5. PUERPERAL PYREXIA
“ A rise of temperature reaching 100.4
degree F or more (Measured orally) on
two seperate occassions at 24 hours
apart (excluding first 24 hours) within
first 10 days following delivery is called
Puerperal pyrexia”
➢In some countries postabortal fever
is also included.
7. PUERPERAL SEPSIS
“An infection of the genital tract which
occurs as a complication of delivery is
termed puerperal sepsis.”
➢Puerperal pyrexia is considered to
be due to genital tract infection unless
proved otherwise.
8. INCEDENCE
❖There had been marked decline in
puerperal sepsis during the past few years
due to:-
Improved obstetric care
Availability of wider range of antibiotics
10. PREDISPOSING FACTORS
➢Damage of Cervicovaginal
mucous membrane
➢Large placental wound surface area
➢Blood clots presents at placental site
ANTEPARTUM FACTORS:
✓Malnutrition and anemia
✓Preterm labour
✓PROM
✓Chronic illness
✓Prolonged rupture of membrane >18 hours
11. INTRAPARTUM FACTORS:
✓Repeated vaginal examinations
✓Prolonged rupture of membranes
✓Dehydration and keto- acidosis
during labour
✓Traumatic operative delivery
✓Hemorrhage
✓Retained bits of placenta or membranes
✓Placenta previa
✓Cesarean Section delivery
13. AEROBIC:-
▪ Streptococcus hemolytic group- A
▪ Streptococcus hemolytic group - B
▪Others: Streptococcus pyogenus, aureus,
E coli, Pseudomonas, chlamydia
ANAEROBIC:-
▪ Streptococcus, peptococcus, bacteriodes
14. MODE OF INFECTION
➢Puerperal sepsis is essentially a
wound infection
➢Placental site, lacerations of the
genital tract or cesarean section
wounds
➢It may get infected by
ENDOGENOUS or EXOGENOUS
organisms.
16. 1. LOCAL INFECTION
✓Slight temperature rise
✓Generalized malaise
✓Headache
✓Redness and swelling to local wound
✓Pus formation
17. 2. UTERINE INFECTION
MILD:-
▪ Rise in temperature and pulse rate
▪ Offensive and copious lochial discharge
▪ Subinvoluted and tender uterus
SEVERE:-
▪Acute onset with high grade temperature
with chills and rigor
▪ Rapid pulse rate
▪ Scanty and orderless lochia
20. PROPHYLAXIS
ANTENATAL:
✓Improvement of nutritional status
✓Eradication of any septic status
INTRANATAL:
✓Full surgical asepsis during labour
✓Prophylactic antibiotics: Cefriaxone 1g
IV immediate after cord clamping and
second dose: after 8 hour is recommended
21. POSTNATAL:
✓Aseptic precautions atleast one week
following delivery
✓Too many visitors are restricted
✓Sterilized senitory pads are to be used
✓Infected babies and mothers should
be in isolated room
22. GENERAL CARE:-
➢Isolation of the patient
➢Adequate fluid and calorie (IV)
➢Anemia is to be corrected
➢Progress chart should be
maintained
TREATMENT
24. ANTIBIOTICS
➢Gentamicin, 2 mg/kg IV loading dose
followed by 1.5 mg/kg IV every 8 hours
➢Ampicillin, 1g IV every 6 hours
➢Clindamycin 900 mg, IV every 8 hours
➢Cefotaxime 1 g, 8 hourly IV is an
alternative
➢Metrinidazole 0.5 g IV, 8 hourly
➢continue atleast 7-8 days
26. PERINEAL WOUND:-
❑Stiches of perineal wound may have to
be removed to facilitate drainage of pus
and relieve pain
❑Wound has to be cleaned with sitz bath
several times per day and dressed with
antiseptic ointment or powder
❑After the infection is controlled,
secondary suture may be given on later
date
SURGICAL TREATMENT
27. RETAINED UTERINE PRODUCTS:-
❑With diameter of 3 cm or less may be
disregarded or left alone
❑Otherwise surgical evacuation after
antibiotic coverage for 24 hours should be
done to avoid risk of septicemia
SEPTIC THROMBOPHLEBITIS:-
❑IV Heparin for 7-10 days
28. PELVIC ABCESS:-
❑Drainage by colpotomy under ultrasound
guidance
WOUND DEHISCENCE:
➢Dehiscence of episiotomy or abdominal
wound following cesarean section:-
❑Scrubbing the wound
❑Debridement of all necrotic tissues
❑Secondary suture
29. LAPROTOMY:
✓Has got limited indications
✓IV fluids and antibiotics usually
controls the peritonitis
✓When the peritonitis is unresponsible
to antibiotics laprotomy is indicated
HYSTERECTOMY:
✓In case of uterine rupture or perforation
✓Multiple abcess, gangrenous uterus
✓Ruptured tubo-ovarian abcess
30. NECROTYSING FACITIS:
❑Wound scrubbing
❑Debridement of all necrotic tissues
❑Use of effective antimicrobial agents
BACTEREMIC OR SEPTIC SHOCK:
❑Fluid and electrolyte balance
❑Respiratory supports
❑Circulatory support (dopamine/ dobutamine)
❑Infection control
35. SYMPTOMS
➢May be asymptomatic sometimes
➢Abnormal Lochial Discharge : Excessive or
prolonged
➢Irregular at times Excessive Uterine Bleeding
➢Irregular Cramp like Pain (Retained bits)
➢Rise of Temperature in case of Sepsis
37. MANAGEMENT
✓Antibiotics in case of infection
✓Exploration of uterus for
retained products
✓Pessary in prolapse or retroversion
✓Methargin to enhance
involution process
39. URINARY TRACT INFECTION
➢Most common cause of
puerperal pyrexia
➢Incedence 1-5 %
➢May be because of consequences
of: Reccurence of previous cystitis
or pyelitis, asymptomatic bacteriuria
➢First time because of:
Frequent catheterization,
stasis of urine
43. RETENTION OF URINE
Common complication in early
puerperium.
