RENAL DISORDERS





6.1 Urinary Tract Infections

6.2 Chronic Kidney Disease

6.3 Dialysis in Pregnancy

6.4 Renal Transplantation

6.5 Nephrotic Syndrome





6.1 Urinary Tract Infections







Incidence

1–3% of pregnancies are complicated by urinary tract infection, 2–10% by asymptomatic bacteriuria1

Risk for Childbearing

Moderate Risk





EXPLANATION OF CONDITION


Urinary tract infection (UTI) is caused by bacteria in the urinary tract. Bacteria usually originate from the bowel and the most common causative organism is Escherichia coli, which accounts for 80–90% of all acute UTI. In pregnancy UTI may be manifest as the urethral syndrome, acute cystitis (2% of all pregnancies) or acute pyelonephritis (1–3% of pregnancies).


Features of the urethral syndrome are frequency and dysuria, whereas those of acute cystitis include frequency, urgency and dysuria, offensive smelling urine, haematuria and suprapubic discomfort. Urethral syndrome may be caused by sexually transmitted genital infections such as Chlamydia trachomatis. Acute pyelonephritis may present with pyrexia, rigors, abdominal/flank pain, nausea and vomiting1–4.


The presence of >105/ml of the same bacterial species in a midstream specimen of urine (MSU) in the absence of symptoms is called asymptomatic bacteriuria (ABU). This is of greatest significance in pregnancy, and in non-pregnant individuals with structurally abnormal urinary tracts, renal stones or diabetes mellitus2,5,6.


COMPLICATIONS



  • Acute symptomatic urinary tract infection

    • developed by ≥30% of women with asymptomatic bacteriuria
    • can lead to pyelonephritis
    • untreated infection may cause kidney damage2,5,6

  • Acute cystitis

    • not usually dangerous but may cause significant discomfort and inconvenience
    • usually an isolated event but can be recurrent and may follow sexual intercourse
    • if untreated may progress to acute pyelonephritis

  • Pre-term labour

    • in many non-pregnant women uncomplicated asymptomatic bacteriuria resolves spontaneously
    • in pregnancy ABU is associated with premature delivery and low birth weight and is therefore treated with antibiotics
    • ABU occurs in 2–10% of all pregnancies1

  • Acute pyelonephritis

    • a more serious infection
    • if very severe, or inadequately treated, septicaemia may result in acute renal failure, multiple organ failure and death
    • repeated episodes of acute pyelonephritis may be associated with the development of renal scars4

NON-PREGNANCY TREATMENT AND CARE



  • Identify causative organism by testing an MSU, and treat with appropriate antibiotics
  • On completion of antibiotic therapy, an MSU is retested to ensure that the urine is now free of infection
  • Treatment is not required in non-pregnant women with uncomplicated asymptomatic bacteriuria
  • Affected individuals should be warned to be alert for symptoms suggestive of active urinary infection

Advise on ways to reduce the risk of recurrent UTI:



  • Drink 2 l of fluid daily, with frequent voiding of urine
  • Wipe from ‘front to back’ after passing urine
  • Void to empty the bladder after intercourse
  • Drinking cranberry juice may reduce the risk; the dosage is unclear, but approximately 200–300 ml (or by capsule), daily appears to be potentially effective7–9
  • Consider prophylactic antibiotics if recurrent UTI

If UTI is recurrent, consider investigation of underlying cause, such as renal stones or ureteric reflux, with:



  • Renal ultrasound
  • Abdominal X-ray
  • Cystoscopy

Acute pyelonephritis may require:



  • Hospitalisation
  • Intravenous hydration, monitor fluid balance
  • Intravenous antibiotics, changing to oral antibiotics when infection is controlled
  • Monitor U&E, urine and blood cultures
  • Four-hourly observation of temperature

PRE-CONCEPTION ISSUES AND CARE



  • Investigate renal function, and possible underlying causes, prior to pregnancy if recurrent infections have occurred
  • Treat and eliminate infections
  • Women at risk should be counselled regarding the need for regular urine culture, and the possible requirement for antibiotic therapy during pregnancy
  • Advise that there is an increased risk of UTI in pregnancy. This is as a result of relaxation and dilation of the ureters due to hormonal changes and compression at the pelvic brim by the enlarging uterus and ovarian vein2. As the pregnancy advances, upward displacement of the bladder into the abdomen results in elongation of the urethra. Under these circumstances, incomplete bladder emptying allows urinary stasis, which in turn encourages infection. If this is accompanied by vesicoureteral reflux ascending bacterial migration and infection is facilitated2






