Research Article Volume 12 Issue 3
1Pediatric Gastroenterology Unit, Department of Pediatrics, Botucatu Medical School - São Paulo State University, Brazil
2University/ Hospital of Botucatu Medical School, São Paulo State University, Botucatu, Brazil
3Pediatric Gastroenterology Unit,. University/ Hospital of Botucatu Medical School, São Paulo State University, Botucatu, Brazil
Correspondence: Nilton Carlos Machado, Pediatric Gastroenterology, Hepatology and Nutrition, Department of Pediatrics, Botucatu Medical School – UNESP, Av. Prof. Montenegro, Distrito de Rubião Junior, s/n, Botucatu, São Paulo, 18618-687, Brazil
Received: October 25, 2022 | Published: November 8, 2022
Citation: Carvalho MA, de Jesus CDF, Penatti DA, et al. Comparison of two self-report pain intensity scales in children and adolescents with chronic abdominal pain associated with Helicobacter pylori-dyspepsia and Irritable bowel syndrome. J Pediatr Neonatal Care. 2022;12(3):164-168. DOI: 10.15406/jpnc.2022.12.00474
Purpose: To evaluate pain intensity and the agreement between the Visual Analogue Scale (VAS) and Faces Pain Scale (FAS) in children/adolescents with Chronic Abdominal Pain (CAP) both in Irritable Bowel Syndrome (IBS) and Helicobacter pylori dyspepsia (HpD).
Methods: Single-centre, observational, cross-sectional study including 217 children/adolescents. Inclusion criteria: age (4-15 years); HpD diagnosis established with endoscopy and histopathological biopsies. IBS diagnosis based on Rome IV criteria. Exclusion criteria: chronic disorders (genetic, metabolic, cardiac, hepatic, renal diseases). In a standardized form, data was achieved, and children marked the "pain over the past month".
Results: The age of first symptoms, first visits, pain (epigastric, retrosternal, nocturnal pain, burning), vomiting, and anorexia were higher in HpD than in IBS children. The pain intensity was categorized as severe (7-10) for the majority of children both in FAS and VAS scales (p>.05). Also, analysis between IBS and HpD concerning sex, first child, age at first visit (≤10 y or >10y), overweight/obese, average BMI child, and the number of episodes of pain during the week (p>0.05). There was a positive and statistically significant correlation between FAS and VAS pain intensity in IBS (All children, male and female) and HpD group (only for All children). On Bland-Altman plots of VAS vs FAS, the 2SD values of differences between scales were: IBS (3.8) and HpD (3.4) group. The calculated limits of agreement (95% CIs) exceeded the a priori limits of acceptability for all measured parameters, indicating that the scales are not interchangeable.
Conclusions: Pain scales were, without difficulty performed, widely accepted and provided evidence that FAS and VAS are valid measures for assessing pain intensity in children with CAP. However, both VAS and FAS did not discriminate IBS from HpD, and the scales are not interchangeable.
Keywords:abdominal pain, pain measurement, irritable bowel syndrome, Helicobacter pylori, gastritis, dyspepsia, children
CAP, chronic abdominal pain; FAPDS, functional abdominal pain disorders; IBS, irritable bowel syndrome; HpD, helicobacter pylori-associated dyspepsia; VAS, visual analogue scale; FAS, facial affective scale; WHO, world health organization; BMI, body mass index; IQR, interquartile range
Chronic Abdominal Pain (CAP) is a common problem in children and adolescents. A meta-analysis of epidemiologic studies on abdominal pain noted a global pooled prevalence of 13.5%. It evidenced that most children seeking healthcare advice for their CAP suffered from Functional Abdominal Pain Disorders (FAPDs). Irritable Bowel Syndrome (IBS) was the most prevalent (8.8%) and considered the prototypical of FAPDs.1 Although IBS is a multi-symptom disorder characterized by the absence of biochemical, anatomical, or metabolic findings, abdominal pain is a predominant feature.
