Abstract
Self-management and independence behaviors are associated with improved health conditions common to spina bifida such as skin integrity and bowel and bladder management. While most children with spina bifida ultimately achieve basic self-care behaviors, (e.g., dressing appropriately, planning activities with peers, or cooking pre-planned meals), they often lag 2–5 years behind their typically-developing peers in these activities [1]. Valid and reliable condition-specific assessments of self-management and independence are critical to optimizing outcomes for this population. Partnerships among parents, clinicians, and youths with spina bifida are essential to implementing tailored interventions based on these assessments. The guidelines delineated in this article are informed by current self-management research for people with spina bifida and offer recommendations to promote self-management and independence across the lifespan.
Keywords: Myelomeningocele, spina bifida, self-management, independence, guidelines, neural tube defects
1. Introduction
Research suggests that more than 75% of individuals born with spina bifida [SB] will survive into adulthood [2] with evidence underscoring the critical importance of self-management in extending life expectancy. According to the Guidelines for the Care of People with Spina Bifida [3]:
Self-management for youth and emerging adults with Spina Bifida is an active daily and flexible process in which youth and their parents share responsibility and decision-making for managing their condition, health, and well-being through a wide range of knowledge, attitudes, activities, and skills. The goal of this increasing responsibility is to develop the self-management behaviors needed to achieve independence and transition to adulthood and independent living [4, 5].
Self-management may also be thought of as the interaction of health behaviors that affected individuals and families engage in to care for a chronic condition [6]. Within the SB population, effective self-management is particularly important for preventing co-morbidities and secondary complications such as skin breakdown, renal dysfunction, and bladder and bowel incontinence [7, 8]. Self-management is also central to a successful transition from adolescence into emerging adulthood, participating fully in society, and combating vulnerability, stigma, and discrimination. SB is a congenital condition; therefore the building blocks of self-management must begin early in childhood and in partnership with families and multi-disciplinary providers [9]. Therefore, these guidelines begin in infancy and progress through adulthood.
Child autonomy provides a critical foundation for developing self-management and independence. For all children, autonomy begins early and is fostered by opportunities to make choices and to develop a sense of mastery. Most children with SB ultimately achieve basic self-management and independence behaviors (e.g., dressing appropriately, planning activities with peers, or cooking pre-planned meals) yet often lag 2–5 years behind their typically-developing peers in these behaviors [1]. This gap may be due to the child’s difficulties performing common everyday motor and processing activities in efficient and independent ways [1]. Adaptation of performance and initiation of new steps may be especially challenging [10].
Social skills in children are also important building blocks for independence. Many children with SB need assistance building adaptive social behaviors in peer interactions, specifically basic social skills such as reading social cues, clarity of thought, and collaboration [10]. Monitoring self-management learning is needed for all with cognitive functioning challenges, especially those with executive functioning, inattention, and working memory issues [11, 12, 13, 14, 15]. Educational programs in the home, school, and broader community that offer opportunities to practice new behaviors are critical.
Youth with SB often do not enter adolescence with a comprehensive knowledge base of how to self-manage their condition (i.e. watching for signs of skin breakdown, bowel problems, shunt failure, and urinary tract infections) yet most develop this knowledge before age eighteen [1, 4, 16]. Advanced self-management behaviors for community living (i.e., managing a bank account, cooking independently) are typically achieved by peers without complex disabilities by age 18, but not as commonly by individuals with SB [1]. It is not clear if these difficulties reflect a delay in development for youth with SB or are due to a lack of expectations and support in the home, school, health system, or broader community. However, research suggests healthy family functioning characterized by open communication and shared decision-making is related to more optimal self-management outcomes across all developmental stages [13, 16].
