the rest of week 5 Flashcards

1
Q

what is amniotic fluid embolism (APE) or anaphylactoid syndrome?

A

Introduction of amniotic fluid into the circulation of the labouring patient during labour, during birth, or within 30 minutes after birth.

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2
Q

clinical manifestations of AFE

A

-Respiratory distress
-Restlessness
-Dyspnea
-Cyanosis
-Pulmonary edema
-Respiratory arrest
-Circulatory collapse
-Hypotension
-Tachycardia
-Shock
-Cardiac arrest
-Hemorrhage
-Coagulation failure
-Uterine atony
-mortality rate is 61% or higher

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3
Q

risk factors for AFE

A

advanced age, non-White race, placenta previa, pre-eclampsia, and forceps-assisted or Caesarean birth.

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4
Q

interventions for AFE

A

-Oxygenate.
-Administer oxygen by nonrebreather face mask (10 L/min) or resuscitation bag delivering 100% oxygen.
-Prepare for intubation and mechanical ventilation.
-Initiate or assist with cardiopulmonary resuscitation. -Tilt pregnant patient 30 degrees to side to displace uterus.
-replace fluid loss via IV
-administer blood- packed cells, fresh frozen plasma
-insert in-dwelling catheter and measure hourly urine output
-FHR/maternal status
-prepare for emergency birth once pt’s condition has stabilized

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5
Q

what is the bishop score?

A

-to see if induction is successful
-includes, dilation, effacement, station, consistency, position

Cervical ripeness is the most important predictor of successful induction.

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6
Q

chemical method of induction -Cervical ripening agents

A

Chemical agents: ripens the cervix, making it softer and causing it to begin to dilate and efface; it stimulates uterine contractions
-prostaglandins E2
-cervidil insert and prepidil gel

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7
Q

Cervidil insert

A

placed transvaginally into the posterior fornix of the vagina. removed after 12 hours or at the onset of active labour or abnormal fetal heart rate and patterns occur.

Keep the Cervidil insert frozen until just before insertion and warming is needed.
-Have the patient void before insertion.
-Prepare to pull the string to remove the insert if significant adverse effects occur. Delay initiation of oxytocin for induction of labour for 6 hours after last instillation of gel or at least 30 to 60 minutes after removal of the insert

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8
Q

Prepidil Gel

A

administered through a syringe into the vaginal canal just below the internal cervical os.

Bring the Prepidil gel to room temperature just before administration avoid force with hot water or microwave
-have the pt void before insertion
-Assist the patient in maintaining a supine position with lateral tilt for at least 30 minutes after insertion of gel or for 2 hours after placement of insert.

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9
Q

methods of induction: mechanical

A

-to to ripen the cervix by stimulating the release of endogenous prostaglandins
-balloon catheters (like a foley) is inserted through the intracervical canal
-catheter balloon is inflated above the internal cervical os with 30 to 50 mL of sterile water.
-pressure and stretching of the lower uterine segment and cervix stimulates the released of endogenous prostaglandins
-balloon will fall out when dilation is 3cm or removed after 24 hours

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10
Q

what are the contraindications for mechanical methods of induction?

A

-low-lying placenta
-antepartum haemorrhage
-rupture of membranes
-evidence of lower tract genital infection

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11
Q

Hydroscopic dilators

A

-Hydroscopic dilators-substances that absorb fluid from surrounding tissues and enlarge
-Laminaria tents (natural cervical dilators made from desiccated seaweed)
-Lamicel synthetic dilators containing magnesium sulphate
-inserted into the endocervix without rupturing the membranes
-expand as fluid is absorb, causing cervical dilation and the release of endogenous prostaglandins.

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12
Q

methods of Induction: Mechanical and physical methods

A

-sexual intercourse (prostaglandins in the semen and stimulation of contractions with orgasm)
-nipple stimulation (release of endogenous oxytocin from the pituitary gland)
-ambulation/walking (gravity applies pressure to the cervix, which stimulates the secretion of endogenous oxytocin)

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13
Q

Methods of Induction: Alternative and Amniotomy

A

Amniotomy: artificial rupture of membranes [AROM]
when do we initiate this:
-presenting part of the fetus should be engaged and well applied to the cervix
-there is no active infection of the genital tract like herpes
-HIV status is negative or viral load is low
-labour usually begins 12 hours of the rupture but we can’t predict outcome of brith or time which is why we combine it with oxytocin

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14
Q

assessment after giving amniotomy?

A

-color, odour, amount, consistency, meconium or blood

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15
Q

what are the complications of amniotomy?

