Health related quality of life in children with constipation-associated fecal incontinence

Marloes E J Bongers, Marieke van Dijk Marc A BenningaMartha A Grootenhuis

Abstract

Objectives: With a disease-specific questionnaire, this study aimed to evaluate health-related quality of life (HRQoL) in children with constipation in association with clinical characteristics.

Study design: Children with constipation-associated fecal incontinence (n = 114), 8 to 18 years, filled out the Defecation Disorder List at a Dutch tertiary hospital. Correlations and linear regression analysis between clinical characteristics and scores on emotional and social functioning were calculated. Specific concerns of children were described by individual item scores of these domains.

Results: Higher frequency of fecal incontinence episodes was associated with lower emotional and social functioning. Linear regression analysis showed a significant association between social functioning and fecal incontinence, but the variance of the model was low (adjusted R(2)= 0.08). Between 70% to 80% of children were concerned about experiencing fecal incontinence unnoticeably and the attendant social consequences. Children did not report having fewer friends and participated well in social events.

Conclusion: Lower HRQoL regarding disease-specific emotional and social functioning was reported in children with frequent episodes of constipation-associated fecal incontinence. However, other nonspecified factors may also influence HRQoL of these children. Most children reported relatively more emotional concerns than social consequences.

Click the link for access to full text article: https://pubmed.ncbi.nlm.nih.gov/19150085/

Conventional treatment of functional constipation has a positive impact on the behavioural difficulties in children with and without faecal incontinence

Line ModinIda Skytte Jakobsen,  Marianne Skytte Jakobsen

Abstract

Aim: Constipation studies have only evaluated behavioural difficulties in children with faecal incontinence. This study evaluated changes in behavioural difficulties in childhood with functional constipation (FC) with and without faecal incontinence, based on treatment outcomes.

Methods: Children aged five to 16 years who fulfilled the Rome III criteria for FC received conventional treatment. The Strength and Difficulties Questionnaire was completed at inclusion and at the 12-month follow-up.

Results: We included 116 children. The behaviour scores decreased in successfully treated boys (10.3 versus 7.9; p < 0.001) and girls (10.0 versus 7.4; p = 0.0001) with and without faecal incontinence. There was no decrease in the behaviour scores in children with unsuccessful outcomes. Unsuccessfully treated boys had significantly higher behaviour scores than successfully treated boys at inclusion (13.2 versus 10.3; p = 0.006) and after 12 months (11.4 versus 7.9; p = 0.02). No difference was found between unsuccessfully treated and successfully treated girls at inclusion (10.5 versus 10.0; p = 0.77) or after 12 months (10.3 versus 7.4; p = 0.18).

Conclusion: Our findings indicate that conventional treatment of FC had a positive impact on behavioural difficulties in constipated children with and without faecal incontinence. This study highlights the importance of proactive detection and treatment of FC in paediatric patients.

Click the link for access to full text article:

https://pubmed.ncbi.nlm.nih.gov/26913469/

The Uniformed Services Constipation Action Plan: An Effective Tool for the Management of Children with Functional Constipation

Patrick T. Reeves, et al.

Objective: To implement and to evaluate the effectiveness of the Uniformed Services Constipation Action Plan (USCAP) in our gastroenterology clinic for children with functional constipation.

Study design: This implementation science study included toilet-trained subjects aged 4 years and older who met the Rome IV criteria for functional constipation. Children were block randomized to receive either the USCAP or control. All clinic functional constipation plans recommended subjects continue pharmacotherapy for 4 months. Endpoints measured were clinical outcomes (resolution of functional constipation and achievement of a Pediatric Bristol Stool Form Scale [PBSFS] score of 3 or 4), patient-related outcomes (health-related quality of life [HRQoL] total scale score), and health confidence outcomes (Health Confidence Score [HCS]).

Results: Fifty-seven treatment group subjects (44%) received a USCAP (52% male; mean age, 10.9 [4.9] years) compared with 73 controls (56%; 48% male; mean age,10.9 [5.3] years). A PBSFS score of 3 or 4 was achieved by 77% of the treatment group compared with 59% of controls (P = .03). Subjects from the treatment group were more likely than the controls to endorse adherence to the 4-month course of pharmacotherapy (P < .001). Subjects who received a USCAP had greater improvements in HRQoL total scale score by the end of the project (P = .04).