Since there is evidence that responsibility in the home (e.g., chores and general decision-making) promotes self-management and skill-building, individuals and families should be encouraged to expand the range of everyday living skills and responsibilities for youth with SB [1, 16, 17, 18, 19, 20, 21]. These findings are complicated by longitudinal studies indicating that older school-age children with SB perceive themselves as being more independent relative to parent assessment [21]. Moreover, while health care providers expect school-age and older children to perform self-management behaviors related to bladder programs, bowel programs, skin checks, and prevention of other secondary conditions [22], older children have reported that self-catheterization and bowel programs were a challenge and often required parent involvement [4]. In addition, both the families and children have had difficulty carrying out diet recommendations, bowel programs, and skin care [23]. Thus, tailored interventions are needed to support growth in these areas [23].
Adolescents with SB transitioning to emerging adulthood are generally poorly prepared to self-manage their condition or live independently and are therefore at risk for preventable secondary conditions such as skin breakdown and UTIs [24]. This vulnerability appears to persist into adulthood [25]. Other research has identified associations between lower self-management behaviors and higher hospitalization rates in this population [7, 26]. However, there is evidence that improved self-management in young adults is associated with decreased depressive symptomology [27]. In addition, there is evidence in other conditions such as asthma that increased self-management improves health outcomes and healthcare utilization [28, 29, 30, 31]. Most adults with SB over 18 years of age have not achieved optimal independence milestones in education, employment, and independent living [32]. However, they were reported to have higher independence than those with other severe conditions such as fragile X syndrome or muscular dystrophy [33].
Self-management interventions for youth with SB and other chronic health conditions generally show significant improvement in at least one area, although a short workshop-based intervention for older children with SB yielded no significant differences in intervention and control groups [34, 35]. Family-oriented self-management interventions may be most effective in younger adolescents [36]. Camp-based psychosocial interventions promoting skills-development in goal-setting and problem-solving have shown promise in developmentally-diverse samples of children, adolescents, and adults with SB [11, 37]. Another intervention using a problem-solving model combining education and home/community practice similarly improved perceived family stress associated with SB condition management but not youth self-management [36]. Rehabilitation interventions in young and middle-aged adults have improved all aspects of self-management and independence, with moderate- to large-effect sizes including self-efficacy, management of bowel and bladder incontinence, cognitive function, and psychosocial symptoms [8, 26]. Although tested mostly in adults, technology-based interventions hold promise for expanding self-management behaviors in youth as well [20, 38, 39, 40, 41, 42].
1.1. Guidelines, goals and outcomes
The goals and desired outcomes of the Self- Management and Independence Guidelines were developed to be both practical and aspirational.
1.1.1. Primary outcomes
The aspirational objectives of these guidelines were to improve our developmental methodology to facilitate children and adults with spina bifida to:
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Perform effective self-management behaviors at the highest level of their abilities.
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Achieve optimal independent living and employment, as well as maximal participation in society.
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Develop autonomy, responsibility, and other foundational skills for self-management and independent living.
1.1.2. Secondary outcomes
The guidelines address practical goals to achieve these aspirational objectives, including:
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Interventions that address the foundational skills necessary for complex self-management and independence behaviors are introduced throughout the lifespan, as appropriate.
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Targeted foundational skills include executive functioning skills, self-efficacy, self-regulation, and engaging in social activities.
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Self-management and independence goals are evaluated yearly with the family, child, adolescent, and adult.
1.1.3. Tertiary outcomes
By supporting development of these important self-management and independence skills, the guidelines aim to promote independent behaviors and activities of adolescents and adults with SB, including:
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Adults over 18 with SB who have a guardian responsible for their health care perform self-management behaviors in the areas of medication management, prevention of complications, implementation of bladder and bowel programs, skin surveillance, and have the ability to communicate their findings to their guardians and/or health care providers at their highest level of ability.
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Adults over 18 with SB who do not need a guardian are fully responsible to self-manage their condition and independence (e.g., making appointments, ordering medications, arranging for transportation, conducting basic living skills like cooking and doing the laundry, managing money, managing insurance, and communicating with their health care provider).