A

-Chorioamnionitis resulting from prolonged rupture without labour.
-Variable FHR deceleration patterns may due occur due to cord compression resulting from umbilical cord prolapse or decreased amniotic fluid.

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16
Q

Oxytocin

A

-Stimulates uterine contractions
-Used for induction or augmentation of labour
-Administered IV in saline or lactated Ringers via a pump
-goal of oxytocin administration is to produce acceptable uterine contractions as evidenced by a consistent pattern of three to five contractions every 10 minutes

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17
Q

dosage of oxytocin

A

-The IV solution containing oxytocin should be mixed in a standard concentration. Concentrations often used are 10 units in 1 000 mL of fluid, 20 units in 1 000 mL of fluid, or 30 units in 500 mL of fluid.
* Isotonic IV solutions (e.g., 0.9% sodium chloride, lactated Ringer’s) are used to avoid electrolyte imbalance.
* Oxytocin is administered intravenously through a secondary line connected to the main line at the proximal port (connection closest to the IV insertion site). Oxytocin is always administered by pump.
* Oxytocin administration is started at a low-dose or high-dose regimen. Dosage is increased per protocol until an adequate contraction pa ern is established.
* The goal of oxytocin administration is to produce acceptable uterine contractions as evidenced by a consistent pa ern of three to five contractions every 10 minutes.
* Once labour is established, oxytocin is maintained at or decreased to a rate adequate for continued labour progress.

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18
Q

oxytocin indications

A

-Suspected fetal jeopardy (e.g., intrauterine growth restriction)
-Inadequate uterine contractions; dystocia
-Prelabour rupture of membranes
-Post-term pregnancy
-Chorioamnionitis
-Medical concerns in pregnant patient (e.g., severe Rh isoimmunization, inadequately controlled diabetes, chronic renal disease, or chronic pulmonary disease)
-Gestational hypertension (e.g., pre-eclampsia, eclampsia)
-Fetal death

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19
Q

Contraindications of oxytocin

A

-Abnormal fetal heart rate
-Cephalopelvic disproportion, prolapsed cord, transverse lie
-Placenta previa or vasa previa
-Prior classic uterine incision or other uterine surgery
-Active genital herpes infection
-Invasive cancer of the cervix – bc risk of bleeding
-Previous uterine rupture

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20
Q

oxytocin reportable condition (immediate)

A

-Uterine tachysystole (with or without FHR changes)
-Abnormal fetal heart rate and pattern (absent baseline variability and any of the following:
recurrent late decelerations,
recurrent variable decelerations
-bradycardia prolonged decelerations)
-Suspected uterine rupture
-Inadequate uterine response at 30 mU/min

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21
Q

nursing care during oxytocin

A

-Assess level of the labouring patient’s discomfort and pain and the effectiveness of pain management.
-Monitor fetal status using electronic fetal monitoring and evaluate tracing
every 15 minutes and with every change in dose during the first stage of labour
every 5 minutes during the active pushing phase of the second stage of labour.
-Monitor the contraction pattern and uterine resting tone
every 15 minutes and with every change in dose during the first stage of labour and every 5 minutes during the second stage of labour.
-Monitor blood pressure, pulse, and respirations every 30 to 60 minutes and with every change in dose.
-Assess intake and output; limit IV intake to 1 000 mL in 8 hours; urine output should be 120 mL or more every 4 hours.
-Monitor for adverse effects, including nausea, vomiting, headache, and hypotension.
Observe emotional responses of labouring patient and their partner.

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22
Q

Measures if any reportable conditions should occur w/ oxytocin

A

-Discontinue use of oxytocin per hospital protocol and notify primary care provider immediately:
-Turn patient onto lateral position.
-Give IV bolus if patient is hypovolemic or hypotensive.
-If there is evidence of hypoxia or hypovolemia in the patient, administer oxygen by nonrebreather face mask at 8 to 10 units/min or per protocol or primary health care provider’s order. Oxygen is reserved for maternal resuscitation in the presence of maternal hypoxia or hypovolemia, NOT for fetal resuscitation.
-Prepare to administer nitroglycerine (causes vasodilation), if ordered, to decrease uterine activity.
-Continue monitoring fetal heart rate and pattern and uterine activity.
-give oxygen to mum not baby

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23
Q

Augmentation of Labour

A

Stimulation of uterine contractions after labour has started spontaneously but progress is unsatisfactory.
-Implemented for management of hypotonic uterine dysfunction

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24
Q

Common augmentation methods

A

-Oxytocin infusion
-Amniotomy
-Noninvasive methods-emptying the bladder, ambulation, position changes, relaxation measures, nourishment, hydration, and hydrotherap

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25
Q

external cephalic version

A

-manual turning of a fetus from breech to transverse to cephalic/vertex

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26
Q

what are the contraindications of external cephalic version?

