labor: monitor cardiac output closely

  • Skin Disorders: normal changes with pregnancy o Pruritus gravidarum (severe itching):  Usually disappears shortly after birth  Can reoccur in 50% future pregnancies o Polymorphic eruption of pregnancy (PEP):  Usually does NOT recur in other pregnancies  Itchy bumpy rash on stretch marks o Treatment:  Both symptomatic tx with:  Skin lubrication, topical antipruritic, and oral antihistamines  Ultraviolet light and careful exposure to sunlight decrease itching
  • Substance Use Disorders: o Prescription or illicit drugs, tobacco, alcohol, marijuana, cocaine, meth o Prevalence:  Continues to grow in the US  Usage is usually higher in 1st & 2nd trimester o Maternal and Fetal Effects of Selected Drugs:  Most associated with low birth weight and preterm birth  IUGR o Barriers to Treatment r/t:  Social stigma, labeling, and guilt are significant barriers to receiving necessary care  Fear losing other children or criminal prosecution  Lack of treatment options o Legal Considerations:  Defined as child abuse in 23 states  Should be aware of current laws in your practicing state o Screening:  Recommend screening everyone at first prenatal visit  Discussion of past and present use of tobacco, alcohol, & other drugs o Prescription medications and OTC o Herbal remedies

 Requires lots of education on risks of use  4 Ps Plus: parents, partners, past, and pregnancy, depression/domestic violence  CRAFFT substance abuse screen for adolescents & young adults o Assessment:  Comprehensive med history and complete physical exam  Lab for syphilis, hep B & C, and HIV  CBC & TB  Gonorrhea & chlamydia o Interventions:  Education on risks, treatment, referrals o Follow-up care: With known SUD  Home assessment  Social services interview  Family or support identified  Home nurse visit

o Identifying and Preventing Preeclampsia:  BP should be monitored and urine should be checked for protein at each prenatal visit  No specific test; diagnosis relies on identification of S/S  Women at risk of developing preeclampsia may receive low-dose aspirin daily between 12-28 weeks gestation o Assessment:  BP should be taken with a manual BP cuff  Edema, DTR, presence (or absence) of clonus, proteinuria (at least 1+ on dipstick or >300mg)  Examination should include assessment for severe features including:  Headache, epigastric pain, RUQ pain, and visual disturbances o Interventions:  Gestational hypertension and preeclampsia without severe features:  Close monitoring of the mother and fetus  May be appropriate for home care  Woman should be hospitalized if severe features develop  Maternal assessment includes: o Monitoring of BP, labs, maternal weight & careful monitoring for severe features  Fetal assessment includes; o Daily kick counts, serial nonstress tests, serial ultrasound, and monitoring of amniotic fluid levels  Complete/partial bed rest recommended  Gestational hypertension and preeclampsia with severe features:  Increased risks of maternal and fetal mortality/morbidity  Requires IMMEDIATE HOSPITALIZATION  Mag sulfate used to prevent seizure activity (decreases CNS excitability)  Serial labs are necessary  Fetal assessment = essential o Frequent monitoring to identify and respond to s/s of magnesium toxicity  Calcium gluconate: antidote to mag sulfate o Should be readily available in case of toxicity o Mag crosses placenta and can impact fetus (EFM strip)  Hydralazine, labetalol, nifedipine to control BP

  • Eclampsia: o Immediate care:  Time the seizure, protect patient safety- side rails up & padded  After seizure- lower HOB and turn to left side; ensure airway (ABC)  Call code if needed; IV line should be placed  If mag is running, increase mag; recurrent seizures  lorazepam

 After woman stabilized, assess fetal well-being; membranes may have ruptured (CHECK MEMBRANES)  Determine best route for delivery (vaginal vs c-section)

  • Hyperemesis Gravidarum (HG): o Etiology:  Nausea develops between 4-8 weeks gestation (normal)  HG = severe N/V that results in weight loss, electrolyte imbalance, nutritional deficiencies & ketonuria o Clinical manifestations:  Significant weight loss & dehydration  May also have low BP and increase pulse  Dry mucous membranes, poor skin turgor, electrolyte imbalances o Assessment:  Frequency/severity/duration of episodes of n/v and description of vomitus  Any diarrhea or other GI disturbances  Precipitating/alleviating factors  Pharmacological/nonpharmacological measures used  Complete physical exam & prepregnancy weight o Interventions:  Initial care:  IV therapy for fluid and electrolyte replacement o May be inpatient or outpatient  May also need antiemetic medication, corticosteroids, antacids, and GERD medication  Once vomiting controlled, small frequent meals should be started  Need for plenty of rest  Follow-up care:  Small, frequent meals  Notify provider if vomiting returns
  • Early Pregnancy Bleeding: o Spontaneous abortion/miscarriage:  A pregnancy that ends due to natural causes before the age of viability (before 20 weeks)  10-15% of all pregnancies end in miscarriage  80% of miscarriages occur before 12 weeks  Different types of miscarriage require different care  When speaking with the patient/family, term miscarriage should be used o Cervical Insufficiency: a.k. incompetent cervix  One cause of late miscarriage  May be cause of recurrent late miscarriage  Can be diagnosed through obstetric history, speculum exam, or by visual inspection of the cervix on ultrasound

