The following excerpt is taken from Chapter 3 of Autistic Spectrum
Disorders: Understanding the Diagnosis & Getting Help
Mitzi Waltz, copyright 2002 by O'Reilly & Associates, Inc. For book
orders/information, call 1-800-998-9938. Permission is granted to
print and distribute this excerpt for noncommercial use as long as the
above source is included. The information in this article is meant to
educate and should not be used as an alternative for professional
medical care.
Usually, the first person to hear the concerns of a young child's
parents is a pediatrician. In this age of managed care, the
pediatrician takes on more importance than ever: Not only is she the
doctor who knows the most about how a particular child's development
compares to the norm, but she is almost always the primary care
provider (PCP) designated by health insurance plans. She generally
serves as a gatekeeper to more advanced care, making referrals to
medical and therapeutic specialists as needed.
In an ideal world, pediatricians would be quick to see the early
signs of ASDs, and would guide parents toward the best medical
resources available. Sometimes that's how it works.
Elaine's pediatrician recognized developmental problems quite
early. He said that she did not speak because she couldn't, not
because she didn't want to, and advised me to have her seen by
St. Mary's Hospital for Early Intervention. At St. Mary's, Elaine was
seen by a neurologist, a speech expert, and countless doctors. They
couldn't agree on a label--only the neurologist felt certain that it
was PDD-NOS. Luckily, they did agree on recommendations for
treatment. --Sarah, mother of two-year-old Elaine (diagnosed PDD-NOS,
possible oral-motor apraxia)
Because parents know the most about their child, they play a
key role. To assure a proper diagnosis, parents need to make their
concerns crystal clear.
That isn't always easy. Many pediatricians complain that parents
seem almost apologetic about being in their offices, don't ask enough
questions, and don't volunteer important information unless asked. By
and large, that's learned behavior, ingrained over a lifetime of
rushed appointments with harried doctors.
It's true that the typical sore-throat appointment is a ten-minute
affair these days, but when you have greater concerns it's okay to ask
for more one-on-one time with the doctor. There's no need to feel
guilty, because doctors are accustomed to scheduling longer sessions
for some types of appointments. Practitioners should reassure parents
about this point.
You're not asking the pediatrician to diagnose an ASD
, you're looking for a referral--but before such a referral can be
approved, the doctor must be sure that specialized diagnostic help is
required. Ask the pediatrician's office for a consultation appointment
of at least thirty minutes (more would be nice).
Why do you need to go beyond the pediatrician? Because while
pediatricians are indeed experts in the typical problems of
children--croup, the flu, pinworms, diaper rashes, and all the
rest--they receive very little training in neurological or psychiatric
disorders. In fact, a study by Elizabeth Costello, Ph.D., associate
professor of child and adolescent psychiatry at Duke University, found
that a large HMO's pediatricians were only able to identify 17 percent
of the children who presented with psychiatric disorders. In addition,
that 17 percent tended to be children with the most common problems,
including bedwetting and learning disabilities.1
Pediatricians also have their own opinions about disability. Some know
very little about available services, and assume that only the
severely disabled are eligible for assistance.
We began asking our pediatrician questions about Joseph's
language regression at fifteen months, but she ignored our concerns
because she felt his skill with letters and numbers precluded any
developmental disability. She actually discouraged us from seeking
Early Intervention when he was twenty-four months old. She said we
might be uncomfortable since "the other children are more severely
impaired." --Jennifer, mother of three-year-old Joseph (Aspergers-like
and autistic-like features, diagnosis still in progress)
Use your consultation appointment as
efficiently as possible. Accurate, detailed records are the most
important thing parents can contribute at this appointment. These
should include the usual "baby book" milestones (first step, first
word, etc.) as well as notes about anything unusual parents have
observed. Areas the pediatrician is likely to ask about include
patient and family medical history, speech, relationships with family
members and peers, play patterns, and interests. You may want to
consult the diagnostic questionnaires, under Resources on this
site, to see the kinds of questions a doctor might ask.
