ABSTRACT
OBJECTIVE: To evaluate the psychological development of patients with congenital central hypoventilation syndrome (CCHS). METHODS: We performed a questionnaire-based survey of 17 patients with CCHS aged over 7 years and assessed their clinical course, respiratory management, and psychological development. RESULTS: CCHS was present at birth in 15 patients, of which eight presented with respiratory failure with a low Apgar score. Twelve patients required mechanical ventilation with intubation, and five received mask ventilation. All patients with intubation underwent tracheostomy between 1 and 12 months of age (median 5.5 months), and most of them had associated conditions such as Hirschsprung disease. Four of 12 patients with intubation were eventually switched to mask ventilation and one to diaphragm pacing and mask ventilation. The patients undergoing mask ventilation had relatively milder disease severity and had fewer complications than did the patients with intubation. The psychological development of patients who received tracheostomy ranged from normal to severe retardation. Retardation was more likely to be severe in patients who received tracheostomy in late infancy. All patients who received mask ventilation experienced borderline to moderate psychological retardation. This effect could be attributed to poor compliance with mask fitting. CONCLUSION: Our findings suggest that the psychological development of CCHS patients was influenced by hypoxia; tracheostomy and strict respiratory management since the neonatal period were needed for neurological protection.
Subject(s)
Hypoventilation/congenital , Respiration , Sleep Apnea, Central/physiopathology , Sleep Apnea, Central/psychology , Adolescent , Child , Female , Humans , Hypoventilation/complications , Hypoventilation/physiopathology , Hypoventilation/psychology , Intellectual Disability/complications , Japan , Male , Respiration, Artificial , Sleep Apnea, Central/complications , Tracheostomy , Young AdultABSTRACT
OBJECTIVE: The nutritive evaluation and the serum carnitine values were measured for persons with severe motor and intellectual disabilities with enteral (tube) feeding. METHODS: In Shimada Rehabilitation Center, twenty one people who had serum albumin levels of 3.4 g/dl or less, and were taking nutrition with enteral (tube) feeding, were tested. Body weight, blood samples, and serum carnitine levels were measured. RESULTS: The total carnitine value was less than the standard value in 19 patients. The total carnitine value decreased in the group taking valporate sodium (VPA), compared to the values from the group non-taking VPA. CONCLUSIONS: From our evaluation, we think that daily carnitine supplements is essential for persons with sever motor and intellectual disabilities taking VPA to maintain carnitine levels in the blood, and regular urine test should be done for earlier detection secondary lack complications from the secondary lack of carnitine.
Subject(s)
Carnitine/blood , Disabled Persons , Enteral Nutrition , Adolescent , Adult , Aged , Aged, 80 and over , Cerebral Palsy/blood , Cerebral Palsy/therapy , Chromosome Aberrations , Female , Humans , Male , Middle Aged , Valproic Acid/therapeutic useABSTRACT
Hoffmann reflex (H reflex) is an electrically elicited spinal monosynaptic reflex. H reflex was examined in 18 patients with spastic quadriplegia who had perinatal or postnatal problems. H reflex was elicitable in 11 patients for the abductor pollicis brevis (61.1%), 10 for the abductor digiti minimi (55.6%) and 16 for the abductor hallucis (88.9%). Because the abductor pollicis brevis and the abductor digiti minimi do not exhibit H reflex in normal subjects, it was suggested that the excitability of alpha motor neurons innervating these muscles was increased. H reflex was not detected for the extensor digitorum brevis in any patients, indicating the difference in the excitability among alpha motor neurons. In some patients, H reflex did not disappear under supramaximal stimuli. We conclude that the mechanism of evolution of H reflex in patients with spastic quadriplegia is different from that in normal subjects.
Subject(s)
H-Reflex , Muscle, Skeletal/innervation , Quadriplegia/physiopathology , Adolescent , Child , Electric Stimulation , Female , Humans , Male , Motor Neurons/physiology , Muscle, Skeletal/physiopathology , Young AdultABSTRACT
We examined the present situation of children and adolescents with psycho-motor disabilities, and their parents by means of a questionnaire survey. The survey was conducted on the family members of outpatients, 116 males and 86 females. About half the patients were older than 15 years of age. The families of 128 patients did not use a home help service such as home nursing or a regional care service. Many family members had chronic ailments. The families of only 45 patients expressed that it would be better if their children would live in a care home in the future. We must develop a versatile system with social support and medical care for such cases.
Subject(s)
Child Rearing , Disabled Children/statistics & numerical data , Home Nursing , Parents/psychology , Psychomotor Disorders , Adolescent , Adult , Caregivers/psychology , Child , Child, Preschool , Female , Health Services Needs and Demand , Humans , Infant , Male , Psychomotor Disorders/epidemiology , Surveys and QuestionnairesABSTRACT
This is a report of the setting up of a day group service system for severely disabled children, the "Koala Club". The "Koala Club" was started in 1993, and has been running outside of the hospital since 1997. A support group for the "Koala Club" was established in 1999. Currently 13 children attend the "Koala Club". The staff of the "Koala Club" consists of one coordinater, four nurses and eight care workers. The medical care is fulfilled by nurses. The "Koala Club" open two days a week. It has been supervised by a doctor and a case worker. There is an important role for physicians in the regional care of disabled children.