▪ Consultation Liaison: Consultation in Pediatrics



▪ Consultation Liaison: Consultation in Pediatrics





GENERAL PRINCIPLES AND MODELS OF CONSULTATION

Chronic medical illness increases the risk for psychiatric conditions in children and adolescents, with rates two- to fourfold those in the general population. Concomitant medical illness may color the presentation of behavioral difficulties. Further complications can arise given the significant stress experienced by parents and other family members (e.g., with higher rates of stress-related symptoms and even posttraumatic stress disorder [PTSD]). Consultation issues can arise in different contexts (e.g., outpatient or emergency settings) but most typically arise in the context of pediatric inpatient hospitalization. As described in Chapter 23, different models of care and options for treatment can arise, and an understanding of the nature of the differences between medical and psychiatric models of care is important.

A typical medical consultation in pediatrics can often be obtained quickly with a treatment plan rapidly in place, but in psychiatry, even when the initial assessment is expeditious, intervention may be a long-term process. Other issues include sensitivities to issues of confidentiality and privacy. An appreciation of both the biomedical and biopsychosocial approaches is helpful in providing effective consultation. Some appreciation of the nature of underlying medical conditions may be highly relevant (e.g., are symptoms a feature of the underlying disorder or might they be a manifestation of treatment?). In some circumstances, such as head trauma or central nervous system (CNS) radiation as part of cancer treatment, the potential brain contributions to behavioral difficulties may be easy to appreciate.

Medical procedures may be painful and stressful and are often associated with behavioral and emotional difficulties. Similarly, acute and chronic medical problems can represent different challenges for children and family members. Previous patterns of coping may be used with varying degrees of success. The reactions and behaviors of parents may also be important factors in relation to levels of distress in the child. Peer relationships may also be important (e.g., management of type I diabetes in which the availability of more supportive peers results in better control). The age and cognitive level of the child also have an impact on children’s understanding of and responses to illness and medical procedures. Using Piaget’s approach (see Chapter 2), Lewis (2002) noted the ways in which children’s cognition color their responses
to illness, physical functioning, and disease; this can inform intervention. Over time, children have an increased ability to understand cause and effect, but children in the phase of concrete operations (roughly early primary school) may see their illness as a punishment and may benefit from an explanation. In contrast, adolescents are capable of abstract thought and have a more adult understanding of pathophysiology, although in adolescents, a sense of invulnerability may complicate compliance with medical treatments.

Mental health professionals can provide a broad range of services with either a narrow or broad focus. Consultants must be aware of the context in which they are asked to consult and be familiar with the range of problems frequently encountered along with their potential treatments. For psychiatrists, a familiarity with issues of differential diagnosis and potential behavioral and psychiatric symptoms and complications associated with specific illnesses and treatments is important. In addition to work around a specific case, consultants are ideally involved on a longer term basis, providing suggestions for programmatic approaches designed to minimize stress, maximize coping, and facilitate outcomes.

Mental health professionals can draw on a number of treatments that have been used with support, to varying degrees, in the research literature. These include treatments for pain, encopresis, and obesity as well as interventions specific to disease such as sickle cell disease and other conditions. Methods from cognitive behavior therapy (CBT; see Chapter 22) have been adapted for procedure-related pain. These methods may also help ensure adherence to treatment for children with asthma, juvenile rheumatoid arthritis, and type 1 diabetes. A range of theories and model approaches exist for pediatric consultation (Table 25.1).

The Resource Consultation Model (also referred to as the Independent Functions Model) usually focuses on a specific diagnostic concern with a goal of obtaining diagnostic clarification, recommendations, and potential resources both for the medical team and family with usually no further involvement of the consultant. This is the approach similar to that of other specialists who consult with the primary care provider. Although it has the potential to serve, over time, as a bridge to other more complex models of consultation, this model has limitations intrinsic to limited contact and a highly specific and narrow focus (e.g., it might not address relevant system issues). In contrast, the process (or educative) model may involve work primarily with the medical staff with, potentially, little or no actual contact with the patient. In this approach, the consultant provides relevant information to the primary provider. Broadly viewed, this model includes a range of educational activities and has the great potential advantage of “spreading the wealth” of information broadly. Limitations stem from the problems of variable knowledge base on the parts of the primary care providers and potential lack of specificity to the individual child’s problems. In the collaborative team model, there is a sharing of responsibility and decision making and more intensive collaboration between the mental health consultant and medical personnel. If things go well, this model has the potential for influencing an entire system of care but it does, of course, intrinsically require a substantial commitment on the part of all concerned. Other approaches have attempted to take a broader systems perspective looking, for example, at how the family, school, and medical care system all interact to influence care. The family systems framework considers differences in family interaction and communication as well as disease management practices. Involving schools and the educational system may also be important. Some psychiatric and developmental problems have clear implications for school-based services, and children with medical conditions can also present issues relative to school reentry after illness or hospitalization. These issues are becoming increasingly common as children with serious medical illnesses are surviving more frequently and may present to schools with problems that impact their ability to profit from usual educational programs, as we discuss at the end of this chapter. Issues of school-based consultation are addressed subsequently in this chapter.