A

-multiple fetuses- think of dana
-non-assuring fetal stauts
-placenta previa

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27
Q

what are the complications associated with external cephalic version?

A

-prelabour rupture of membranes
-changes in the fetuses heart rate
-placenta abruption
-placenta previa
-preterm labour
-PROM
-cord prolapse bc u are moving the baby
-multiple gestations
-uteroplacental insufficiency
-fetomaternal hemorrhage
-high risk of c-section

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28
Q

required assessment before external cephalic version

A

-rule out placenta previa
-determine the fetal position
-locate the umbilical cord bc we don’t want it to prolapse
-detect multiple gestation or any fetal abnormalities
-measure fetal dimensions

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29
Q

induction of labour for pre-eclampsia

A

-Pre-eclampsia >37 weeks
-Significant maternal disease not responding to treatment
-Significant but stable antepartum hemorrhage
-Chorioamnionitis
-Suspected fetal compromise
-Term prelabour rupture of membranes (PROM) with maternal group B streptococcus (GBS) colonization

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30
Q

Contraindications for induction of labour

A

-Suspected fetal macrosomia
*Absence of fetal or maternal indication
*Caregiver or patient convenience

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31
Q

Operative Vaginal Births: Forceps-assisted birth maternal indication

A

-prolonged second stage of labour
-need to shorten the second stage of labour for maternal reason like exhaustion, cardiopulmonary disease, cerebrovascular disease)

32
Q

Operative Vaginal Births: Forceps/Vacuum Assisted birth -assisted birth fetal indication

A

-abnormal FHR tracing, abnormal presentation
-arrest of rotation
-delivery of head in a breech presentation

33
Q

Operative Vaginal Births: Forceps-assisted key considerations

A
  • members must be ruptured
    -assessment of adequacy of pelvis relation fetal head circumferences
    -fully dilated cervix w/ head engaged
    -empty bladder
34
Q

Nursing care: operative vaginal birth -forceps

A

-Postpartum and newborn assessment
-assessed for vaginal and cervical lacerations
-bleeding due to lacerations
-urinary retention due to bladder injuries or urethral
-injuries; hematoma formation in the pelvic soft tissues
-assessed newborn for bruising or abrasions at the site of the blade applications
-facial palsy resulting from pressure of the blades on -the facial nerve (cranial nerve VII)
-subdural hematoma.

35
Q

Operative Vaginal Births: Vacuum Assisted Birth

A

-Attachment of vacuum cup to fetal head, using negative pressure to assist birth of head

36
Q

Vacuum Assisted Birth- Nursing Care

A

-FHR monitoring
-Newborn assessment for signs of trauma, infection and cerebral irritation (seizures, lethargy, increased irritability or poor feeding)

37
Q

Risk to newborn: vacuum assisted birth

A

Risk to newborn: cephalhematoma, scalp lacerations, subdural hematoma-

38
Q

Caesarean Birth

A

Birth of a fetus through a transabdominal incision of the uterus- can be vertical or horizontal
-if scheduled c-section- labour and vaginal birth are contraindicated
-if unplanned c-section- changes in labouring patient’s and family expectations
-forced: to protect the well-being of labouring patient and the fetus (to save mum and baby)

39
Q

complications of Caesarean birth

A

-anaesthesia events
-hemorrhage
-bowel or bladder injury
-amniotic fluid embolism
-air embolism
and then possible postpartum complications: atelectasis, endometritis, UTI, abdominal wound hematoma formation, dehiscence, infection, thromboembolic disease, bowel dysfunction

40
Q

Recommended Measures to Safely Reduce the Primary Caesarean Birth Rate

A

-Offer external cephalic version for breech presentation.
-Offer the option of labour for patients with twin gestations when the first twin is in cephalic presentation.
-Avoid Caesarean birth for suspected fetal macrosomia unless the estimated fetal weight is at least 5 000 g in patients without diabetes and at least 4500 g in patients with diabetes.
-Offer operative (forceps- or vacuum-assisted) vaginal birth, performed by an experienced, well-trained physician.

41
Q

Trial of labour after caesarean : TOLAC

A

A patient who has had a previous low-segment Caesarean birth may be a candidate for a TOLAC

42
Q

Indications for primary Caesarean birth

A

-Dystocia
-breech presentation
-abnormal FHR pattern often are nonrecurring.