In contrast, non-ulcer Helicobacter pylori-associated dyspepsia (HpD) is one of the most common diagnoses in our outpatient clinic.2,3 Also, abdominal pain is the primary clinical manifestation of Helicobacter pylori infection in children, but it is not specific.2–4 Indeed, these two etiologies have distinct pathophysiological underlying mechanisms.5,6
On the other hand, pain is a complex, multidimensional phenomenon, and its assessment includes an estimation of the intensity and its impact on pain-related domains, such as emotional, physical, and social functioning.7 Accordingly, by age five years and older, most children can express pain verbally and indicate the severity using pain-rating scales if age-appropriate tools are used.8 Thus, pain intensity is likely the most accessible dimension to assess, and pain rating scales have a central place in clinical practice. Self-report approaches are acceptable for measuring pain,9 and many face scales were developed for measuring pain intensity in children.10,11 Currently, five measures of pediatric pain intensity have been recommended for use in systematic reviews or by expert panels,9,12 of which only 3, the Numeric Rating Scale, Visual Analogue Scale (VAS), and Faces Pain Scale (FPS), were the most mentioned.13,14
Aims
To evaluate the intensity of pain and the agreement between the Visual Analogue Scale and a Faces Pain Scale in children with CAP, both IBS and HpD.
The study was a single-centre, observational, cross-sectional study including consecutive cases of children/adolescents referred between 2017 to 2019 from the Brazilian Public Health System (SUS) seen for initial evaluation of CAP at Outpatient Pediatric Gastroenterology Clinic of Botucatu Medical School, Botucatu, Sao Paulo, Brazil. All children/adolescents were in the same geographic area. Inclusion criteria: CAP defined according to Apley and Naish15 and Von Baeyer & Walker;16 aged between 4-15 years; HpD diagnosis established with serology, endoscopy, and confirmed in a histopathological study of gastric biopsies.2,3 Diagnosis of IBS is based on Rome IV criteria.17 Exclusion criteria: chronic disorders (genetic, metabolic, immune, cardiac, hepatic or renal diseases, neurodevelopment delay, and previous surgery) and patients unable to self-report pain. The medical institutional review board approved this study. The parent or legal guardian consent to the study.
Procedures
The data extraction from a patient interview and electronic medical records was based on a standardized form that included information on demographics, clinical findings, and alarm symptoms and signs. Patients were stratified by sex (male vs female) and age (≤ 10 y vs >10 y), according to Riley et al.18 Diagnosis was performed based on a protocol established for CAP.19 Complete blood cell count, C-reactive protein, urinalysis, stool for ova & parasites, and Helicobacter pylori serology were done in all patients. Another diagnostic test was completed at the discretion of the gastroenterology team. The patients' final diagnoses were determined after four months of follow-up by two experienced pediatric gastroenterologists (MAC, NCM). They collaborated on the design, planning, and execution of the study. Afterwards, patients were allocated to the HpD and IBS groups. All data was continuously stored in a databank and entered into an Excel spreadsheet program (Microsoft, Redmond, WA). Data were entered by one author and checked by another author.
Pain evaluation
Patients were assessed for pain by the study's authors, and scores were documented in the medical record. Children mark the "pain over the past month"20 on two scales at the first visit: The VAS21 and the FAS.11,22 The VAS is a 10-cm line, anchored by verbal descriptors, with the endpoint 0 for "no pain" and 10 for "worst pain". Participants mark across a 10-cm line at a point corresponding to the pain intensity level. The distance in centimetres from the low anchor of the VAS to the patient's mark is a numeric index of pain severity.23 On the other side of the sheet, the FAS11,22 was evaluated. It consists of nine faces depicting varying levels of distress, ranging from no pain (far left face) to much pain (far right face). Children choose a face that appears similar when they have pain. Numerical values for faces vary from 0.4 to 9.7. The intensity of pain was: absence of pain (0), mild pain (1-3), moderate pain (4-6), and severe pain (7-10), both in FAS and VAS in a 0 to 10 numeric rating scale.20
Anthropometric data
Experienced pediatric nurses obtained anthropometric measurements of body weight (kilograms) and height (centimetres) according to World Health Organization guidelines.24 BMI (kg/m2) and z-score were evaluated according to de Onis et al.25 and WHO AnthroPlus.26 Each child was classified as Obesity (z-score >2), Overweight (z-score between 1 and 2), and, Normal BMI (z-score between -2 and +1). All data were adjusted for sex and age. Then the patients were stratified into two groups: Obesity/Overweight and Normal BMI.
Statistical methods
The analysis was performed using GraphPad Prism version 7.00 for Windows (GraphPad Software, San Diego, CA). Shapiro–Wilk tested the normality of data distribution. Continuous variables were expressed as the median and interquartile range (IQR) and analyzed by the Mann-Whitney test. Fisher's exact test analyzed the categorical data in count and per cent. Spearman's Correlation assessed associations between VAS and FAS pain scales. Results were converted into a numeric value of 0 to 100, the agreement between scores evaluated with the Bland-Altman method, and 95% lower and upper limits reported. We defined a priori the maximum limit of agreement at 2.0 mm, and a value of p <0.05 was considered significant.