Conclusions: The USCAP is a simple, inexpensive tool that has the potential to improve global outcomes for functional constipation in children and should be recommended as standard clinical practice.

 

For access to full text, click this link:

https://pubmed.ncbi.nlm.nih.gov/36115625/

To see the Vermont Continence Project’s “Constipation Traffic Lights Form and a plain language video describing its use, go to Constipation Treatment: Bowel Maintenance

Paediatrics: how to manage functional constipation

Alexander KC Leung, corresponding author and Kam Lun Hon

Abstract

Background: Despite being a common problem in childhood, functional constipation is often difficult to manage. This article provides a narrative updated review on the evaluation, diagnosis and management of childhood functional constipation.

Methods: A PubMed search was performed with Clinical Queries using the key term ‘functional constipation’. The search strategy included clinical trials, meta-analyses, randomized controlled trials, observational studies and reviews. The search was restricted to the English literature and to the paediatric population. The information retrieved from the above search was used in the compilation of the present article.

Results: A detailed history and thorough physical examination are important in the evaluation of a child with constipation to establish the diagnosis of functional constipation as per the Rome IV criteria and to catch ‘red flags’ suggestive of organic causes of constipation. These ‘red flags’ include delayed passage of meconium, ribbon stool, rectal bleeding/blood in the stool unless attributable to an anal fissure, failure to thrive, severe abdominal distension, absent anal wink/cremasteric reflex, tight and empty rectum on digital examination and explosive expulsion of liquid stool and gas on withdrawal of the finger, hair tuft/dimple/lipoma/haemangioma in the lumbosacral area, and an anteriorly displaced anus. For functional constipation, pharmacological therapy consists of faecal disimpaction and maintenance therapy. This can be effectively accomplished with oral medications, rectal medications or a combination of both. The most commonly used and most effective laxative is polyethylene glycol. Non-pharmacological management consists of education, behavioural modification and dietary interventions. The combination of pharmacological therapy and non-pharmacological management increases the chance of success.

Conclusion: Polyethylene glycol is the medication of first choice for both disimpaction and maintenance therapy. If polyethylene glycol is not available or is poorly tolerated, lactulose is the preferred alternative. Other laxatives may be considered as second-line therapy if treatment with osmotic laxatives fails or is insufficient. Maintenance treatment should be continued for at least 2 months. Early treatment will result in a faster and shorter treatment course.

Click link to access full text:

https://pubmed.ncbi.nlm.nih.gov/33828605/

Parents’ Experiences and Information Needs While Caring for a Child With Functional Constipation: A Systematic Review

Alison P, Thompson, Eytan Wine, Shannon E MacDonald, Alyson Campbell, Shannon D. Scott

Abstract

Pediatric functional constipation (FC) reportedly affects at least 1 in 10 children worldwide. Parent and family education is a key component for successful treatment, yet there is little research exploring what information families need and how to best support them. The aim of this review is to synthesize current evidence on the experiences and information needs of parents caring for a child with FC. We systematically searched published research and completed screening against a priori inclusion criteria. Thirteen studies (n = 10 quantitative, n = 3 qualitative) were included. We found 2 main themes, precarious footing and profound and pervasive effects. Heavy caregiving burdens fueled doubts, misinformation, relationship breakdown, and treatment deviation. In light of clinical recommendations, our findings reveal a potential mismatch between parents’ needs and care provision for FC. It is likely that both parents and health care providers would benefit from resources and interventions to improve care related to pediatric FC.

Click Link for full text access:

https://pubmed.ncbi.nlm.nih.gov/33026251/

Planning for Setbacks

Did you know that 40-50% children treated for constipation will have a relapse in the first 1-5 years? We encourage parents to do what you can to prevent relapses, but also to prepare yourself for what might happen. This video from Vermont Continence Project nurse consultant, Kelly Savitri, RN, offers helpful suggestions to keep things moving smoothly.

 

A full transcript of the video appears below.

Continue reading “Planning for Setbacks”

Picky Eating & Continence Challenges, Part 1

Most parents know that their child’s diet plays a role in their elimination health and habits. What do you do if your child won’t eat those foods that help improve elimination? This video from Vermont Continence Project nutrition consultant, Kelli Borgman, RD, describes the things that stand in the way of children developing healthy eating habits. Watch this before Picky Eating and Continence Challenges, Part 2, where we suggest some ways you can adapt foods and mealtimes to help your picky eater.

