Renal Disorders in
Pregnancy
DR. Shamsa Tariq
Associate Professor RMC
Physiological Adaptation








Dramatic dilatation of the urinary collecting system
during pregnancy.
Renal plasma flow rises by 60-80% by the second
trimester.
RPF falls throughout the third trimester but maintained at
50% greater than prepregnancy levels.
GFR increases significantly and creatinine clearance
rises by 50%.
Fall in Urea and Creatinine level
Pretein excretion is increased up to 300 mg per 24
hours.
80% of women develop edema due to physiological
increase in sodium retention.
Renal Disorders


Urinary tract infection



Chronic renal disease



Acute renal failure



Pregnancy in renal transplant recipient
Urinary Tract Infection


Asymptomatic bacteriuria



Acute cystitis



Acute pyelonephritis
Asymptomatic Bacteriuria
Incidence





This ranges from 2 to 10%
40% will develop symptomatic urinary-tract infection in
pregnancy.
Women with history of previous urinary-tract infection
have a 10-fold increased risk of developing cystitis or
acute pyelonephritis in pregnancy.
Pathogenesis



75-90% due to E coli, probably derived from large bowel
Colonization of urinary tract results from ascending
infection from the perineum and is related to sexual
intercourse.

Diagnosis




Most women with asymptomatic bacteriuria are found to
be infected during early pregnancy and very few
subsequently acquire asymptomatic bacteriuria
Bacteriuria is only considered significant if the colony
count exceeds 100,000/ml on a MSU
Management




The choice of antibiotic depends on culture/sensitivity
Ampicillin, amoxicillin, Augmentin and the cephalosporin
are safe and appropriate antibiotics in pregnancy.
Treatment should be continued for 2 weeks in the first
instance and regular urinary culture required.
Acute Cystitis
Incidence
Cystitis complicates 1% of pregnancies

Clinical features
Urinary frequency, dysuria, haemeturia and
suprapubic pain

Diagnosis
Significant bacteriuria on MSU
Management


Same as asymptomatic bacteriuria
Several non-pharmacological maneuvers may help to
prevent recurrent infection in women with recurrent
urinary-tract infections in pregnancy.

These include:
 Increase fluid intake
 Emptying the bladder following sexual intercourse
Acute Pyelonephritis
Incidence



This complicates 1-2% of pregnancies
More common in pregnancy ( physiological dilatation of
the upper renal tract).

Clinical Features







Fever
Loin and abdominal pain
Vomiting
Rigors
Proteinuria
Haematuria
Risk increases in women
 On steroid therapy

With polycystic kidneys
 Congenital abnormalities of renal tract
 Urinary-tract calculi
 Diabetes
Diagnosis
Significant bacteriuria on MSU specimen.
Differential diagnosis
 Pneumonia
 Viral infections
 Cholecystitis , biliary colic
 Acute appendicitis
 Gastroenteritis,
 Placental abruption
 Degenerating uterine fibroid.
Blood cultures and a full blood count is
recommended
Management


Should be after hospitalization



I/V Antibiotic Penicillin and cephalosporin are the Ist
choice.
Chronic Renal Disease
Pregnancy with Chronic Renal
Disease
Effects of Pregnancy
The risks include:
 Accelerated decline in renal function
 Rising hypertension
 Worsening proteinuria
Effects of chronic renal disease on pregnancy
The risks includes:
 Miscarriage
 Pre-eclampsia
 Intrauterine growth retardation
 Preterm delivery
 Fetal death
Factors Influencing Outcome


The presence and degree of renal impairment



The presence and severity of proteinuria



The underlying type of chronic renal disease
Degree of Renal Impairment


Mild renal impairment (plasma creatinine <125 umol/I)



Moderate renal impairment (plasma creatinine 125-250
umol/I)



Severe renal impairment (plasma creatinine >250 umol/I)
In general, women without hypertension or renal
impairment prior to conception have successful
pregnancies, and pregnancy does not adversely
influence the progression of the renal disease.
Specific Types of Renal Disease


Glomerulonephritis



Reflux nephropathy



Diabetic nephropathy



SLE nephritis



Polycystic kidney disease (PKD)
Management








Women with chronic renal disease should be managed
jointly by obstetricians and physicians
Preconceptual assessment of renal functions and blood
pressure should be made.
In view of the increased risk of pre-eclampsia, treatment
with low dose aspirin should be considered especially in
those with hypertension, renal impairment or a previous
poor obstetric history.
Careful monitoring and control of blood pressure both
prepregnancy and antenatally is important.




