A parent or legal guardian must accompany children under age 18 to the Preoperative Clinic or the Admitting Office to provide consent for medical treatments and procedures during hospitalization. In general, the hospital cannot provide treatment without consent from a parent or legal guardian.
If your child is 18 years or older and is able, he or she can consent to treatment. If, however, a patient 18 years or older and is emotionally or mentally limited, he or she may not be able to consent to treatment, and parents will need court-ordered guardianship to consent for them. In such cases, please bring the legal papers documenting your guardianship or authority to consent to a child's care with you to the hospital. If the Massachusetts Department of Social Services (DSS) is involved with your child, contact your case worker to ask about the role of DSS in any decisions regarding the hospital experience.
All patients age 18 or older should read the Massachusetts Health Care Proxy Form. The federal Patient Self-Determination Act and the associated Massachusetts Health Care Proxy Act state that patients age 18 or older may name another person to act as an agent if they become unable to make decisions about their care. This person would be responsible for making all medical decisions, including those involving life-sustaining medical treatment, in agreement with his or her understanding of the patient's wishes. For more information about these and other hospital policies and procedures, see Patient Relations.
Consenting to a test, procedure, or surgery is an important decision. Before you consent, it is essential to have a conversation with the physician (or other provider) who is recommending and/or performing the procedure so you can fully understand what is involved and have all of your questions answered.
No. It is impossible to guarantee the outcome or to eliminate every risk. However, the doctor has recommended the procedure because he/she thinks the advantages to your child outweigh the risks.
Many procedures require more than one pair of hands. Your doctor may be helped by other fully trained doctors, doctors in training, nurse practitioners, physician assistants and other healthcare providers. Sometimes the team who assists your doctor will change during the procedure.
No one can assist your doctor unless they are legally allowed to do so here at Boston Children’s Hospital.
In most cases, nobody will watch except the care team.
Sometimes there are other observers. The only people who are allowed to watch are medical students on approved training rotations and others who have formal guest privileges at Boston Children’s. For example, surgeons from around the world often visit to watch our teams at work.
Please tell us and we will respect your wishes.
However, please consider that by allowing students and others to watch your child’s procedure, you will be helping us train those who will care for the next generation of children.
The doctor will ask you to explain the procedure back to him/her to make sure we have done a good job of explaining things to you. We want you to be able to tell us your understanding of:
It is rare for the doctor to change the plan during a procedure. In most cases, the doctor would contact you in the family waiting area before making a major change in plan.
Sometimes doctors will find something they were not expecting and need to change the plan.
In an emergency, the doctors will respond immediately, and may not have time to contact you first. Emergencies are rare. However, our job is to prepare for any event, no matter how uncommon
Blood and blood products are given to improve the oxygen supply to the body. They help to correct bleeding problems and can be life-saving.
Tissues that are removed during surgery are tested and examined by a special physician (pathologist) to ensure there are no unexpected problems. This examination is an essential part of your child’s care.
Boston Children’s Hospital, like other research hospitals, may use tissue (that would otherwise be disposed of) for research into causes and cures for disease or for teaching purposes. Any tissue that we use for research will be de-identified, which means that we can not identify which patient it came from.
In many procedures, pictures or video records of the findings are considered “standard” and are needed for best care. For example, doctors may need pictures to tell if your child’s condition has changed over time. Pictures and video are used only to care for your child, or to teach others. When they are used for teaching purposes, all identifying information (such as names and addresses) is removed.
Tell your doctor. Some parts may be crossed out before you sign. Other parts (such as permission for my doctor to change the plan if he/she finds other problems during the procedure) cannot be removed.
A Spanish version of this is available from your provider.
Please send comments or questions to familyed@childrens.harvard.edu.