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Individuals with SB interact effectively with family, health care providers, and others in the external environment in an independent manner.
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Table 2, continued | |||
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| Age group | Guidelines | Evidence | |
| 6–12 years11 months | 4. | Serve as a resource to school systems regarding transportation, learning skills, health issues, and development of self-management skills. | Clinical consensus |
| 5. | Emphasize positive attitudes, self-esteem, assertiveness, sell-efficacy, and self-empowerment. | Clinical consensus | |
| 6. | Assess peer relationships and encourage peer social involvement. | Evidence [4, 10]Mental Health Guidelines [62] | |
| 7. | Assess for potential patient, family, or environmental barriers to developing autonomy and independence (including family stress and conflict) and address in action plan. | Evidence [21, 36, 58] | |
| 8. | Assess bladder and bowel management programs for eventual independent self-management. | Evidence [66] | |
| 9. | Consider using an age- and condition-appropriate assessment instrument especially if the child has executive-functioning impairments (Table 3). | Evidence [1, 12, 15, 59, 60, 61] | |
| 10. | Discuss with parents the need to help their child develop basic money management skills [1]. If the child has an Individualized Educational Plan (IEP), encourage parents and the school to include money management skills in the child’s IEP. | Evidence [1] Clinical consensus | |
| 11. | Encourage families to facilitate their child’s language performance by creating intellectually- and culturally-enhancing activities in the child’s typical environment. | Evidence [67] | |
| 12. | Set beginning expectations for independent living. | Clinical consensus | |
| 13. | Encourage use of technology to enhance self-management. | Clinical consensus | |
| 13–17 years11 months | 1. | Evaluate self-management in appropriate areas (e.g. managing medications, prevention of complications, skin care, equipment care, bowel and bladder care, and making health care appointments). Assess self-efficacy for these activities, considering that the child’s ability to assume responsibility for health care encounters and other self-management of spina bifida can progress. Full responsibility for self-management is critical for successful transition. | Evidence [1, 17, 18, 23, 38, 64, 65, 68] |
| 2. | Assist families in knowing how to incrementally involve the child in organizing self-management activities. Specifically, encourage transition to having the child complete these activities initially with parental oversight and eventually independently. | Evidence [12, 17, 18, 19] | |
| 3. | Initiate a discussion and develop action plans to address deficits in self-management and independence skills, abilities, and behaviors as needed. | Clinical consensus | |
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Evidence [13, 60, 32, 46, 69] | ||
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Evidence [21, 23, 66, 70, 71] | ||
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Evidence [6, 16] | ||
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Evidence [12, 13, 14, 15] Neuropsychology Guidelines [63] | ||
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Evidence [72] Clinical consensus | ||
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Evidence [1, 16, 32, 46, 73] | ||
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Evidence [16] | ||
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Clinical consensus | ||
| 4. | Encourage participation in IEP/504 planning that addresses self-management and transition skills. For those with an IEP, transition planning must be initiated by age 14. | Transition guidelines [74] | |
| 5. | Support family functioning strengths related to self-management (navigating family stress, conflict, satisfaction, and family resources). | Evidence [36, 75] | |
| 6. | Involve the local Department of Vocational Rehabilitation and include vocational counseling in transition team planning. | Clinical consensus | |
| 7. | When it is developmentally appropriate, include time alone with the child to discuss self-management and independence topics as part of the visit. | Clinical consensus | |
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Table 2, continued | |||
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| Age group | Guidelines | Evidence | |
| 13–17 years11 months | 8. | Discuss sexuality, contraception (including latex allergy precautions), marriage, childbearing issues, genetic counseling, and folic acid supplementation. | Latex and Latex AllergyGuidelines [76] Men’s Health Guidelines [77] Sexual Health and Education Guidelines [78] Women’s Health Guidelines [79] |
| 9. | Assess individual and system barriers to self-management and transition from pediatric to adult health care (e.g., responsibility for health management, advocacy, assertiveness, and insufficient adult services). | Evidence [73, 80] | |