TABLE 25.1 COMPARING AND CONTRASTING CONSULTATION MODELS WITH PEDIATRICS









































Model


Consultee


Nature


Methods


Duration


Resource consultation


Patient


Contact with patient and pediatrician


Telephone, face-to-face; “curbside” consultation


Limited; as needed


Process—educative consultation


Pediatrician


Contact with pediatrician


Educational


Ongoing relationship with pediatrician


Collaborative team


Patient and treatment team (e.g., pediatrician; nursing staff)


Contact with patient and health care providers


Interdisciplinary and multidisciplinary approach; “shared caregiving”


Ongoing relationships with teams of health care providers


Family systems consultation


Patient, family, and staff


Contact with patient, family, and health care providers; entire system is unit of consultation


Joining with family; acknowledge strengths and competencies of family


Time limited


Multisystemic


Hospital and other systems


Contact with patient, family, health care providers, other systems (e.g., school settings)


Consultation with multiple care providers within and outside of the hospital setting


Proposed model; unknown


Reprinted from Campbell, J. M., & Cardona, L. (2007). The consultation and liaison process to pediatrics. In A. Martin & F. Volkmar (Eds.), Lewis’s Child and Adolescent Psychiatry: A Comprehensive Textbook, 4th edition, p. 917. Philadelphia: Lippincott Williams & Wilkins.




PEDIATRIC INPATIENT CONSULTATION

Various issues and problems may serve to elicit requests for consultation relative to inpatients in pediatric settings (Table 25.2). These requests can vary from consultation on aspects of management of behavioral difficulties, issues of differential diagnosis, adherence to treatment, and so forth. Some of the more frequent requests involve issues of depression and suicidal ideality, management of anxiety and psychiatric symptoms, and lack of adherence to treatment. Referral rates vary widely and may be more frequent in some service areas than others (e.g., hematology, oncology, and general pediatric services are common sources of referral). It is common for patients referred to psychiatric consultation to have longer lengths of stay, reflecting various factors. On the other hand, various factors may make referral less likely, and much of the available literature suggests that this is indeed the case.








TABLE 25.2 FREQUENT CONSULTATION REQUESTS ACROSS THREE PEDIATRIC SETTINGS





















Setting


Presenting Concerns (%)1


Primary Clinical Activities


Primary care


Heterogeneity of concerns:




  1. Behavioral noncompliance (16.2)



  2. Tantrums (12.8)



  3. Aggression (8.1)


Assessment; parent guidance; psychotherapy


Inpatient ward


Heterogeneity of concerns:




  1. Adjustment problems (14.9)



  2. Noncompliance (13.3)



  3. Depression or suicide (12.9)



  4. Anxiety (6.6)



  5. Pain management (6.6)



  6. Parent coping (6.2)


Wide range of activities: assessment; time-limited psychotherapy; staff consultation; psychopharmacological consultation; parent guidance


Emergency department




  1. Suicidal behaviors (47%)



  2. Oppositional behavior (24%)



  3. Threats of violence or aggression (17%)


Assessment, diagnosis, and disposition


1 Percentages reported are from Carter et al. (2003) and Drotar, Spirito, and Stancin’s (2003) review. Reprinted from Campbell, J. M., & Cardona, L. (2007). The consultation and liaison process to pediatrics. In A. Martin & F. Volkmar (Eds.), Lewis’s Child and Adolescent Psychiatry: A Comprehensive Textbook, 4th edition, p. 918. Philadelphia: Lippincott Williams & Wilkins.



