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Psychiatric Times. Vol. 23 No. 6
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Essential Issues in Pediatric Psychosomatic Medicine

By Maryland Pao, MD, Elizabeth D. Ballard, and Haniya Raza, DO, MPH | May 1, 2006

Treatment nonadherence

Nonadherence with treatment, another common reason for a psychosomatic consultation request, can range from 11% to 93% in pediatric patients. It adversely affects treatment response, increases the need for additional prescriptions, and may extend the course of illness.15Factors such as age, culture, patient and family characteristics, and dosage and means of administration of medication can all affect adherence. Furthermore, child psychopathology such as oppositional defiant disorder has been associated with a higher rate of nonadherence with medical regimens.16 Thus, multiple factors need to be considered when evaluating nonadherence.

Psychiatric disorders

Many of the psychiatric disorders seen in adult psychosomatic medicine practice are also seen in practices involving children and adolescents, although research on the prevalence of specific conditions is sparse. Delirium is relatively common and has a similar presentation to that seen in adults. Certain symptoms, such as disorientation and psychosis, appear to be less common or more difficult to assess in pediatric patients, while delirium associated with organic causes, including medication toxicity, infection, and metabolic imbalances, is comparable in prevalence to adult delirium.17 Strategies for treating delirium include reorienting the child through reassurance, use of familiar objects, and clocks and calendars (when age appropriate) in the hospital room. When pharmacologic treatment is indicated, typical and atypical antipsychotic medications are used.17

Other psychiatric conditions that may be encountered in chronically ill children include depression, anxiety, somatization, and illness falsification. Assessing psychiatric illness is often difficult because of physical symptoms that interfere with diagnostic measures; this can lead to both overdiagnosis and underdiagnosis. Depression appears to be similarly prevalent in chronically ill and healthy children; in children with chronic illness, it can lead to complications in medical outcomes and increased disability.18

Somatization can occur when a child learns that reporting physical symptoms garners more attention than reporting emotional distress.19 Illness falsification, though rare in children, may manifest as factitious fevers, self-induced rashes, or deliberately manipulated insulin levels.20 Somatization, illness falsification, and Munchausen syndrome by proxy (illness falsification by caretaker) can all lead to unneeded treatment and, in extreme cases, death. Management of these disorders requires a clear understanding of the delicate interplay between biologic, psychological, and social factors that affect psychiatric symptoms.

Use of psychotropic medication

Psychotropic medications for symptoms as well as syndromes can be quite helpful in improving the quality of life of many patients. The prevalence of psychotropic use in the general pediatric population is estimated to be around 6%,21 but the prevalence of psychotropic medication use in medically ill children is not well documented. Table 2 shows psychotropic medications with their FDA approval status for use in children and adolescents.