| 10. | Encourage the use of technology to enhance self-management. | Evidence [38, 39, 40, 42, 81] | |
| 11. | Share expectations and resources for future independent living, transition to college or employment. | Evidence [19, 24] | |
| 12. | Provide consultation to adult providers with limited skill in providing care to those with congenital conditions such as spina bifida. | Evidence [73] Transition Guidelines [74] | |
| 18 years | 1. | Evaluate full responsibility for implementing condition-specific self-management behaviors in appropriate areas, as needed (e.g. managing medications, preventing complications, monitoring skin care, maintaining equipment, bowel and bladder care, and ability to make health care appointments). | Evidence [1, 17, 18, 23, 38, 60, 61, 65, 68] |
| 2. | Reinforce the need for daily skin assessment, given the high incidence of skin breakdown on lower extremities (e.g. due to poor fitting leg braces) and risk for wound-related hospitalization. | Evidence [38, 26, 36] Integument [Skin} Guidelines [70] | |
| 3. | Evaluate if the adult has expanded self-management to encompass everyday living activities such as laundry, meal preparation, managing finances, making health care appointment, and ordering supplies. | Clinical consensus | |
| 4. | Initiate a discussion and develop an action plans to address deficits in self-management skills, abilities, and behaviors as needed. | Clinical consensus | |
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Evidence [13, 60, 69, 75] | ||
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Evidence [16, 64] | ||
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Evidence [4, 24, 68] Neuropsychology Guidelines [63] | ||
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Clinical consensus | ||
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Clinical consensus | ||
| 5. | Encourage the use of technology in developing basic self-management skills. For instance, using email, a personal online health record, or patient portal to contact the clinic coordinator and physician with questions. Offer alternatives if this form of access is not available or appropriate. | Clinical consensus | |
| 6. | Encourage the use of technology programs to enhance self-management outcomes [e.g. using mobile health (mHealth) or telehealth tools to monitor skin breakdown or report response to medication for UTI]. | Evidence [10, 38, 39, 40, 42, 82] | |
| 7. | Expand the discussion of sexuality, contraception (including latex allergy precautions), marriage, childbearing issues, genetic counseling, and folic acid supplementation. | Sexual Health and Education Guidelines [78] | |
| 8. | Expand the discussion on child rearing and parenting issues and resources as appropriate. | Clinical consensus | |
| 9. | Discuss strategies for safe infant handling (e.g., holding an infant if you use a wheelchair or accessing a crib or car seat) with parents or expectant parents with mobility limitations. | Clinical consensus | |
| 10. | Encourage involvement in empowerment activities and organizations (e.g., sports, mentoring, camps, and local, national and international spina bifida, and other disability organizations). | Evidence [11] | |
| 11. | Support family functioning strengths related to self-management including family satisfaction and family resources. | Evidence [58, 75, 83] | |
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Table 2, continued | |||
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| Age group | Guidelines | Evidence | |
| 18 years | 12. | Assess individual and system barriers to self-management (e.g., difficulties with self-advocacy, assertiveness, and insufficient adult services). | Evidence [20, 21, 37, 75] |
| 13. | Refer to vocational rehabilitation, independent living centers, or other community agencies as appropriate. | Clinical consensus | |
| 14. | Provide information about accessible housing, financing, and appropriate outside agencies. | Clinical consensus | |
| 15. | Encourage planning and use of support services (e.g., in a college setting, services for students with disabilities) for self-management and independence in new environments. | Clinical consensus | |
| 16. | Encourage the use of wellness programs. | Evidence [39] | |
| 17. | Evaluate and support patients as their parents and caregivers age and assist individuals with spina bifida with planning for changes in self-management and independence when their parents and caregivers will not be available. | Clinical consensus | |
2. Methods
