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Brief Reports

Indian Pediatrics 2002; 39:834-838  

Growth Status of Children with Cerebral Palsy*

 

Mustafa Ozturk, Selami Akkus, Mehmet Ali Malas and Ahmet Nesimi Kisioglu

 

From the Department of Public Health, School of Medicine, University of Suleyman Demirel, Isparta, Turkey.

Correspondence to: Dr. Mustafa Ozturk, Suleyman Demirel Universitesi, Tip Fakultesi, Halk Sagligi Anabilim Dali 32040 Isparta, Turkiye

E-mail: [email protected]

Manuscript received: November 12, 2001, Initial review completed: December 20, 2001;

Revision accepted: March 1, 2002.

 

The aim of this study was to evaluate growth status of the children with cerebral palsy (CP) in Isparta Province, Turkey. Forty three children with CP (24 male 19 female; mean (SD) age 8.1±4.2 years) were included in this study. 32.6% of the children were quadriplegic, 44.2% diplegic and 14.0% hemiplegic. All caregivers were interviewed and anthropometric measurements of the children with CP were performed. The ratio of weight for age and height for age z scores under –2 SD were higher in males, 7-16 age groups, quagriplegics, and having oromotor dysfunction. This study showed that the children with CP in our region have suffered from growth failure.

Key words: Anthropometric measurements. Cerebral palsy, Growth status.

Cerebral palsy (CP) is a disorder especially affecting the ability to control movement and posture. Depending on the location and extent of the damage, cerebral palsy can be mild or severe. It is sometimes associated with other problems such as seizures, mental retardation, hearing and vision problems, communication problems, etc.

It has been well documented in the literature that the children with CP are frequently associated with poor growth. The main cause of growth failure in the children with CP is inadequate nutritional intake resulting from feeding difficulties(1-5). The majority of the studies on growth status of children with CP have been performed in western countries. In this study, we aimed to evaluate the anthropometric growth of the children with CP in our region.

Subjects and Methods

Forty three children with CP admitted to the Isparta Spastic Children’s Center were included. No patient had any other chronic systemic illness (cardiac, renal), or history regarding use of medication (e.g., steroids) that are known to affect growth. The diagnosis of CP was based on a neurologic examination. Severity of impairments were evaluated according to the Gross Motor Function Classification System (GMFCS)(6).

All caregivers were interviewed and informed consent obtained. Information on demographic characteristics and feeding disorders was gathered using a questionnaire. Patients with tongue thrust, fluid or food loss, coughing and gagging during eating, excessive time requirement for meals, and difficulty in consuming textured foods were considered to have oromotor dysfunction(2-3). None of the children with CP were receiving feeds through nasogastric tubes.

Measurements of weight, height, lower-leg lengths and skinfold thickness (triceps, biceps, suprailiac and subscapular) were performed using standard methods(7-8). Weight was measured on an electronic scale. A Holtain skinfold caliper was used to measure skinfold thickness. Percentage body fat, fat mass and fat-free mass were calculated from two skinfold thicknesses (triceps and subscapular) using the equations of Slaughter, et al.(9). ANTHRO software program (Version 1.02, World Health Organization, Geneva 1999) that uses reference data of the National Center for Health Statistics (NCHS) was used for calculation of z scores of weight for age (WAz), height for age (HAz) and weight for height (WHz) . Statistical analysis was completed on the Statistical Package for Social Sciences (Version 7.51).

Results

The mean age of patients was 8.1 ± 4.2 years (range 1.2 to 16.1 years); 55.8% were male. Of 43 patients, 32.6% had quadriplegia, 44.2% diplegia and 14.0% hemiplegia; 81.4% of all patients were spastic. There was no significant difference between male and female children in the ratios of GMFCS level, while frequency of oromotor dysfunction was higher in males (P < 0.01).

Table I shows the mean anthropometric measurements and the variables derived from skinfold thickness. The proportion of patients with WAz, HAz and WHz scores below –2 SD was 34.9%, 30.2% and 9.3% respectively.

