User login
Anticholinergics reduce symptoms of overactive bladder
Anticholinergic drugs such as tolterodine and oxybutynin produce a small effect on the symptoms of overactive bladder, decreasing slightly the number of episodes of leakage and the frequency of urination. The standard conservative intervention of bladder retraining has not been compared with anticholinergic drugs and their effect in combination has not been studied.
Anticholinergic drugs such as tolterodine and oxybutynin produce a small effect on the symptoms of overactive bladder, decreasing slightly the number of episodes of leakage and the frequency of urination. The standard conservative intervention of bladder retraining has not been compared with anticholinergic drugs and their effect in combination has not been studied.
Anticholinergic drugs such as tolterodine and oxybutynin produce a small effect on the symptoms of overactive bladder, decreasing slightly the number of episodes of leakage and the frequency of urination. The standard conservative intervention of bladder retraining has not been compared with anticholinergic drugs and their effect in combination has not been studied.
Flu shot or FluMist?
Lipid-lowering: Can ezetimibe help close the treatment gap?
Trichotillomania: A Review and Case Report
Don’t be fooled by hypochondria
A hypochondria “checklist” can help you sort through many overlapping medical and psychiatric disorders and increase your chances of making an accurate diagnosis. Then—by addressing hypochondria’s cognitive dysfunction—you can help patients achieve partial or full remission and change their distressing behaviors.
We offer a checklist that is useful in our practice and suggest behavioral therapies and medications that can help calm these patients’ excessive, unwarranted fears.
WORKING AS A TEAM
Ideal approach. Because hypochondriasis has features of medical and mental illness, working with the patient’s primary care physician is ideal. Physicians often consider these patients difficult because they demand a lot of time, support, and reassurance. Together, you can:
- offer the patient a healthy level of compassion and empathy to establish a positive therapeutic alliance
- set appropriate time limits and guidelines for the patient’s care
- dissuade patients from “doctor shopping”
- set limits on how often patients may visit their doctors and request reassurance.
Hypochondriasis: Persistent, unwarranted distress
Hypochondriasis is an excessive and persistent fear or belief that one has a serious illness, despite medical reassurance and lack of diagnostic findings that would warrant the health concern. If a medical disorder is present, the distress and preoccupation exceed what the patient’s physician considers reasonable. Illness preoccupation is intense enough to cause great distress or to interfere with daily functioning and may cause the person to miss work or cancel social engagements.1
DSM-IV criteria. A patient’s fear or conviction that he or she has a serious health threat must persist at least 6 months and may be accompanied by specific somatic symptoms, vague symptoms,1 or no symptoms.2 Hypochondriacal preoccupation may be stable over time, where one illness concern dominates, or it may shift—from fear of AIDS to fear of a heart attack.
A common disorder. Hypochondriasis occurs in 4 to 6% of the general medical population. In psychiatric or medical clinics, women are identified as having hypochondriasis three to four times more often than men. Average age of onset is in the early 20s.3
For example, you may indicate to the patient, “I will reassure you only at office visits (not by phone), the office visits will be limited to once a month, and during each visit I will reassure you no more than once.”
A doctor-patient relationship based on mutual trust and respect is vital when you treat a patient with hypochondriasis. You can help primary care physicians provide more empathic treatment by explaining that patients do not feign or desire this distressing condition.
DIAGNOSTIC FEATURES
Patients with hypochondriasis tend to be hyper-vigilant about normal physiologic fluctuations and bodily sensations, often misinterpreting them as life-threatening or serious enough to require immediate medical attention. This excessive focus on benign symptoms (such as an accelerated heart rate, sweating, or a bump on the skin) and the cognitive distortion of their significance result in increased anxiety, bodily checking, and doctor visits (Box).1-4
Presentations. Hypochondriasis has three common presentations: disease conviction, disease fear, and bodily preoccupation (Table 1).5 Psychiatrists are most likely to see disease fear, as patients with this predominant symptom tend to realize that fear plays too prominent a role in their lives. Physicians in medical practice are more likely to encounter patients with high levels of disease conviction or somatic preoccupation.
Psychiatric comorbidity. Hypochondriasis is highly comorbid with Axis I and Axis II disorders, which complicate treatment. Nearly one-half of patients with hypochondriasis also have dysthymia (45%) or major depression (43%). Other comorbidities include phobias (38%), somatization disorder (21%), panic disorder (17%), and obsessive-compulsive disorder (8%).6 Patients with hypochondriasis are three times more likely than the general population to have personality disorders;6,7 the prognosis is believed to be more promising for patients without personality disorders.
Distinguishing between primary and secondary hypochondriasis is important. Treating a primary psychiatric disorder often alleviates the symptoms of secondary hypochondriasis, particularly when hypochondriasis masks depression.
HYPOCHONDRIASIS CHECKLIST
Underlying medical disorder? Before diagnosing hypochondriasis, review the medical workup for underlying disease or illness. Medical conditions sometimes go undetected when physicians assume that complaints are an expression of longstanding hypochondriasis.
Table 1
Three common presentations of hypochondriasis
Predominant symptom | Characterization |
---|---|
Disease conviction | Patient may appear delusional in believing he or she has a disease and in persistent efforts to find a doctor who will make the “accurate” diagnosis |
Disease fear | Patient may avoid doctors because of fear associated with confirmation of a dreaded disease |
Bodily preoccupation | Patient may complain of multiple somatic symptoms, which mask underlying fear or belief of having a serious disease |
Sometimes a patient may become anxious when mild or vague signs and symptoms do not yet meet established diagnostic criteria for a medical disorder. An effective approach is to provide ongoing support, avoid excessive diagnostic tests, and help the patient make the best use of his or her functional capacities while living with uncertainty.
Functional somatic syndrome? Fibromyalgia and chronic fatigue syndrome do not represent hypochondriasis,8 although they may be exacerbated by comorbid psychiatric disorders. Both disorders have diagnostic criteria and specified courses and have been studied to identify psychiatric comorbidity.
Transient or sustained? After it is clear that the patient is not suffering from a medical problem, determine whether hypochondriasis is transient or fully diagnostic:
- If transient, the patient may only need to be educated about how overattention may amplify symptoms; reassure him or her that a full medical workup has been negative.
- If fully diagnostic, reassurance may work for only a few days or weeks; the return of the fear or conviction helps establish the diagnosis.
Somatoform disorder? Distinguish hypochondriasis from other somatoform disorders (Table 2). In practice, the terms “hypochondriac” and “somatizer” are commonly used interchangeably, but the distinction needs to be clear. Hypochondriasis is primarily a disorder of abnormal cognition, in which symptom meaning is of greatest concern. Somatization is primarily a disorder of abnormal sensation, in which the symptoms themselves are the overwhelming focus of attention.
Anxiety disorder? Patients with generalized anxiety disorder may worry about illness, but they also worry about other life issues. Patients with panic disorder may have intense hypochondriacal concerns (such as having a heart attack), but these worries tend to be related to panic symptoms and resolve when the panic disorder is treated.
Obsessive compulsive disorder? Like obsessive-compulsive disorder (OCD), hypochondriasis is characterized by recurrent intrusive thoughts that create heightened anxiety and distress. To relieve their anxiety, patients with hypochondriasis engage in compulsions, such as:
- undergoing extensive medical tests
- seeking habitual reassurance from doctors and family
- consulting medical literature
- performing repeated body checks for perceived lumps or bumps
- avoiding activities that trigger their health-related stress.9
Table 2
How to distinguish somatoform disorders
Disorder | Patient focuses on… |
---|---|
Hypochondriasis | physical symptoms’ meaning (abnormal cognition) |
Somatization disorder | multiple unexplained physical symptoms (abnormal sensation) |
Body dysmorphic disorder | perceived abnormal bodily appearance |
Conversion disorder | motor or sensory function abnormalities that develop soon after life stressors or conflict |
Pain disorder | intense pain, in which psychological factors contribute to pain onset, severity, or maintenance |
OCD and hypochondriasis also may share the diagnostic feature of pathologic doubt; patients’ uncertainty in appraising a situation leads to additional checking and reassurance-seeking behaviors. The immediate relief gained by these compulsions reinforces the patient’s urge to engage in more maladaptive behaviors and sends a stronger message to the brain that these behaviors are needed to prevent harm.