Keeping a daily diary is an excellent way to prepare for a
diagnostic evaluation. Many families have learned a great deal during
this process as well. If possible, record activities, diet, and
behaviors each day for a period of two weeks or more, with the time
and duration of activities and behaviors noted. Not only can this
diary provide a very complete picture of the child to a professional,
it can also help to identify patterns. Some families have identified
food allergies this way, or gotten data they needed to create the most
beneficial daily routine for their child.
If the child has seen other doctors, releases must be signed to
have any useful records transferred to the pediatrician. Older
children may have school records that would be helpful, and these can
also be transferred if a signed release is on file. Transfers always
seem to take longer than you would expect, so get releases taken care
of early, and make sure records were sent and received. Alternatively,
if you have your own copies of these records (and you should), you may
photocopy and deliver them yourself.
If possible, provide your information to the pediatrician at least a week before the consultation appointment. Include a request that she read the material in advance and review the patient's medical file before the meeting. The goal is to put your child's case on the pediatrician's front burner and to ensure that when the appointment takes place, the details are fresh in her mind.
You should also summarize their concerns in writing. The
records already mentioned can help you gather your thoughts. You don't
have to be an eloquent writer to express what worries you. You can jot
down a simple numbered list rather than writing whole paragraphs if
you prefer. It may help to compare your child to his or her siblings,
or to other children in the day-care center, school or
neighborhood. Some parents may want to send their summary of concerns
to the doctor in advance; others may prefer to use it as an agenda for
discussion during the consultation session.
You may also want to discuss your concerns in advance with an
advice nurse or another person, such as a physician's assistant, who
works closely with the pediatrician. In large medical practices or
HMOs, nurses are an important part of the organization, and can be
important allies for parents who need referrals to specialists or even
just a listening ear.
As you prepare for it, keep in mind that the consultation
appointment is only a preliminary step toward your real goal: a
multidisciplinary evaluation.
The consultation appointment
A consultation appointment is different from a regular visit to the
pediatrician. Unless the doctor happens to notice something of medical
concern, there will be no need to do the usual eye, ear, and mouth
exam, or to check height and weight. In fact, the appointment may take
place in a meeting room or office rather than in an examination room.
When you come, bring any records you have
gathered, copies of your earlier letter (just in case it never reached
the doctor), your summary of concerns, and any questions that you want
to ask. Bringing a small notebook can help you keep
a record of the discussion. If your child tends to be difficult to
manage, bring a bag of toys or books that are likely to help keep him
calm. Parents may want to choose playthings that will help the doctor
see where the child is at developmentally, such as a doll or stuffed
animal.
If the consultation seems to be getting off to an awkward start,
start the ball rolling by referring to your summary of concerns or
your list of questions. Always keep your goal in mind:
You're there to make a case for referral, and
your observations are the evidence you'll need to convince the
pediatrician. Think of yourself as a salesperson, trying to convince a
customer. You want to be the one in charge of this meeting, and
keeping that image in your mind can help.
Most pediatricians will use the consultation appointment to
listen to your concerns, discuss the issues raised, and recommend the next course of
action. Some will use a set of standard questions about behavior and
development to screen the patient. For children, the Pediatric Symptom
Checklist (PSC) is one of the most common screening tools used. It's a
list of thirty-five questions created by Dr. Michael S. Jellinek of
Harvard Medical School, and has proven to be about 95 percent
effective at catching psychiatric disorders in children.
Checklists and guidelines are great, but there's really no
substitute for knowledge and experience. As parents interviewed make
painfully clear, some pediatricians are reluctant or unable to
recognize ASDs, even when faced with a non-verbal three-year-old who
spends the entire consultation appointment screaming or dissembling
the doctor's scale. You may hear phrases like "your child just needs
to be disciplined more strictly," "he'll grow out of it," or "let's
wait and see." There are several responses you can make:
- Go back over your evidence, showing that your child is having more
than one developmental problem, and explaining how it is affecting her
life. If you feel comfortable doing so, you may also want to mention
how it is affecting your family life.
- Set a "wait and see" timetable. Ask the pediatrician which
important milestones (such as meaningful speech) should be passed
within the next three months, and secure a promise that if these goals
have not been met, a referral will be made. This approach may be
appropriate for very young children whose possible impairments are
subtle.