CAUSES:
❖Bruising
❖Edema of bladder neck
❖Reflex from the perineal injury
❖Anaccustamized position
44. TREATMENT
✓Indwelling catheter for 48 hours
✓Following removal catheter
recidual urine is to be measured
✓If it is more than 100 ml drainage
is resumed
✓Appropriate urinary antiseptics up to
5- 7 days
45. INCONTENENCE OF URINE
➢Not a common symptom following
birth
It may be:-
✓Stress incontenence (late puerperium)
✓overflow incontenence (
following retention of urine)
✓True incontenence (soon following
labour)
46. SUPRESSION OF URINE
➢“If the 24 hours urine excretion is less
than 400 ml or less, supression of urine
is dagnosed.”
➢The cause is to be sought for and
appropriate management is instituted.
49. BREAST ENGORGEMENT
➢Breast engorgement is due to
exaggerated normal venous and
lymphatic engorgement of the breasts
which precedes lactation.
➢This in turn prevents escape of
milk from the lacteal system
50. ➢The primiparous patient and the
patient with inelastic breasts are more
likely develop breast engorgement
➢Engorgement is an indication that
the baby is not in step with stage of
lactation
ONSET:
• It usually manifests after the milk
secretion starts ( 3r
dand 4th day
postpartm)
53. TREATMENT:
❑Support with the binders
❑Mannual expression of milk
❑Administer analgesics for pain
❑Frequently and regular feeding the
baby
❑In severe cases gentle use of breast
pump
❑Hot application
56. SYMPTOMS
➢Condition may remain asymptomatic
➢Sometimes painful when feeding
the baby
➢When infected, the infection may
spread to the deeper tissue proceding
mastitis
57. PROPHYLAXIS
❑Local cleanliness during pregnancy
and puerperium
❑Clean the crusts before and after
feeding
❑Application of lotion to soothen the
epithelium
58. TREATMENT
✓Correct attachement during feeding
✓Purified lanonin with mother's milk
applied 3 or 4 times a day for healing
✓In severe
cases
expression of
milk by breast
pump
59. ✓For inflammed
nipple and areola
miconazole lotion
is applied
✓Apply
nipple
shields
✓If persistant...
biopsy is needed
60. RETRACTED AND FLAT NIPPLE
➢Commonly seen in primiparous
mother
➢Manual expression of milk is initiated
❖Correction of retracted nipple
61.
62. ACUTE MASTITIS
➢Incidence of mastitis is 2-5 %
in lactating
➢Less than 1% in nonlactating mother
Organisms involved are...
▪ Streptococcus aureus,
▪ S. epidermidis and
▪ Streptococci viridans
63.
64. Mode of infection:-
Two different types of mastitis based on
location of infection.
1.Infection that involves the breast
paranchymal tissues leading to cellulitis.
(lacteal system remains unaffected)
2.Infection up to lactefarous ducts...lead
to development of primary mammary
adenitis
65. Source of infection : infant's nose/mouth
➢Noninfected mastitis is due to
milk stasis.