Ironically, the emergence of a real medical ailment—despite hypochondriacal worry—may force the patient to re-evaluate the usefulness of behaviors motivated by trying to avoid harm. A hypochondriacal patient who was diagnosed with optic neuritis and possible multiple sclerosis recently said to these authors, “I had always thought that by being vigilant I could keep illnesses away. Now I know that’s not true.”
Although hypochondriasis and OCD have similarities, certain clinical distinctions exist. Patients with hypochondriasis worry about having an illness, whereas OCD patients with somatic obsessions fear developing or transmitting an illness. A hypochondriacal patient might fear having AIDS or cancer despite reassurance from doctors, while an OCD patient more typically would fear contracting or transmitting the disease (a contamination obsession) and would engage in excessive behaviors to reduce the risk of developing the disease.
Depressive disorder? Unlike the anxious-worrying version of hypochondriasis, the depressive version is more fatalistic. Patients may be convinced they are dying of a dreaded disease, often believing it to be punishment for an indiscretion, such as marital infidelity. Or they may suddenly become hypochondriacal with mild depressive features, unaware that the actual problem is unresolved bereavement (hypochondriasis with secondary depression). The appropriate diagnosis is primary depressive disorder with secondary hypochondriacal features when depression dominates the presentation and preceded the illness fears.
Table 3
Recommended dosages for treating primary hypochondriasis
Drug | Starting dosage | Maximum dosage |
---|---|---|
Fluoxetine | 10 mg/d if panic symptoms are present; 20 mg/d otherwise | 80 mg/d |
Fluvoxamine | 50 mg at bedtime | 150 mg bid |
Nefazodone | 100 mg bid | 300 mg bid |
Paroxetine | 20 mg once daily | 50 mg once daily |
Delusional disorder? To distinguish hypochondriasis from delusional disorder (somatic type), consider the patient’s pattern of insight:
- Hypochondriacal patients often vacillate between poor and excellent insight, depending on their distress level.10 They may acknowledge the irrationality of their fears, then later be convinced they have a disease.
- Patients with delusional disorder are convinced they have a serious health threat, despite the absence of medical confirmation. These patients are considered to have a primary psychotic disorder that requires antipsychotic treatment.
TREATING PRIMARY SYMPTOMS
Drug therapy. When hypochondriasis is secondary—such as to depression or panic disorder—treat the primary condition first.11,12 For primary hypochondriasis, selective serotonin reuptake inhibitors (SSRIs) such as fluoxetine, paroxetine, or fluvoxamine have shown benefit, mostly in open-label studies. An uncontrolled case series suggests that nefazodone—with mixed serotonin reuptake inhibition and agonist properties—also may help patients with hypochondriasis.13 In the only published controlled study, fluoxetine was more effective than placebo for treating hypochondriasis.10
Continue drug therapy, when used, for at least 8 weeks, with each dosage maintained for at least 4 weeks. If patients do not respond to lower SSRI dosages, increase to the higher dosages reported to be more effective for OCD (Table 3).14
Except for primary illness phobia, hypochondriasis has not been shown to respond to tricyclics, benzodiazepines, or dopaminergic blockers. In our experience, electroconvulsive therapy—although inadequately studied—may help treat patients with severe, treatment-refractory hypochondriasis with marked somatization.
Psychotherapy. Cognitive-behavioral therapy (CBT)—challenging patients’ irrational fears about illness and teaching them problem-solving tools—is effective in treating hypochondriasis.15 CBT can help patients understand that distorted thoughts lead to their sad or anxious moods.
Instructing patients to keep thought diaries can help them identify irrational fears and use cognitive restructuring to correct their faulty schemas. Tailor your cognitive therapy techniques to target the patient’s level of insight at the time of therapy.
Effective behavioral techniques may include setting limits on doctor visits, checking behaviors, reassurance seeking, etc. Repeated exposure to feared stimuli such as needles, white lab coats, blood pressure cuffs, medical dialogue, or hospital wards can help the patient habituate to the anxiety.
Relaxation techniques, a healthy diet, and exercise are also useful. Relaxation exercises—such as diaphragmatic breathing, progressive muscle relaxation, and visual imagery—may help patients manage anxiety by reducing CNS and autonomic nervous system arousal.
Bottom line
Hypochondriasis’ cognitive dysfunction is treatable, once an accurate diagnosis is made. Using a checklist can help you differentiate hypochondriasis from other medical and psychiatric disorders. A trusting doctor-patient relationship enhances outcome.
Related resources
- Fallon BA., Feinstein SB. Hypochondriasis: clinical, theoretical, and therapeutic aspects. In: Oldham J (ed). Review of psychiatry (vol. 20) Washington, DC: American Psychiatric Press, 2001:27-60.
- Cantor C, Fallon BA. Phantom illness: shattering the myth of hypochondria Boston: Houghton Mifflin Company, 1996.
- Starcevic V, Lipsitt DR (eds). Hypochondriasis: modern perspectives on an ancient malady New York: Oxford University Press, 2001.
Drug brand names
- Fluoxetine • Prozac
- Fluvoxamine • Luvox
- Nefazodone • Serzone
- Paroxetine • Paxil
1. Diagnostic and statistical manual of mental disorders (4th ed-text revision). Washington, DC: American Psychiatric Association, 2000.
2. Task Force on DSM-IV. DSM-IV options book. Washington DC: American Psychiatric Association, 1991.
3. Barsky AJ, Wyshak G, Klerman GL, Lathan KS. The prevalence of hypochondriasis in medical outpatients. Soc Psychiatry Psychiatr Epidemiol 1990;25(2):89-94.
4. Salkovskis PM, Clark DM. Panic and hypochondriasis. Adv Behav Res Ther 1993;15:23-48.
5. Pilowsky I. Dimensions of hypochondriasis. Br J Psychiatry 1967;113(494):89-93.
6. Barsky AJ, Wyshak G, Klerman GL. Psychiatric comorbidity in DSM-III-R hypochondriasis. Arch Gen Psychiatry 1992;49(2):101-8.
7. Kellner R. The prognosis of treated hypochondriasis: a clinical study. Acta Psychiatr Scand 1983;67(2):69-79.
8. Noyes R, Jr, Kathol RG, Fisher M, Phillips BM, et al. The validity of DSM-III-R hypochondriasis. Arch Gen Psychiatry 1993;50(12):961-70.
9. Fallon BA, Qureshi AI, Laje G, Klein B. Hypochondriasis and its relationship to obsessive-compulsive disorder. Psychiatr Clin North Am 2000;23(3):605-16.
10. Fallon BA, Schneier FR, Marshall R, Campeas R, et al. The pharmacotherapy of hypochondriasis. Psychopharmacol Bull 1996;32:607-11.
11. Kellner R, Fava GA, Lisansky J, et al. Hypochondriacal fears and beliefs in DSM-III melancholia: changes with amitriptyline. J Affect Disord 1986;10(1):21-6.
12. Noyes R, Jr, Reich J, Clancy J, O’Gorman TW. Reduction in hypochondriasis with treatment of panic disorder. Br J Psychiatry 1986;149:631-5(erratum in Br J Psychiatry 1987;150:273).
