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• UTI is defined as the presence of at least
100,000 organisms per milliliter of urine in an
asymptomatic patient.
• more than 100 organisms/mL of urine with
accompanying pyuria (> 7 white blood cells
[WBCs]/mL) in a symptomatic patient.
• Infections result from ascending colonization of
the urinary tract, primarily by existing vaginal,
perineal, and fecal flora.
• urinary retention caused by the weight of the
enlarging uterus
• urinary stasis due to progesterone-induced
ureteral smooth muscle relaxation.
• Blood-volume expansion is accompanied by
increases in the glomerular filtration rate and
urinary output
• Loss of ureteral tone combined with increased
urinary tract volume results in urinary stasis,
which can lead to dilatation of the ureters, renal
pelvis, and calyces.
• Urinary stasis and the presence of vesicoureteral
reflux predispose some women to upper urinary
tract infections (UTIs) and acute pyelonephritis.
• E.coli is the most common cause of urinary tract
infection (UTI).
• Cesarean delivery
• Preeclampsia
Presentation
• Cystitis(1%)- suprapubic pain,
frequency,dysuria,urgency,haematuria, proteinuria.
• Pyelonephritis(2%)- fever,rigor ,tachycardia, loin pain
,vomiting
Management
• The urine should be cultured at the booking visit, and
asymptomatic bacteriuria is treated.
• In pyelonephritis, treat with intravenous antibiotics.
• Affect 0.2% of pregnant women.
• Dependent on the degree of hypertension and
renal impairment.
• Creatinine level is more than 200 mmol/L.
• Occurs in late pregnancy
• Aetiology:
• 1. reflux nephropathy
• 2. diabetes
• 3. systemic lupus erythromatosus (SLE)
• 4.Glomerulonephritis.
• 5. polycystic kidney disease.
• Classification:
• mild, moderate or severe depending on the serum
creatinine.
• creatinine depends on the muscle mass i.e. a figure
representing moderate impairment in an 85-kg may
represent severe impairment for a 50-kg woman.
• - mild impairment (creatinine < 125 μmol/l):
tolerate pregnancy well with no renal function
deterioration.
• - severe renal impairment (creatinine > 250
μmol/l): at increased risk of permanent loss of
function during and after pregnancy and even
end stage of renal failure.
• 1. PET, IUGR, spontaneous and iatrogenic premature
delivery.
• - severe renal impairment + hypertension have < 50 %
chance of successful pregnancy because of severe,
early-onset of PET with severe IUGR.
• - premature delivery is justified in rapidly worsening
renal function to avoid dialysis even in the absence of
PET.
• 2. severe renal impairment → polyhydramnios and risk
of cord prolapse due to fetal polyuria in response to high
osmotic load from increased maternal urea.
• 3. nephrotic syndrome and heavy protienuria → severe
hypoalbuminria with associated risks of pulmonary
oedema and thrombosis.
MANAGEMENT
• Ultrasound for fetal growth
• Measurement of renal
function
• Screening for urinary
infection
• Control of hypertension
• Dialysis (severe)
PRESENTATION
• tiredness
• swollen ankles, feet or
hands (due to water
retention)
• shortness of breath
• nausea
• blood in the urine
• Pregnancy increases the risk of venous
thromboembolism (VTE) 4- to 5-fold over that in
the nonpregnant state.
• The 2 manifestations of VTE are deep venous
thrombosis (DVT) and pulmonary embolus (PE).
• Blood clotting factors are increased,fibrinolytic
activity is reduced and blood flow is altered by
mechanical obstuction and immobility.
• Women with inherited prothrombotic conditions
and those with a family or personal history are
prone to thromboses.
• Pulmonary embolus is important cause of
maternal death.
• DVT: leg pain and discomfort (the left is more
commonly affected), swelling, tenderness,
oedema, increased temperature and a raised
white cell count. There may also be abdominal
pain.
• PE: dyspnoea, pleuritic chest pain, haemoptysis,
faintness, collapse.
DIAGNOSIS
• In non-pregnant women
Chest x-ray
Arterial blood gas analysis
Computed tomography
VQ scanning
urgent compression
duplex ultrasound scan.
MANAGEMENT
• Treated with
subcuatneous LMWH.
• Doses are adjusted
according to the anti-
Factor 10a.
• Treatment should be stop
before labour and
restarted and continued
into the puerperium.