➢Feeding from the affected breast
can solve the problem
ONSET:
❖In superficial cellulitis, onset is acute
during first 2-4 weeks postpartum
❖However it may occurs after several
weeks also
70. MANAGEMENT
❑Support by binders
❑Plenty of oral fluids
❑Good attachment when feeding the
baby
❑Initiate feeding from uninfected breast
first to establish let down
❑The infected site is emptied manually
with each feed
❑Dicloxacilin is the drug of choice. 500
mg 6 hourly. erythromycin is
71. • Antibiotic therapy is to continue up to 7
days
• Analgesics
• Milk flow is maintained by feeding the
baby
• It will prevent proloferation of
staphylococcus in the stagnant milk
• The ingested staphylococcus will
digested without any harm
72. BREAST ABCESS
FEATURES ARE:
✓Flushed breasts not responding
to antibiotics
✓Browny edema on the overlying skin
✓Marked tenderness with fluctuation
✓Swinging temperature
73. MANAGEMENT
❑Incision and drainage under general
anesthesia
❑Deep radial incision extending from
near the areolar margin to prevent
injury of the lacteferous ducts
❑Incision perpendicular to the
lactiferous duct can increase the risk of
fistula formation and ductal occlusion
74. ❑Finger exploration has to be done to
break the walls of loculi.
❑The cavilty is loosely packed with
gause which should be replaced after
24 hoursby a smaller pack
❑Continue till it heals up
❑Abcess can also be drained by serial
percutaneous niddle aspiration under
ultrasound guidance
❑Surgical draiange is commonly done
75. ❑Breast feeding is contonued at
uninvolved side
❑The infected side is mechanically
expressed by pump every two hourly
and with every let down
❑Reccurence risk is about 10 %
❑Once cellulitis resolved breast feeding
from the involved side may be resumed
76. BREAST PAIN
May be due to....
✓Engorgement
✓Infection ( candida albicans)
✓Nipple trauma
✓Mastitis
✓Occasionally on letching-on or
let down reflex
78. LACTATION FAILURE
CAUSES ARE:
➢Infrequent suckling
➢Depression or anxiety state in
puerperium
➢Unwilling to nursing
➢Ill development of nipples
➢Endogenous supression of prolactin
➢Prolactin inhibition
79. MANAGEMENT
ANTENATAL:
❑Counsell mother regading benefits of
nursing her baby
❑To take care of any breast abnormality..
breast engorgement
❑Maintaining adequate breast hygiene
specially in last two months of
pregnancy
80. PUERPERIUM:
➢Encourage adequate fluid intake
➢To nurse the baby regularly
➢Treat the painfull local lesions
to prevent nursing phobia
➢Metoclopramide 10 g thrice
daily, intranasal oxytocin and
sulpiride
( selective dopamine intagonist) has
been found to increase milk production.
➢They act by stimulating
prolactin secretion
83. RISK FACTORS
Vascular stasis
Hypercoagulopathy of blood
Vascular endothelial trauma
Other pregnancy related factors
Venous thrombo-embolic disease like..
deep vein thrombosis, thrombophlebitis,
pulmonary embolism
84. This stasis causes damage to the
endothelial cells
Thrombophilias are hypercoaguable states
in pregnancy that increase the risk of
venous thrombosis (inheritate/ acquired)
85. OTHER ACQUIRED RISK FACTORS
Advanced age and
parity
Operative delivery
Obesity
Anemia
Heart disease
Infection- pevic celluitis
Trauma to the venous
wall
Immobility and smoking
86. DEEP VEIN THROMBOSIS
➢Clinical diagnosis is unreliable.
➢In majority it remains asymptomatic
SYMPTOMS INCLUDE:
✓Pain in the caff muscles
✓On examination asymmentric
leg edema
✓A positive Homan's sign
88. PELVIC THROMBOPHLEBITIS
➢Originates in the thrombosed veins at
placental site by organism such as an
anaerobic streptococci or
bacteriosides
➢When localised in the pelvis
called pelvic thrombophlebitis.
➢There is specific features but it is
suspected when there is constatnt
fever instead of antibiotics
administration
89. EXTRA PELVIC SPREAD
➢Through the right ovarian vein to
inferior vana cava and hence to the
lungs
➢Through left ovarian vein to left
renal vein and hence to the left
kidney
➢Retrograde extension to iliofemoral
veins to produce the clinical
pathological entity called “phlegmasia
alba dolens” ( adjacent cellulitis in
90. CLINICAL FEATURES:
✓Usually develops in second week
of puerperium
✓Mild pyrexia
✓High grade fever with chills and rigor
✓Constitutional disturbances like...
headache, malaise, rising pulse rate
✓Swelling, pain, white , cold
over affected leg
92. MANAGEMENT
❑Bed rest with foot end kept higher to
heart level
❑Pain management
❑Antibiotics
❑Anticoagulants- Heparin- 15000 units IV
followed by 10,000 units 6-8 hourly for
4 to 6 injections. up to 7 to 10 days
❑Administartion of fibrinolytic agents
❑Venous thrombectomy
93. PULMONARY EMBOLISM
➢Most leading cause of maternal
deaths
➢Classical symptoms of
massive pulmonary embolism
are...