The methods for the review of the literature and development of the recommendations were designed by the Executive Committee of the SB Guidelines [43]. Independence had been a topic in previous guidelines, however self-management was added in this edition. The central staff conducted a search of the literature from 2006 to 2016 using the search terms “independence and spina bifida” or “independence and myelomeningocele”. This search yielded 18 studies that addressed independence. In addition, because the search for self-management studies was inadvertently omitted from the central search process, one author (Au 2) conducted a search of three databases, PubMed, CINAHL, and Psychinfo for the dates 2006–2016 using the terms “spina bifida and self-management or spina bifida and independence.” This search yielded an additional 25 studies. References of these publications were searched for any earlier self-management studies; three additional studies were added. In addition, later during the review process two studies were identified and included. Early in the literature review, it became apparent that the recommendations of the self-management and independence working groups were similar. Therefore, the decision was made to combine the two sections. The blended working group consisted of: a PhD social worker, a PhD physical therapist, a PhD nurse, a rehabilitation physician, and a developmental pediatrician. Forty-eight studies informed the combined recommendations. In addition to the age-specific recommendations, the combined work group created a table describing the SB self-management instruments identified in this search and seven additional generic self-management instruments with references supporting their reliability and validity. Clinical questions were created to guide the organization of the guidelines (Table 1). The results of the 48 studies that addressed these concepts along with expert opinion informed the guidelines.
Table 1.
Clinical questions that informed the self-management and independence guidelines
| Age group | Clinical questions |
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| 0–11 months |
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| 1–2 years11 months |
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| 3–5 years11 months |
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| 6–12 years11 months |
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| 13–17 years11 months |
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| 18 years |
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3. Results
Evidence continues to mount in support of assessment and education of families and children/adolescents/young adults with SB around self-management issues (Table 2). The importance of these issues in adulthood is undisputed. Using valid and reliable tools to measure these concepts is well-supported (Table 3). Evidence is emerging for the success of community-based educational and training programs to improve self-management. More research is needed to support and refine these programs. In addition, we do not yet know the most effective developmental steps that encourage independence from a young age in this population.
Table 2.
Self-management guidelines
| Age group | Guidelines | Evidence | |
|---|---|---|---|
| 0–11 months | 1. | Provide instruction and support to families regarding knowledge and skills needed to manage their child’s spina bifida and related issues. | Clinical consensus |
| 2. | Provide orientation to families that include the expectation for eventual self-management and independence according to the individual’s age and the status of their spina bifida. | Prenatal Counseling Guidelines [57] | |
| 3. | Encourage families to expect participation in activities of daily life including tasks such as picking up toys, cleaning up, and imitative housework. | Clinical consensus Family Functioning Guidelines [58] | |
| 4. | Evaluate and support family function. | Clinical consensus Appendix: EarlyIntervention Services, Individual-ized Educational Plans [IEP] and504 Plans [59] Clinical consensus | |
| 5. | Identify and make referrals to early intervention programs. | Clinical consensus Appendix: Early Intervention Services, Individualized Educational Plans [IEP] and 504 Plans [59] | |
| 1–2 yrs11 months | 1. | Provide instruction and support to families regarding knowledge and skills needed to manage their child’s spina bifida and related issues. | Clinical consensus |
| 2. | Provide anticipatory guidance regarding developmental needs of children (such as exploration of environment, routines, and age-appropriate choices). | Clinical consensus | |
| 3. | Teach families to offer daily age-appropriate choices such as choosing between two articles of clothing, two cereals for breakfast, or two books to read. | Clinical consensus | |
| 4. | Encourage families to expect participation in daily life activities, including tasks such as picking up toys, cleaning up, and imitating housework. | Clinical consensus | |
| 5. | Identify and make referrals to early education programs. | Clinical consensus Appendix: Early Intervention Services, Individualized Educational Plans (IEP) and 504 Plans [59] | |
| 3–5 years11 months | 1. | Provide instruction and support to families regarding knowledge, skills, and behaviors needed to manage their child’s spina bifida and related issues. | Clinical consensus |
| 2. | Discuss the need to expand the range of daily life activities and chores, as well as strategies to accommodate the child’s learning style and/or mobility. | Evidence [60, 61] | |
