Incontinentia pigmenti burden scale: designing a family burden questionnaire
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Incontentia pigmenti (IP) is a rare multisystem disorder of ectodermal origin comprising skin, dental, ocular and central nervous system features. Symptomatic treatments are adapted to each family according to the patient’s disability. Due to its rarity, the family IP burden in its broadest sense (psychological, social, economic and physical) has not yet been evaluated.
To design a questionnaire allowing assessing the family burden of IP (F’BoIP).
A questionnaire was developed using a standardized methodology for designing quality of life questionnaires according to the following steps: conception, development, and validation. A multidisciplinary working group was designed, including experts in questionnaire development, dermatologists specialised in IP patient care and representatives of the French IP association. A cultural and linguistic validation into US English was conducted, based on the original French version.
A 20-item conceptual questionnaire was generated. Subsequent confirmatory analyses produced a 20-item questionnaire grouped into four domains, demonstrating internal consistency (Cronbach’s alpha: 0.93), reproducibility and high reliability. The F’BoIP questionnaire significantly correlated with other validated questionnaires: Family Dermatology Life Quality Index (F-DLQI), Perceived Stress Scale (PSS) and SF-12 mental and SF12 physical scores, indicating good external validity.
The F’BoIP questionnaire is the first specific tool to assess the family burden of IP and can be used by both family members of IP patients and by health care professionals. It is a valuable tool which evaluates medical and nonmedical strategies to improve the daily life of families affected by this orphan disease.
KeywordsIncontinentia pigmenti Disease burden Quality of life Orphan disease
Bayesian information criterion
Central nervous system
European Medicine Agency
Food and Drug Administration
Family-Dermatology Life Quality Index
Institut für Qualität und Wirtschaftlichkeit im Gesundheitswesen
Mental composite score
National Institute for Health and Care Excellence
Physical composite score
Perceived Stress Scale
Quality of Life
Root mean square error of approximation
IP, or Bloch-Sulzberger syndrome, is a rare multisystem disorder of ectodermal origin comprising skin, dental, ocular and central nervous system features such as seizures, spastic paralysis, microcephaly and intellectual disability. IP is an X-linked dominant genodermatosis. It affects exclusively female patients and is usually lethal in utero in males . The condition is caused by a genetic mutation in the IKBKG gene located on the X chromosome . This gene is known as nuclear factor-kappa B (NF-kappaB) essential modulator (NEMO), required for activating the transcription of factor NF-kappaB. The NF-kappaB pathway plays a central role in the expression of numerous genes pertaining to the immune system, including those involved in embryonic development and the development of bone, skin, mammary glands and the central nervous system (CNS). NF-kappaB activation is defective in IP cells.
Skin manifestations are the first diagnostic signs observed at birth or during early life. They are subdivided into four stages, comprising blisters, hyperkeratotic lesions, hyperpigmentation and, lastly, atrophic lesions . These skin lesions follow Blaschko lines, virtual lines thought to represent the clonal boundaries of cells migrating from the neural crest. While lesions resolve spontaneously, residual hyper- or hypopigmentation can persist throughout life.
Clinical IP diagnosis is based on major and minor criteria associated with the skin lesions . In addition, minor criteria include extracutaneous disease lesions [3, 4]. Its severity is related to ocular or neurological impairment. While no specific treatment is available, symptomatic measures are adapted to each family, according to the patient’s disability. Scientific literature has reported about 1000 cases of IP worldwide ..
To date, individual patient disease burden has already been evaluated in many skin diseases, such as psoriasis, infantile haemangioma, hereditary ichthyoses, atopic dermatitis, vitiligo, albinism and palmoplantar keratoderma [5, 6, 7, 8, 9, 10, 11].
But, burden and reduced quality of life (QoL) are not only limited to patients, family members and caregivers may also be impacted, and in some situations the QoL of a partner or a parent may even be more impaired than that of the patient. As such, family members and caregivers may experience a major impact on their lives such as physical and mental exhaustion, social disruption, marital problems and financial implications [12, 13].