The fetus should be monitored with regular ultrasound
assessment of growth and Doppler assessment of
uterine and umbilical circulation.
Admission should be considered if the woman develops
worsening hypertension, deteriorating renal function or
proteinuria, or superimposed eclampsia.
Acute Renal Failure
Incidence


Rare in pregnancy <0.005%

Clinical Features




Anuria/oliguria
urea, creatinine rises
Decreased GFR
Causes
Infection




Septic abortion
Puerperal sepsis
Rarely acute pyelonephritis

Blood Loss



Postpartum hemorrhage
Abruption
Volume Contraction




Pre-eclampsia
Eclampsia (6%)
Hypermesis gravidarum

Post-renal Failure


Ureteric damage or obstruction

Pre-eclampsia
HELLP Syndrome



7% have actual renal failure
Thrombotic thrombocytopenic purura/hemolytic
uraemic syndrome (TTP/HUS)

Management


This depend on underlying cause
Pregnancy in Renal
Transplant
Recipients


Women receiving renal transplants should be warned
that as renal function returns to normal, ovulation,
menstruation and fertility also resume.



Women desiring pregnancy are usually advised to wait
about 1-2 years after transplantation.
Effects of pregnancy on renal transplants





Pregnancy probably has no adverse long-term effect
Renal allograft adapt to pregnancy
About 15% of women develop significant impairment
About 40% develop proteinuria towards term
Effect of renal transplants on pregnancy




The chance of successful outcome is >90%, but this is
reduced to 70% if complications occur before 28 weeks’
gestation.
The complication rate is higher for diabetics.
Antenatal Management









Women should be managed jointly by nephrologists and
obstetricians with expertise in the care of pregnant renal
transplant recipients.
Careful monitoring and control of blood pressure is
important.
Regular assessment of RFTs by creatinine clearance
and 24 hour protein excretion, as well as serum
creatinine and urea is essential.
A FBC and LFTs should also be checked regularly.
Anemia is common and haematinics should be
prescribed.
The fetus should be monitored with regular ultrasound
assessment of growth and Doppler assessment of
uterine Sand umbilical circulation.
Immunosuppressive Therapy




The doses of immunosuppressive drugs are maintained
at prepregnancy
Levels which should preferably be:
Prednisolone, <15 mg/day plus either
Azathioprine, <2 mg/kg/day
Cyclosporin A, 2-4 mg/kg/day
Delivery






Caesarean section is only required for obstetric
indications.
Prophylactic antibiotics should be given to cover any
surgical procedure including episiotomy.
Parental steroids are necessary to cover labour, as with
any woman on maintenance steroids.
Neonatal Problems
These are largely related to prematurely but also include
the following:
 Thymic atrophy
 Transient leukopenia or thrombocytopenia
 Depressed haemopoiesis
Renal disorders in pregnancy