| 3. | Provide anticipatory guidance so that autonomy skills are maximized when positive behaviors are reinforced, and clear and consistent consequences for inappropriate behavior are used. | Clinical consensus Mental Health Guidelines [62], Neuropsychology Guidelines [63] | |
| 4. | Refer to community resources such as early education programs that promote autonomy, self-efficacy, and other foundational independence skills. | Clinical consensus Appendix: Early Intervention Services, Individualized Educational Plans (IEP) and 504 Plans [59] | |
| 6–12 years11 months | 1. | Provide instruction and support to children and families regarding the knowledge and skills needed to manage spina bifida and related independence issues. Teach the child basic self-management skills, including skills to prevent secondary conditions (clean intermittent catheterization, skin care, equipment care, bowel and bladder care, wheelchair maintenance, and propulsion) based on individual abilities. Focus on self-efficacy. Children with spina bifida may develop foundational skills and self-management behaviors at a slightly later age (2–5 year delay) and may need more deliberate practice. However, most self-management behaviors are achievable by adults with spina bifida. | Evidence [1, 16, 17, 18, 23, 64, 65] Neuropsychology Guidelines [63] |
| 2. | Assist families in learning how to incrementally involve the child in organizing schoolwork and self-management activities. Specifically, encourage transition to having the child complete these activities initially with parental oversight and eventually independently. | Evidence [12, 17, 18, 38] | |
| 3. | Discuss the need to expand the range of daily life activities and chores as well as strategies to accommodate the child’s learning style and/or mobility. | Evidence [60, 61] | |
Table 3.
| Name of instrument Citation | Short description: Number of items; age range; type of instrument; subscales | Psychometric evidence: reliability and validity | Recommended use |
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| Spina bifida-specific instrument developed with samples of youth with spina bifida | |||
| KKIS-SB Kennedy Krieger Independence Scales-Spina Bifida (KKIS-SB) The Kennedy Krieger Independence Scales-Spina Bifida Version: A Measure of Executive Components of Self-Management (KKIS-SB) [13]. |
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Evidence reported [13]
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4. Discussion
There are several themes that have emerged from these guidelines. While it is important to understand the risk factors that complicate self-management such as level of the lesion, cognitive ability, and functional mobility, the trajectory of self-management skill development can be positively impacted independent of these complicating elements. Families and clinicians must work together to assess child readiness for self-management and collaboratively cultivate those skills over time. Clinicians should consider using one of the valid and reliable generic or SB-specific measures of self-management and independence [13, 44, 45, 46]. Clinical assessment of the level of self-management and independence in those with SB should specifically distinguish between the skills and behaviors the individual knows how to do and the behaviors they actually execute independently [47]. The evidence supports the need to have a structured, planned, and incremental approach to building self-management and independence skills beginning in early childhood, conveying expectations for developmentally-appropriate household responsibilities, and increasingly involving the child in their care. Plans that accommodate cognitive learning styles or executive functioning status and purposefully, incrementally increase skills with multiple opportunities to practice new behaviors are central to achieve successful self-management and independence. While the science of self-management for individuals with SB is not completely established, the general health behavior literature supports the powerful effect of expectations and self-efficacy [48, 49]. The expectation that children with spina bifida will grow into independent teenagers and adults must be supported by health care providers starting in infancy and increasing over time [50]. Typical developmentally appropriate expectations of putting away toys for preschoolers and participating in chores for children set the stage for the development of later skills and confidence. Facilitating both toddlers’ and older children’s decision-making ability is necessary for building skills needed for managing the challenges of SB [51]. Similar to school teachers assessing and addressing the unique learning needs of children with SB, clinicians and families should engage in intentional and targeted planning for self-management skill development. This plan needs to integrate and address the child’s challenges with executive functioning, working memory, or other unique learning needs, as well as attend to the child’s inherent strengths and interests.