The study evaluated pain intensity in a convenience sample of 217 children/adolescents with CAP. In Table 1, the first symptoms and first visit age; epigastric, retrosternal, nocturnal pain; burning, vomiting, and anorexia were higher in HpD than in IBS children. The prevalence of Obesity/Overweight was 23% and 27%, respectively, for IBS and HpD, with the non–statistical difference between groups.
Variable |
IBS (n=128) |
HpD (n=89) |
p value |
Median (IQR) or n (%) |
|||
Child characteristics |
|||
Age at first visit, years |
9.7 (7.2 - 11.0) |
10.1 (8.7 - 13.0) |
** |
Age at first symptoms, years |
7.2 (5.1 - 9.9) |
8.3 (6.8 - 10.8) |
* |
Duration of symptoms, months |
12 (6 - 36) |
12 (6 - 36) |
- |
Pain duration ≤12 months |
62 (48) |
50 (56) |
- |
Pain duration ≤10 months |
39 (30) |
30 (34) |
- |
Female sex |
87 (68) |
65 (73) |
- |
First-born child |
65 (51) |
38 (43) |
- |
Pain characteristics |
|||
Frequency (weekly) |
3.5 (3.5 - 14) |
3.5 (3.5 - 14) |
- |
Epigastric |
31 (24) |
77 (87) |
*** |
Periumbilical |
66 (52) |
8 (9) |
*** |
Retrosternal irradiation |
5 (4) |
44 (49) |
*** |
Burning type |
1 (0.8) |
43 (48) |
*** |
Nocturnal |
11 (9) |
40 (45) |
*** |
Vomiting |
37 (29) |
48 (54) |
*** |
Anorexia |
28 (22) |
46 (52) |
*** |
Nutritional status |
|||
z Weight/Age |
0 (-0.63 - 0.83) |
0.09 (-0.56 - 1.14) |
- |
z Height /Age |
-0.15 (-0.89 - 0.62) |
-0.15 (-0.56 - 0.82) |
- |
z BMI/Age |
0.04 (-0.63 - 1.00) |
0.44 (-0.69 - 1.07) |
- |
Overweight and Obese |
30 (23) |
24 (27) |
- |
Parental age, years |
|||
Mother |
33 (28 - 37) |
32 (29 - 37) |
- |
Father |
37 (32 - 41) |
37 (32 - 43) |
- |
Residence characteristics |
|||
Number of children |
2 (1 - 3) |
2 (1 - 3) |
- |
Number of persons |
4 (4 - 5) |
4 (4 - 5) |
- |
Number of rooms |
5 (4 - 6) |
5 (4 - 6) |
- |
Crowding index (person/room) |
0.8 (0.6 - 1.1) |
0.8 (0.6 - 1) |
- |
Table 1 Baseline characteristics of children with Irritable Bowel Syndrome and Helicobacter pylori associated dyspepsia
IBS, irritable bowel syndrome; HpD, helicobacter pylori associated dyspepsia; IQR, interquartile range; - not significant; *p<0.05; **p<0.005; ***p<0.0005; p value by Fisher’s exact test or Mann-Whitney test
Table 2 compares pain rating scales of children with IBS and HpD. The pain intensity evaluated with FAS or VAS was not statistically different between IBS and HpD groups concerning sex, first child, age at first visit (≤10 y or >10y), Overweight/Obese, Normal BMI child, and the number of episodes of pain during the week. Conversely, in Pain intensity/duration ≤12 months, HpD was higher than IBS children with booth FAS and VAS scales. The pain intensity was categorized as severe (7-10) for the majority of children I both in scales, with no statistical differences.