Pregnancy Issues

All pregnant women should be offered routine screening for asymptomatic bacteriuria by an MSU culture in early pregnancy, followed by prompt treatment. UTI in pregnancy has been shown to be associated with pre-term birth and low birth weight, although this is controversial1,3,4.

Generally, if adequately treated, there are no significant effects on the fetus. If the mother has reflux nephropathy as a predisposing cause for UTI there is an increased risk that the baby may also suffer from this condition.

If the organism responsible for the UTI is Group B Streptococcus (GBS), this will need to be treated with antibiotics at the time of diagnosis. Intrapartum antibiotics will also be advised. GBS bacteriuria is associated with an increased risk of early onset neonatal sepsis; although the risk is increased, it is not quantified10.










Medical Management and Care


  • Treat confirmed UTI including asymptomatic bacteriuria, promptly11
  • Ensure antibiotic chosen is safe in pregnancy
  • Avoid trimethoprim in the first trimester, as it is a folate antagonist12
  • Augmentin increases the risk of neonatal necrotising enterocolitis if taken around the time of a premature delivery13
  • Consider prophylactic antibiotics to prevent recurrent UTI
  • In the case of acute pyelonephritis, hospitalise, commence iv antibiotics, converting to oral when tolerated, iv hydration and adequate analgesia
  • Monitor renal function and consider renal ultrasound

Midwifery Management and Care

Monthly MSU – more frequently if clinically indicated by:


  • Dysuria
  • Increased frequency of micturition
  • Urine dipstick positive for haematuria/proteinuria or nitrates
  • Lower abdominal pain or renal tenderness
  • Pyrexia

Always do a test of cure MSU after any treatment of UTI and encourage compliance with prescribed antibiotic regime.

Advise:


  • Drinking 2 l of fluid daily
  • Empty bladder after intercourse
  • Always wipe from front to back after urinating
  • Drinking 200–300 ml cranberry juice (or capsule) daily may reduce the risk of recurrent UTI7–9

If GBS is the causative organism, inform the woman, placing an alert note on the case notes for antibiotic cover in labour10.

Pyelonephritis:


  • Refer to hospital if acute pyelonephritis suspected
  • Administer analgesia and antibiotics as prescribed
  • Observations: hourly temperature, BP, pulse
  • Record fluid balance accurately










Labour Issues

If the mother has a UTI in labour, and is pyrexic and tachycardic, this may result in fetal tachycardia. In this case electronic monitoring of the fetal heart rate in labour is indicated.

Urinary catheterisation increases the risk of UTI, so avoid if possible, but if this is required utilise a strict aseptic technique.










Medical Management and Care


  • Commence antibiotics and monitor fetal wellbeing especially if the mother is pyrexic in labour. Otherwise manage as normal.

Midwifery Management and Care


  • Encourage regular emptying of the bladder
  • Good hygiene practices such as offering the mother soap and water for hand washing after using a bedpan
  • Avoid urinary catheterisation as this increases the risk of UTI
  • Administer any prescribed treatment
  • Ensure adequate hydration, if pyrexic iv fluid may be required










Postpartum Issues

If mother has recurrent UTI due to reflux nephropathy, then there is a risk that the baby could also have this condition.

Early detection and prompt treatment of urinary infections in the newborn can help prevent renal scarring and chronic kidney disease later in life.