A full transcript of the video appears below.

Hello, I’m Kelli Borgman. I’m a dietitian consultant with the Vermont Continence Project. In this video, I’m going to talk about picky eating as it relates to continence challenges, and a general framework to start thinking about how to best support your child.

Picky eating can be so challenging day to day, and both parents and kids can have a lot of worry, stress or strong reactions around it. It’s also quite a personal topic. Each child’s or family has their own story about how picky eating came to be an issue, how each family member is dealing with it and what’s being done about it, if anything, and how picky relating eating relates to the emotional and communication dynamics within the family system. Family cultural or personal beliefs and ethics about food and health all play a part too.

When a child continually refuses foods, you purchase and prepare with care, parents and caregivers feel frustrated, powerless, hopeless, or just annoyed. Sometimes it can come with a lot of shame or you feel like you’re a bad parent. This is made worse when parents and children have conflict about food and eating. So I really want to start off by saying there are no right answers and each child and parent needs personalized support. Please know it’s okay to put on the brakes and of trying to get your child to eat specific foods in a similar way to how you might be rethinking teaching, toileting.

Parents often wonder if their child’s picky eating is typical. Feeding therapists may describe children as being picky eaters or extremely picky eaters. So this is kind of a busy slide. But I wanted to give you some context for caregivers to know which category their child can fall in. I hope it will validate the experience you’re having and give some clarity on how to best support your child’s eating. So just to compare picky eating affects about half of children at some point. It starts around 15 to 18 months, once calorie needs decrease past infancy. Picky eaters do have favorite foods, which are often carbs. They drop new foods but are able to pick up new ones. They often will reintroduce dropped foods in time and over several days will eat foods from all food groups. They can be hesitant to accept new foods. They can accept varied textures, and they will often eat enough at school or daycare.

In comparison, extreme picky eaters impacts a smaller amount of children, and this is nondisabled children about 13%. It usually starts earlier than 15 months. They might have favorite foods, but there’s more rigidity in their choices. They drop foods but aren’t as able to pick up new ones. They won’t often reintroduce dropped foods, and over day’s time, they will avoid foods from certain food groups and not get the variety.

They generally have a fear of new foods or have food anxiety. They won’t often accept varied textures and will often struggle to eat enough at school or daycare. If you think your child falls into the picky eater category, there’s some great information in the video called Picky Eaters, Part Two about the parent child feeding relationship. That will likely be a great foundation to think about extremely picky eaters generally need more accommodation and support, so consider working with a pediatric feeding therapist and dietitian team. These are the kids that can have more severe malnutrition or at risk for longer term disordered eating patterns. Please note the data from these stats are commonly cited and accepted in the scientific literature. Of course, children don’t always neatly fall into one category or another and disabled or neurodivergent children are often underrepresented or not acknowledged. So it’s hard to apply this data to include all kids experience with picky eating or more extreme picky eating.

So when thinking of the long term nutrition goals related to GI health, we of course want to help support their GI tract to function optimally and optimally function functioning GI system is able to uptake the amount of nutrition they need to play, grow and learn. So for most kids this means working on increasing fiber, fluid, or variety, or a combination of these.

If your child’s daily eating choices don’t currently meet 100% of what the GI tract requires to function optimally, medications and supplements should be used to support each child’s body, mind and emotions where they are right now.

So what makes healthy, healthy relationship to food possible? Really, a more regulated nervous system stimulates appetite and allows more flexible thinking and openness to foods. The enteric nervous system, shown in a picture here, innervates the entire GI tract, and is the largest and most complex unit of the entire nervous system outside the brain. It’s all quite connected, literally. Appetite, curiosity, and interest in more quantity or variety will often dramatically increase when we think about nervous system balance and meeting their emotional needs at the table, too.

In my work with families over the years, I’ve noticed a common theme amongst the extreme picky eaters parents often report, and I can see during mealtime observations that children display lots of non-verbal and verbal communication that indicates they’re getting disregulated and upset. The causes of upset are usually what foods are offered or not offered, or the caregivers involvement in their mealtime.