Variable |
FAS |
VAS |
||||
Median (IQR) or n (%) |
Median (IQR) or n (%) |
|||||
IBS (n=128) |
HpD (n=89) |
p |
IBS (n=128) |
HpD (n=89) |
p |
|
All children |
8.2 (7.8 - 9) |
8.2 (7.8 - 9) |
- |
7.6 (5.4 - 9.7) |
7.7 (6.5 - 9.4) |
- |
Pain scores |
||||||
0 |
0 |
0 |
- |
1 (1) |
0 |
- |
1-3 |
1 (1) |
0 |
- |
10 (8) |
2 (2) |
- |
4-6 |
23 (18) |
11 (12) |
- |
29 (23) |
17 (19) |
- |
7-10 |
104 (81) |
78 (88) |
88 (68) |
70 (79) |
- |
|
Sex |
||||||
Male |
7.8 (6.9 - 9.3) |
7.8 (7.8 - 8.8) |
- |
7.6 (5.3 - 9.3) |
7.6 (5.1 - 9.3) |
- |
Female |
8.2 (7.8 - 9) |
8.2 (7.8 - 9) |
- |
7.7 (5.6 - 9.9) |
7.7 (7.4 - 9.4) |
- |
First child |
||||||
Yes |
8.2 (7.8 - 9.7) |
8.2 (7.8 - 9) |
- |
8 (6 - 9.7) |
7.8 (7.6 - 10) |
- |
No |
7.8 (7.8 - 9) |
8.2 (7.8 - 9) |
- |
7.6 (5.2 - 9.7) |
7.6 (5.2 - 8.3) |
- |
Age |
||||||
≤10 years |
8.2 (7.8 - 9) |
8 (7.8 - 9) |
- |
8 (5.1 - 9.9) |
7.7 (6.6 - 10) |
- |
>10 years |
8.2 (7.8 - 9) |
8.2 (7.8 - 9) |
- |
7.6 (6 - 9.2) |
7.6 (5.5 - 8.3) |
- |
Pain intensity/duration |
||||||
≤12 months |
7.8 (7.8 - 9) |
8.2 (7.8 - 9.7) |
* |
7.5 (5.0 - 9.0) |
7.7 (7.4 - 10) |
* |
>12 months |
8.2 (7.8 - 9.7) |
7.8 (7.8 - 8.2) |
* |
8 (6.3 - 10) |
7.6 (5.1 - 8.2) |
- |
Nutritional status |
||||||
Overweight/Obese |
8 (7.8 - 9) |
8.2 (7.8 - 9.7) |
- |
7.8 (6.6 - 9.6) |
7.6 (6.5 - 9.3) |
- |
Normal |
8.2 (7.8 - 9.7) |
8.2 (7.8 - 9) |
- |
7.6 (5.3 - 9.7) |
7.7 (6.0 - 9.9) |
- |
Weekly pain frequency |
||||||
≤3.5 |
7.8 (7.8 - 9) |
8.2 (7.8 - 9.7) |
- |
7.6 (5 - 9.5) |
7.7 (6.7 - 9.5) |
- |
>3.5 |
8.2 (7.8 - 9.7) |
8.2 (7.8 - 9) |
- |
8 (6.6 - 9.8) |
7.7 (5.2 - 9.5) |
- |
Table 2 Comparison of children with Irritable Bowel Syndrome and Helicobacter pylori associated dyspepsia by pain rating scales
IBS, irritable bowel syndrome; HpD, helicobacter pylori associated dyspepsia; IQR, interquartile range; FAS, facial affective scale; VAS, visual analog scale; - not significant; *p<0.05; p value by Fisher’s exact test or Mann-Whitney test
Table 3 displayed a positive and statistically significant pain intensity correlation between FAS and VAS scales for All children, Male and Female, in IBS and only for All children in the HpD group. On Bland-Altman plots of VAS vs FAS, the 2SD values of differences between scales were respectively 3.8 for the IBS and 3.4 for the HpD group. The calculated limits of agreement (95% CIs) exceeded the a priori limits of acceptability for all measured parameters, indicating that the scales are not interchangeable. The percentages of all children with differences of more than 2 points between scales were respectively 22.5% and 25%.