However, a few instruments to assess the impact of skin diseases on patients’ family members, such as the Family Dermatology Life Quality Index (F-DLQI), have been developed to date . Existing instruments to assess family burden in dermatology have been recently reviewed by Sampogna et al. .
According to our literature search, no specific instrument exists to assess the burden and impact on QoL of parents of IP patients. However, such a tool would be useful for both parents of IP patients and clinicians in charge of patient management. The instrument could, to begin with, serve as a way of describing the IP parents’ perceptions. Secondly, it could be used as a tool in the follow-up of any changes in the patient’s medical and non-medical care. As part of its research activities, the French national network of expert centres for rare skin disorders has developed three different questionnaires for rare skin diseases [7, 10, 11].
The objective of the present study was to develop a self-administered questionnaire in order to assess the individual family burden in an IP patient cohort (F’BoIP). The second objective was to ensure that this questionnaire could be used by as many IP families as possible, following cultural and linguistic validation into US English based on the original F’BoIP.
Material and methods
The self-administered F’BoIP questionnaire was designed using a standard methodology for designing QoL questionnaires . The methodology was based on three distinct phases: conception, development and validation. To ensure the questionnaire’s validity, a multidisciplinary working group was created including experts in the design and development of questionnaires, such as healthcare professionals (physicians and public-health specialists). Moreover, three “expert parents”, active members of the French Association of IP Patients, participated in this working group.
The questionnaire was built in a question and answer format. Response modalities were determined via expert consensus and took the form of a 7-point Likert scale, often used in self-completion questionnaires: “never” (0), “rarely” (1), “sometimes” (2), “often” (3), “very often” (4), “constantly” (5) and “not concerned” (0). To prevent confusion with any changes in perception due to symptoms related to comorbidities, the majority of questions included the wording “IP of your child.”
During the conceptual phase, a series of interviews with dermatologists, patient-reported outcome (PRO) experts and IP parents was conducted to comprehensively collect the parents’ perceptions and complaints as an initial wording report. Based on this initial wording report, the working group drew up a list of items that were reformulated as simple questions that would be easily understood. Nine interviews of patient family members (both parents, or only mother or father) were then conducted. Patients were selected in collaboration with the French association of IP patients which only proposed the questionnaire to parents of previously diagnosed IP patients. This ensured broad recruitment and the guarantee of diversity in patients in terms of geographical location, as well as age and sociological status. Thus, a semi-structured questionnaire was built. It discussed specific themes using closed-ended questions with a choice of predetermined answers. The final choice of questions was made by the working group who analysed the initial wording report semantically. The wording of each question was examined, thereby allowing regrouping questions if their similarities were proved too strong.
During this phase the conceptual questionnaire was administered to a random sample of parents of IP patients (n = 114). This was followed by an exploratory factor analysis in order to reveal latent constructs, assigning each item to its respective domain or dimension.
A principal component analysis using a varimax orthogonal rotation was performed, to determine to which domain or dimension each question belonged . Whenever questions could be linked to several dimensions, questions were allocated to the dimensions deemed to be the most semantically relevant by the expert working group.
To evaluate the questionnaire’s internal consistency, the homogeneity of the items in each dimension was tested using Cronbach’s alpha coefficient . Scores in the higher ranges (>0.7) generally suggested that the items measured the same entity, indicating good homogeneity.
To demonstrate the questionnaire’s unidimensionality, a higher order factor confirmatory analysis was performed, aiming to confirm that dimensions could be combined into one single score. The model’s goodness-of-fit was assessed using several criteria, the Bentler comparative fit index and Bentler-Bonett non-normed fit index . Criteria for a model’s goodness-of-fit were defined as a Bentler comparative fit and Bentler-Bonett non-normed fit index both >0.90. The root mean square error of approximation (RMSEA) was to be about 0.05 or at the very least <0.08, with 0.05 contained within the confidence interval.
To determine the questionnaire’s external validity, all participants were asked to complete three validated self-administered questionnaires: a 12-Item Short Form Health Survey (SF12), a F- DLQI questionnaire and a PSS [12, 18, 19].