 
Table 2
Psychotropic medications with FDA approval status for use in children and adolescents
Class   Medications   FDA labeled for use in children
Anti-
depressants
Amitriptyline (generic) 12 y and older, for depression, polyneuropathy
  Bupropion (Wellbutrin, Zyban) No
  Citalopram (Celexa) No
  Desipramine (Norpramin, generic) No
  Doxepine (Adepin, Sinequan, generic) 12 y and older, for mixed anxiety and depressive disorder
  Escitalopram (Lexapro) No
  Fluoxetine (Prozac, generic) 7 - 17 y, for depression, OCD
  Fluvoxamine (Luvox) 8 y and older, for OCD
  Mirtazapine(Drug information on mirtazapine) (Remeron) No
  Nortriptyline (Pamelor, generic) No
  Sertraline (Zoloft) 6 - 17 y, for OCD
  Paroxetine (Paxil, generic) No
  Trazodone (Desyrel) No
  Venlafaxine (Effexor) No
Anxiolytics Alprazolam (Xanax, generic)
No
  Clonazepam (Klonopin, generic) Up to 10 y, or 30 kg, for epilepsy
  Lorazepam (Ativan, generic) 12 y and older, for insomnia (oral), anesthesia premedication (oral)
Mood stabilizers Carbamazepine (Tegretol, generic) 12 y and older, for depression, polyneuropathy
  Gabapentin (Neurontin) 3 - 12 y, for partial seizures
  Lamotrigine (Lamictal) 2 y and older, for partial seizures
  Lithium (Eskalith, generic) 12 y and older, for bipolar disorder
  Oxcarbazepine (Trileptal) 4 - 16 y, for epilepsy
  Valproate (Depakote, Depacon, generic) 10 y and older, for migraine prophylaxis, epilepsy
Anti-psychotics Aripiprazole (Abilify) No
  Chlorpromazine (Thorazine) 6 mo and older, for anxiety about presurgery
1 - 12 y, for behavioral syndrome
Pediatric, for nausea and vomiting, tetanus
  Droperidol (Inapsine) 2 y and older, for prophylaxis of postoperative nausea and vomiting
  Haloperidol (Haldol, generic) 3 y and older, for delirium, Tourette syndrome, severe problematic behavior
  Olanzapine (Zyprexa) No
  Quetiapine (Seroquel) No
  Risperidone (Risperdal) No
  Thioridazine (Mellaril, generic) 2 y and older, for schizophrenia
  Ziprasidone (Geodon) No
Stimulants Dextroamphetamine (Adderall, generic) 3 y and older, for ADHD, narcolepsy
  Methylphenidate (Concerta, Ritalin, generic) 6 y and older, for ADHD, narcolepsy
Other Atomoxetine (Strattera) 6 y and older, for ADHD
  Clonidine (Catapres) Pediatric, for epidural for pain relief
  Guanfacine (Tenex)
Propranolol(Drug information on propranolol) (Inderal,
12 y and older, for hypertension
  Propranolol (Inderal, generic) Pediatric, for hypertension
 
OCD, obsessive-compulsive disorder; ADHD, attention-deficit/hyperactivity disorder.

Terminal illness

Terminal illness and the death of a child is a sad and inevitable aspect of pediatric hospital consultation that provokes significant anxiety in the patient, family, and caregivers. Informing a child that he or she is going to die is difficult, but parents rarely regret sharing this information with the child.22 Children in different developmental stages have differing conceptions or misunderstandings of death and may be helped by frank conversations with family or by play therapy facilitated by pediatric psychosomatic medicine specialists. Comfort is another important issue at the end of life; parents have reported that at the end of life, their child had a great deal of suffering from pain, dyspnea, or fatigue and had “no fun.”23 Psychiatrists can provide treatment for a dying child while also offering support to the family and hospital staff.

Conclusion

With evolving innovations in medical technology and rapid advances in neuroscience and molecular genetics, a comprehensive and integrative field such as pediatric psychosomatic medicine can only be expected to expand. Recent research on cytokine-induced sickness behavior24 and the periodic identification of novel genetic markers in patients with chronic diseases provide new information that may help in the development of future treatments.

Clinicians providing psychiatric care must always remain vigilant in understanding how these treatments are experienced by children and their families. Early identification of psychiatric symptomatology will enhance outcomes in at-risk children. Appropriate diagnosis of mental disorders, prompt psychiatric treatment, and recognition of normal developmental processes in children and adolescents are critical aspects of caring for the whole child.

Terminal illness

Terminal illness and the death of a child is a sad and inevitable aspect of pediatric hospital consultation that provokes significant anxiety in the patient, family, and caregivers. Informing a child that he or she is going to die is difficult, but parents rarely regret sharing this information with the child.22 Children in different developmental stages have differing conceptions or misunderstandings of death and may be helped by frank conversations with family or by play therapy facilitated by pediatric psychosomatic medicine specialists. Comfort is another important issue at the end of life; parents have reported that at the end of life, their child had a great deal of suffering from pain, dyspnea, or fatigue and had “no fun.”23 Psychiatrists can provide treatment for a dying child while also offering support to the family and hospital staff.

Conclusion

With evolving innovations in medical technology and rapid advances in neuroscience and molecular genetics, a comprehensive and integrative field such as pediatric psychosomatic medicine can only be expected to expand. Recent research on cytokine-induced sickness behavior24 and the periodic identification of novel genetic markers in patients with chronic diseases provide new information that may help in the development of future treatments.

Clinicians providing psychiatric care must always remain vigilant in understanding how these treatments are experienced by children and their families. Early identification of psychiatric symptomatology will enhance outcomes in at-risk children. Appropriate diagnosis of mental disorders, prompt psychiatric treatment, and recognition of normal developmental processes in children and adolescents are critical aspects of caring for the whole child.