13. Kjernisted KD, Ennis MW, Lander M. An open-label clinical trial of nefazodone in hypochondriasis. Psychosomatics 2002;43:290-4.
14. Fallon BA. Pharmacologic strategies for hypochondriasis. In: Starcevic V, Lipsitt DR (eds). Hypochondriasis: modern perspectives on an ancient malady. New York: Oxford University Press, 2001;329-51.
15. Warwick HMC, Salkovskis PM. Hypochondriasis. In: Scott J, Williams JMG, Beck AT (eds). Cognitive therapy in clinical practice: an illustrative casebook. London; Routledge, 1989;78-102.
A hypochondria “checklist” can help you sort through many overlapping medical and psychiatric disorders and increase your chances of making an accurate diagnosis. Then—by addressing hypochondria’s cognitive dysfunction—you can help patients achieve partial or full remission and change their distressing behaviors.
We offer a checklist that is useful in our practice and suggest behavioral therapies and medications that can help calm these patients’ excessive, unwarranted fears.
WORKING AS A TEAM
Ideal approach. Because hypochondriasis has features of medical and mental illness, working with the patient’s primary care physician is ideal. Physicians often consider these patients difficult because they demand a lot of time, support, and reassurance. Together, you can:
- offer the patient a healthy level of compassion and empathy to establish a positive therapeutic alliance
- set appropriate time limits and guidelines for the patient’s care
- dissuade patients from “doctor shopping”
- set limits on how often patients may visit their doctors and request reassurance.
Hypochondriasis: Persistent, unwarranted distress
Hypochondriasis is an excessive and persistent fear or belief that one has a serious illness, despite medical reassurance and lack of diagnostic findings that would warrant the health concern. If a medical disorder is present, the distress and preoccupation exceed what the patient’s physician considers reasonable. Illness preoccupation is intense enough to cause great distress or to interfere with daily functioning and may cause the person to miss work or cancel social engagements.1
DSM-IV criteria. A patient’s fear or conviction that he or she has a serious health threat must persist at least 6 months and may be accompanied by specific somatic symptoms, vague symptoms,1 or no symptoms.2 Hypochondriacal preoccupation may be stable over time, where one illness concern dominates, or it may shift—from fear of AIDS to fear of a heart attack.
A common disorder. Hypochondriasis occurs in 4 to 6% of the general medical population. In psychiatric or medical clinics, women are identified as having hypochondriasis three to four times more often than men. Average age of onset is in the early 20s.3
For example, you may indicate to the patient, “I will reassure you only at office visits (not by phone), the office visits will be limited to once a month, and during each visit I will reassure you no more than once.”
A doctor-patient relationship based on mutual trust and respect is vital when you treat a patient with hypochondriasis. You can help primary care physicians provide more empathic treatment by explaining that patients do not feign or desire this distressing condition.
DIAGNOSTIC FEATURES
Patients with hypochondriasis tend to be hyper-vigilant about normal physiologic fluctuations and bodily sensations, often misinterpreting them as life-threatening or serious enough to require immediate medical attention. This excessive focus on benign symptoms (such as an accelerated heart rate, sweating, or a bump on the skin) and the cognitive distortion of their significance result in increased anxiety, bodily checking, and doctor visits (Box).1-4
Presentations. Hypochondriasis has three common presentations: disease conviction, disease fear, and bodily preoccupation (Table 1).5 Psychiatrists are most likely to see disease fear, as patients with this predominant symptom tend to realize that fear plays too prominent a role in their lives. Physicians in medical practice are more likely to encounter patients with high levels of disease conviction or somatic preoccupation.
Psychiatric comorbidity. Hypochondriasis is highly comorbid with Axis I and Axis II disorders, which complicate treatment. Nearly one-half of patients with hypochondriasis also have dysthymia (45%) or major depression (43%). Other comorbidities include phobias (38%), somatization disorder (21%), panic disorder (17%), and obsessive-compulsive disorder (8%).6 Patients with hypochondriasis are three times more likely than the general population to have personality disorders;6,7 the prognosis is believed to be more promising for patients without personality disorders.
Distinguishing between primary and secondary hypochondriasis is important. Treating a primary psychiatric disorder often alleviates the symptoms of secondary hypochondriasis, particularly when hypochondriasis masks depression.
HYPOCHONDRIASIS CHECKLIST
Underlying medical disorder? Before diagnosing hypochondriasis, review the medical workup for underlying disease or illness. Medical conditions sometimes go undetected when physicians assume that complaints are an expression of longstanding hypochondriasis.
Table 1
Three common presentations of hypochondriasis
Predominant symptom | Characterization |
---|---|
Disease conviction | Patient may appear delusional in believing he or she has a disease and in persistent efforts to find a doctor who will make the “accurate” diagnosis |
Disease fear | Patient may avoid doctors because of fear associated with confirmation of a dreaded disease |
Bodily preoccupation | Patient may complain of multiple somatic symptoms, which mask underlying fear or belief of having a serious disease |
Sometimes a patient may become anxious when mild or vague signs and symptoms do not yet meet established diagnostic criteria for a medical disorder. An effective approach is to provide ongoing support, avoid excessive diagnostic tests, and help the patient make the best use of his or her functional capacities while living with uncertainty.
Functional somatic syndrome? Fibromyalgia and chronic fatigue syndrome do not represent hypochondriasis,8 although they may be exacerbated by comorbid psychiatric disorders. Both disorders have diagnostic criteria and specified courses and have been studied to identify psychiatric comorbidity.
Transient or sustained? After it is clear that the patient is not suffering from a medical problem, determine whether hypochondriasis is transient or fully diagnostic:
- If transient, the patient may only need to be educated about how overattention may amplify symptoms; reassure him or her that a full medical workup has been negative.
- If fully diagnostic, reassurance may work for only a few days or weeks; the return of the fear or conviction helps establish the diagnosis.
Somatoform disorder? Distinguish hypochondriasis from other somatoform disorders (Table 2). In practice, the terms “hypochondriac” and “somatizer” are commonly used interchangeably, but the distinction needs to be clear. Hypochondriasis is primarily a disorder of abnormal cognition, in which symptom meaning is of greatest concern. Somatization is primarily a disorder of abnormal sensation, in which the symptoms themselves are the overwhelming focus of attention.
Anxiety disorder? Patients with generalized anxiety disorder may worry about illness, but they also worry about other life issues. Patients with panic disorder may have intense hypochondriacal concerns (such as having a heart attack), but these worries tend to be related to panic symptoms and resolve when the panic disorder is treated.
Obsessive compulsive disorder? Like obsessive-compulsive disorder (OCD), hypochondriasis is characterized by recurrent intrusive thoughts that create heightened anxiety and distress. To relieve their anxiety, patients with hypochondriasis engage in compulsions, such as:
- undergoing extensive medical tests
- seeking habitual reassurance from doctors and family
- consulting medical literature
- performing repeated body checks for perceived lumps or bumps
- avoiding activities that trigger their health-related stress.9
Table 2
How to distinguish somatoform disorders
Disorder | Patient focuses on… |
---|---|
Hypochondriasis | physical symptoms’ meaning (abnormal cognition) |
Somatization disorder | multiple unexplained physical symptoms (abnormal sensation) |
Body dysmorphic disorder | perceived abnormal bodily appearance |
Conversion disorder | motor or sensory function abnormalities that develop soon after life stressors or conflict |
Pain disorder | intense pain, in which psychological factors contribute to pain onset, severity, or maintenance |
OCD and hypochondriasis also may share the diagnostic feature of pathologic doubt; patients’ uncertainty in appraising a situation leads to additional checking and reassurance-seeking behaviors. The immediate relief gained by these compulsions reinforces the patient’s urge to engage in more maladaptive behaviors and sends a stronger message to the brain that these behaviors are needed to prevent harm.