The SF12 is a short version of the SF-36, a well-known quality of life tool. Based on 12 questions, a physical composite score (PCS) and mental composite score (MCS) were calculated.
The FDLQI is a questionnaire designed for adults (more than 16 years of age), family members or partners of patients (of any age) with any skin disease. The F-DLQI represents the sum of all scores (0–30); results can equally be expressed as percentages (0–100%).
The PSS, developed by Cohen et al. in 1983, is the most widely-used psychological instrument for measuring the perception of stress. Composed of 10 items, rated from “never” to “often”, the PSS measures the degree to which situations in one’s own life are perceived as stressful. The total score ranges from 10 to 50; the higher the score, the higher the stress.
Pearson correlation was calculated to assess the validity between the F’BoIP and the three other questionnaires.
All data were analysed using SAS software Version 9.4 (SAS Institute, Cary, NC, USA) for Windows, with a significance level set at 0.05.
To assess reproducibility, test-retest analyses were carried out. Participants answered the questionnaire once and then again after a 10 to 12-day interval. Using these means, answers obtained were compared and the reliability of measurements confirmed.
Translation, cross-cultural adaptation and cognitive debriefing
The validated methodology was applied to generate a US English-language version, according to the recommendations of the ISPOR task force . This process, comprising a meticulous 9-step procedure, refined the translation while taking into account subtle nuances of the source document.
Principles of Good Practice for the Translation and Cultural Adaptation Process for Patient-Reported Outcomes (PRO) Measures 
Evaluation of the source text from a linguistic and cultural point of view including definition of concepts
Forward translation into the required target language by two independent translators
Comparison of the two forward translations to provide the best adapted and to produce a draft versions of the text
Translation of the draft forward translation back into the targeted language without reference to the original language
Back translation review
Comparison of the original text and the back translation to verify if changes are required to the draft forward version
Analysis and implementation of back translation review report
Analysis of the back translation review report to verify if changes are required to draft forward version
Clinical review and cognitive debriefing
Review of cognitive debriefing or clinical review results
Review of results from the cognitive debriefing or clinical review to identify translation modifications necessary for improvement
This phase involved IP patients’ parents who expressed and shared their perceptions and complaints regarding their children’s IP. The research resulted in an initial wording report. Several exchanges and one-to-one discussions between IP dermatologists, sociologists and experts in healthcare-related outcomes contributed to further consolidating this initial verbatim report. A 21-item questionnaire was then drawn up, thereby defining the conceptual questionnaire.
Socio-economic status and age of parents, disease manifestations and management details of IP-affected children
One of the parents with IP
Living in a couple
Average parents’ age
41.7 ± 12.8
High income group
Low income group
Higher education qualification
100% health insurance cover
Diagnosis made by a dermatologist
Satisfied overall with care provided
Satisfied with medical care provided by your physician
Followed by an ophthalmologist
Followed by a psychologist
Followed by a speech therapist
Followed by an occupational therapist
Followed by a massage therapist
Attended a therapy education programme
Contact with an association
In 26 of all cases, the mother was affected and in 7 cases a brother or a sister. The different scores were calculated for both groups: the 26 families where one of the parents was affected by IP compared to the 35 families with no affected parents. However, the sample was too small to show any significant difference. QoL was slightly more impacted if one of the parents was affected; in this group also stress, evaluated by the PSS questionnaire, appeared somewhat more pronounced.
Comparison of mean scores of newly developed F’BoIP questionnaire compared to F-DLQI, stress evaluated by PSS, and SF12 Mental and Physical dimension
SF12 Mental dimension
SF12 Physical dimension
32.31 ± 19.28
6.62 ± 8.51
28.48 ± 8.34
50.64 ± 9.52
39.90 ± 11.83
N = 61
Parents not affected
33.83 ± 18.66
6.35 ± 8.57
27.00 ± 9.07
49.61 ± 9.39
42.04 ± 12.66
N = 35
30.27 ± 20.26
7.00 ± 8.59
30.58 ± 6.81
52.10 ± 9.71
36.86 ± 10.04
N = 26
Exploratory factor analysis
Dimension 1, with eight questions regarding social life and family life
Dimension 2, with six questions regarding professional life and renunciation
Dimension 3, with five questions regarding daily life
Dimension 4, with two questions regarding economic impact
Loading of questions on factors after rotation
The confirmatory analysis showed that the question “Have you ever been affected by the looks others give your child because of his/her IP?” was non-relevant. This question was therefore removed, resulting in a final questionnaire of 20 items, grouped into four dimensions. Thus, only Dimension 1 was modified from eight to seven questions.
