Dr. Tamar Shalem Shaare Zedek Medical Center. Puerperium Post Partum Hemorrhage (PPH) ...
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Transcript of Dr. Tamar Shalem Shaare Zedek Medical Center. Puerperium Post Partum Hemorrhage (PPH) ...
PUERPERIUM& Post Partum Hemorrhage
Dr. Tamar ShalemShaare Zedek Medical Center
Puerperium
Post Partum Hemorrhage (PPH)
Abnormalities of the Puerperium
PUERPERIUM
Puerperium defines as a period of 6 weeks following delivery, in which
a number of changes in anatomy and physiology occur.
DEFINITION
ANATOMIC CHANGES REPRODUCTIVE SYSTEM
Weight
Pregravid uterus: 50 - 100 g Uterus at term: 1000 - 2000 g
Length Non-pregnant : 6 - 8 cm
At term: 40 cm
UTERUS
UTERUS
Size
after 24 h Reduced to 20 w gestation
after 48 h Reduced to 14 w gestation
descends to pelvic cavity within 2 w
returns to non-pregnant size within 4 w
UTERUS
Within 2-3 days patients begin to passvaginal discharge Called lochia.
Definition: the superficial necrotic layer of
pregnant endometrium (decidua).
Contains: RBC / WBC Decidua Epithelial cells Bacteria
UTERUS
Stages: lochia rubra (days 1-4) lochia serosa (days 5-7) lochia alba (days 7-14)
vaginal discharge is normal up to 6 w.
CERVIX
Following parturition the cervix is very
distensible, thin and flabby even with a well
contracted uterus, and may show tears
along its margins.
Dilated state: 2-3 cm after few days 1 cm at 1 w non-pregnancy state in 6-
12w
VAGINA
Following parturition the vagina ishyperemic - swollen - smooth.
The normal rugae reappear within 3 w.
The edema usually resolve by 6 w.
SYSTEMIC CHANGES
•CARDIOVASCULAR CHANGES•URINARY TRACT CHANGES •HEMOTHOLOGICAL CHANGES
CARDIOVASCULAR CHANGES
The significantly altered cardiovascular
system returns to a non-pregnant state
2-3 w after delivery.
Blood volume decreases by 33% in 72 h
due to blood loss and diuresis.
Increased heart rate and cardiac output
return to baseline within 2 w.
URINARY TRACT CHANGES
In the first days after labor: Over distention of bladder Incomplete emptying Traumatic bacteruria
URINARY TRACT CHANGES
Risk Factors for complicationsEpidural analgesiaVolume overloadPitocin (ADH effect)Episiotomy & lacerations
URINARY TRACT CHANGES
Puerperal diuresis usually occurs after2-5 days after labor.
Structural changes : Dilatation of bladder, Ureters and renal pelvis may persist for 3
m or more.
HEMATHOLOGICAL CHANGES
Blood count:
Leukocytosis (up to 30,000)LymphopeniaThrombocytosis
Blood volume: returns to normal in 1 w – increased
Hct.
CLINICAL & PHYSIOLOGICAL ASPECTS
Gustav Climt
WEIGHT LOSS
5-6 Kg - immediately fetus
amniotic fluid placenta
blood loss
2-3 Kg - within few days diuresis
PAINS
After pains (multipara >> nullipara)
Breast enlargement
Post spinal headache
Episiotomy/and lacerations
POST-PARTUM BLUES
Mild depression after labor is very common, lasts 2-3 days, and is self-limited.
Factors:•emotional letdown•pains of early puerperium• fatigue & loss of sleep•anxiety over taking care of the baby•defected self imaging
Mild depression after labor is very common, lasts 2-3 days, and is self-limited.
Factors:• emotional letdown• pains of early puerperium• fatigue & loss of sleep• anxiety over taking care of the baby• defected self imaging
POST-PARTUM BLUES
Treatment:anticipation, recognition & reassurance.
Attention :If the symptoms lasts more than 10 days or getting worse:Consider post-partum psychosis.
טיפול ביולדת לאחר לידה השגחה בחדר לידה לשעה-שעתיים )ניטור סימנים
וכמות דימום(
וידוא מתן שתן - למניעת .overflow incontinence
מוביליזציה מהירה
מתן זריקת anti D לאמהות שהןRh שליליות שעות מהלידה(.72 חיובי )תוך Rh להן תינוקות
.חיסון אדמת/ וריצלה
הטיפול ביולדת לאחר לידה ש' לאחר לידה נרתיקית ללא סיבוכים.48שחרור - ימים לאחר ניתוח קיסרי ללא סיבוכים.5
הנחיות בשחרור לגבי מצבים בהם יש לפנות לרופא:חום, דימום משמעותי, כאב ונפיחות ברגליים וקוצ"נ.