Ironically, the emergence of a real medical ailment—despite hypochondriacal worry—may force the patient to re-evaluate the usefulness of behaviors motivated by trying to avoid harm. A hypochondriacal patient who was diagnosed with optic neuritis and possible multiple sclerosis recently said to these authors, “I had always thought that by being vigilant I could keep illnesses away. Now I know that’s not true.”
Although hypochondriasis and OCD have similarities, certain clinical distinctions exist. Patients with hypochondriasis worry about having an illness, whereas OCD patients with somatic obsessions fear developing or transmitting an illness. A hypochondriacal patient might fear having AIDS or cancer despite reassurance from doctors, while an OCD patient more typically would fear contracting or transmitting the disease (a contamination obsession) and would engage in excessive behaviors to reduce the risk of developing the disease.
Depressive disorder? Unlike the anxious-worrying version of hypochondriasis, the depressive version is more fatalistic. Patients may be convinced they are dying of a dreaded disease, often believing it to be punishment for an indiscretion, such as marital infidelity. Or they may suddenly become hypochondriacal with mild depressive features, unaware that the actual problem is unresolved bereavement (hypochondriasis with secondary depression). The appropriate diagnosis is primary depressive disorder with secondary hypochondriacal features when depression dominates the presentation and preceded the illness fears.
Table 3
Recommended dosages for treating primary hypochondriasis
Drug | Starting dosage | Maximum dosage |
---|---|---|
Fluoxetine | 10 mg/d if panic symptoms are present; 20 mg/d otherwise | 80 mg/d |
Fluvoxamine | 50 mg at bedtime | 150 mg bid |
Nefazodone | 100 mg bid | 300 mg bid |
Paroxetine | 20 mg once daily | 50 mg once daily |
Delusional disorder? To distinguish hypochondriasis from delusional disorder (somatic type), consider the patient’s pattern of insight:
- Hypochondriacal patients often vacillate between poor and excellent insight, depending on their distress level.10 They may acknowledge the irrationality of their fears, then later be convinced they have a disease.
- Patients with delusional disorder are convinced they have a serious health threat, despite the absence of medical confirmation. These patients are considered to have a primary psychotic disorder that requires antipsychotic treatment.
TREATING PRIMARY SYMPTOMS
Drug therapy. When hypochondriasis is secondary—such as to depression or panic disorder—treat the primary condition first.11,12 For primary hypochondriasis, selective serotonin reuptake inhibitors (SSRIs) such as fluoxetine, paroxetine, or fluvoxamine have shown benefit, mostly in open-label studies. An uncontrolled case series suggests that nefazodone—with mixed serotonin reuptake inhibition and agonist properties—also may help patients with hypochondriasis.13 In the only published controlled study, fluoxetine was more effective than placebo for treating hypochondriasis.10
Continue drug therapy, when used, for at least 8 weeks, with each dosage maintained for at least 4 weeks. If patients do not respond to lower SSRI dosages, increase to the higher dosages reported to be more effective for OCD (Table 3).14
Except for primary illness phobia, hypochondriasis has not been shown to respond to tricyclics, benzodiazepines, or dopaminergic blockers. In our experience, electroconvulsive therapy—although inadequately studied—may help treat patients with severe, treatment-refractory hypochondriasis with marked somatization.
Psychotherapy. Cognitive-behavioral therapy (CBT)—challenging patients’ irrational fears about illness and teaching them problem-solving tools—is effective in treating hypochondriasis.15 CBT can help patients understand that distorted thoughts lead to their sad or anxious moods.
Instructing patients to keep thought diaries can help them identify irrational fears and use cognitive restructuring to correct their faulty schemas. Tailor your cognitive therapy techniques to target the patient’s level of insight at the time of therapy.
Effective behavioral techniques may include setting limits on doctor visits, checking behaviors, reassurance seeking, etc. Repeated exposure to feared stimuli such as needles, white lab coats, blood pressure cuffs, medical dialogue, or hospital wards can help the patient habituate to the anxiety.
Relaxation techniques, a healthy diet, and exercise are also useful. Relaxation exercises—such as diaphragmatic breathing, progressive muscle relaxation, and visual imagery—may help patients manage anxiety by reducing CNS and autonomic nervous system arousal.
Bottom line
Hypochondriasis’ cognitive dysfunction is treatable, once an accurate diagnosis is made. Using a checklist can help you differentiate hypochondriasis from other medical and psychiatric disorders. A trusting doctor-patient relationship enhances outcome.
Related resources
- Fallon BA., Feinstein SB. Hypochondriasis: clinical, theoretical, and therapeutic aspects. In: Oldham J (ed). Review of psychiatry (vol. 20) Washington, DC: American Psychiatric Press, 2001:27-60.
- Cantor C, Fallon BA. Phantom illness: shattering the myth of hypochondria Boston: Houghton Mifflin Company, 1996.
- Starcevic V, Lipsitt DR (eds). Hypochondriasis: modern perspectives on an ancient malady New York: Oxford University Press, 2001.
Drug brand names
- Fluoxetine • Prozac
- Fluvoxamine • Luvox
- Nefazodone • Serzone
- Paroxetine • Paxil
A hypochondria “checklist” can help you sort through many overlapping medical and psychiatric disorders and increase your chances of making an accurate diagnosis. Then—by addressing hypochondria’s cognitive dysfunction—you can help patients achieve partial or full remission and change their distressing behaviors.
We offer a checklist that is useful in our practice and suggest behavioral therapies and medications that can help calm these patients’ excessive, unwarranted fears.
WORKING AS A TEAM
Ideal approach. Because hypochondriasis has features of medical and mental illness, working with the patient’s primary care physician is ideal. Physicians often consider these patients difficult because they demand a lot of time, support, and reassurance. Together, you can:
- offer the patient a healthy level of compassion and empathy to establish a positive therapeutic alliance
- set appropriate time limits and guidelines for the patient’s care
- dissuade patients from “doctor shopping”
- set limits on how often patients may visit their doctors and request reassurance.
Hypochondriasis: Persistent, unwarranted distress
Hypochondriasis is an excessive and persistent fear or belief that one has a serious illness, despite medical reassurance and lack of diagnostic findings that would warrant the health concern. If a medical disorder is present, the distress and preoccupation exceed what the patient’s physician considers reasonable. Illness preoccupation is intense enough to cause great distress or to interfere with daily functioning and may cause the person to miss work or cancel social engagements.1
DSM-IV criteria. A patient’s fear or conviction that he or she has a serious health threat must persist at least 6 months and may be accompanied by specific somatic symptoms, vague symptoms,1 or no symptoms.2 Hypochondriacal preoccupation may be stable over time, where one illness concern dominates, or it may shift—from fear of AIDS to fear of a heart attack.
A common disorder. Hypochondriasis occurs in 4 to 6% of the general medical population. In psychiatric or medical clinics, women are identified as having hypochondriasis three to four times more often than men. Average age of onset is in the early 20s.3
For example, you may indicate to the patient, “I will reassure you only at office visits (not by phone), the office visits will be limited to once a month, and during each visit I will reassure you no more than once.”
A doctor-patient relationship based on mutual trust and respect is vital when you treat a patient with hypochondriasis. You can help primary care physicians provide more empathic treatment by explaining that patients do not feign or desire this distressing condition.