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Medical problem in pregnancy

  • 1.
  • 2. • UTI is defined as the presence of at least 100,000 organisms per milliliter of urine in an asymptomatic patient. • more than 100 organisms/mL of urine with accompanying pyuria (> 7 white blood cells [WBCs]/mL) in a symptomatic patient.
  • 3. • Infections result from ascending colonization of the urinary tract, primarily by existing vaginal, perineal, and fecal flora. • urinary retention caused by the weight of the enlarging uterus • urinary stasis due to progesterone-induced ureteral smooth muscle relaxation. • Blood-volume expansion is accompanied by increases in the glomerular filtration rate and urinary output
  • 4. • Loss of ureteral tone combined with increased urinary tract volume results in urinary stasis, which can lead to dilatation of the ureters, renal pelvis, and calyces. • Urinary stasis and the presence of vesicoureteral reflux predispose some women to upper urinary tract infections (UTIs) and acute pyelonephritis.
  • 5. • E.coli is the most common cause of urinary tract infection (UTI). • Cesarean delivery • Preeclampsia
  • 6. Presentation • Cystitis(1%)- suprapubic pain, frequency,dysuria,urgency,haematuria, proteinuria. • Pyelonephritis(2%)- fever,rigor ,tachycardia, loin pain ,vomiting Management • The urine should be cultured at the booking visit, and asymptomatic bacteriuria is treated. • In pyelonephritis, treat with intravenous antibiotics.
  • 7. • Affect 0.2% of pregnant women. • Dependent on the degree of hypertension and renal impairment. • Creatinine level is more than 200 mmol/L. • Occurs in late pregnancy
  • 8. • Aetiology: • 1. reflux nephropathy • 2. diabetes • 3. systemic lupus erythromatosus (SLE) • 4.Glomerulonephritis. • 5. polycystic kidney disease. • Classification: • mild, moderate or severe depending on the serum creatinine. • creatinine depends on the muscle mass i.e. a figure representing moderate impairment in an 85-kg may represent severe impairment for a 50-kg woman.
  • 9. • - mild impairment (creatinine < 125 μmol/l): tolerate pregnancy well with no renal function deterioration. • - severe renal impairment (creatinine > 250 μmol/l): at increased risk of permanent loss of function during and after pregnancy and even end stage of renal failure.
  • 10. • 1. PET, IUGR, spontaneous and iatrogenic premature delivery. • - severe renal impairment + hypertension have < 50 % chance of successful pregnancy because of severe, early-onset of PET with severe IUGR. • - premature delivery is justified in rapidly worsening renal function to avoid dialysis even in the absence of PET. • 2. severe renal impairment → polyhydramnios and risk of cord prolapse due to fetal polyuria in response to high osmotic load from increased maternal urea. • 3. nephrotic syndrome and heavy protienuria → severe hypoalbuminria with associated risks of pulmonary oedema and thrombosis.
  • 11. MANAGEMENT • Ultrasound for fetal growth • Measurement of renal function • Screening for urinary infection • Control of hypertension • Dialysis (severe) PRESENTATION • tiredness • swollen ankles, feet or hands (due to water retention) • shortness of breath • nausea • blood in the urine
  • 12. • Pregnancy increases the risk of venous thromboembolism (VTE) 4- to 5-fold over that in the nonpregnant state. • The 2 manifestations of VTE are deep venous thrombosis (DVT) and pulmonary embolus (PE). • Blood clotting factors are increased,fibrinolytic activity is reduced and blood flow is altered by mechanical obstuction and immobility.
  • 13. • Women with inherited prothrombotic conditions and those with a family or personal history are prone to thromboses. • Pulmonary embolus is important cause of maternal death.
  • 14. • DVT: leg pain and discomfort (the left is more commonly affected), swelling, tenderness, oedema, increased temperature and a raised white cell count. There may also be abdominal pain. • PE: dyspnoea, pleuritic chest pain, haemoptysis, faintness, collapse.
  • 15. DIAGNOSIS • In non-pregnant women Chest x-ray Arterial blood gas analysis Computed tomography VQ scanning urgent compression duplex ultrasound scan. MANAGEMENT • Treated with subcuatneous LMWH. • Doses are adjusted according to the anti- Factor 10a. • Treatment should be stop before labour and restarted and continued into the puerperium.