Medical Management and Care


  • Liaise with the GP if there have been recurrent UTIs in pregnancy
  • If UTI persists postpartum further investigation is warranted
  • A renal ultrasound scan, for reflux nephropathy, should be arranged for the baby

Midwifery Management and Care


  • Postnatal care can usually be managed from a normal perspective by the midwife
  • Enquires about the occurrence and symptoms of micturition should form part of routine postnatal care, and be acted upon if the mother reports symptoms such as dysuria.
  • Encourage the mother to drink regular fluids, especially if breast-feeding
  • The mother may need reassurance that antibiotics are safe to be taken when breast-feeding





6.2 Chronic Kidney Disease







Incidence

11% of UK adult population may have CKD1

Risk for Childbearing

High Risk





EXPLANATION OF CONDITION


Chronic kidney disease (CKD) implies longstanding kidney problems often, but not always, associated with loss of excretory function. CKD is classified according to estimated glomerular filtration rate (eGFR). Five stages are recognised:



1. NormalGFR >90 ml/min/1.73 m2 with other evidence of chronic kidney damage*

2. Mild impairmentGFR 60–89 ml/min/1.73 m2 with other evidence of chronic kidney damage*

3. Moderate impairmentGFR 30–59 ml/min/1.73 m2

4. Severe impairmentGFR 15–29 ml/min/1.73 m2

5. Established renal failureGFR <15 ml/min/1.73 m2 or on dialysis
Other evidence may be urinary dipstick abnormalities or structural abnormalities detected by ultrasound scanning

Estimated GFR is automatically reported by chemical pathology laboratories using a formulaic calculation based on serum creatinine2, but it is not validated in pregnancy.


Proteinuria in the first trimester of pregnancy may be the first indication of CKD, as this is often the first time a woman’s urine has been tested.


COMPLICATIONS



  • Hypertension – common with CKD
  • Fluid retention – may cause ankle oedema and contribute to hypertension
  • Anaemia – increased risk as the kidney produces erythropoietin which stimulates the bone marrow to produce red blood cells; erythropoietin is often deficient
  • Heavy proteinuria – in the nephrotic range (>3 g per 24 hours); can cause hypoalbuminaemia and oedema
  • Metabolic acidosis – can develop
  • Renal bone disease – may occur
  • UTI – increased risk of infection
  • Impaired renal function – this may relentlessly and predictably deteriorate over time
  • Patients may be given dietary restrictions to help control BP and potassium levels within safe limits

NON-PREGNANCY TREATMENT AND CARE



  • Investigations into the cause of CKD may include renal ultrasound scanning or occasionally renal biopsy
  • Some causes of CKD may require specific treatments, such as immunosuppression with steroids
  • Regular monitoring of renal function in nephrology clinic or primary care
  • Antihypertensive medication
  • Diuretics to treat fluid retention
  • Subcutaneous erythropoietin for anaemia
  • Referral to a dietician if dietary restrictions are required to maintain safe blood chemistry levels
  • Patient education about disease and treatment
  • Dialysis or transplantation is required for stage 5 CKD

PRE-CONCEPTION ISSUES AND CARE



  • Referral to a renal/obstetric or maternal medicine clinic for personalised specialised advice and counselling
  • The predicted outcome of a pregnancy depends on, and is directly proportional to:

    • how well controlled the BP is at booking
    • the level of renal impairment
    • magnitude of proteinuria
    • the underlying disorder responsible for CKD3–6

  • Ascertain cause of CKD; if actively under investigation it is prudent to await results before conception
  • Always consider previous obstetric history and underlying medical conditions, e.g. patients with lupus nephritis could also have antiphospholipid syndrome7
  • With progressively worsening CKD, decreasing fertility and need for early conception is balanced against the risk of deteriorating renal function in a pregnancy
  • Optimal BP control is essential, and alteration to medications may be required

    • ACE inhibitors are commonly used for patients in CRF because of their protective effect on the kidneys, but they are contraindicated in pregnancy as they cause fetal anuria and subsequent oligohydramnios8

  • Heavily proteinuric patients are at increased risk of thrombo-embolism in pregnancy

    • prophylactic daily injections of low-molecular-weight heparin might be considered if they become preg­nant; must be balanced against the increased risk of bleeding9

  • Some individuals have familial renal disease and may require referral to clinical genetics for counselling
  • Pre-eclampsia risk increases with CKD, being difficult to differentiate from deterioration of underlying CKD
  • Increased risk of UTI, so regular MSU testing required with early treatment of symptoms
  • If there is significant proteinuria, it may be difficult to measure accurately the alpha-feta protein (AFP) level

    • meaningful interpretation of Down’s syndrome screen­ing blood test, usually offered around the 15th week of pregnancy, may not be possible
    • if the kidney is leaking protein, AFP may also, theoretically, be lost in the urine

  • Once pregnant, the woman will need to have regular hospital appointments, at a specialised centre






Pregnancy Issues

If the woman did not receive pre-conceptual counselling she should be made fully aware of the effect and risks of pregnancy upon herself, her renal function and her fetus.