Various guidelines for conducting a psychiatric consultation have been proposed (see Campbell and Cardona, 2007). Generally, the consultant seeks to define the specific, explicit question being asked; reviews the record; and talks with the staff before actually interviewing the patient, parents, or both. After this, there may be suggestions for additional tests or assessments and perhaps coordination with other agencies or providers (e.g., schools or mental health service providers). The consultant should be continuously aware of potential issues of coordination and communication (or lack thereof) because these impact the patient. There will usually be a feedback with specific recommendations. Depending on the context, services may be provided, and the consultant will wish to follow up on the assessment.

Clarification of the referral question is the first step in the process. The consultant should be aware of both the explicit and implicit issues raised at the time of referral (e.g., the explicit question might concern the child or may be more truly focused on the parents). As part of this process, the consultant can also elicit exactly what has been told to the child and family about the consultation and be sure that they have been adequately prepared for it. As part of the review of the medical record, the consultant should be particularly alert to issues of poor or miscommunication and fragmentation of care that can potentially play an important role; this becomes particularly important in more complicated situations in which multiple medical subspecialties are involved. The observations of nurses in the record or in discussion provide important information on the child’s functioning and behavior. The consultant should be alert to potential behavioral or psychiatric effects of medications or medication combinations or the after effects of such agents (e.g., withdrawal symptoms). Often, the parents are interviewed before the child; as relevant, others “stake holders” (state child protective service agencies, foster parents, teachers, and others) may also provide important information. The consultant should aim to obtain a concise summary of the child’s history with emphasis on special issues such as vulnerabilities or difficulties antedating the current hospitalization, family and social factors that may relate to the referral, community and financial resources, and so on.

The interview with the child typically includes a comprehensive mental status examination appropriate to the child’s age and level of functioning (see Chapter 3). Observation of the child in the hospital setting can provide important information. At times, specific self-report inventories might be administered. If there are questions of potential CNS dysfunction or delirium, repeated interviews are essential to document baseline function and changes.

Depending on the situation, the consultant might ask for further procedures or tests (e.g., neuroimaging or electroencephalography [EEG]). Sometimes neuropsychological testing may be needed for children who have experienced CNS insults. The consultant has an important role in attempting to understand the relationships between the patient and family and other systems of care (educational, medical, or otherwise) that pose potential obstacles.

Even before the consultant places a formal summary of his or her assessment in the patient’s record, it is important that the results be communicated to both the medical staff and to the patient and family. The consultant should conduct a direct discussion of the various factors that are contributing to current difficulties and attempt to foster a thoughtful discussion with both the medical staff and the family about these issues.

As noted in Chapters 21, 22 and 23, a range of treatment procedures have been developed to help children and families coping with both acute and chronic illness. CBT methods can be used to help children deal with pain and anxiety around anticipated medical procedures. Other approaches can be used to target issues of treatment noncompliance within a family context. Depending on the context, psychopharmacological intervention may provide significant benefit (e.g., in management of anxiety, depression, or agitation). Although some interventions can
be instituted within a hospital settings others may require helping families access community- and school-based services.

Many barriers to providing effective consultation services exist. These include a shortage of potential consultants, limited insurance reimbursement, and differences in models of service delivery in the pediatric and mental health systems. The pace of pediatric care moves much more quickly than that of mental health work, and an adequate psychiatric consultation can take several hours. Other issues have to do with resistance, on the part of families and medical professionals, to use of mental health services. The complex issues of confidentiality (see Chapter 26) can also be an issue. Pediatricians and primary care providers may complain about a lack of willingness to share results and recommendations; this is particularly unfortunate given the importance of primary care providers in providing comprehensive care. The consultant should attempt to keep the assessment and recommendations understandable, action oriented, and concise. Lewis (2002) has suggested that on larger inpatient services, the occasional, or frequent, presence of the consultant can reduce barriers to communication and facilitate improved service delivery. This is most practical in teaching hospital settings.


Pediatric Oncology

Around one in 6500 children and adolescents are diagnosed with cancer each year, and despite many advances in treatment, pediatric cancer remains the leading cause of disease-related death in children ages 1 to 14 years (Zebrack, 2007). Advances in treatment have increased long-term survival and, in many cases, recovery. With increased survival rates, the emphasis of intervention programs has, to a considerable extent, changed to include a more developmental and family-focused approach to care with greater attention to foster coping and dealing with stress-related symptoms and disorders Much of the available research literature focuses on children of middle school age with comparatively less on preschool and young school-age populations, reflecting, at least in some part, complexities related to assessment, consent, and so forth. The growing recognition of the importance of family and family factors reflects a greater awareness of the challenges pediatric cancer poses for parents and siblings. Similarly, the older literature, which emphasized only the stressful aspects of cancer, has come to a fuller appreciation of the range of outcomes, including positive outcomes, that may come with coping with pediatric cancer.

