management of chronic complications of sickle cell disease
Last reviewed 01/2018
- chronic pain
- often caused by orthopaedic conditions such as avascular necrosis, vertebral collapse, or chronic arthritis (1)
- chronic pain is difficult to eradicate and the goal should be to minimise
the suffering as much as possible
- medium- to long-acting opiates (orally or transdermally) should be used
- prescribe an alternative analgesia for "breakthrough" pain
- if NSAID's are used, should be limited to standard doses and defined periods and if given for longer periods, monitor renal function every 3 months (2)
- non pharmacological therapies such as massage, psychological coping strategies, including distraction techniques should be encouraged in children (3)
- yearly (or more frequently in special cases) assessment, medication
review, and health education should be provided to the patient
- career/vocational and employment advice
- occupational, psychological therapy (2)
- inform about the importance of avoiding factors that may exacerbate
pain e.g. - cold weather, high-impact exercise or sports, weight management
and dehydration (2,3)
- nutrition and growth
- height and weight should be measured at each visit
- if the child is hospitalized for frequent and long periods, consider referral to a dietician for extra calorie input
- zinc supplementation in case of growth retardation and vitamin D deficiencies should be treated (3)
- folic acid supplementation is recommended for all patients with SCD (although it may mask megaloblastic anaemia caused by cobalamin deficiency) (2)
- refer children with no physical signs of puberty at 14 years in a girl
and 14.5 years in a boy to a paediatric endocrinologist
- nocturnal enuresis
- inform the parents that nocturnal enuresis is common in SCD (specially in boys with HbSS) and most will resolve spontaneously
- advice on techniques to achieve continence e.g - intermittent alarms and parental waking to achieve continence
- if children do not respond to routine advice, consider oral or nasal desmopressin
- refer to
- an ENT specialist if the history is suggestive of obstructive apnoea and snoring
- a specialist management (e.g. an enuresis clinic) if there is no
response to basic measures after the age of 7 years (3)
- cerebrovascular disease
- all children with SCD aged over 2 years should undergo annual transcranial Doppler imaging (3)
- parents/carers should be educated about symptoms and signs of stroke and what action should be taken if a child develops neurological symptoms (3)
- a first episode of acute severe headache, or a significant change in the type of headache may indicate intracranial haemorrhage or venous sinus thrombosis and these patients should be admitted for urgent assessment (2)
- the mean blood pressure in SCD patients is lower when compared to age and sex matched controls hence more aggressive management of systemic hypertension is required on detection (2)
- regular blood transfusion should be offered throughout childhood for
secondary prevention of stroke (3)
- eye complications
- prevention of developing complications is the most effective therapy
- all SCD patients must be evaluated by an ophthalmologist annually
- patients with acute loss of vision (due to occlusion of the central
retinal artery) should be treated with immediate blood transfusion and
referral to an ophthalmologist
- leg ulcers
- should be managed by a multidisciplinary team with expertise in leg ulcer management
- could be treated with frequent dressing, support bandages, physiotherapy and antibiotics if infected (Topical antibiotics should be avoided)(3)
- blood transfusion could be considered in patients who fail to respond
(2)
- priapism
- boys and their parents/carers should be educated that priapism is a complication of SCD and to seek treatment early and should attend hospital as an emergency if priapism persists for more than 2 hours
- for minor events (occurring for less than 3 hours) - bladder emptying, exercise such as jogging, warm baths and analgesia may be useful
- for stuttering priapism oral etilefrine may be beneficial(3)
- chronic lung disease
- in patients with chronic lung disease advice about smoking cessation, vaccinations (should be kept up to date), avoiding, or getting early treatment for chest infections (2)
- Trans-thoracic echocardiography should be done to screen pulmonary hypertension every 1-2 years (2)
- refer patients with suspected pulmonary hypertension to a specialist
- liver disease
- an ultrasound of liver and biliary tree should be carried out in patients with recurrent abdominal pain
- in symptomatic biliary disease, consider elective cholecystectomy
Reference:
- 1. Claster S, Vichinsky EP. Managing sickle cell disease. BMJ. 2003;327(7424):1151-5.
- 2. Sickle Cell Society 2008. Standards for the clinical care of adults with sickle cell disease in the UK
- 3. NHS Sickle Cell and Thalassaemia Screening Programme 2009. Sickle cell and Thalssaemia. Handbook for laboratories