Their sensory and nervous systems are ringing alarm bells that the situation isn’t comfortable or safe, or they have fears that their needs aren’t going to be met. So why do kids avoid healthy foods First, Kids, just like adults, use food for emotional comfort. There’s nothing pathological or wrong about this. This is human nature. So if emotional needs are perceived to be threatened or needs aren’t getting met, children will often revert to their comfort foods to regain that sense of calm and relax by filling their belly with foods or drinks that satisfy that sense of emotional safety or control and help them regulate their nervous systems.

Sometimes, especially at specific times of the day, such as lunchtime at school or at dinner, they might come to the table with a dysregulated nervous system already, or they perceive a threat to be coming. They might also be seeking comfort in a specific experience through their food, which is often the case. Like for the afternoon snack, they’ll be more rigid with their choices and behavior the more their nervous system is dysregulated. There are likely sensory needs and preferences they’re also turning into tuning in to. These sensory preferences are unique to your child, their natural likes and dislikes, what foods they’ve been exposed to so far, and in what frequency, as well as how comfortable they are with varied sensations. They also may have or have had in the past.

Oral motor skill difficulties:less processed foods are generally more challenging to eat. Fresh produce and whole grains are often presented in forms that are much harder to chew, and mixed texture foods are just more complicated for your mouth to manage. They naturally start to avoid what they’re not yet competent at, especially if the adults are around them, aren’t quite catching on to what a challenge it actually is for them. Imagine if you were continually offered whole apples when you actually have the ability for applesauce or offered steak when you’re really only able to handle meatloaf.

Most kids that are picky eaters benefit from a flexible routine where they can generally feel safe and predictably get their needs met. There are a lot of challenging, competing time priorities for families and kids, so being able to slow down and really focus on a food routine can be challenging. Oftentimes we talk about eating together as a family and how great that is, but when kids are hungry and want food immediately during busy days, parents often focus on getting the child what they need quickly versus actually being able to sit down and eat with them. Meals can be fast paced and just feel more stressful for many reasons, which virtually eliminates curiosity and appetite for many children. Also, irregularly timed meals and snacks can cause extreme blood sugar, highs and lows. Even without diabetes, blood sugar lows can be felt as alarm bells to the nervous system, which can lead to eating processed foods and snacks that quickly calm the body and resolve the low blood sugar. They will get confirmation these foods feel good to their body and that the processed foods meet their safety and hangry needs for other kids or regularly timed meals and snacks means grazing or whatever or whatever kind of eating. When grazing occurs, the gut doesn’t get a chance to rest, and some rest between meals and snacks is optimal for the GI tract to move food efficiently through.

Foods offered at daycare or school can also be a big part of the picture for some kids. They can undereat at school or will only eat snacks or drink milk or juice. This may be partly due to nervous system dysregulation or because lower preference foods are being offered during meals. Some kids also start to associate eating with the urge to poop, which they’re usually trying to avoid at school. So this will lead the child right back into the constipation, carousel and undernutrition, which can lead to more extreme picky eating and a negative behavior loop or cycle being established.

So in summary, what makes eating healthy foods possible a healthy relationship to food, responsive and attuned caregivers who sense when their child is disregulated at a meal and try to learn why taking small steps at the right time. So when the child’s nervous system feels more safe and regulated, when you take those small steps, consider offering choices that match their dietary needs and sensory preference preferences, which we’ll talk more about in the next video.

And the last point is true. Treating GI distress and constipation adequately. Don’t underestimate how constipation and other GI issues can be the underlying cause of picky eating kids quickly learn to kind of sort of eat to avoid that discomfort. So recognizing and treating GI concerns adequately is key.

Thank you for taking the time to watch this. The information contained in this video is for informational purposes only. It is not a substitute for professional health or medical advice, diagnosis or treatment. Always seek the advice of your physician or other qualified health care provider.

 

Urination Questions and Concerns

What are signs that your child’s urination is healthy? This video describes the signs of healthy urination, and indicators that your child’s urination is not functioning quite right.

A full transcript appears below.

00:00:00:00 – 00:00:26:00
Unknown
Hi, my name is Haya Lickteig. I’m an occupational therapist and I’m the director of the Vermont Continence Project. In this video, Urination questions and Concerns, we are going to talk about some signs that you may need to pay more attention to your child’s bladder function or may want to check in with your child’s medical provider. First, let’s review how the bladder works.

