The survey allows us to have a truthful view on one of the major problems that incur in the life of people dealing with spina bifida. The data collected shows how the urinary and fecal incontinence and constipation affect the day of these people. The high prevalence of incontinence observed is in line with the data reported for children and adolescents signed in the United States Spina Bifida Patient Registry (NSBPR): the 58% struggle with urinary incontinence and the 50% with fecal incontinence (8). These problems lead the lives of the people with spina bifida, and so, the education is crucial and fundamental. Most of these people was educated by the medical staff on how to perform the self-catheterization technique and the 34,8% only was trained by their parents. The self-catheterization is a fundamental technique to manage bladder incontinence and obtain a much bigger independence, limiting unpleasant situations such as discharge as much as possible (9). A recent study observed that the impact of incontinence on quality of life was noted only starting at 10 years old and increases in adolescence, when it corresponds to the discomfort reported by adults (5). This suggests that the impact on the quality of life may be age-dependent phenomenon.
Since self-catheterization, and potentially other self-care activities, begin at about 9 years old, it is plausible that an increasingly more independent child exposed to more peer interactions in school, could live a condition of diversity as opposed to other children and so affect the quality of their life(10).
It is fundamental that the parent of a children dealing with spina bifida is capable of educating them into practicing self-catheterization, even if it takes time; it is important to encourage the child to actively take part into empty the bladder as soon as possible. Catheterization will then become a natural step if the child starts practicing at an early age, as a 2018 study shows complications (infections, reflux.) and improve quality of life (11). It is important to find tricks that help the child remember when to perform self-catheterization in specific time intervals, for example it can be done in relation to other activities (meals, snacks) that respects these intervals of time, usually no more than every 6–7 hours or one could use reminders on their phone. The child must take the responsibility of empty the bladder; this will contribute on gaining more confidence and autonomy in life. Of course, the training of the parents must be done by the medical staff, which has to be available to fix any issue that might come up in the first phases of the practice. Struggling with urinary incontinence can be embarrassing and isolating, and this can impact on physical and mental health, having a negative impact on the quality of life. There are proofs that testify how urinary and fecal incontinence not only interfere with the daily activities but they’re also associated to a lower self-confidence and participation in social activities as well(12).The nursing staff not only has to teach how to perform self-catheterization, but it also has to educate the people affected with spina bifida on how to follow an appropriate diet, because by doing so they could improve some issues linked to incontinence and the well-being of the person. The survey shows that only a small part, the 8%, actually drinks 2L of water a day, the 13,6% drinks 0.5L, the 36,8% drinks 1L while the remaining 41,6% drinks 1.5L. Unlike what one might think (just as one of the interviewed claimed), drinking little water isn’t really an effective fix for urinary incontinence. That is because the body requires the right amount of liquids to keep hydrated and to not face dehydration. Furthermore, drinking little water leads to more concentrated urine, which can favor the proliferation of bacteria and create unpleasant infections that might worsen the problem of incontinence. Drinking enough is then so important: it is suggested to drink at least a liter and a half per day, which equals eight cups of water. Another recommendation is to eat healthy, eating a lot of fruit and vegetables as well, and be careful not to exceed with certain foods and drinks such as chocolate, tea, coffee, spicy foods and alcohol, as they actually irritate the bladder walls and can worsen urinary discharge.
We’ve already seen that people dealing with spina bifida show a neurogenic bowel, which is a colon dysfunction (that implies constipation, fecal incontinence, and problems with defecations) due to the loss of the sensory and motor control, or both. With regards to the prevention for fecal incontinence, we can intervene by educating the patients into being careful to certain conditions that may favor it: in the case of constipation, one might need to add fiber into their diet and an adequate amount of water, more than 2L; in the case of soft or liquid stools (which can easily cause incontinence) it is recommended to reduce or, sometimes, avoid foods or drinks that can irritate the bowel such as alcohol, caffeine, species, spicy and smoky foods which can flame the bowel. From the results showed in the survey, we can observe the aspects on which the nursing staff has to intervene for the management and education of people dealing with spina bifida from a very young age, with the aim to reaching a condition of autonomy and independence in adulthood. Transanal irrigation or colon retrograde irrigation (TAI) is a practice used to assist the feces evacuation from the bowel through the introduction of water in the colon through the anus. In patients dealing with constipation of fecal incontinence, the regular use of transanal irrigation can help stabilize the proper bowel functionalities. This helps the people develop an adequate management of their bowel functions, setting and choosing the right place and time for evacuation. As it was already noted, the 56,7% claims not to be autonomous when it comes to rectal irrigation, and this is something that needs to be taken care of, with a bigger intervention from the sanitary staff and the patients and their families. This is fundamental for the people dealing with spina bifida because, by reducing as much as possible the probability of discharge and/or constipation, leads to them feeling much more self-confident into participating in social life and build social relationship, improving the quality of life. As other studies suggest (13), many participants (almost 50%) were heavily dependent on their caregivers for the management and the support. This information has implications for the future disposal of clinical services to improve the results reached by the patients. A comprehensive ID ambulatory care continuum model should be able to facilitate the management and treatment of common clinical issues, such as urinary tract infections (UTI), pressure areas, neurogenic bowel, sexual dysfunction, and secondary conditions resulting from “overuse” syndromes and “ageing” with disability (14). This study has some potential limitations: first, selection bias cannot be ruled out, as participants were a selective cohort of people belonging to ASBI that decided autonomously to file the survey anonymously, limiting the possibility of generalizing the results. We acknowledge that other factors may have impacted bowel/bladder and psychological issues in participants and were not studied. However, patient self-report and care report were considered. Important outcomes, such as impact on careers and families and analysis of costs associated with are, were beyond the scope of this study.