Table I– Anthropometric Measurements
Measurement
Mean (n=43)
(SD)
Weight (kg)
22.3
(11.3)
Height (cm)
116.3
(22.3)
Weight for age Z score
–1.5
(0.9)
Height for age Z core
–1.6
(1.3)
Weight for height Z score
–0.4
(1.2)
Biceps skinfold (mm)
4.0
(1.6)
Triceps skinfold (mm)
6.6
(2.6)
Subscapular skinfold (mm)
5.2 
(2.3)
Suprailiac skinfold (mm)
4.3
(2.5)
Body fat (%)
11.2
(4.1)
Fat mass (kg)
2.7
(2.4)
Fat-free mass (kg)
19.6
(9.3) 

Lower-leg lengths(8) below the 2.5th centile was seen in 32.6% patients. There was a significant correlation between height and lower-leg length (r = 0.83, P < 0.001).

Table II shows the distribution of mean z scores in relation to some characteristics. Both HAz and WHz scores were significantly lower in 7-16 yr old (P < 0.05). Mean fat mass and body fat were higher in females (P < 001). Similarly, the proportion of patients with WAz and HAz scores under –2 SD were higher in males, patients 7-16 yr of age, quadriplegics, having GMFCS levels III-V, and having oromotor dysfunction.

Table II-WAz, HAz and WHz scores, and Body Fat Measurements in Relation to 
Clinical Characteristics
	
 

Means (SD)a

Characteristics
n
WAz
HAz
WHz
FM (kg)
FFM (kg)
BF (%)
Gender
Male
24
–1.7(0.8)
–1.8(1.1)
–0.6(1.0)
2.0(1.0)
19.2(8.1)
9.7(2.1)
Female
19
–1.3(0.9)
–1.4(1.4)
–0.2(1.4)
3.6(3.3)*
20.2(10.7)
13.2(5.1)**
Age groups
1-6 years
16
–1.4(0.8)
–0.9(1.2)
–0.1(1.3)
1.4(0.3)
11.9(1.7)
10.4(1.7)
7-16 years
27
–1.6(0.9)
–2.0(1.1)*
–1.0(0.9)*
3.5(2.7)**
24.2(8.8)***
11.7(4.9)
Diagnosis
Quadriplegia
14
–1.8(0.9)
–2.1(1.3)
–0.6(1.0)
2.0(1.0)
19.4(8.0)
9.5(2.1)
Others
29
–1.4(0.9)
–1.4(1.2)
–0.3(1.3)
3.1(2.8)
19.7(10.0)
12.0(4.5)*
GMFCS level
I-II
23
–1.5(0.9)
–1.4(1.0)
–0.4(1.3)
2.9(2.5)
20.4(10.3)
11.5(4.6)
III-V
20
–1.6(0.9)
–1.9(1.5)
–0.5(1.2)
2.5(2.3)
18.7(8.1)
10.8(3.4)
Oromotor dysfunction
Yes
23
–1.7(1.0)
–1.9(1.3)
–0.5(1.2)
2.6(2.4)
19.0(8.6)
10.9(4.0)
No
20
–1.3(0.7)
–1.3(1.1)
–0.3(1.2)
2.9(2.5)
20.3(10.2)
11.6(4.3)
Total
43
–1.5(0.9)
–1.6(1.3)
–0.4(1.2)
2.7(2.4)
19.6(9.3)
11.2(4.1)
unpaired t test, *P<0.05, **P<0.01, ***P<0.001
WAz, HAz, WHz scores: weight for age, height for age, weight for height standard deviation scores.
FM: fat mass; FFM: free fat mass; BF: body fat

Discussion

Accurate measurement of linear growth by height in children with CP may be difficult due to frequent occurrence of joint contractures. It is suggested that linear growth may be assessed using upper-arm and lower-leg lengths(8). We found a significant correlation between height and lower leg length measurements in our subjects.

Growth retardation in the children with CP has been well documented in the literature. Stallings, et al.(2), reported that there was a strong relationship between linear growth measured with upper arm and lower leg length, neuromotor involvement and nutritional status in the children with quadriplegic CP. Among 171 patients attending a pediatric rehabilitation center, the mean z scores of height and weight were found to be as –1.7 ± 1.9 and –1.6 ± 1.8 respectively(10). The proportions of the children below the 2.5th centile for normal height and weight were 38%, and 42%, respectively in this study(10). Similar figures are reported by other workers(11).