The process of developing self-management skills is one that needs to be addressed early and include multiple supervised opportunities for practice in the home, healthcare provider’s office, and broader community. Ideally, these building blocks are core components of clinical encounters and addressed in a systematic and incremental manner during both primary and specialty care visits or through other regular self-management interventions or programs specifically tailored for individuals with SB and their caregivers. It is also important to continue to work on developing these self-management skills incrementally as adolescents age into adulthood, while at the same time assessing and planning for any self-management supports a young adult with SB will need to maintain optimal health and independence as an adult.
Multiple research gaps were identified by the working group. A critical need is to understand what foundational skills and abilities in young children with SB facilitate the development of self-management and independence behaviors in later childhood and adulthood. Once those foundational skills are identified, interventions that optimize the development of these skills and abilities need to be evaluated. The complex timing and skills needed for incremental transfer of responsibility for condition self-management in adolescents is unknown. In addition, the multi-faceted and multi-level barriers and facilitators for developing autonomy, self-management, and independent living skills across the lifespan need to be better delineated. Increased attention should also be placed on testing interventions aimed at closing the gap between self-management behaviors in individuals with SB and their typically-developing peers. Similarly, family-centered interventions that identify the support needs of parents and facilitate parental transition from direct care to coach and
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Table 3, continued | |||
| Name of instrument Citation | Short description: Number of items; age range; type of instrument; subscales | Psychometric evidence: reliability and validity | Recommended use |
| AMIS II(Interview)The Development of the AdolescentYoung Adult Self-Management and Independence Scale-AMIS II: Psychometric Data [46]. |
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Evidence reported [46] Initial psychometric analysis with a sample of 201 adolescents/young adults ages 12–25 with spina bifida and 129 of their parents. Reliability
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Table 3, continued | |||
| Name of instrument Citation | Short description: Number of items; age range; type of instrument; subscales | Psychometric evidence: reliability and validity | Recommended use |
| Medical Self-Management andTransition ReadinessMeasurement of medical self-management and transition readiness among Canadian adolescents with special health care needs [86]. |
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Evidence reported [86]:
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Table 3, continued | |||
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| Name of instrument Citation | Short description: Number of items; age range; type of instrument; subscales | Psychometric evidence: reliability and validity | Recommended use |
| Spina Bifida Self-ManagementProfile (SBSMP)Sharing of Spina Bifida Responsibilities Scale (SOSBMR)Spina Bifida Independence Scales (SBIS)Condition self-management in pediatric spina bifida: A longitudinal investigation of medical adherence, responsibility-sharing, and independence skills [23]. |
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Evidence reported [23]:
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| Generic Self-Management/Transition Readiness Instruments. No reported use in spina bifida | |||
| TRAQ(Transition Readiness Assess-ment Questionnaire)Measures the transition-readiness of youth with special health care needs [69]. |
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Evidence reported [69]
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Table 3, continued | |||
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| Name of instrument Citation | Short description: Number of items; age range; type of instrument; subscales | Psychometric evidence: reliability and validity | Recommended use |
| UNC TR(x)ANSITIONscale.A clinical tool to measure health care transition components from pediatric to adult care [87]. |
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Evidence reported [87]:
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| PEDI-CATPediatric Evaluation of Disability Inventory (PEDI) Computer Aided Test (CAT) [60, 61]. |
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Evidence reported [60]:
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Table 3, continued | |||
| Name of instrument Citation | Short description: Number of items; age range; type of instrument; subscales | Psychometric evidence: reliability and validity | Recommended use |
| STARxSelf-Management and Transition to Adulthood with Rx TreatmentSelf-management and transition readiness assessment: development, reliability, and factor structure of the STARx questionnaire [89]. |
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Evidence Reported [89, 90]:
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Legend: Table 3 used with permission and obtained from Guidelines for the Care of People with Spina Bifida 2018: (https://www.spinabifidaassociation.org/guidelines/). Additional resource: The SBA “Beyond Crayons” resources are useful in developing the knowledge, self-efficacy, attitudes and skills necessary for self-management. They can be found here: https://www. spinabifidaassociation.org/resource/beyond-crayons-resource-packet/.