DIAGNOSTIC FEATURES
Patients with hypochondriasis tend to be hyper-vigilant about normal physiologic fluctuations and bodily sensations, often misinterpreting them as life-threatening or serious enough to require immediate medical attention. This excessive focus on benign symptoms (such as an accelerated heart rate, sweating, or a bump on the skin) and the cognitive distortion of their significance result in increased anxiety, bodily checking, and doctor visits (Box).1-4
Presentations. Hypochondriasis has three common presentations: disease conviction, disease fear, and bodily preoccupation (Table 1).5 Psychiatrists are most likely to see disease fear, as patients with this predominant symptom tend to realize that fear plays too prominent a role in their lives. Physicians in medical practice are more likely to encounter patients with high levels of disease conviction or somatic preoccupation.
Psychiatric comorbidity. Hypochondriasis is highly comorbid with Axis I and Axis II disorders, which complicate treatment. Nearly one-half of patients with hypochondriasis also have dysthymia (45%) or major depression (43%). Other comorbidities include phobias (38%), somatization disorder (21%), panic disorder (17%), and obsessive-compulsive disorder (8%).6 Patients with hypochondriasis are three times more likely than the general population to have personality disorders;6,7 the prognosis is believed to be more promising for patients without personality disorders.
Distinguishing between primary and secondary hypochondriasis is important. Treating a primary psychiatric disorder often alleviates the symptoms of secondary hypochondriasis, particularly when hypochondriasis masks depression.
HYPOCHONDRIASIS CHECKLIST
Underlying medical disorder? Before diagnosing hypochondriasis, review the medical workup for underlying disease or illness. Medical conditions sometimes go undetected when physicians assume that complaints are an expression of longstanding hypochondriasis.
Table 1
Three common presentations of hypochondriasis
Predominant symptom | Characterization |
---|---|
Disease conviction | Patient may appear delusional in believing he or she has a disease and in persistent efforts to find a doctor who will make the “accurate” diagnosis |
Disease fear | Patient may avoid doctors because of fear associated with confirmation of a dreaded disease |
Bodily preoccupation | Patient may complain of multiple somatic symptoms, which mask underlying fear or belief of having a serious disease |
Sometimes a patient may become anxious when mild or vague signs and symptoms do not yet meet established diagnostic criteria for a medical disorder. An effective approach is to provide ongoing support, avoid excessive diagnostic tests, and help the patient make the best use of his or her functional capacities while living with uncertainty.
Functional somatic syndrome? Fibromyalgia and chronic fatigue syndrome do not represent hypochondriasis,8 although they may be exacerbated by comorbid psychiatric disorders. Both disorders have diagnostic criteria and specified courses and have been studied to identify psychiatric comorbidity.
Transient or sustained? After it is clear that the patient is not suffering from a medical problem, determine whether hypochondriasis is transient or fully diagnostic:
- If transient, the patient may only need to be educated about how overattention may amplify symptoms; reassure him or her that a full medical workup has been negative.
- If fully diagnostic, reassurance may work for only a few days or weeks; the return of the fear or conviction helps establish the diagnosis.
Somatoform disorder? Distinguish hypochondriasis from other somatoform disorders (Table 2). In practice, the terms “hypochondriac” and “somatizer” are commonly used interchangeably, but the distinction needs to be clear. Hypochondriasis is primarily a disorder of abnormal cognition, in which symptom meaning is of greatest concern. Somatization is primarily a disorder of abnormal sensation, in which the symptoms themselves are the overwhelming focus of attention.
Anxiety disorder? Patients with generalized anxiety disorder may worry about illness, but they also worry about other life issues. Patients with panic disorder may have intense hypochondriacal concerns (such as having a heart attack), but these worries tend to be related to panic symptoms and resolve when the panic disorder is treated.
Obsessive compulsive disorder? Like obsessive-compulsive disorder (OCD), hypochondriasis is characterized by recurrent intrusive thoughts that create heightened anxiety and distress. To relieve their anxiety, patients with hypochondriasis engage in compulsions, such as:
- undergoing extensive medical tests
- seeking habitual reassurance from doctors and family
- consulting medical literature
- performing repeated body checks for perceived lumps or bumps
- avoiding activities that trigger their health-related stress.9
Table 2
How to distinguish somatoform disorders
Disorder | Patient focuses on… |
---|---|
Hypochondriasis | physical symptoms’ meaning (abnormal cognition) |
Somatization disorder | multiple unexplained physical symptoms (abnormal sensation) |
Body dysmorphic disorder | perceived abnormal bodily appearance |
Conversion disorder | motor or sensory function abnormalities that develop soon after life stressors or conflict |
Pain disorder | intense pain, in which psychological factors contribute to pain onset, severity, or maintenance |
OCD and hypochondriasis also may share the diagnostic feature of pathologic doubt; patients’ uncertainty in appraising a situation leads to additional checking and reassurance-seeking behaviors. The immediate relief gained by these compulsions reinforces the patient’s urge to engage in more maladaptive behaviors and sends a stronger message to the brain that these behaviors are needed to prevent harm.
Ironically, the emergence of a real medical ailment—despite hypochondriacal worry—may force the patient to re-evaluate the usefulness of behaviors motivated by trying to avoid harm. A hypochondriacal patient who was diagnosed with optic neuritis and possible multiple sclerosis recently said to these authors, “I had always thought that by being vigilant I could keep illnesses away. Now I know that’s not true.”
Although hypochondriasis and OCD have similarities, certain clinical distinctions exist. Patients with hypochondriasis worry about having an illness, whereas OCD patients with somatic obsessions fear developing or transmitting an illness. A hypochondriacal patient might fear having AIDS or cancer despite reassurance from doctors, while an OCD patient more typically would fear contracting or transmitting the disease (a contamination obsession) and would engage in excessive behaviors to reduce the risk of developing the disease.
Depressive disorder? Unlike the anxious-worrying version of hypochondriasis, the depressive version is more fatalistic. Patients may be convinced they are dying of a dreaded disease, often believing it to be punishment for an indiscretion, such as marital infidelity. Or they may suddenly become hypochondriacal with mild depressive features, unaware that the actual problem is unresolved bereavement (hypochondriasis with secondary depression). The appropriate diagnosis is primary depressive disorder with secondary hypochondriacal features when depression dominates the presentation and preceded the illness fears.
Table 3
Recommended dosages for treating primary hypochondriasis
Drug | Starting dosage | Maximum dosage |
---|---|---|
Fluoxetine | 10 mg/d if panic symptoms are present; 20 mg/d otherwise | 80 mg/d |
Fluvoxamine | 50 mg at bedtime | 150 mg bid |
Nefazodone | 100 mg bid | 300 mg bid |
Paroxetine | 20 mg once daily | 50 mg once daily |
Delusional disorder? To distinguish hypochondriasis from delusional disorder (somatic type), consider the patient’s pattern of insight:
- Hypochondriacal patients often vacillate between poor and excellent insight, depending on their distress level.10 They may acknowledge the irrationality of their fears, then later be convinced they have a disease.
- Patients with delusional disorder are convinced they have a serious health threat, despite the absence of medical confirmation. These patients are considered to have a primary psychotic disorder that requires antipsychotic treatment.
TREATING PRIMARY SYMPTOMS
Drug therapy. When hypochondriasis is secondary—such as to depression or panic disorder—treat the primary condition first.11,12 For primary hypochondriasis, selective serotonin reuptake inhibitors (SSRIs) such as fluoxetine, paroxetine, or fluvoxamine have shown benefit, mostly in open-label studies. An uncontrolled case series suggests that nefazodone—with mixed serotonin reuptake inhibition and agonist properties—also may help patients with hypochondriasis.13 In the only published controlled study, fluoxetine was more effective than placebo for treating hypochondriasis.10
Continue drug therapy, when used, for at least 8 weeks, with each dosage maintained for at least 4 weeks. If patients do not respond to lower SSRI dosages, increase to the higher dosages reported to be more effective for OCD (Table 3).14
Except for primary illness phobia, hypochondriasis has not been shown to respond to tricyclics, benzodiazepines, or dopaminergic blockers. In our experience, electroconvulsive therapy—although inadequately studied—may help treat patients with severe, treatment-refractory hypochondriasis with marked somatization.
