Complications

Complication
Timeframe
Likelihood
short term
medium

Small head suggesting microcephaly reflects poor brain growth.

short term
medium

Increased head circumference is indicative of hydrocephalus requiring a ventriculoperitoneal shunt.

long term
high

A low visual acuity can be present in up to 75% of patients with CP. Common with premature birth history. Patients with spastic quadriplegia have higher rates of visual impairment.

Evaluation of vision loss

long term
high

Around 50% of people with CP have intellectual disability (IQ below 70).[56]

long term
high

Excessive drooling (sialorrhea) is a common problem, affecting around half of people with CP.[238] It can be treated with oral medication (glycopyrrolate or trihexyphenidyl), scopolamine patches, injection of botulinum toxin into the salivary glands, or surgical procedures.[239][240][241][242][243][244][245][246]

long term
medium

Orthopedic consultation should be sought and treatment including vitamin D and calcium therapy commenced. Additional medications such as pamidronate or other bisphosphonates may also be considered, although evidence for efficacy is limited.[247][248]

Osteoporosis

long term
low

Hearing impairment occurs in around 10% of people with CP, and is more commonly associated with dyskinetic or ataxic CP than spastic CP. Regular ongoing hearing assessment is necessary.[56]

Evaluation of hearing loss

long term
low

The possibility of cervical myelopathy should be considered in patients with slow, insidious degradation of function in the absence of trauma or other clear antecedent event. Loss of ambulation, upper-extremity function, and bowel or bladder control is not part of the natural history of CP.

Radiographs and cervical magnetic resonance imaging can confirm cervical myelopathy. It is most commonly seen in patients with dyskinesia but has been reported in patients with spasticity.[249][250]

variable
high

Gastrointestinal and feeding problems are observed in 50% of patients.

Patients with spastic quadriplegia have higher rates of oral-motor impairment.

The patient presents with poor sucking, swallowing, or chewing. An individualized plan should address factors such as posture, food textures, specialized equipment, feeding technique, and the mealtime environment.[56]

If oral intake is insufficient to provide adequate nutrition after assessment and nutritional interventions, percutaneous gastrostomy insertion may be considered. A review of interventions for feeding and nutrition in CP concluded that gastrostomy-fed children gained weight, but the effects on other measures of growth and development were less clear.[226] Substantial numbers of children remained underweight, although normal reference standards for children with CP are lacking.

Special methods may have to be used in the nutritional assessment of CP patients if height and weight cannot easily be measured.[56][232]

variable
high

Behavior problems are 5 times more likely in children with CP. These are addressed by psychosocial approaches such as parental counseling and more direct interventions with the children themselves.[233]

variable
high

Frequently observed due to poor oral and pharyngeal motor control secondary to spasticity, weakness, or dyskinesia. Patients with spastic quadriplegia have higher rates of oral-motor impairment.

The child should be assessed for swallowing difficulties while eating (including any choking, coughing, gagging, or vomiting), and for other risk factors.[224] Aspiration may be silent with no symptoms.

Patients suspected of aspiration should undergo swallowing studies. Follow-up requires observation for pneumonia, asthma, or chronic lower respiratory infections.[234]

variable
high

Poor growth is common in children with CP and particularly in those with quadriplegic involvement. All children should have serial height, weight, and head circumference measured on age- and sex-specific growth charts. Nutritional needs should be addressed.[222]

variable
high

Observed in up to 40% of patients with CP; more common in dyskinetic than in spastic CP. Patients require treatment with anticonvulsant medications. Electroencephalogram is performed to evaluate patients with epilepsy.[71]

variable
high

Up to 60% of children and young people with CP have chronic constipation.[56]

variable
high

Sleep issues are common in patients with CP but are infrequently studied in this population. Sleep hygiene should be optimized. There is some evidence that melatonin may be beneficial in improving sleep patterns.[236] Referral to specialist sleep services should be considered if sleep disturbances are ongoing.[56]

variable
medium

Observed in 25% of patients.

variable
medium

GERD is associated with anemia, malnutrition, recurrent upper respiratory infections, and low bodyweight.[235] Gastrointestinal swallow studies are indicated in patients suspected with GERD.

variable
medium

Patients with CP have an increased prevalence of mental health, psychological, and emotional problems (including depression, anxiety, and conduct disorders) which may have a substantial impact on quality of life. Specialist psychological assessment and ongoing management may be required.[56][107]

variable
medium

Weight bearing (e.g., using standers or walkers) should be maximized to avoid osteopenia. Basic calcium and vitamin D intake should be assessed for the recommended daily intake. Avoidance of excessive intake should be ensured to prevent renal stone formation.[234][237]

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