Model assessment parameters
Synthesis of adjustments made
Higher order factor criteria
Ratio of chi-sq to degrees of freedom
Pr > Khi-2
Goodness of fit index (GFI)
Adjusted goodness of fit index (AGFI)
About 0.05 and at the very least under 0.08.
Inferior limit of the 90% RMSEA confidence interval (CI)
Superior limit of the 90% RMSEA confidence interval (CI)
Akaike information criterion
The lowest value possible of the models tested
Bentler comparative fit index
Bentler-Bonett non-normed index
Cronbach’s alpha coefficient reached 0.93 for the entire questionnaire, reflecting its excellent internal coherence. Moreover, intra-dimensional coherences showed good reliability (α > 0.72).
Correlations between scores
Pearson correlation coefficients, N = 58a
Probability > |r| under H0: Rho = 0
SF12 mental score
SF12 physical score
SF12 mental score
SF12 physical score
A closer correlation was expected and reached with the F-DLQI questionnaire and the PSS questionnaire (specific instruments) than with SF12 (generic instrument). Furthermore, a correlation with the F-DLQI, specific to dermatology, proved to be the closest.
A greater correlation was expected and shown with the mental dimension of SF12 than with the physical dimension. Indeed, the physical dimension has been affected to a limited extent as most of the families were quite young. Thus, QoL impairment concerned more a psychological fatigue rather than a physical fatigue.
The test-retest reliability was assessed, based on test results from 20 subjects undergoing testing on both Day 0 and Day 10. Results demonstrated a very good reproducibility, with an intra-class correlation of each dimension exceeding 0.85 for each domain.
Cognitive debriefing, translation and cross-cultural adaptation
Cognitive debriefing did not result in any changes regarding the questions’ wording. The original French version of the F’BoIP questionnaire was translated and underwent linguistic and cultural validation into US English.
The total F’BoIP score was obtained by summing up scores for each of the 20 questions as defined in the aforementioned method description, with “never” or “not applicable”, which scored 0, “rarely” 1, “sometimes” 2, “often” 3, “very often” 4, and “constantly” 5.
Final validated version of the IP Family Burden questionnaire
Score from 0 to 5
Have you ever felt that it is unfair when thinking about your child having incontinentia pigmenti?
Have you noticed family tension due to your child’s incontinentia pigmenti?
Have you noticed marital problems due to your child’s incontinentia pigmenti?
Have you been embarrassed by the glances of others due to his/her incontinentia pigmenti?
Due to your child’s incontinentia pigmenti, have you felt the need to keep to yourself?
Have you experienced a feeling of guilt due to your child’s incontinentia pigmenti?
Have you been forced to reconsider your future plans because of your child’s incontinentia pigmenti?
Have you ever hesitated to buy any medication that is not covered by your insurance?
Have you had to give up dental care due to your child’s incontinentia pigmenti?
Have you behaved in a neglectful way toward your other children because of your child’s incontinentia pigmenti?
Have you been distracted at work because of your child’s incontinentia pigmenti?
Have you needed to miss work to take your child to the doctor?
Have you had to stop working due to your child’s incontintentia pigmenti?
Do you think you have “overprotected” your child due to his/her incontintentia pigmenti?
Has your child’s incontintentia pigmenti upset your daily life?
Has facing the required care support (psychologists, orthoptics, psychomotor therapy) made you feel mentally drained?
Does the care that you have to give tire you out?
Have you been hurt by the teasing your children have experienced from other children?
Have you ever had the impression that your child’s incontintentia pigmenti is increasingly expensive?