שבועות מהלידה.6 ביקורת גניקולוג - • יחסי מין -רצוי להימנע מיחסי מין עד לביקורת גניקולוג• שב'.6-8 מחזור - בלא מניקות יחלו מחזורי ביוץ תוך •
חד'.6 בהנקה מלאה יחלו מחזורי ביוץ לאחר אמצעי מניעה - במניקות גלולות על בסיס פרוגסטרון או •
IUD.
POSTPARTUM HEMORRHAGE
POSTPARTUM HEMORRHAGE
Early PPH occurs during the first 24 h after delivery.Late PPHoccurs after 24 h but before 6 weeks afterdelivery .Definition:1. more than 500cc blood loss at delivery.2. 10% change in Hct in Post Partum
period. 3. a need for blood transfusion.
POSTPARTUM HEMORRHAGE
incidence:The overall incidence for all deliveries: Early PPH 3-6% Late PPH 0.5-1.3%
Mortality: PPH contributes 30% of 500,000
pregnancy relateddeaths that occur each year worldwide.
Incidence
Vaginal delivery- 5–8%. PPH is the most common cause of
excessive blood loss in pregnancy. PPH is the main cause for transfusions in
pregnant women. 3rd leading cause of mortality in the USA.
1/6 of maternal deaths. In less-developed countries, hemorrhage is a
leading causes of death.
POSTPARTUM HEMORRHAGE
Early PPH - etiologies:
Uterine atony- 50%Lower genital tract laceration –
20%Retained placental fragment – 5-
10%Uterine ruptureUterine inversionPlacenta accretaHereditary coagulopathy
POSTPARTUM HEMORRHAGE
Risk Factors
Coagulopathy Hemorrhage/blood transfusion during previous pregnancy Anemia Grand multiparity Multiple gestation/ large infant/ polyhydramnios Dysfunctional labor Oxytocin induction or augmentation of labor Rapid or tumultuous labor PET / eclampsia Vaginal delivery after previous cesarean birth General anesthesia for delivery Forceps delivery
Uterine atony
.
Uterine atony Predisposing causes:
excessive manipulation of the uterus general anesthesia uterine overdistention )twins or polyhydramnios( prolonged labor grand multiparity uterine leiomyomas operative delivery and intrauterine manipulation, oxytocin induction or augmentation of labor previous hemorrhage in the third stage uterine infection extravasation of blood into the myometrium )Couvelaire
uterus( intrinsic myometrial dysfunction.
POSTPARTUM HEMORRHAGE
Late PPH - etiologies:
• Infections• Retained placental fragments
•Hereditary coagulopathy
POSTPARTUM HEMORRHAGE - complications
Postpartum hypotension may lead to partial or total necrosis of the anterior pituitary gland and cause postpartum panhypopituitarism, or Sheehan's syndrome. failure to lactate amenorrhea decreased breast size loss of pubic and axillary hair hypothyroidism adrenal insufficiency
The condition is rare )< 1:10,000 deliveries )
Treatment
Predelivery Blood type & cross-matched test Large bore IV Blood reserve in blood bank
Third stage of labor Uterotonic agents Manual removal of placenta Repair of lacerations/ Episiotomy Evaluation of persistent bleeding
Treatment
Measures to control bleeding Manual exploration of the uterus )&birth
canal( Bi manual pressure & massage Uterine packing Uterotonic agents Blood replacement Radiographic embolization of pelvic
vessels Operative management
Treatment
Operative management Uterine artery ligation B-Lynch suture Internal artery ligation Hysterectomy
Uterine artery ligation
B-Lynch suture
Internal Iliac artery ligation
Abnormalities of the Puerperium
Puerperal fever Endometritis
Cesarean section wound infection Episiotomy infection Analgesia complications
Puerperal Fever
Puerperal morbidity due to infection has occurred if the patient's temperature is higher than 38 °C on 2 separate occasions at least 24 hours apart following the first 24 hours after delivery.
Morbidity and Mortality
Major cause of morbidity associated with childbirth.
8% of maternal death.