- If the pediatrician says he knows nothing about autistic spectrum disorders, suggest that he do some research. The organization First Signs, online at
http://www.firstsigns.org,
sends out an excellent kit for pediatricians that includes diagnostic information in written for and on video. You might even order one for the doctor yourself.
- Ask the reluctant pediatrician for a referral to a developmental
pediatrician (see below).
- Go up the chain of command in the health-care organization, if you
are using a managed care or HMO practitioner. In medical groups there
is a board that takes patient complaints under consideration. You can
petition the board to approve your referral even if the pediatrician
refuses. Usually this is done in writing, not in person.
- Ask the doctor to put his refusal to refer in writing. This may
not be something he'd like to commit to paper, so you might end up
getting the referral after all.
- If the doctor does put his refusal in writing, you can choose to
call your diagnostic facility of choice and set up an appointment with
the appropriate evaluation team directly. Be prepared to pay for this
visit out-of-pocket. However, if the team confirms your suspicions,
you should be able to bill your insurance company for reimbursement
due to refusal of an appropriate referral.
- If the pediatrician won't refer, but won't put his refusal in
writing either, you can still "self-refer," but it will be harder to
get reimbursed. You should send a letter to the pediatrician
explaining why you have made this choice over his objections. Send a
copy to your insurance company as well. This creates a paper record,
allowing you to later pursue a claim for improper refusal later on, if
warranted.
Referral to a developmental pediatrician, a doctor who
specializes in treating the health problems of children with
developmental delays or handicaps, presents a less-expensive
alternative. For you, seeing another pediatrician may seem like one
more hurdle to jump on the way to the diagnostic team. Your reluctant
pediatrician, on the other hand, will probably like the idea. If your
concerns are valid, the developmental pediatrician can explain the
reasons to your regular pediatrician, and can provide information
about the best resources available locally for full diagnosis and
treatment.
Developmental pediatricians are much more familiar with
neurological problems, medications, and current research on
disabilities. They tend to work closely with specialists, including
neurologists, psychopharmacologists, psychiatrists, and therapists of
various types. In fact, you may want to continue seeing the
developmental pediatrician on a long-term basis, once the diagnostic
process is complete.
Roadblocks to referral
Most doctors in the U.S. share the risks and expenses of caring for
special-needs patients, including specialist referrals, with business
partners or an HMO group. Doctors who make too many referrals can face
financial penalties, even if the extra services were absolutely
necessary for the patients' health. Physicians may also feel
constrained by directives from insurance companies, which want to
minimize expenses. The health-care structure in America can make
convincing your pediatrician to send you to an expensive facility a
little difficult.
Low-income Americans who are uninsured face the biggest roadblock
of all: lack of access to health care. They may be able to obtain
diagnostic help through the school district or through public Early
Intervention programs for pre-school children. The school district may
also provide some diagnostic and therapeutic assistance, especially in
the areas of speech, occupational, and physical therapy that relates
to classroom performance. There are also special medical programs
available for low-income families and for children with handicapping
conditions.
In Canada and Europe, where the single-payer system of nationalized
health-care predominates, doctors have a different set of constraints
on their ability to make referrals. Resources are focused on providing
basic health-care to everyone, so specialists are rarer and harder to
access than in the U.S. Parents may be forced to pay out-of-pocket to
doctors who practice outside the national health-care scheme. The
expenses can be considerable. Some families have been able to gain
more-timely access with help from a sympathetic social worker or
health visitor, or have called on disability advocacy groups for
assistance.
In countries where neither the private insurance nor the
single-payer model predominates, parents should seek out--and pay
for--a specialist directly, without going through a preliminary
consultation appointment. Reduced-fee or free help may be available
through state-run hospitals and clinics, medical facilities run by
religious orders or charities, or individual physicians who are
willing to take a case at a lower cost than usual.
1. Elizabeth Costello et al., "The Great Smoky Mountains Study of
Youth: Functional Impairment and Serious Emotional Disturbance (SED)"
Archives of General Psychiatry (1988): 1107-1116.