The time of initial diagnosis can be one of stress and confusion. It is helpful for the child to know, in developmentally appropriate ways, exactly what his or her condition is. Often, other information will have been gleaned from what they have overhead parents or staff members say, or information provided may be partial (often in the misguided attempt not to burden the child). This is also a time of stress for parents and siblings, whose needs should be attended to as well.

The many and sometimes painful procedures involved in cancer treatments pose other burdens. These can be compounded by isolation from peers, sometimes by isolation from family members, and the child’s lack of participation in his or her usual daily activities.

As children begin to know other children undergoing treatment, they may also experience the death of friends and be reminded of the seriousness of their illness. Children and adolescents are frequently amenable to straightforward discussion of relevant issues with mental health professionals and others. Their ability to participate in discussion with medical staff may also help lessen their anxiety. In the absence of such information and involvement, children may (and often will) think the worst. They may develop symptoms of stress such as nausea and vomiting in anticipation of treatment. The latter may result from the associations of chemotherapy with specific environmental stimuli.

As with other chronic diseases, lack of adherence to treatments is frequent and can take many forms, ranging from overt treatment refusal and “forgetting” medications and appointments to uses of unproven, alternative treatments. Engaging the child and adolescent in the process through conversations and participation in decision making helps prevent these problems. Other issues may arise around cultural differences and beliefs; it is important for treating
physicians and the team to understand how specific cultural issues might impact compliance with treatment.

Repeated school absence is often unavoidable, but lack of attendance creates several issues. It tends to isolate the child from peers, prevents the child from engaging in usual activities, and places the child at academic risk (sometimes further compounded by side effects of treatments). In some hospitals, the availability of a teacher may help the child maintain at least some continuity with homework. In other instances, the school district may be able to help provide services. Other problems may be encountered as the child returns to school;, changes in appearance or ability to participate in usual activities, issues of anxiety or depression, or even cognitive changes brought about by the chemotherapy may all have an impact. The child may be worried about being able to fit in with peers or feel embarrassed about his or her appearance. Having peers remain involved with the child through the hospitalization as much as possible will help the reentry process. Side effects of CNS treatments can impact various cognitive abilities, and attention; memory; and learning math, handwriting, and organization skills may be adversely impacted. These issues may be most dramatic in association with CNS irradiation and younger age (younger than 6 years).

Parents face many issues as they cope with the child’s cancer. They must balance the needs of the child with the rest of the family. Siblings may feel (often accurately) that they are receiving less attention and may have their own issues in understanding the sibling’s condition as they cope with feelings of anger, frustration, isolation, and sometimes resentment and jealousy. Even when things go well, the experience for siblings can be highly stressful. Siblings may seek to protect both their brother or sister and the parents. Sometimes, particularly when good lines of communication can remain open, siblings may ultimately view the experience as one that helped them grow closer to family members. Issues for parents include tensions around trying to maintain normative activities and parental role and coping with the stress of a child with cancer. Other problems can include overprotectiveness, long-term worries about the child’s future, and so forth. Marital issues can arise and be compounded by stress and this can exacerbate preexisting problems.

The child, siblings, and parents may report various problems at the time of initial diagnosis and treatment. The data on these issues is somewhat mixed, presumably given individual differences, age of child, and differences in cancer and cancer treatment. Symptoms can include anxiety, depression, and regression in the child with cancer, and these difficulties may be related to the length of treatment. School reentry can be a further stress for the child. For some children, difficulties may be manifest somewhat later. Some studies have reported reasonably normative functioning after treatment, and symptoms often improve with time. There is some suggestion that for some children, the experience of surviving cancer may be associated with increased levels of maturity and emotional development.

As expected, parents experience various reactions. Feelings of initial shock, confusion, and denial may give way to anxiety, depression, grief, and anger. For some parents, issues of stress and anxiety persist even when the child does well, and there is some suggestion or increased risk for various problems, including PTSD, depression, anxiety, and marital difficulties. In many instances, parents are, however, able to cope well, although residual fears can remain. Studies of differences between fathers and mothers have produced mixed results, perhaps reflecting the effects of different stressors based on roles in the family. Fathers may have more difficulty talking about their experiences than mothers.