Psychotherapy. Cognitive-behavioral therapy (CBT)—challenging patients’ irrational fears about illness and teaching them problem-solving tools—is effective in treating hypochondriasis.15 CBT can help patients understand that distorted thoughts lead to their sad or anxious moods.
Instructing patients to keep thought diaries can help them identify irrational fears and use cognitive restructuring to correct their faulty schemas. Tailor your cognitive therapy techniques to target the patient’s level of insight at the time of therapy.
Effective behavioral techniques may include setting limits on doctor visits, checking behaviors, reassurance seeking, etc. Repeated exposure to feared stimuli such as needles, white lab coats, blood pressure cuffs, medical dialogue, or hospital wards can help the patient habituate to the anxiety.
Relaxation techniques, a healthy diet, and exercise are also useful. Relaxation exercises—such as diaphragmatic breathing, progressive muscle relaxation, and visual imagery—may help patients manage anxiety by reducing CNS and autonomic nervous system arousal.
Bottom line
Hypochondriasis’ cognitive dysfunction is treatable, once an accurate diagnosis is made. Using a checklist can help you differentiate hypochondriasis from other medical and psychiatric disorders. A trusting doctor-patient relationship enhances outcome.
Related resources
- Fallon BA., Feinstein SB. Hypochondriasis: clinical, theoretical, and therapeutic aspects. In: Oldham J (ed). Review of psychiatry (vol. 20) Washington, DC: American Psychiatric Press, 2001:27-60.
- Cantor C, Fallon BA. Phantom illness: shattering the myth of hypochondria Boston: Houghton Mifflin Company, 1996.
- Starcevic V, Lipsitt DR (eds). Hypochondriasis: modern perspectives on an ancient malady New York: Oxford University Press, 2001.
Drug brand names
- Fluoxetine • Prozac
- Fluvoxamine • Luvox
- Nefazodone • Serzone
- Paroxetine • Paxil
1. Diagnostic and statistical manual of mental disorders (4th ed-text revision). Washington, DC: American Psychiatric Association, 2000.
2. Task Force on DSM-IV. DSM-IV options book. Washington DC: American Psychiatric Association, 1991.
3. Barsky AJ, Wyshak G, Klerman GL, Lathan KS. The prevalence of hypochondriasis in medical outpatients. Soc Psychiatry Psychiatr Epidemiol 1990;25(2):89-94.
4. Salkovskis PM, Clark DM. Panic and hypochondriasis. Adv Behav Res Ther 1993;15:23-48.
5. Pilowsky I. Dimensions of hypochondriasis. Br J Psychiatry 1967;113(494):89-93.
6. Barsky AJ, Wyshak G, Klerman GL. Psychiatric comorbidity in DSM-III-R hypochondriasis. Arch Gen Psychiatry 1992;49(2):101-8.
7. Kellner R. The prognosis of treated hypochondriasis: a clinical study. Acta Psychiatr Scand 1983;67(2):69-79.
8. Noyes R, Jr, Kathol RG, Fisher M, Phillips BM, et al. The validity of DSM-III-R hypochondriasis. Arch Gen Psychiatry 1993;50(12):961-70.
9. Fallon BA, Qureshi AI, Laje G, Klein B. Hypochondriasis and its relationship to obsessive-compulsive disorder. Psychiatr Clin North Am 2000;23(3):605-16.
10. Fallon BA, Schneier FR, Marshall R, Campeas R, et al. The pharmacotherapy of hypochondriasis. Psychopharmacol Bull 1996;32:607-11.
11. Kellner R, Fava GA, Lisansky J, et al. Hypochondriacal fears and beliefs in DSM-III melancholia: changes with amitriptyline. J Affect Disord 1986;10(1):21-6.
12. Noyes R, Jr, Reich J, Clancy J, O’Gorman TW. Reduction in hypochondriasis with treatment of panic disorder. Br J Psychiatry 1986;149:631-5(erratum in Br J Psychiatry 1987;150:273).
13. Kjernisted KD, Ennis MW, Lander M. An open-label clinical trial of nefazodone in hypochondriasis. Psychosomatics 2002;43:290-4.
14. Fallon BA. Pharmacologic strategies for hypochondriasis. In: Starcevic V, Lipsitt DR (eds). Hypochondriasis: modern perspectives on an ancient malady. New York: Oxford University Press, 2001;329-51.
15. Warwick HMC, Salkovskis PM. Hypochondriasis. In: Scott J, Williams JMG, Beck AT (eds). Cognitive therapy in clinical practice: an illustrative casebook. London; Routledge, 1989;78-102.
1. Diagnostic and statistical manual of mental disorders (4th ed-text revision). Washington, DC: American Psychiatric Association, 2000.
2. Task Force on DSM-IV. DSM-IV options book. Washington DC: American Psychiatric Association, 1991.
3. Barsky AJ, Wyshak G, Klerman GL, Lathan KS. The prevalence of hypochondriasis in medical outpatients. Soc Psychiatry Psychiatr Epidemiol 1990;25(2):89-94.
4. Salkovskis PM, Clark DM. Panic and hypochondriasis. Adv Behav Res Ther 1993;15:23-48.
5. Pilowsky I. Dimensions of hypochondriasis. Br J Psychiatry 1967;113(494):89-93.
6. Barsky AJ, Wyshak G, Klerman GL. Psychiatric comorbidity in DSM-III-R hypochondriasis. Arch Gen Psychiatry 1992;49(2):101-8.
7. Kellner R. The prognosis of treated hypochondriasis: a clinical study. Acta Psychiatr Scand 1983;67(2):69-79.
8. Noyes R, Jr, Kathol RG, Fisher M, Phillips BM, et al. The validity of DSM-III-R hypochondriasis. Arch Gen Psychiatry 1993;50(12):961-70.
9. Fallon BA, Qureshi AI, Laje G, Klein B. Hypochondriasis and its relationship to obsessive-compulsive disorder. Psychiatr Clin North Am 2000;23(3):605-16.
10. Fallon BA, Schneier FR, Marshall R, Campeas R, et al. The pharmacotherapy of hypochondriasis. Psychopharmacol Bull 1996;32:607-11.
11. Kellner R, Fava GA, Lisansky J, et al. Hypochondriacal fears and beliefs in DSM-III melancholia: changes with amitriptyline. J Affect Disord 1986;10(1):21-6.
12. Noyes R, Jr, Reich J, Clancy J, O’Gorman TW. Reduction in hypochondriasis with treatment of panic disorder. Br J Psychiatry 1986;149:631-5(erratum in Br J Psychiatry 1987;150:273).
13. Kjernisted KD, Ennis MW, Lander M. An open-label clinical trial of nefazodone in hypochondriasis. Psychosomatics 2002;43:290-4.
14. Fallon BA. Pharmacologic strategies for hypochondriasis. In: Starcevic V, Lipsitt DR (eds). Hypochondriasis: modern perspectives on an ancient malady. New York: Oxford University Press, 2001;329-51.
15. Warwick HMC, Salkovskis PM. Hypochondriasis. In: Scott J, Williams JMG, Beck AT (eds). Cognitive therapy in clinical practice: an illustrative casebook. London; Routledge, 1989;78-102.
Update on contraception: Benefits and risks of the new formulations
New contraceptives for women
Is there a role for metformin or acarbose as a weight-loss agent in the absence of diabetes?