The woman should be managed at a maternal medicine or renal/obstetric clinic.

In pregnancy, CKD is associated with:


  • IUGR
  • Pre-eclampsia
  • Premature delivery
  • Fetal loss
  • UTI
  • Deteriorating renal function3–6

The predicted outcome of the pregnancy is directly proportional to BP control at booking, the degree of hypertension, the level of renal impairment, magnitude of proteinuria and the underlying disorder responsible for CKD3–6.

Close supervision of renal function, BP and proteinuria are required.

Although eGFR is now reported as a measure of renal function with all requests for serum creatinine, eGFR is not validated as an accurate measure of renal function in pregnancy2.










Medical Management and Care


  • Specific treatment for underlying renal disease should continue
  • Commence 75 mg daily of aspirin, to reduce the risks of pre-eclampsia10
  • Monitoring renal function necessitates regular blood testing
  • Careful BP monitoring is required (see Chapter 3.1)
  • Current medications should be reviewed; some agents may need to be omitted or changed to those which are safe for pregnancy
  • Administration of erythropoietin may be required to treat anaemia
  • Monitor urine for increasing protein excretion
  • If heavily proteinuric and/or there is a low serum albumin, it may be necessary for the mother to commence anticoagulant therapy9
  • Monitor renal function carefully by serum creatinine
  • Declining renal function may occasionally necessitate institution of dialysis during pregnancy
  • Regular fetal growth scans

Midwifery Management and Care


  • Early referral to a renal/obstetric or maternal medicine clinic
  • Baseline U&E and LFT with booking blood tests
  • Advise about alternative screening methods for Down’s syndrome if the serum test was unreliable due to heavy proteinuria; an alternative is nuchal translucency scanning
  • Monthly MSU
  • Advise the woman about the signs and symptoms of pre-eclampsia
  • Encourage compliance with prescribed medications and reassure regarding the safety of the drugs for the fetus, and whilst breast-feeding
  • Refer to the pharmacist if further information is required
  • Teach administration of anticoagulant injections, if prescribed, and give information about the symptoms of DVT and PE; reinforce with general advice about reducing the risk of thrombosis9










Labour Issues

There is no reason why the patient should not have a normal vaginal delivery. However, the woman will be at increased risk of an emergency LSCS, or induction of labour for either maternal or fetal complications.

The ergometrine component of Syntometrine is associated with hypertensive episodes.










Medical Management and Care


  • Monitor renal function and BP carefully
  • Strict fluid balance
  • Monitor fetal wellbeing, being vigilant for fetal distress

Midwifery Management and Care


  • If the fetus is premature or growth restricted then continuous fetal monitoring will be indicated
  • If the woman is hypertensive, oxytocin will be required for active third-stage management instead of Syntometrine










Postpartum Issues

There is still potential in the immediate postnatal period for instability in the maternal renal function and BP control.

The baby will require a renal ultrasound if the mother has ureteric reflux, because of the familial nature of these conditions.

If the woman suffers from uncontrolled hypertension, or is breast-feeding, the combined oestrogen and progesterone oral contraceptive will be contraindicated.










Medical Management and Care


  • Monitor renal function carefully in immediate postpartum period
  • BP should be well controlled
  • Recommence and change to pre-pregnancy medication if required (avoiding nephrotoxic medications). However, this may be delayed if the mother wishes to breast-feed, dependent upon any contraindications
  • Ensure adequate hydration
  • Send notification to the woman’s lead nephrologist and GP detailing care and pregnancy outcome
  • Arrange a renal ultrasound for the baby if required

Midwifery Management and Care


  • Follow-up appointment should be arranged in the mother’s routine nephrology department
  • If alterations are made to hypertensive treatment, more frequent BP monitoring should be arranged
  • The woman will not be suitable for an early discharge
  • Discuss the alternative methods of contraception available





6.3 Dialysis in Pregnancy







Incidence

Uncommon – less than 1% of women of childbearing age on dialysis become pregnant each year.