|
FAS vs VAS |
||||
Spearman correlation |
Bland-Altman test |
||||
|
n |
r |
p |
MD±SD |
LA 95% |
IBS |
|||||
All children |
128 |
0.60 (0.47 - 0.70) |
*** |
-0.7±1,9 |
-7.7 |
Male |
41 |
0.52 (0.25 - 0.72) |
*** |
-0.7± 2.0 |
-8.1 |
Female |
87 |
0.63 (0.48 - 0.74) |
*** |
-0.7±1.9 |
-7.6 |
HpD |
|||||
All children |
89 |
0.43 (0.20 - 0.61) |
*** |
0.6±1.7 |
-6.8 |
Male |
24 |
0.55 (0.14 - 0.80) |
* |
-0.9± 1.7 |
-6.7 |
Female |
65 |
0.35 (0.05 - 0.59) |
* |
-0.4± 1.7 |
-6.9 |
Table 3 Pain intensity correlations and agreement between Facial Affective Scale and Visual Analog, Scale for children with Irritable Bowel Syndrome and Helicobacter pylori associated dyspepsia
IBS, irritable bowel syndrome; HpD, helicobacter pylori associated dyspepsia; FAS, facial affective scale; VAS, visual analog scale; *p<0.05; ***p<0.0005; r, correlation coefficient; MD, mean difference; LA 95%, limits of agreement of 95%
The current pre-pandemic COVID-19, single-centre, a cross-sectional study evaluated the intensity of pain and the agreement between the VAS and FPS in children with CAP. HpD children were significantly younger at the age of first symptoms and age at the first visit and more symptomatic (with retrosternal pain, burning, pain that awakens the child, vomiting, and anorexia). However, pain intensity assessed by VAS and FAS did not discriminate the subgroups of IBS and HpD children and are valid measures for assessing pain in children with CAP, but not interchangeable scales.
There has yet to be a consensus on how pain intensity changes classifications from mild to moderate or moderate to severe in pediatric chronic pain.27 However, Powell et al.28 determined that the minimum clinically significant difference in VAS pain scores for children aged 8 to 15 years (on a 100-mm VAS scale) is 10 mm (95% confidence interval, 7 to 12 mm). The current study noted subjects' tendency to cluster data around 2 to 3 points for FAS and VAS (median between 7 and 8, and IQR between 6 and 9) according to previous studies.11,29,30 Also, a positive and highly significant correlation between the two scales for all IBS and HpD children. Former studies demonstrated that it was highly correlated with VAS31,32 and validated over time.33,34 Given the lack of agreement between FAS and VAS in the current study, it is advisable using the same scale on an outcome measure in research or pediatric chronic pain clinics.32
The present study has some limitations. First, children were enrolled in a tertiary abdominal pain clinic, and the findings may not be generalizable. Second, pain scales were not re-applied to analyze treatment response and efficacy. Third, the study employed a unidimensional assessment tool. Current guidelines suggest using a multidimensional tool that combines behavioural, contextual, and physiologic information available to the subjects describing their perceptions. Fourth, psychological and social factors, including fear, knowledge, and previous experiences of pain, culture and learning, were not evaluated.8 Some strengths: first, there was consistency and uniformity in demographics, anthropometrics, and clinical data collection using a well-defined form. Second, non-ulcer Helicobacter pylori gastritis was established with serology, endoscopy, and histopathological analysis. Third, pain intensity scales were easily administered, widely accepted, and with no stressful conditions during the first visit.
Chronic pain is a biopsychosocial phenomenon resulting from the dynamic integration of biological, psychological and socio-cultural contexts. Therefore, these factors are not independent and interact in various ways to shape the child's experience of pain. Thus, CAP is challenging to manage, and comorbid symptoms and behaviours can add to overall suffering and discomfort, dramatically reducing the quality of life.7 Pain is considered the "fifth vital sign" in medical care.35 Consequently, pain assessment is vital for effective pain management. Many single-item pain measures are used for this purpose, and unidimensional pain scales routinely assess pediatric chronic pain. The most commonly used pain scales include VASs and FPS,8,36,37 as used in this study. VAS is considered appropriate for children above seven37 and FPS for above four34 years. The VAS is conceptually complex and requires translating a subjective sensory experience into a linear format.38 However; VAS is the gold standard for a child older than six. Markedly, children generally prefer FPS when the choice is offered.9,39,40
In conclusion, pain scales were, without difficulty performed, widely accepted and provided evidence that FAS and VAS are valid measures for assessing pain intensity in children with CAP. However, both VAS and FAS did not discriminate IBS from HpD, and the scales are not interchangeable.
Carvalho MA contributed on the conception of the work, analysis and interpretation of the data, drafted the initial manuscript and revised the article critically; Carine Dias Ferreira de Jesus, Debora Avellaneda Penatti, Juliana Tedesco Dias performed the collection of the data and drafted the initial manuscript; Machado NC contributed on the conception of the work, analysis and interpretation of the data, drafted the initial manuscript and revised it critically.
None.
None.
The authors declare no conflict of interest.
©2022 Carvalho, et al. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.