Dr Pao is deputy clinical director, National Institute of Mental Health (NIMH) Clinical Research Center, Bethesda, Md. Ms Ballard is a research associate at NIMH. Dr Raza is a psychiatry resident at NIMH. The authors have no conflicts to disclose.
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References
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3. American Academy of Pediatrics, Committee on Psychosocial Aspects of Child and Family Health. The new morbidity revisited: a renewed commitment to the psychosocial aspects of pediatric care. Pediatrics. 2001;108:1227-1230.
4. Knapp PK, Harris ES, Consultation-liaison in child psychiatry: a review of the past 10 years, part I: clinical findings. J Am Acad Child Adolesc Psychiatry. 1998;37:17-25.
5. Gitlin DF, Levenson JL, Lyketsos CG. Psychosomatic medicine: a new psychiatric subspecialty. Acad Psychiatry. 2004;28:4-11.
6. Caspi A, Sugden K, Moffitt TE, et al. Influence of life stress on depression: moderation by a polymorphism in the 5-HTT gene. Science. 2003;301:386-389.
7. Sharpe D, Rossiter L. Siblings of children with a chronic illness: a meta-analysis. J Pediatr Psychol. 2002;27:699-710.
8. Wamboldt MZ, Wamboldt FS. Role of the family in the onset and outcome of childhood disorders: selected research findings. J Am Acad Child Adolesc Psychiatry. 2000;39:1212-1219.
9. Kain ZN, Caldwell-Andrews A, Wang SM. Psychological preparation of the parent and pediatric surgical patient. Anesthesiol Clin North America. 2002;20:29-44.
10. Fitzgerald M, Beggs S. The neurobiology of pain: developmental aspects. Neuroscientist. 2001;7:246- 257.
11. National Child Traumatic Stress Network. Medical Events & Traumatic Stress in Children and Families. 2005. Available at http://www.nctsnet.org/nccts/nav.do?pid=typ_mt. Accessed March 10, 2006.
12. Bennett DS. Depression among children with chronic medical problems: a meta-analysis. J Pediatr Psychol. 1994;19:149-169.
13. Phipps S, Srivastava DK. Repressive adaptation in children with cancer. Health Psychol. 1997;16:521-528.
14. Klinnert MD, Nelson HS, Price MR, et al. Onset and persistence of childhood asthma: predictors from infancy. Pediatrics. 2001;108:E69.
15. Winnick S, Lucas DO, Hartman AL, Toll D. How do you improve compliance? Pediatrics. 2005;115: e718-e724.
16. Bernstein GA, Anderson LK, Hektner JM, Realmuto GM. Imipramine compliance in adolescents. J Am Acad Child Adolesc Psychiatry. 2000;39:284-291.
17. Turkel SB, Tavare CJ. Delirium in children and adolescents. J Neuropsychiatry Clin Neurosci. 2003; 15:431-435.
18. Shemesh E, Bartell A, Newcorn JH. Assessment and treatment of depression in medically ill children. Curr Psychiatry Rep. 2002;4:88-92.
19. Silber TJ, Pao M. Somatization disorders in children and adolescents. Pediatr Rev. 2003;24:255-64.
20. Libow JA. Child and adolescent illness falsification. Pediatrics. 2000;105:336-342.
21. Zito JM, Safer DJ, Dosreis S, et al. Psychotropic practice patterns for youth: a 10 year perspective. Arch Pediatr Adolesc Med. 2003;157:17-25.
22. Kreicbergs U, Valdimarsdottir U, Onelov E, et al. Talking about death with children who have severe malignant disease. N Engl J Med. 2004;351:1175- 1186.
23. Wolfe J, Grier HE, Klar N et al. Symptoms and suffering at the end of life in children with cancer. N Engl J Med. 2000;342:326-333.
24. Konsman JP, Parnet P, Dantzer R. Cytokineinduced sickness behaviour: mechanisms and implications. Trends Neurosci. 2000;25:154-159.
25. Koopman HM, Baars RM, Chaplin J, Zwinderman KH. Illness through the eyes of the child: the development of children's understanding of the causes of illness. Patient Educ Couns. 2004;55:363-370.


 
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