Have you had to dedicate a portion of your budget to cover the costs of care for your child?
Skin diseases do not only psychosocially affect the patient, but also impact the entire family’s functioning. Today, the individual disease burden is increasingly investigated. “Individual burden” accounts for the broadest aspects of disease-related disability, covering psychological, physical, social and economic factors, simultaneously taking into account QoL, community integration, organization of everyday life, as well as medical resource consumption. Using questionnaires may allow evaluating this overarching burden, especially among patients with a particular disease [5, 6, 7, 8, 9, 10, 11].
IP impacts the family’s lifestyle and quality of life heavily. As a result, family members have to reorganize their life, overcome the stress of diagnostic procedures and integrate the notion of chronicity and absence of curative treatments into their daily life.
Based on advances made in QoL research over the last decades, health-care professionals and regulatory agencies, such as the US Food and Drug Administration (FDA) and the European Medicine Agency (EMA), currently face complex issues related to the development of health-related quality of life claims for both product labelling and promotion . In this context, Leidy et al. generated recommendations for the healthcare industry to ensure that all health-related QoL claims are based on rigorously-designed studies, with appropriate methodology and instruments . Development in the clinical research field has led to the widespread use of questionnaires and this trend is most likely to continue in the near future. The reason for this is the increasing relevance of data that are both closer to clinical practice and increasingly needed to achieve market access. At present, QoL, patient wellbeing, and patient-centred outcomes are requested by reimbursement agencies, such as NICE in the UK and IQWIG in Germany .
To our knowledge, no specific instrument exists that is able to assess the overall burden of parents of children with IP. This paper provides an easy-to-use questionnaire which assesses the individual disease burden of parents of IP patients. The questionnaire is currently available in French and US English and can be translated and culturally and linguistically validated into other languages, such as German, Spanish, etc. The 9-step methodology required to generate linguistically-validated and cross-culturally-adapted F’BoIP versions into other languages is well-established. With its 20 items and six possible answers for each question, our questionnaire is relatively short, understandable and easy to use. F’BoIP is a robust tool with an internal consistency exceeding the minimum reliability criterion of 0.90 for individual analysis.
The main limitation of our study is the relatively small sample size of 61 parents. However, as IP is a rare disease, a small sample size is not surprising.
We believe that the objective evaluation of the IP burden will enhance communication between patients, parents and healthcare providers, thereby improving information transfer and creating a real opportunity for practitioners to gain better understanding of certain issues brought up by the patients or their families.
Moreover, F’BoIP may allow the development of new patient management approaches and the improvement of existing patients’ health, care and daily-life.
F’BoIP demonstrates feasibility, validity and discriminant reliability. It can therefore be used to understand the multidimensional nature of IP better, in addition to the individual burden of the parents of patients suffering from this condition. Moreover, it may play a role in the decision-making process. Additional research to develop a version of the instrument for children to use in the future is currently ongoing.
The authors thank the patient association for helping and supporting this project. Moreover, the authors acknowledge the editing assistance of Karl Patrick Göritz, SMWS Scientific and Medical Writing Services, France.
CT, SH and CB conceived the study, participated in its design and coordination and helped drafting the manuscript. CB, and CT participated in the design of the study and conceptual phase. MB performed the statistical analysis. All authors read, commented on, and approved the final manuscript.
The project has received public funding from Fimarad (French network of rare skin disorders, Necker Hospital, Paris, France).
Ethics approval and consent to participate
The questionnaire construction was carried out as part of the RADICO-FARD project, which obtained a favorable opinion from the Committee for the Protection of Individuals (CPP Ouest V, Rennes) on July 31, 2017.
The questionnaire was proposed by the patient association, and at no time did the authors of the project or the persons in charge of the analgesia statistics know the identity of the responders.
There was no way to make a connection between the answers obtained and the person who answered the questionnaire.
The respondents were provided with an information sheet before giving their consent. This information sheet as well as the consent form clearly explained the purpose of the project and guaranteed the anonymity of the responses.
Consent for publication
The authors declare that they have no competing interests.
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