Renal disorders in pregnancy

  • 1.
    Renal Disorders in Pregnancy DR.Shamsa Tariq Associate Professor RMC
  • 2.
    Physiological Adaptation        Dramatic dilatationof the urinary collecting system during pregnancy. Renal plasma flow rises by 60-80% by the second trimester. RPF falls throughout the third trimester but maintained at 50% greater than prepregnancy levels. GFR increases significantly and creatinine clearance rises by 50%. Fall in Urea and Creatinine level Pretein excretion is increased up to 300 mg per 24 hours. 80% of women develop edema due to physiological increase in sodium retention.
  • 3.
    Renal Disorders  Urinary tractinfection  Chronic renal disease  Acute renal failure  Pregnancy in renal transplant recipient
  • 4.
    Urinary Tract Infection  Asymptomaticbacteriuria  Acute cystitis  Acute pyelonephritis
  • 5.
    Asymptomatic Bacteriuria Incidence    This rangesfrom 2 to 10% 40% will develop symptomatic urinary-tract infection in pregnancy. Women with history of previous urinary-tract infection have a 10-fold increased risk of developing cystitis or acute pyelonephritis in pregnancy.
  • 6.
    Pathogenesis   75-90% due toE coli, probably derived from large bowel Colonization of urinary tract results from ascending infection from the perineum and is related to sexual intercourse. Diagnosis   Most women with asymptomatic bacteriuria are found to be infected during early pregnancy and very few subsequently acquire asymptomatic bacteriuria Bacteriuria is only considered significant if the colony count exceeds 100,000/ml on a MSU
  • 7.
    Management    The choice ofantibiotic depends on culture/sensitivity Ampicillin, amoxicillin, Augmentin and the cephalosporin are safe and appropriate antibiotics in pregnancy. Treatment should be continued for 2 weeks in the first instance and regular urinary culture required.
  • 8.
    Acute Cystitis Incidence Cystitis complicates1% of pregnancies Clinical features Urinary frequency, dysuria, haemeturia and suprapubic pain Diagnosis Significant bacteriuria on MSU
  • 9.
    Management  Same as asymptomaticbacteriuria Several non-pharmacological maneuvers may help to prevent recurrent infection in women with recurrent urinary-tract infections in pregnancy. These include:  Increase fluid intake  Emptying the bladder following sexual intercourse
  • 10.
    Acute Pyelonephritis Incidence   This complicates1-2% of pregnancies More common in pregnancy ( physiological dilatation of the upper renal tract). Clinical Features       Fever Loin and abdominal pain Vomiting Rigors Proteinuria Haematuria
  • 11.
    Risk increases inwomen  On steroid therapy  With polycystic kidneys  Congenital abnormalities of renal tract  Urinary-tract calculi  Diabetes
  • 12.
    Diagnosis Significant bacteriuria onMSU specimen. Differential diagnosis  Pneumonia  Viral infections  Cholecystitis , biliary colic  Acute appendicitis  Gastroenteritis,  Placental abruption  Degenerating uterine fibroid. Blood cultures and a full blood count is recommended
  • 13.
    Management  Should be afterhospitalization  I/V Antibiotic Penicillin and cephalosporin are the Ist choice.
  • 14.
  • 15.
    Pregnancy with ChronicRenal Disease Effects of Pregnancy The risks include:  Accelerated decline in renal function  Rising hypertension  Worsening proteinuria
  • 16.
    Effects of chronicrenal disease on pregnancy The risks includes:  Miscarriage  Pre-eclampsia  Intrauterine growth retardation  Preterm delivery  Fetal death
  • 17.
    Factors Influencing Outcome  Thepresence and degree of renal impairment  The presence and severity of proteinuria  The underlying type of chronic renal disease
  • 18.
    Degree of RenalImpairment  Mild renal impairment (plasma creatinine <125 umol/I)  Moderate renal impairment (plasma creatinine 125-250 umol/I)  Severe renal impairment (plasma creatinine >250 umol/I)
  • 19.
    In general, womenwithout hypertension or renal impairment prior to conception have successful pregnancies, and pregnancy does not adversely influence the progression of the renal disease.
  • 20.
    Specific Types ofRenal Disease  Glomerulonephritis  Reflux nephropathy  Diabetic nephropathy  SLE nephritis  Polycystic kidney disease (PKD)
  • 21.
    Management     Women with chronicrenal disease should be managed jointly by obstetricians and physicians Preconceptual assessment of renal functions and blood pressure should be made. In view of the increased risk of pre-eclampsia, treatment with low dose aspirin should be considered especially in those with hypertension, renal impairment or a previous poor obstetric history. Careful monitoring and control of blood pressure both prepregnancy and antenatally is important.
  • 22.
      The fetus shouldbe monitored with regular ultrasound assessment of growth and Doppler assessment of uterine and umbilical circulation. Admission should be considered if the woman develops worsening hypertension, deteriorating renal function or proteinuria, or superimposed eclampsia.
  • 23.
  • 24.
    Incidence  Rare in pregnancy<0.005% Clinical Features    Anuria/oliguria urea, creatinine rises Decreased GFR
  • 25.
    Causes Infection    Septic abortion Puerperal sepsis Rarelyacute pyelonephritis Blood Loss   Postpartum hemorrhage Abruption
  • 26.
    Volume Contraction    Pre-eclampsia Eclampsia (6%) Hypermesisgravidarum Post-renal Failure  Ureteric damage or obstruction Pre-eclampsia
  • 27.
    HELLP Syndrome   7% haveactual renal failure Thrombotic thrombocytopenic purura/hemolytic uraemic syndrome (TTP/HUS) Management  This depend on underlying cause
  • 28.
  • 29.
     Women receiving renaltransplants should be warned that as renal function returns to normal, ovulation, menstruation and fertility also resume.  Women desiring pregnancy are usually advised to wait about 1-2 years after transplantation.
  • 30.
    Effects of pregnancyon renal transplants     Pregnancy probably has no adverse long-term effect Renal allograft adapt to pregnancy About 15% of women develop significant impairment About 40% develop proteinuria towards term
  • 31.
    Effect of renaltransplants on pregnancy   The chance of successful outcome is >90%, but this is reduced to 70% if complications occur before 28 weeks’ gestation. The complication rate is higher for diabetics.
  • 32.
    Antenatal Management      Women shouldbe managed jointly by nephrologists and obstetricians with expertise in the care of pregnant renal transplant recipients. Careful monitoring and control of blood pressure is important. Regular assessment of RFTs by creatinine clearance and 24 hour protein excretion, as well as serum creatinine and urea is essential. A FBC and LFTs should also be checked regularly. Anemia is common and haematinics should be prescribed. The fetus should be monitored with regular ultrasound assessment of growth and Doppler assessment of uterine Sand umbilical circulation.
  • 33.
    Immunosuppressive Therapy   The dosesof immunosuppressive drugs are maintained at prepregnancy Levels which should preferably be: Prednisolone, <15 mg/day plus either Azathioprine, <2 mg/kg/day Cyclosporin A, 2-4 mg/kg/day
  • 34.
    Delivery    Caesarean section isonly required for obstetric indications. Prophylactic antibiotics should be given to cover any surgical procedure including episiotomy. Parental steroids are necessary to cover labour, as with any woman on maintenance steroids.
  • 35.
    Neonatal Problems These arelargely related to prematurely but also include the following:  Thymic atrophy  Transient leukopenia or thrombocytopenia  Depressed haemopoiesis