Sodium oxybate: A new way to treat narcolepsy
Existing drug treatments for narcolepsy enhance daytime alertness, and most improve cataplexy, sleep paralysis, and hypnagogic/hypnopompic hallucinations. None of these agents, however, target the nocturnal sleep deficits that lead to daytime symptoms.
Sodium oxybate, one of the most controversial medications to receive FDA approval in recent years (Table 1), has been found to reduce daytime sleepiness and cataplexy by improving nighttime sleep in patients with narcolepsy.
ABOUT SODIUM OXYBATE
Sodium oxybate is also known as gamma-hydroxybutyrate (GHB). An illegal form of GHB—the so-called “date rape drug”—is produced and used illicitly, typically at parties and nightclubs. Some users hide the fast-acting, sedating drug in a cocktail, rendering victims unable to defend against an assault or to recall details leading to the assault.1
Some athletes believe GHB enhances on-field performance by increasing production of growth hormone. Enhanced growth hormone release has no known clinical significance or effect on athletic performance, however.
Table 1
Sodium oxybate: Fast facts
Drug brand name: Xyrem |
Class: CNS depressant |
FDA-approved indications: Treatment of cataplexy |
Approval date: July 17, 2002 |
Manufacturer: Orphan Medical |
Dosing forms: 180 mL oral solution at a concentration of 0.5 grams/mL |
Recommended dosage: Start at 2.25 grams at bedtime; repeat dose overnight (4.5 grams/d total). Dosage can be increased to 9 grams/d (4.5 grams per dose) by increments of 0.75 grams per dose every 2 weeks. A dropper is supplied to facilitate measurement. |
The U.S. Drug Enforcement Agency (DEA) considers GHB a Schedule 1 (illegal) drug. DEA considers the prescription version a Schedule 3 drug, meaning it can be prescribed with refills as long as a DEA number is listed on the prescription. To prevent misuse, a central pharmacy dispenses sodium oxybate and mandates use of a specific prescription form to verify the physician’s familiarity with the medication. Psychiatrists can call (866) 997-3688 to obtain the form.
Table 2
Sodium oxybate dosing recommendations for patients
|
Sodium oxybate is the only agent FDA-approved for treating cataplexy—muscle weakness common among patients with narcolepsy.
HOW IT WORKS
Developed as an anesthetic, sodium oxybate induces deep sleep and at higher doses causes amnesia.
Derived from gamma-aminobutyric acid (GABA), sodium oxybate’s mechanism of action is unknown. Some believe it binds to the GABA B receptor and partially inhibits the NMDA and AMPA receptor-mediated excitatory neurons in the hippocampus.2
Food alters its bioavailability, so sodium oxybate should be taken several hours after meals to prevent delays in absorption and effect. Patients taking it should not eat at bedtime.
The agent’s pharmacokinetics are nonlinear, meaning that if the dose is doubled, the medication effect is tripled or quadrupled. For this reason, dosage increases must be small (no more than 0.75 grams for each dose) and gradual (at intervals of at least 2 weeks). The medication reaches peak plasma concentration within 30 to 75 minutes, so patients should not take the medication until they are in bed. Its 1-hour half-life explains its brief duration of action and need for repeat dosing overnight (Table 2).
Sodium oxybate does not modify the activity of any cytochrome P-450 enzymes. The medication is high in sodium (0.5 grams in a 3-gram dose) and has a salty taste. Use caution when considering the agent for patients with hypertension or on low-sodium diets.
Sodium oxybate’s safety has not been adequately tested in patients younger than 18 or older than 65 or in those with dementia and other disease processes. Because the drug is metabolized by the liver, the manufacturer recommends prescribing one-half the starting dosage to patients with significant hepatic impairment.
EFFICACY
Sodium oxybate has been shown to indirectly reduce frequency of cataplexy by improving nocturnal sleep:
- In a placebo-controlled, 4-week trial, 136 patients received either placebo or sodium oxybate at bedtime and again overnight in two equally divided doses of 3, 6, or 9 grams each. Patients who received the medication experienced less-frequent cataplexy, reduced daytime sleepiness, and fewer unplanned daytime naps and nocturnal awakenings.3
- A placebo-controlled trial that followed 55 patients for more than 3 years demonstrated long-term efficacy based on the patients’ cataplexy diaries (mean duration of treatment 21 months). Cataplexy returned after abrupt discontinuation.4
Unlike patients with most other disorders, those with narcolepsy generally are willing to repeat a medication overnight. They awaken easily at night—often without an alarm. Patients taking the medication report that they fall asleep again more readily and experience dramatically improved sleep quality and duration.
TOLERABILITY
Sodium oxybate has been well tolerated in relatively small clinical trials.
In the 4-week, placebo-controlled trial,3 nausea, headache, dizziness, and enuresis were most frequently reported. Out of 136 participants, 1 withdrew because of acute confusion and 9 others left because of mild to moderate adverse events. Twelve others experienced one episode of enuresis—probably because they did not fully awaken from deep sleep when developing urinary urgency. Advise patients taking sodium oxybate to urinate before going to bed.
The medication’s propensity to increase slow-wave sleep may cause sleepwalking. Sleepwalking was reported in 32% of patients in one long-term, uncontrolled study.5 If a patient with a history of sleepwalking needs sodium oxybate, advise against sleeping in upper bunks and other dangerous settings, and recommend precautions such as locking doors.
Because of sodium oxybate’s sedating properties, concomitant use of alcohol, barbiturates, and benzodiazepines should be discouraged.
ABUSE POTENTIAL
As discussed, GHB has a high abuse potential with effects such as euphoria, relaxation, and heightened sexual feelings.
Tolerance and dependence has not been reported with sodium oxybate when used as prescribed. A withdrawal state—similar to alcohol and sedative/hypnotic withdrawal and marked by anxiety, tremor, agitation, and delirium—has been reported with GHB abuse (although other chemicals often are used simultaneously in such cases). Narcolepsy patients in clinical trials have abruptly discontinued sodium oxybate after months of use without significant withdrawal.4
Related resources
- Narcolepsy Network Inc. www.narcolepsynetwork.org
Disclosure
Dr. Krahn reports no financial relationship with Orphan Medical or with manufacturers of competing products.
1. Galloway GP, Frederick SL, Staggers FE, Jr, et al. Gamma-hydroxybutyrate: an emerging drug of abuse that causes physical dependence. Addiction 1997;92(1):89-96.
2. Cammalleri M, Brancucci A, Berton F, et al. Gamma-hydroxybutyrate reduces GABA(A)-mediated inhibitory postsynaptic potentials in the CA1 region of hippocampus. Neuropsychopharmacology. 2002;27(9):960-9.
3. U.S. Xyrem Multicenter Study Group. A randomized, double blind, placebo-controlled multicenter trial comparing the effects of three doses of orally administered sodium oxybate with placebo for the treatment of narcolepsy. Sleep 2002;25(1):42-9.
4. U.S. Xyrem Multi-Center Study Group. The abrupt cessation of therapeutically administered sodium oxybate (GHB) does not cause withdrawal symptoms. J Toxicol Clin Toxicol 2003;41:131-5.
5. Physicians’ Desk Reference (57th ed). Montvale, NJ: Thomson Healthcare, 2003.
6. Mitler MM, Hayduk R. Benefits and risks of pharmacotherapy for narcolepsy. Drug Saf. 2002;25(11):791-809.
Existing drug treatments for narcolepsy enhance daytime alertness, and most improve cataplexy, sleep paralysis, and hypnagogic/hypnopompic hallucinations. None of these agents, however, target the nocturnal sleep deficits that lead to daytime symptoms.
Sodium oxybate, one of the most controversial medications to receive FDA approval in recent years (Table 1), has been found to reduce daytime sleepiness and cataplexy by improving nighttime sleep in patients with narcolepsy.