Problems in siblings include both internalizing and externalizing difficulties. These can also include posttraumatic stress symptoms, but many siblings do reasonably well. Adolescent siblings may be at somewhat higher risk for difficulties. There is some suggestion of a gender difference, with sisters reporting more physical complaints but with behavioral and social difficulties more common in brothers.

Several steps can be taken to help children cope as well as possible with the experience of cancer and its treatment. The differing “worlds” of normal life and cancer treatment pose obstacles for children, most of whom wish to resume a normal life as quickly as and as much as possible. Often, there is a wish not to be perceived as different. To this end, school attendance remains important. As much as possible, school attendance on a regular basis is helpful and
prevents peer isolation and facilitates positive coping. Communication issues with schools can be a problem for parents who understandably can be very concerned about what information they need to provide. The child must decide if and how to share information with peers. For many children, participation in special oncology camps and activities can also be helpful.

Many children with pediatric cancer fall within the “other health impaired” category in qualifying for needed additional services. Parents should provide sufficient information about the child’s illness and its treatment to help teachers and others provide appropriate educational services. Sometimes special resources are provided to school personnel through oncology programs, or a visit from a staff member to the school may be used.

Historically, it was often the case that children were told very little about their condition. Other care providers chose to wait for children to ask about their condition, and still others, particularly more recently, take a much more active stance relative to sharing information. The latter procedure has been recommended by the International Society of Pediatric Oncologists after a meeting with the parents and several studies suggesting better outcomes with more open communication about the cancer within the family.

Psychosocial outcomes depend on several factors. These include the child’s age and developmental level and the degree to which the child is comfortable knowing about his or her illness. For some children, a degree of denial around medical procedures may be more adaptive, but for others, a straightforward, honest discussion of what is involved may reduce anxiety and fear. Open communication should be encouraged, and the questions of the child should be addressed in a supportive but honest way appropriate to the child’s level of understanding. Sometimes a videotape will be made of the diagnostic conference held with the treating team and parents and child; this tape can then be taken home for review and discussion.

Children can have many ways of coping positively, including searching for more information, using humor and optimism, or denial and withdrawal. Factors that facilitate adjustment and coping include faith in the competence of the team; open communication; and supporting positive coping, along with emotional support and continued social supports for the child. Positive parent coping is associated with positive coping in the child.

For some children, the experience of childhood cancer becomes an opportunity for spiritual as well as emotional growth. This may be particularly true in families that have been involved in church and similar groups. Support of siblings can include support groups. Parents should be encouraged to use the resources available to them. For some, this may take the form of more formal psychotherapy, but for others, support from friends and parents of other children may be helpful and sufficient. In particular, parent support groups can be helpful (e.g., http://www.candlelighters.org). Over time, many parents of children who have survived cancer report positive aspects of the experience.


Pediatric Transplantation

There have been major advances in pediatric transplantation over the past decades with successful solid organ and bone marrow transplant procedures now frequent. The first of these procedures involved cardiac transplants in infants, which were beset but a host of problems. The introduction of the immunosuppressant cyclosporine in 1980 marked a major turning point and paved the way for improved outcome and quality of life. Similar advances have occurred in bone marrow transplantation, which had its origins in children. Transplantation procedures with children and adolescents have many similarities and a few differences from adults. Issues of suitability and preparation are relevant to all groups, but for youth, compliance issues, attention to developmental needs and status, and psychosocial issues can be more important. Over time, pediatricians, surgeons, and transplant specialists have become more interested in obtaining appropriate mental health supports for children and youth.

There are similarities and differences between transplant of bone marrow and solid organs. Children coping with these procedures are, depending on their cognitive level, acutely aware of their medical status and potential risk. Both they and their family are under very considerable stress, and the range of treatment options, with their associated risks and potential benefits,
provide other challenges. Decisions can lead to a lifetime commitment to antirejection medications, which have short and longer term side effects. It is typical for families to have concern about future academic and reproductive success. The side effects associated with antirejection agents and with the corticosteroids can include agitation, mood problems, paranoid thinking, and cognitive changes. For children and adolescents with preexisting psychiatric problems, these may be exacerbated. Mental health consultants must be aware of the potential range of adverse effects. Potential problems can also arise because of drug interactions. Mental health consultants have an important role in assessing potential side effects, both in terms of risk and as these emerge.