consultant are presently limited in scope and availability. It is also important to determine if routine clinical assessments of self-management behaviors that result in the development of action plans tailored toward the adolescent and their family yield improved outcomes. It is unclear if these types of interventions enhancing self-management and independence can be delivered in the clinical setting or if alternative structures need to be developed, such as implementation within school settings. Further, the optimal structures for coordinated, comprehensive transition to adult care have yet to be determined. As longevity in SB increases, understanding the self-management and independence needs in young, middle-age, and older adults with SB as they age becomes imperative. Finally, the role of the health care provider and the larger health care system in optimizing self-management and independence outcomes needs to be explored.
Addressing these gaps should provide a map for future care-providers to effectively help families prepare children with SB to become independent. In the meantime, it is hoped that these guidelines will steer care-givers to have developmentally appropriate expectations for the development of self-management skills. Since the publication of the guidelines, there has been emerging evidence which, in the view of the authors, is currently shaping the dialogue relevant to these guidelines [52, 53, 54]. These findings will need to be integrated into ongoing care.
Two additional publications build on Self- Management and Independence Work Group’s work. Both reflect the importance of assessment in order to meet the person with SB at the appropriate readiness level for change in this area [55, 56].
Acknowledgments
This edition of the Journal of Pediatric Rehabilitation Medicine includes manuscripts based on the most recent “Guidelines For the Care of People with Spina Bifida,” developed by the Spina Bifida Association. Thank you to the Spina Bifida Association for allowing the guidelines to be published in this forum and making them Open Access.
The Spina Bifida Association has already embarked on a systematic process for reviewing and updating the guidelines. Future guidelines updates will be made available as they are completed.
Executive Committee
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Timothy J. Brei, MD, Spina Bifida Association Medical Director; Developmental Pediatrician, Professor, Seattle Children’s Hospital
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Sara Struwe, MPA, Spina Bifida Association President & Chief Executive Officer
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Patricia Beierwaltes, DNP, CPNP, Guideline Steering Committee Co-Chair; Associate Professor, Nursing, Minnesota State University, Mankato
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Brad E. Dicianno, MD, Guideline Steering Committee Co-Chair; Associate Medical Director and Chair of Spina Bifida Association’s Professional Advisory Council; Associate Professor, Department of Physical Medicine and Rehabilitation, University of Pittsburgh School of Medicine
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Nienke Dosa MD, MPH, Guideline Steering Committee Co-Chair; Upstate Foundation Professor of Child Health Policy; SUNY Upstate Medical University
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Lisa Raman, RN, MScANP, MEd, former Spina Bifida Association Director, Patient and Clinical Services
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Jerome B. Chelliah, MD, MPH, Johns Hopkins Bloomberg School of Public Health
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Julie Bolen, PhD, MPH, Lead Health Scientist, Rare Disorders Health Outcomes Team, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention
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Adrienne Herron, PhD Behavioral Scientist, Intervention Research Team, National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention, Centers for Disease Control and Prevention
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Judy Thibadeau, RN, MN, Spina Bifida Association Director, Research and Services; former Health Scientist, National Spina Bifida Program, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention
Funding
The development of these Guidelines was supported in part by Cooperative Agreement UO1DD001077, funded by the Centers for Disease Control and Prevention. Its contents are solely the responsibility of the authors and do not necessarily represent the official view of the Centers for Disease Control and Prevention or the Department of Health and Human Services.
Conflict of interest
The authors declare no conflicts of interest.
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