It has been reported that patients with CP have growth failure when compared with age and sex-matched healthy children, and have different body compositions. Stallings, et al(3) reported lower WAz and HAz scores, and body fat, fat mass and fat-free mass in children with spastic quadriplegic CP in comparison to normals. More children are malnourished in the developing countries, including Turkey, as compared to the NCHS reference population(12,13). Although we did not make a comparison between the children with CP and a control group, we believe that the z scores in our patients were significantly lower than healthy Turkish children.

Krick and Van Duyn(14) found that children with CP and oromotor dysfunction had significantly reduced weight and height than their age-and sex-matched counterparts without such impairment. Our results confirm those reported previously since the proportion of patients with WAz and HAz scores below –2 SD were higher in these with oromotor dysfunction.

Contributors: MO coordinated the study and drafted the paper, he will act as the guarantor for the paper. SA participated in data analysis and drafting the paper. MAM participated in data collection and analysis. ANK contributed in data analysis and drafting the paper.

Funding: None.

Competing interests: None stated.

 

Key Messages

• Children with cerebral palsy suffer from growth failure.

• Qromotor dysfunction might contribute to growth failure in some patients.

 

 References


1. Shapiro BK, Green P, Krick J, Allen D, Capute AJ. Growth of severely impaired children: neurological versus nutritional factors. Dev Med Child Neurol 1986; 28: 729-733.

2. Stallings VA, Charney EB, Davies JC, Cronk CE. Nutrition-related growth failure of children with quadriplegic cerebral palsy. Dev Med Child Neurol 1993; 35: 126-138.

3. Stalling VA, Zemel BS, Davies JC, Cronk CE, Charney EB. Energy expenditure of children and adolescents with severe disabilities: a cerebral palsy model. Am J Clin Nutr 1994; 64: 627-634.

4. Troughton KEV, Hill AE. Relation between objectively measured feeding competence and nutrition in children with cerebral palsy. Dev Med Child Neurol 2001; 43: 187-190.

5. Pai M, Alur M, Wirz S, Filteau S, Pagedar S, Yousafzai A. A pilot study of the nutritional status of disabled and non-diabled children living in Dharavi, Mumbai. Indian Pediatr 2001; 38: 60-65.

6. Palisano R, Rosenbaum P, Walter S, Russell D, Wood E, Galuppi B. Development and reliability of a system to classify gross motor function in children with cerebral palsy. Dev Med Child Neurol 1997; 39: 214-223.

7. Cameron N. The methods of auxological anthrompometry. In: Human Growth , vol 2, Eds. Falkner F, Tanner JM. New York, Plenum Press, 1986; pp 3-43.

8. Spender WQ, Cronk CE, Charney EB, Stallings VA. Assessment of linear growth of children with cerebral palsy: use of alternative measures to height or length. Dev Med Child Neurol 1989; 31: 206-214.

9. Slaughter M, Lohman T, Boileau R, et al. Skinfold equations for estimation of body fatness in children and youth. Hum Biol 1988; 60: 709-723.

10. Stevenson RD, Hayes RP, Cater LV, Blackman CA. Clinical correlates of linear growth in children with cerebral palsy. Dev Med Child Neurol 1994; 36: 135-142.

11. Johnson RK, Maeda M. Establishing outpatient nutrition services for children with cerebral palsy. J Am Diet Assoc 1989; 89: 504-506.

12. Dindar H, Yucesan S, Olcay I, et al. Physical growth measurements of 18,719 primary school children living in Adana, Turkey. Turk J Pediatr 1989; 31: 45-56.

13. Gangil A, Patwari AK, Aneja S, Ahuja B, Anand VK. Feeding problems in children with cerebral palsy. Indian Pediatr 2001, 38: 839-846.

14. Krick J, van Duyn MAS. The relationship between oral-motor involvement and growth: a pilot study in cerebral palsy. J Am Diet Assoc 1984; 84: 555-559.

 

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