43
Q

Contraindications – for TOLAC

A

-Previous or suspected classical uterine incision
-Previous inverted T or low vertical uterine incision
-Previous uterine rupture
-Previous major uterine surgery
-Patient requests repeat Caesarean birth
-Inability to perform an emergency Caesarean birth if necessary

44
Q

Postpartum Changes and Ongoing Physical Assessment

A

B = Breasts (firmness) and nipples
U = Uterine fundus (location; consistency)
B = Bladder function (amount; frequency)
B = Bowel function (passing gas or bowel movements)
L = Lochia (amount; colour)
L = Legs (peripheral edema)
E = Episiotomy/Laceration or Caesarean birth incision (perineum: discomfort; condition of repair, if done)
E = Emotional status (mood, fatigue)

45
Q

post delivery cardiac output

A

-return to prelabour values after 1 hour
-HR/BP return to non-pregnant levels w/in a few days

46
Q

post delivery blood

A

-volume returns to normal after 3-4 weeks
-hameatocrit, haemglobin- normal by 8 weeks
-hemorrhoids, varicosities decrease overtime

47
Q

post delivery- respiratory

A

rapidly returns to non-pregnant levels after birth
-immediate decrease in intra-abdominal pressure
-after c-section remind client to cough, turn, deep breath

48
Q

post delivery- endocrine

A

-Once placenta is expelled – decrease in hormones produced by placenta (estrogen, progesterone)
-70% of non-breastfeeding mothers menstruate within first 12 weeks
-In breastfeeding women, return of ovulation depends on breastfeeding patterns.
-Lactational amenorrhea
May ovulate before first menstrual cycle

49
Q

post-delivery uterus-expected findings

A

-loose floppy abdominal skin
-uterus firm and contracting, not boggy (feels spongy) should be midline of abdomen
-boggy uterus may indicate retained placental fragments
-uterus displace to the right may indicate full bladder- and uterus cannot contract well if bladder is full
-uterus should be descending 1 fingerbreadth /per
-afterpains of uterus should resolve 3-7 days

50
Q

post-delivery uterus-unexpected findings

A

-uterine atony-failure of the uterus to contract-lead to postpartum hemorrhage
-distended abdomen and hypoactive bowel sounds
-red, tender, dehiscing incision

51
Q

Abdomen I.A.P.P

A

-Inspect: distension; incision line post C-section for infection, dehiscing,
-Auscultate: all 4 quadrants for bowel sounds
-Palpate: uterine descent in relation to umbilicus; firmness and position-abdominal midline
-Percuss: Drum like sound suggests abdominal gas

-Initially – poor abdominal muscle tone
Takes approx. 6 weeks for wall to tighten to pre-pregnant state

52
Q

post-delivery Vagina

A

-Returns to normal by 6-8 weeks
-Some changes in vaginal rugae
-Dryness until ovulation returns

53
Q

post delivery relieve care

A

-Ice packs for first 24 hrs. (rotate 20 minutes on, 20 minutes off); then warm sitz baths
-Some women find witch hazel pads relieve pain
-Adequate hydration
-Potential need for stool softeners
-Assess pain; discomfort

54
Q

clots are coming out- what should you do?

A

provide a uterine massage and call for help

55
Q

bleeding post delivery

A

-assess ACCO
-should not be foul smelling

56
Q

Lochia rubra -bleeding

A

(3 to 4 days)
Bright red or rust coloured flow
Blood and decidual and trophoblastic debris

57
Q

Lochia serosa (lasting approximately 2 to 4 weeks)-bleeding

A

-Pink, brownish coloured
-Old blood, serum, leukocytes, and debris

58
Q

Lochia alba (4-6 weeks)

A

-Whitish, yellow
-Leukocytes, decidua, epithelial cells, mucus, serum, and bacteria

59
Q

potential signs of PPH (postpartum hemorrhage)

A

-soaking pad 1-2 hours, passing clots the size of a golf ball, SOB, light headed, chest pains, palpitations
Notify HCP immediately
-best time is to discuss this education during peri-care

60
Q

postpartum haemorrhage

A

-loss of 500ml of blood through vaginal delivery or 100ml of blood through c-section
-leading cause of maternal death worldwide
-comes on with little to no symptoms until profound symptoms are visible

61
Q

postpartum haemorrhage and tone:

A

uterine atony- cannot relax/contract= leads to bleeding

62
Q

other causes and risk factors to postpartum haemorrhage

A

-Overdistended uterus—large fetus, multiple fetuses, hydramnios, distension with clots
-Anaesthesia and analgesia—conduction anaesthesia
-Previous history of uterine atony
-High parity
-Prolonged labour, oxytocin-induced labour
-Magnesium sulphate administration during labour or postpartum period
-Chorioamnionitis
-Uterine subinvolution
-Obesity
-Tissue
Retained placental fragments
-Trauma-from the delivery itself-forceps-assisted birth, vacuum-assisted birth, Caesarean birth
-Thrombin-like DIC -Coagulation disorder
-Placental abruption
-Placenta previa

63
Q

primary postpartum haemorrhage

A

-occurs within 24 hours of the birth.
-uterine atony
-genital laceration
-retained products of conception
-placenta accreta/increta
-uterine rupture
-uterine inversion
-Coagulopathy (DIC)

64
Q

secondary postpartum haemorrhage

A

-Secondary PPH occurs more than 24 hours but less than 12 weeks after the birth
-subinvolution of uterus
-retained products of conception
infection
-coagulopathy

65
Q

goal of care in postpartum haemorrhage

A

management of hypovolemic shock involves restoring circulating blood volume and eliminating the cause of the hemorrhage

-Establishing two venous access with a large-bore IV catheter to facilitates
fluid resuscitation
-administration of crystalloids (lactated Ringer’s, normal saline solution)
colloids (albumin) blood, and blood components.
-Packed RBCs are usually infused if the patient is still actively bleeding and no improvement in their condition
-Infusion of fresh frozen plasma may be needed if clotting factors and platelet counts are below normal values

66
Q

Nursing assessment of haemorrhage

A

-Palpation of Pulses (Rate, Quality, Equality), BP, -pulse oximetry
-Skin colour, temperature, turgor
-Level of consciousness
-Heart sounds/murmurs
-Breath sounds
-Anxiety, apprehension, restlessness, disorientation
-Monitor Urinary output
-Monitor hemorrhagic

67
Q

Post vaginal delivery bladder and bowels

A

-Voiding usually occurs within first 6 hrs.
-Usually attempt to empty bladder after 2hrs.
-Potential for bladder distention due to normal postpartum diuresis
-Epidural – potential for urinary retention
-Should have good bowel sounds; be passing gas.

68
Q

Post C-Section- bladder and bowels

A

-Indwelling catheter removed at approx. 12 hrs. post C-section
-Normal bowel sounds within 12-24 hrs. ; bowel movement within 2-3 days
-Urine output of 3 000 mL or more each day during the first 2 to 3 days
-Profuse diaphoresis often occurs, especially at night, for the first 2 to 3 days after birth.
-weight loss of 2 to 3kg during the early puerperium
-spontaneous bowel evacuation may not occur for 2 to 3 days after childbirth
-decreased muscle tone

69
Q

Education/nursing consideration bladder and bowels

A

-Encourage voiding – assess ability to voi
- Should be voiding regularly – minimum 360 cc/12 hrs as full bladder may compromise ability of uterus to contract post delivery
-Remind to pat dry front to back to avoid infection
-Educate Kegel/pelvic muscles exercises to improve tone
-Encourage ambulation
-Encourage adequate fluid and food intake
-Stool softener

70
Q

neurological assessment - post delivery

A

-Pregnancy-related neurological discomforts go away post delivery
-Ongoing headache requires careful assessment.
-postpartum headache is associated with:
-gestational hypertension
-stress
-leakage of cerebrospinal fluid into extradural space during placement of needle for epidural or -spinal anaesthesia.

71
Q

muscusketeal after delivery

A

-Lordosis is reversed in the puerperium
-Joints stabilize by 6-8 weeks
-Size of feet may increase
-Back pain usually resolves in a few weeks or months following birth.

72
Q

immune system after pregnancy

A

-suppressed during pregnancy, gradually returns to its prepregnant
-rebound of the immune system can trigger flare-ups of autoimmune e.g. multiple sclerosis or lupus erythematosus

73
Q

after delivery what is the one thing a nurse should promote?

A

ambulation to prevent DVT, STROKE, CLOTS, Constipation from happening

74
Q

postpartum nursing promotion

A

-promoting rest
-postpartum fatigue (PPF)
-promoting ambulation -prevent falls, prevent VTE (venous thromboembolism)
-promoting exercise
-preventing infection
-promoting perineal care
-hand hygiene
-promoting comfort
-nonpharmacological interventions and pharmacological

75
Q

female genital mutliation

A

partial or removal of the external female genitalia -mainly practiced in Africa but also in 40+ countries