00:00:26:03 – 00:00:55:12
Unknown
Urine is made in the kidneys and drips down, drop by, drop through tubes called ureters. Urine then collected in the bladder, which is basically a muscular pouch like a water balloon while urine is collecting, the walls of the bladder are relaxed and stretching out. At the same time, a muscle at the bottom of the bladder, the urethral sphincter is contracting to hold the bladder shut.

00:00:55:15 – 00:01:19:05
Unknown
When the bladder gets a certain amount of stretch. It sends a message to the brain that says the bladder is full. The muscles then reverse their actions. The muscles at the bottom of the bladder. Relax, allowing the urine to flow out while the walls of the bladder contract or squeezed in to make sure that all the urine comes out.

00:01:19:08 – 00:01:53:23
Unknown
This is similar to releasing the neck of a water balloon and giving the widest part a squeeze to clear it out. While our body controls that sphincter muscle that holds the urine in. It doesn’t voluntarily control the muscle on the inside that squeezes the bladder, an indication that this process is working well is that a person can urinate very soon after sitting on the toilet and that their urine stream has a steady sound which gets sore, start soft, gets loud and then soft again.

00:01:53:25 – 00:02:21:12
Unknown
Holding urine between large urination is also a sign that things are working well. While it’s too complicated to explain why problems occur here. There are some important signs to look for that your child may have a problem or concern with bladder function. If your child urinates very frequently, like more than once an hour, that’s something that we’d want our health care provider to be aware of.

00:02:21:14 – 00:02:50:05
Unknown
If your child regularly goes 4 to 6 hours or more between voids, that’s also something that you’d want your health care provider to be aware of. Parents also see this sometimes when their child wakes up dry, but then doesn’t urinate immediately. Some other signs that you may be on to be aware of are that your child’s urine flow is choppy or weak, which you probably would only know if your child is urinating in the toilet.

00:02:50:07 – 00:03:14:28
Unknown
Your child has trouble making urine come out even when they say they need to go or they appear to need to go. This can also look like a child pushing while trying to pee. If you remember, the act of urinating is not a pushing maneuver. It’s the act of releasing a muscle, and the pushing should be completely done by your body’s own processes.

00:03:15:00 – 00:03:42:08
Unknown
If your child has frequent UTIs, it can be a sign of constipation. Since fecal bacteria coming from the anus can get into the urethra, especially for girls. But it can also be a sign of withheld urine, meaning that the bladder isn’t emptying completely, leading to urine that is staying in the bladder too long and becoming too concentrated. So what to do?

00:03:42:10 – 00:04:21:17
Unknown
A common saying in the world of pelvic health is that the bowel drives the bladder and this means that most bladder symptoms for most people may be tied to something happening in the bowel. We frequently tell parents that most of their child’s bladder symptoms may get better when you treat their constipation. If you’ve treated your child’s constipation comprehensively and consistently for 2 to 3 months or more and you see no improvement in your child’s bladder, that’s when another referral may be appropriate.

00:04:21:20 – 00:04:53:25
Unknown
We’d suggest discussing your treatment options with your child’s provider for some of the available options. Include a consultation with a pediatric urologist or working with a pelvic floor, physical therapist or occupational therapist with expertise in working with children. If you have a child with any of these symptoms, it’s essential to address them before any kind of sitting program.

00:04:53:28 – 00:05:23:05
Unknown
Many of these issues can come from a history of withholding, and a structured program will probably make that worse for your child. If your child already sits on the toilet willingly, it’s really important to use all of the postural supports that we discuss in other videos, such as a footstool and a seat reducer. Thank you for taking the time to watch this.

00:05:23:07 – 00:05:40:01
Unknown
The information contained in this video is for informational purposes only. It is not a substitute for professional health or medical advice, diagnosis or treatment. Always seek the advice of your physician or other qualified health care provider.

 

What is Fiber?

Many of us have heard that fiber is important for elimination health. We might not know what foods have fiber, or how much we need! Kelli Borgman, RD, Nutrition Consultant for the Vermont Continence Project, explains how we can increase the fiber in our child’s diet for overall GI health and wellness.

A full transcript of the video appears below.

Continue reading “What is Fiber?”