Myelodysplasia and Neurogenic Bladder Dysfunction Follow-up
- Author: Terry F Favazza, MD; Chief Editor: Marc Cendron, MD more...
Further Outpatient Care
- General follow-up care
- That patients require lifelong supervision and monitoring of renal function cannot be stressed enough. Renal failure can progress slowly or occur with startling rapidity.
- Check postvoiding residual volumes every 6-12 months and renal function (BUN and creatinine levels) yearly.
- Perform renal ultrasound yearly.
- Many advocate a yearly urodynamic study for the first 5 years of life, followed by biennial evaluation.
- Perform a repeat urodynamic study any time the patient experiences any change in neurologic symptoms.
- Tethered cord
- As children age, different growth rates of the vertebral bodies and the spinal cord can add a dynamic element to the lesion. Fibrosis surrounding the cord at the site of meningocele closure can tether it during growth. This can lead to changes in bowel, bladder, and lower extremity function. If these are noted, evaluation using MRI is indicated.
- From the urologic standpoint, an MRI and a repeat urodynamic study are warranted when the patient has a change in symptoms or undergoes any neurosurgical procedure.
Inpatient & Outpatient Medications
- Antibiotics: Antibiotics are used when indicated to treat acute infections. In patients with vesicoureteral reflux, antibiotics are often used as prophylaxis to prevent UTIs.
- Anticholinergics: Anticholinergic medications help suppress involuntary and uninhibited bladder contractions. This serves to decrease urgency and incontinence and to potentially increase the bladder's functional storage capacity.
- Alpha agonists: The role of alpha agonists is to increase tone at the bladder neck, initiating a state of urinary retention in an effort to decrease incontinence. Thus far, the therapy has had limited use in patients with myelodysplasia.
- Botulinum toxin: Studies have reported the use of botulinum toxin directly injected into the detrusor of children with myelodysplasia with success in treating incontinence.[8, 9, 10, 11, 12] However, this treatment is still in its infancy and not yet widely used.
Prognosis
The prognosis for patients with myelodysplasia has improved dramatically over the past decades.
- Neurosurgical techniques and antibiotics have improved, and far fewer infants die of CNS infections and complications related to closure of the defect.
- Since the introduction of IC, incontinent urinary diversion is no longer performed with the same frequency as in the past, leading to greatly reduced operative morbidity and mortality. Many patients can be treated with CIC alone or with adjunctive pharmacotherapy and never require surgery.
- In selected patients, bladder augmentation and continence surgery may provide medical benefits and an improvement in the patient's quality of life.
Patient Education
Starting at birth and as the patient ages, parents and patients need to be educated regarding the many issues associated with living with myelodysplasia.
- Teach parents and patients the skills of catheterization, how to recognize infection, the need to alleviate constipation, the importance of watching for changes in symptoms, and the facts regarding sexual issues.
- Constantly remind parents and patients of the need to adapt to new problems and the need for lifelong observation by health care providers.
- When they are able, encourage patients to become involved in their own care because, eventually, they will be responsible for looking after themselves.
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