 Diagnosed on ultrasound  Characterized by:  Painless, bright red vaginal bleeding during 2nd or 3rd trimester  May need to be hospitalized for assessment of condition  Should have large bore IV  may require blood replacement if bleeding is significant  May be able to be discharged home  After 36 weeks, Cesarean delivery performed  Woman may experience more bleeding than normal delivery o Abruptio Placentae/Placental abruption:  Premature separation of the placenta from uterine wall  Characterized by:  Painful, DARK RED bleeding, and RIGID/BOARDLIKE ABD  Management depends on severity  Mother & fetus = stable; expectant management indicated  If near term, immediate birth is management of choice  Vaginal Cesarean delivery depend on severity/grade/amount of separation and how much bleeding is occurring  Mother may require blood replacement depending on amount of blood loss and clinical manifestations

  • Clotting Disorders in Pregnancy: o Normal Clotting:  Preserves homeostasis by building a clot in response to an injury to prevent excessive bleeding  Clotting cascade and fibrinolytic system work together o Clotting Problems (DIC):  Often related to preeclampsia and results in both bleeding and clotting at the same time  Clotting factors are used up leaving patient at risk of excessive bleeding  Treatment = correction of underlying cause  Nurse must monitor for s/s of bleeding  May require replacement of blood products  In-dwelling catheter should be placed, and renal function needs to monitored closely

Preterm Labor & Birth: - Preterm Birth vs Low Birth Weight: Preterm refers to gestational age o Preterm infants are smaller than average due to their immature gestational age o Low birth weight may occur for different reasons such as IUGR- something preventing the fetus from growing as expected - Spontaneous vs Indicated preterm birth: o Preterm birth can be natural and spontaneous o Or may occur to resolve maternal/fetal risk factors (preeclampsia) o Causes:  Infection, structural abnormalities of the uterus that affects the uterus or cervix, unexplained vaginal bleeding, genetic predisposition, maternal/fetal stress, uterine overdistention, fetal allergy, decreased/low levels of progesterone o Predicting Spontaneous Preterm Labor & Birth:  Risk factors:  History of a previous spontaneous preterm birth between 16 and 36 weeks of gestation  History of genital tract colonization, infection, or instrumentation  Black race  Bleeding of uncertain origin in pregnancy  Uterine anomaly  Use of assisted reproductive technology  Multifetal gestation  Cigarette smoking, substance abuse  Prepregnancy underweight (BMI <19) and prepregnancy obesity (BMI >30)  Periodontal disease  Limited education and low socioeconomic status  Late entry into prenatal care  High levels of personal stress in one or more domains of life  Cervical length:  Can be an indicator of preterm birth  Length changes before uterine activity begins  Fetal fibronectin- FFN: glycoprotein found in early and late pregnancy  Presence in late 2nd and early 3rd trimester indicate placental inflammation preterm labor  Better indicator of who will NOT go into labor  Women with negative test have <1% chance of going into labor within 2 weeks following the test - Assessment = s/s of labor - Interventions: o Prevention: address known risk factors present in the pregnant client

  • Obstetric Procedures:

  • Version o External: used to turn fetus from breech to cephalic presentation  Success rate is 65% & reduces risk of cesarean delivery by 50%  Ultrasound to confirm presentation is performed followed by an NST  Gentle constant pressure on the abdomen is used to turn the fetus  Usually performed 36-37 weeks gestation o Internal: rarely used, most often with a twin delivery to turn the second twin  Provider inserts hand into uterus to physically turn the fetus  Cesarean is most often used for managing malpresentation in multifetal pregnancy

  • Induction of Labor: chemical or mechanical initiation of labor o Elective induction of labor: when labor is induced without a medical indication  Not recommended before 39 completed weeks of gestation  Success of induction is more likely when cervix is favorable  The Bishop score should be assessed before induction; a score of 8 or more, there is a higher likelihood of vaginal birth o Cervical ripening methods:  Chemical agents (prostaglandins or misoprostol)  Balloon catheters (foley catheter balloon) inserted to canal then inflated  Causes cervix to open in response to mechanical pressure applied by balloon  Sweeping/stripping amniotic membranes not recommended due to side effects & little evidence that it’s effective  Sexual intercourse, nipple stimulation, walking  Amniotomy (artificial ROM) may be used to induce/augment labor o Oxytocin:  Can be administered via IV infusion to stimulate uterine contractions  High alert medication! Requires careful monitoring  Should be given slowly in small increments  Woman should be placed on continuous fetal monitoring when receiving  Nurse will monitor for uterine tachysystole (>5 contractions in 10 mins)

