Your child’s primary physician will monitor weight and length. A dietician can review nutrition. An occupational therapist and speech therapist have training in sensory and motor issues of the mouth for assessing feeding skills. A speech therapist and radiologist can assess for aspiration. An endocrinologist can assess problems that alter growth. A gastroenterologist and/or complex care and palliative care clinicians can help guide the decisions regarding feeding tubes.
Feeding Tubes
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Some children with SNI never have the ability to eat by mouth, and questions about a feeding tube arise early in life. Others will eat by mouth for months or years, and then develop problems with swallowing or not eating enough, which can lead to weight loss or lung infections. Though the age when these changes occur can vary, understanding what nutritional or gastrointestinal needs may arise, and knowing the clinicians who can support you, will give you confidence as you manage and make decisions about your child’s nutritional needs.
A feeding tube is used when a child can’t take in enough food or safely swallow because of an illness or chronic health condition. The tube allows nutrients to go into the body through a small flexible tube without having to be swallowed. In most cases, a feeding tube delivers food into the stomach, but in some cases the tube delivers nutrition into the small intestine in order to avoid problems with vomiting or reflux. Some children with SNI will be fed exclusively by feeding tube. Others fed by feeding tube are able to continue to take food by mouth for taste and pleasure. A speech therapist and radiologist will assess what foods can be safely swallowed. The choices to use a feeding tube and/or allow food by mouth may change over time.
There are different types of feeding tubes. Your child’s medical team will help determine which tube makes the best sense for your child.
G-tube (gastronomy tube)
Tube inserted through the abdominal wall, bringing nutrition directly into the stomach.
GJ tube (gastrostomy-jejunostomy tube)
Tube inserted through the abdominal wall into the stomach, with a longer tube that goes from the stomach into the small intestines.
J-tube (jejunostomy tube)
Tube placed through the abdominal wall that travels into the midsection of the small intestine.
NJ tube (nasojejunal tube)
Thin, soft tube inserted through the nose that travels through the stomach and ends in the jejunum, a part of the small intestine. This type of tube is usually used temporarily, commonly during times of illness when the chance of vomiting is increased.
NG tube (nasogastric tube)
Thin, soft tube inserted through the nose that travels into the stomach. This type of tube is usually used temporarily and may be in place as families decide about a permanent feeding tube.
The question of whether to allow a feeding tube is often one of the most emotional ones for a caregiver who considers feeding their child one of their most important responsibilities. The medical team can help you anticipate what you can expect with or without the tube, so that you can arrive at a decision that feels right for your child and family. It is helpful to take time to discuss what impact the tube might have on your family’s and child’s overall quality of life. Does it take a long time to feed your child–time that you could be spending together in other ways? Will a feeding tube help your child have more energy and be more comfortable? Will it make the delivery of critical medications easier, faster, more effective? Will a feeding tube will cause discomfort and agitation, prolonging the suffering of the child?
Sometimes clinicians suggest that your child “needs” a feeding tube placement. Remember that the need is determined by your goals, so make certain that your clinical team can clarify what the goals are that a feeding tube will accomplish.