There has been a growing awareness of the considerable distress involved in transplantation and risk for posttraumatic stress syndromes. It is important to look for stress-related symptoms in both patients and families because there is some suggestion that the degree to which parents feel traumatized correlates with the outcome (both medical and psychological) of patients. Adolescents face particular challenges given their urge for greater independence and this, combined with denial, can lead to noncompliance with treatment regimens. This is, unfortunately, the frequent cause of graft rejection.

Mental health consultants have an important role in facilitating clear and developmentally appropriate discussions with both the patient and family members. Parents face complex issues. The dilemma centers around tension between wanting children to grow and develop while simultaneously being vigilant for signs of rejection. In some cases, ongoing or new mental health issues complicate treatment. In general, psychotropic medications are used judiciously; it is important to be constantly aware of the potential for psychiatric or behavioral side effects. Careful monitoring and use of lower doses for treatment are good practice. The use of behavioral and psychotherapeutic interventions can be helpful.

Transplantation associated with cancer is associated with an even greater psychological burden. This and the potential negative effects of isolation add to the risk in bone marrow transplantation. For solid organ transplants, the range of conditions encountered is now considerable more varied. The mental health consultant should have a good understanding of the medical and surgical issues associated with the specific disease process and the potential risks and benefits of the transplant. Often, the consultant is asked to participate in the evaluation for children who are being considered for transplantation. This provides an opportunity to
know the patient and family before the transplant, to do a comprehensive assessment, and to educate patient and family regarding the risks and benefits. This also sets the stage for allowing the mental health consultant to coordinate and assist the family in working with the transplant team. Procedures for conducting the initial assessment vary but should be cognizant of the child’s age and level of functioning. Often, psychologists or social workers conduct some psychological and psychosocial assessments. Centers also often have their own unique procedures for screening, and in some cases, histories of substance abuse, active psychosis, or suicidal ideation are viewed as exclusionary criteria.

Contact before the transplant can also have important educative function and can sometimes be therapeutic. Concerns include the presence of significant psychiatric conditions as noted above and any developmental or learning problems that might complicate obtaining informed consent. Any history of psychological treatments or medications should be noted along with any history of substance abuse (the latter is much more likely in adolescents). The assessment can also explore aspects of the child’s relationship with parents, availability of supports, motivations for and expectations of the transplant, and so forth. Assessment of the understanding of the child and parents to the requirements for treatment after the transplant is important.

Procedures involved in the transplant can be traumatic. In some cases, a prolonged period of waiting may precede abrupt availability of a donor organ. Before this happens, it is wise to prepare the child and family for what will happen and develop a “game plan” for coping after an organ becomes available. After the transplant, other issues can arise. The child or adolescent may experience anxiety and stress-related symptoms as well as significant mental status changes. Preparation can help parents recognize signs of complications. For the mental health consultant, an important aspect of the work is developing a consultative relationship with the treatment team. Many different professionals (physicians, nurses, social workers, teachers, child life specialists, physical therapists, and others) can be involved in the child’s care. Many issues can arise as team members develop long-term relationships with children and families. These can be particularly acute when children are not deemed suitable for transplantation because of advanced disease or history of noncompliance.

In some situations, living organ donation is an option (e.g., for kidney, lung, and liver transplants). In such situations, the potential donor must have a comprehensive assessment and assessment of capacities for informed consent. This is particularly important if the living donor is biologically related and some degree of implicit coercion is potentially involved. These issues can also be complicated when a parent is offering to serve as a donor. Living organ donors should understand what is involved and be realistically aware of possible outcomes. Advances in immunosuppression have significantly improved transplant outcomes, but these agents by themselves, or in interaction with other agents, can have significant neuropsychiatric side effects. Issues of drug metabolism are somewhat different in children than in adults given children’s faster rates of hepatic metabolism. Some agents specifically impact drug metabolism, and others potentially increase the risk for graft rejection. Table 25.3 summarizes some of the common side effect profiles. Psychiatric complications can also arise in graft versus host disease, which is sometimes seen in bone marrow transplantation. This can present as delirium and encephalopathy.

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Aug 1, 2016 | Posted by in PSYCHIATRY | Comments Off on ▪ Consultation Liaison: Consultation in Pediatrics

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