Risk for Childbearing

High Risk





EXPLANATION OF CONDITION


Dialysis is a means of removing waste products and water from the body of patients whose kidneys have failed and have lost their ability to excrete water and dissolved waste products as urine (Appendix 6.3.1). These patients would otherwise die.


Two types of dialysis are available.


Haemodialysis


In haemodialysis (HD) blood is circulated through a machine where it is purified before being returned to the patient. This type of dialysis is usually performed on three occasions per week in hospital. HD patients require access to their circulation, usually in the form of an arteriovenous fistula or a semi-permanent plastic catheter inserted into a large vein.


Peritoneal Dialysis


In peritoneal dialysis (PD) the patient has a soft tube inserted into the peritoneal cavity. This is used to drain up to 2.5 l of fluid in and out of the peritoneal cavity, typically four times a day, by patients in their own home.


Each patient has an individual dialysis prescription and a target ‘dry’ weight to ensure that the correct amounts of waste products and fluid are removed by their dialysis.


Women of childbearing age receiving dialysis either have reduced fertility or are infertile.


COMPLICATIONS



  • Dialysis is an imperfect substitute for normally functioning kidneys and dialysis patients have a reduced life expectancy
  • Nearly all dialysis patients are hypertensive and anaemic due to the failure of damaged kidneys to produce erythropoietin
  • Dialysis patients suffer from secondary hyperparathyroidism and renal osteodystrophy
  • Dialysis patients have greatly increased morbidity and mortality, predominantly as a result of infection and especially cardiovascular disease, including heart disease, cerebrovascular disease and peripheral vascular disease
  • Arteriovenous fistulae can clot off and become blocked, and permcaths can become blocked or infected; an urgent alternative has to be arranged
  • Patients receiving peritoneal dialysis can develop peritonitis as a result of bacteria entering the peritoneal cavity through the dialysis tube; treatable with antibiotics but a potentially very serious complication

NON-PREGNANCY TREATMENT AND CARE


The patient needs close supervision and care from a multidisciplinary team including doctors, nurses, dieticians, pharmacists and dialysis technicians.


Treatment



  • Dialysis – to be performed regularly
  • Nearly all patients need antihypertensive medication and erythropoietin injections to prevent severe anaemia
  • Strict dietary restrictions to limit intake of fluid, potassium and phosphate
  • Regular review clinics are required to assess adequacy of dialysis treatment and to prevent dialysis complications

PRE-CONCEPTION ISSUES AND CARE


Because of the low likelihood of pregnancy occurring in women receiving dialysis, very few actually seek pre-conceptual advice. However, conception is possible and those of childbearing age should take appropriate contraception precautions to avoid an unwanted pregnancy.


Psychosexual problems are common in dialysis patients and may limit the ability to conceive.


Refer to a joint renal/obstetric or maternal medicine clinic, where they can be seen jointly by a consultant nephrologist and obstetrician and specialised midwife. In some cases this may involve considerable travelling to the appropriate unit.


Advise that pregnancy is at high risk of problems such as:



  • Anaemia
  • Hypertension
  • Pre-eclampsia
  • IUGR
  • Polyhydramnios
  • Premature labour
  • Haemodialysis – HD requirements will increase, and to help stabilise the blood values dialysis would be performed approximately 6 days a week (compared with three occasions per week as described above)
  • Peritoneal dialysis – As the pregnancy advances, then smaller, more frequent fluid exchanges may need to be performed; changing to haemodialysis may have to be considered
  • If renal transplantation is imminent it may be sensible to wait until after transplantation before trying for a pregnancy
  • Down’s screening tests will not be interpretable in dialysis patients; nuchal translucency screening or diagnostic tests would have to be considered if requested
  • The underlying renal disorder may have an impact on the pregnancy, and this will need to be considered
  • Current medications will need review, and probable alteration, by the renal team




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Aug 8, 2016 | Posted by in GYNECOLOGY | Comments Off on RENAL DISORDERS

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