✓Sudden collapse
✓Acute chest pain
✓Air hunger
✓Death usually occurs within short
time from shock and vagal inhibition
96. MANAGEMENT
❑Prophylactic measures
❑Active treatment:
✓Resuscitation: cardiac massage,
oxygen therapy, heparin bolus IVof 5000
units and morphine 15 mg
✓IV fluids
✓Incase of recurrent .. embolectomy,
placement of caval filters, ligation of inferior
vana cava and ovarian veins
97. OBSTETRIC PALSIES
(Syn.POSTPARTUM TRAUMATIC NEURITIS)
➢The commonest form of obstetric
palsy encountered in puerperium is...
“FOOT DROP”
➢Usually unilateral
➢Appears shortly after delivery/ first
day postpartum
98. ➢It is due to stretching of the
lumbosacral trunk by the prolapsed
intervertebral disc between L5 and S1
➢Backward rotation of the
sacrum during labour may also
be a contributory factor
➢Direct pressure either by fetal head
or forcep blade on the lumbosacral
cord or sacral plexus
99.
100. ➢Condition is usually mild
➢May passed unnoticed
➢Neurological examination reveals
lower motor neurone type of lesions
with placcidity and wasting of muscles
in areas supplied by femoral nerve or
lumbosacral plexus
➢Secondary loss is always present
101. ➢Management of damaged
lumbosacral nerve roots is same as
that of the proplapsed intervertebral
disc in
consultation with an orthopedist
➢Paraplegia due to epidural
hematoma or abcess is rare.
105. ❑ EARLY (WITHIN A WEEK):
–Acute retention of urine
–Urinary tract infection
–Puerperal sepsis
–Breast engorgement
–Mastitis and breast abcess
–Pulmonary infection
–Anuria following abruptio placenta,
mismatched boold transfusion or
eclampsia
108. INTRODUCTION
➢In the first 3 months after delivery, the
incidence of mental illness is high.
➢Overall incidence is about 15-20%.
➢Sleep deprivation, hormone elevation
near the end of gestation and massive
postpartum withdrawal contribute to
the high risk
114. POSTPARTUM DEPRESSION
➢Observed in 10-20 % of mothers
➢More gradual in onset over the first 4-
6 months following delivery or
abortion
➢Changes in the hypothelamo-
pitutary- adrenal axis may be a cause
115. MANIFESTED BY:
✓Loss of energy
✓Loss of appetite
✓Insomnia
✓Social withdrawal
✓Irritability
✓Suicidal attitude
✓Risk of reccurence is 50-100%
in subsequence pregnancies
117. POSTPARTUM PSYCHOSIS
➢Observed in 0.14-0.26 % of mothers
➢Commonly seen in women with
past history and family history
➢Onset is relatively sudden
➢Lasts for 4 days
118. MANIFESTED BY:
✓Fear
✓Restlessness
✓Confusion followed by
hallucination, delusion and
disorientation
✓Suicidal, infanticidal impulses
✓Temporary seperation and clinical
supervision is needed
✓Risk foe reccurence 20-25%
119. MANAGEMENT:
❑A psychiatrist must be consulted urgently
❑Hospitalization is needed
❑Chlopramazine 150 mg stat and 50-150
mg three time /day is started
❑Sublingual estradiol 1 mg TDS
in significant improvement
❑Electro convulsive therapy if remains
unresponsive or in depressive psychosis
❑Lithium in manic depressive psychosis
❑Breast feeding is restricted in case
of lithium administration
120. PSYCHOLOGICAL RESPONSES TO THE
PERINATAL DEATHS AND MANAGEMENT
➢Most perinatal events are joyful
➢But when a fetal /neonatal death
occurs, social attention must be given
to grieving parents and family
➢It may be because of unexcpected
hysterectomy, birth of malformed or
chronically ill infant
➢Prolonged seperation from
chronically ill infant can also cause
grief
121. ➢Physician, nurse and attending
staff must understand patient's
reaction
➢The common maternal
somatic symptoms are...
✓Insomnnia
✓Fatigue
✓Sighing respiration
✓Feeling of guilt
✓Anger
✓Hostility ( feeling of opposition)
122. MANAGEMENT OF PERINATAL GRIEVING
❑Facilitating grieving process with
consolation (comfort), support, sympathy
❑Others are:
1. supporting the couple in seeing/ holding/
taking photographs of infant
2. Autopsy requests
3. Planning investigations
4. Follow up visits
5. Plan for subsequent pregnancy
