BAPS Papers
Quality of life in children with slow transit constipation

https://doi.org/10.1016/j.jpedsurg.2007.10.020Get rights and content

Abstract

Background

Slow transit constipation (STC) causes intractable symptoms not readily responsive to laxatives, diet, or life-style changes. Children with STC have irregular bowel motions associated with colicky abdominal pain and frequent uncontrollable soiling.

This study assessed the physical and psychosocial quality of life (QOL) in children with long-standing (≥2 years) STC vs healthy controls.

Methods

Children (aged 8-18) were recruited from gastrointestinal and surgical clinics and a Scout Jamboree. After informed consent was obtained, the questionnaire (Pediatric Quality of Life Inventory) was administered. This consists of parallel child and parent self-report scales encompassing physical functioning, emotional functioning, social functioning, and school functioning. Higher scores indicate better QOL. P value less than .05 was considered statistically significant.

Results

In 51 children with STC (mean, 11.5 years; male/female, 2:1) and 79 controls (mean, 12.1 years; male/female, 1.9:1), Pediatric Quality of Life Inventory QOL score was significantly lower in the STC group (72.90 vs 85.99; P < .0001). In addition, parents of children with STC reported a significantly lower QOL score than their child compared with the child's own report (64.43 vs 72.90; P = .0034). Parents of controls did not (84.25 vs 85.99; P = .12).

Conclusions

Slow transit constipation is a debilitating condition affecting both physical and emotional functioning in children. Parental perception of QOL is significantly worse, highlighting the considerable family impact of constipation and uncontrollable soiling.

Section snippets

Subjects and methods

After the attainment of informed consent, the questionnaire (Pediatric Quality of Life Inventory [PedsQL]) was administered by 1 of 3 investigators (M.C., C.C., or J.C.). The PedsQL 4.0 Generic Core Scales consist of parallel child and parent self-report scales and have been validated in children and adolescents aged 2 to 18 years [18], [19], [20], [21]. The questionnaires consist of 23 items encompassing (i) physical functioning (8 items); (ii) emotional functioning (5 items); (iii) social

Results

From March 2006 to March 2007, 51 children (34 male, 17 female) with STC and 79 healthy controls (48 male, 31 female) were recruited into the study (Table 1). All children and their parents successfully completed the PedsQL.

Child-reported QOL was significantly lower in children with STC compared with normal children (72.90 vs 85.99; P < .0001) (Fig. 1). Parent-reported QOL was significantly lower for children with STC compared with the control group (64.43 vs 84.25; P < .0001) (Fig. 2).

Discussion

Quality of life can be defined as “an individual's subjective perception of overall wellbeing and satisfaction with life” [23] or “physical, social and emotional aspects of a patient's well being that are important to the individual” [24]. QOL is a multidimensional concept that incorporates the assessment of recognized core domains and indicators.

Many studies have looked at the QOL in children with chronic disease; however, there are few studies that have specifically examined the impact of

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    Presented at the British Association of Paediatric Surgeons meeting, Edinburgh, Scotland, July 17-20, 2007.

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