Puerperal Fever
Main cause: endometritis. UTI is the next most common infection. Neglected or virulent endomyometritis
may progress to more serious infection Generalized sepsis septic pelvic thrombophlebitis pelvic abscess
Extragenital infections are much less common than endometritis and urinary tract infections.
Endometritis
Etiology
Lactobacillus Diphteroides Corynebacterium Staphylococcus Streptococcus* Escherichia*
Gardnerella Klebsiella*Proteus* EubacteriumGaffyka Prevotella
Peptostreptococcus Veillonella Bacteroides Fusobacterium*
Mycoplasma Ureaplasma
Etiology
Almost all postpartum infections are caused by bacteria normally present in the genitalia of pregnant women.
The lochia is an excellent culture medium for organisms ascending from the vagina.
70% of puerperal soft-tissue infections are mixed infections.
Cesarean Section is the most common identifiable risk factor for development of puerperal infection.
Etiology
Risk Factors: prolonged rupture of the membranes )> 24
hours(, chorioamnionitis excessive number of digital vaginal examinations prolonged labor )> 12 hours( toxemia intrauterine pressure catheters )> 8 hours( fetal scalp electrode monitoring preexisting vaginitis or cervicitis operative vaginal deliveries cesarean section intrapartum and postpartum anemia poor nutrition obesity low socioeconomic status coitus near term
Symptoms and Signs
Fever tender uterus lochia may or may not have a foul odor. Leukocytosis )> 10,000/ L( In more severe disease:
high fever, malaise, abdominal tenderness, ileus, hypotension, and generalized sepsis may be seen.
Usually develops on the 2nd or 3rd postpartum day.
Early fever )within hours of delivery( and hypotension are almost pathognomonic for infection with hemolytic streptococci.
Treatment
The choice of antibiotics depends on the suspected causative organisms and the severity of the disease.
Treatment usually starts IV after caltures are taken.
Options:
Clindamycin + Aminoglycoside Single-agent therapy with second or third generation
cephalosporins
Treatment
The response to therapy should be carefully monitored for 24–48 hours.
Deterioration or failure to respond determined both clinically and by laboratory test results requires a complete re-evaluation.
Ampicillin is added when the patient has a less than adequate response to the usual regimen, particularly if Enterococcus spp. are suspected.
Intravenous antibiotics are continued until the patient has been afebrile for 24–48 hours.
Cesarean Section Wound Infection
Wound infection occurs in 4–12% of patients following cesarean section.
Risk factors: obesity diabetes prolonged hospitalization before cesarean section prolonged rupture of the membranes chorioamnionitis endomyometritis prolonged labor emergency CS anemia
Symptoms and Signs
Fever with no apparent cause that persists to the fourth or fifth POD.
Wound erythema and tenderness may not be evident until several days after surgery.
Occasionally, wound infections are manifested by spontaneous drainage.
Cesarean Section Wound Infection
The organisms responsible for most wound infections originate on the patient's skin.
S aureus is the organism most commonly isolated.
Streptococcus species, E coli, and other gram-negative organisms that may originally have colonized the amniotic cavity are also seen.
Rarely- necrotizing fasciitis and the closely related synergistic bacterial gangrene.
Radical debridement of necrotic and infected tissue is the cornerstone of treatment.
Episiotomy Infection
0.5–3% Surprising low incidence. Excellent local blood supply could be the
explanation. Correlates severity of the
laceration/episiotomy Other genital infection increase the risk.
Symptoms and Signs
Pain is the most common symptom. Spontaneous drainage is frequent, so a mass
rarely forms. Incontinence of flatus and stool may be the
presenting symptom of an episiotomy that breaks down and heals spontaneously.
Disruption of the wound and gaping of the incision.
A necrotic membrane may cover the wound and should be debrided if possible.
A careful rectovaginal examination should be performed to determine whether a rectovaginal fistula has formed.
Treatment
Initial treatment is opening and cleaning the wound in order to promote formation of granulation tissue.
Warm baths. Closure of an infected episiotomy is likely to fail
and may make ultimate closure more difficult. Surgical should be undertaken only after
granulation tissue has covered the wound. Increasing trend towards early repair of
episiotomy wound dehiscence.
Urinary Tract Infection
2–4% of women postpartum. Following delivery, the bladder and lower
urinary tract remain somewhat hypotonic, and residual urine and reflux result.
Risk factores: asymptomatic bacteria, chronic UTIs, and anatomic disorders of the bladder, urethra, and kidney.