  • Augmentation of Labor: assisting labor that has already started but is not progressing o Most common methods = amniotomy & oxytocin administration

  • Operative Vaginal Birth: o Forceps-assisted birth: curved blades (forceps) assist to deliver fetal head  Indications: prolonged 2nd stage of labor, fetal compromise o Vacuum-assisted birth: vacuum cup is suctioned onto the fetal head to assist in delivery of the head

  • Cesarean Birth: o Indications: fetal, maternal, or fetal-maternal combined o Elective: c-section without a medical indication o Scheduled: labor/vaginal delivery are contraindicated as with active genital herpes infection, birth is necessary but cannot be induced as with some hypertensive states, repeat c-section o Unplanned: unplanned or emergency cesarean o Forced: legal requirement due to fetal jeopardy such as when the woman refuses and an ethical board must be called into place to advocate for fetal well-being o Surgical techniques: different types of incisions may be used  Low-transverse uterine incision  less risk of uterine rupture w/ subsequent pregnancies  Provides the opportunity to attempt a trial of labor or a vaginal birth after cesarean w/ a late pregnancy  Less blood loss with this incision o Complications & risks:  Risks and complications are similar to other surgeries including bleeding, infection, etc. o Anesthesia: Cesarean may use spinal, epidural, or general anesthesia o Prenatal preparation: prenatal education classes should include discussion of cesarean birth & should emphasize the similarities & differences between different modes of birth

  • Trial of Labor: allowing the mother to labor for a “reasonable” period of time (usually 4- 6 hours) to determine if vaginal birth may be possible

  • Vaginal Birth After Cesarean (VBAC): reasons for primary/previous cesarean should be considered, many indications may not be recurring complications o Not all women are candidates but success rates = 60-80%

  • Obstetric Emergencies:

  • Meconium-Stained Amniotic Fluid: occurs when fetus passes meconium prior to delivery o May or may not be associated with fetal distress o Risk for meconium aspiration after delivery

  • Shoulder Dystocia: anterior shoulder gets “stuck” under the mother’s pubic arch o McRoberts maneuver combined w/ suprapubic pressure may free the shoulder o Increased risk with LGA fetus

  • Prolapsed Umbilical Cord: medical emergency & results in the need for immediate C- section o When presenting part is not well engage, cord may slip out ahead of the fetus when the membranes rupture o Pressure should be applied to presenting fetal part until delivery to relieve compression of the cord & restore fetal blood flow o Cord should not be touched or handled (may cause vessels to spasm)

Was this document helpful?

Topics 5 & 6 - Important information for Final Exam highlighted & bolded within material

Course: Nursing Care of the Childbearing Family (NSG-432)

77 Documents
Students shared 77 documents in this course
Was this document helpful?
Assessment of High-Risk Pregnancy:
- Assessment of Risk Factors:
oBiophysical Factors: those that originate within mother/fetus
Genetic: inherited disorders, chromosomal anomalies, multiple gestation,
large fetal size, ABO incompatibility
Nutrition: adolescents, three pregnancies in 2 years,
tobacco/alcohol/drug use, dietary intake (illness, fads, bariatric surgery),
inadequate or excessive weight gain, low hematocrit (<33%)
Medical & Obstetric: Complications (current or previous), pregnancy-
related illness, previous loss
Polyhydramnios (fetal GI issues) or oligohydramnios (possible fetal
renal issues, PROM, IUGR, maternal hypertension/dehydration,
uteroplacental insufficiency)
IUGR- Intrauterine growth restriction
oMother- hx of HTN, diabetes, cardiac or autoimmune
issues, pulmonary disease
Chromosomal abnormalities:
oAdvanced maternal age
oParental chromosomal rearrangements or previous hx of
this
oPsychosocial factors: behaviors/adverse life events
Smoking, caffeine (recommended no more than 12 oz/day)
Alcohol/drugs
Emotional distress, depression/mental health problems
Psychological status:
History of abuse, social environment, unsafe practice, situational
crises
oSociodemographic Factors:
Low income/Social Determinants of Health (SDOH)
Lack of prenatal care
Age: adolescents – anemia, preeclampsia, CPD
Mature mothers (“advanced age” i.e. over 35) increased risk of genetic
issues, chronic disease
oEnvironmental factors:
Infections, chemicals, pollutants (industrial, at home smoking), cat litter,
gardening
-Antepartum Testing:
oPurpose: to identify those at risk for injury due to interrupted acute or chronic
oxygenation
Diabetes, hypertension, preeclampsia, renal or heart issue, IUGR,
previous stillbirth, poly or oligohydramnios, etc