ABOUT SODIUM OXYBATE
Sodium oxybate is also known as gamma-hydroxybutyrate (GHB). An illegal form of GHB—the so-called “date rape drug”—is produced and used illicitly, typically at parties and nightclubs. Some users hide the fast-acting, sedating drug in a cocktail, rendering victims unable to defend against an assault or to recall details leading to the assault.1
Some athletes believe GHB enhances on-field performance by increasing production of growth hormone. Enhanced growth hormone release has no known clinical significance or effect on athletic performance, however.
Table 1
Sodium oxybate: Fast facts
Drug brand name: Xyrem |
Class: CNS depressant |
FDA-approved indications: Treatment of cataplexy |
Approval date: July 17, 2002 |
Manufacturer: Orphan Medical |
Dosing forms: 180 mL oral solution at a concentration of 0.5 grams/mL |
Recommended dosage: Start at 2.25 grams at bedtime; repeat dose overnight (4.5 grams/d total). Dosage can be increased to 9 grams/d (4.5 grams per dose) by increments of 0.75 grams per dose every 2 weeks. A dropper is supplied to facilitate measurement. |
The U.S. Drug Enforcement Agency (DEA) considers GHB a Schedule 1 (illegal) drug. DEA considers the prescription version a Schedule 3 drug, meaning it can be prescribed with refills as long as a DEA number is listed on the prescription. To prevent misuse, a central pharmacy dispenses sodium oxybate and mandates use of a specific prescription form to verify the physician’s familiarity with the medication. Psychiatrists can call (866) 997-3688 to obtain the form.
Table 2
Sodium oxybate dosing recommendations for patients
|
Sodium oxybate is the only agent FDA-approved for treating cataplexy—muscle weakness common among patients with narcolepsy.
HOW IT WORKS
Developed as an anesthetic, sodium oxybate induces deep sleep and at higher doses causes amnesia.
Derived from gamma-aminobutyric acid (GABA), sodium oxybate’s mechanism of action is unknown. Some believe it binds to the GABA B receptor and partially inhibits the NMDA and AMPA receptor-mediated excitatory neurons in the hippocampus.2
Food alters its bioavailability, so sodium oxybate should be taken several hours after meals to prevent delays in absorption and effect. Patients taking it should not eat at bedtime.
The agent’s pharmacokinetics are nonlinear, meaning that if the dose is doubled, the medication effect is tripled or quadrupled. For this reason, dosage increases must be small (no more than 0.75 grams for each dose) and gradual (at intervals of at least 2 weeks). The medication reaches peak plasma concentration within 30 to 75 minutes, so patients should not take the medication until they are in bed. Its 1-hour half-life explains its brief duration of action and need for repeat dosing overnight (Table 2).
Sodium oxybate does not modify the activity of any cytochrome P-450 enzymes. The medication is high in sodium (0.5 grams in a 3-gram dose) and has a salty taste. Use caution when considering the agent for patients with hypertension or on low-sodium diets.
Sodium oxybate’s safety has not been adequately tested in patients younger than 18 or older than 65 or in those with dementia and other disease processes. Because the drug is metabolized by the liver, the manufacturer recommends prescribing one-half the starting dosage to patients with significant hepatic impairment.
EFFICACY
Sodium oxybate has been shown to indirectly reduce frequency of cataplexy by improving nocturnal sleep:
- In a placebo-controlled, 4-week trial, 136 patients received either placebo or sodium oxybate at bedtime and again overnight in two equally divided doses of 3, 6, or 9 grams each. Patients who received the medication experienced less-frequent cataplexy, reduced daytime sleepiness, and fewer unplanned daytime naps and nocturnal awakenings.3
- A placebo-controlled trial that followed 55 patients for more than 3 years demonstrated long-term efficacy based on the patients’ cataplexy diaries (mean duration of treatment 21 months). Cataplexy returned after abrupt discontinuation.4
Unlike patients with most other disorders, those with narcolepsy generally are willing to repeat a medication overnight. They awaken easily at night—often without an alarm. Patients taking the medication report that they fall asleep again more readily and experience dramatically improved sleep quality and duration.
TOLERABILITY
Sodium oxybate has been well tolerated in relatively small clinical trials.
In the 4-week, placebo-controlled trial,3 nausea, headache, dizziness, and enuresis were most frequently reported. Out of 136 participants, 1 withdrew because of acute confusion and 9 others left because of mild to moderate adverse events. Twelve others experienced one episode of enuresis—probably because they did not fully awaken from deep sleep when developing urinary urgency. Advise patients taking sodium oxybate to urinate before going to bed.
The medication’s propensity to increase slow-wave sleep may cause sleepwalking. Sleepwalking was reported in 32% of patients in one long-term, uncontrolled study.5 If a patient with a history of sleepwalking needs sodium oxybate, advise against sleeping in upper bunks and other dangerous settings, and recommend precautions such as locking doors.
Because of sodium oxybate’s sedating properties, concomitant use of alcohol, barbiturates, and benzodiazepines should be discouraged.
ABUSE POTENTIAL
As discussed, GHB has a high abuse potential with effects such as euphoria, relaxation, and heightened sexual feelings.
Tolerance and dependence has not been reported with sodium oxybate when used as prescribed. A withdrawal state—similar to alcohol and sedative/hypnotic withdrawal and marked by anxiety, tremor, agitation, and delirium—has been reported with GHB abuse (although other chemicals often are used simultaneously in such cases). Narcolepsy patients in clinical trials have abruptly discontinued sodium oxybate after months of use without significant withdrawal.4
Related resources
- Narcolepsy Network Inc. www.narcolepsynetwork.org
Disclosure
Dr. Krahn reports no financial relationship with Orphan Medical or with manufacturers of competing products.
Existing drug treatments for narcolepsy enhance daytime alertness, and most improve cataplexy, sleep paralysis, and hypnagogic/hypnopompic hallucinations. None of these agents, however, target the nocturnal sleep deficits that lead to daytime symptoms.
Sodium oxybate, one of the most controversial medications to receive FDA approval in recent years (Table 1), has been found to reduce daytime sleepiness and cataplexy by improving nighttime sleep in patients with narcolepsy.
ABOUT SODIUM OXYBATE
Sodium oxybate is also known as gamma-hydroxybutyrate (GHB). An illegal form of GHB—the so-called “date rape drug”—is produced and used illicitly, typically at parties and nightclubs. Some users hide the fast-acting, sedating drug in a cocktail, rendering victims unable to defend against an assault or to recall details leading to the assault.1
Some athletes believe GHB enhances on-field performance by increasing production of growth hormone. Enhanced growth hormone release has no known clinical significance or effect on athletic performance, however.
Table 1
Sodium oxybate: Fast facts
Drug brand name: Xyrem |
Class: CNS depressant |
FDA-approved indications: Treatment of cataplexy |
Approval date: July 17, 2002 |
Manufacturer: Orphan Medical |
Dosing forms: 180 mL oral solution at a concentration of 0.5 grams/mL |
Recommended dosage: Start at 2.25 grams at bedtime; repeat dose overnight (4.5 grams/d total). Dosage can be increased to 9 grams/d (4.5 grams per dose) by increments of 0.75 grams per dose every 2 weeks. A dropper is supplied to facilitate measurement. |
The U.S. Drug Enforcement Agency (DEA) considers GHB a Schedule 1 (illegal) drug. DEA considers the prescription version a Schedule 3 drug, meaning it can be prescribed with refills as long as a DEA number is listed on the prescription. To prevent misuse, a central pharmacy dispenses sodium oxybate and mandates use of a specific prescription form to verify the physician’s familiarity with the medication. Psychiatrists can call (866) 997-3688 to obtain the form.
Table 2
Sodium oxybate dosing recommendations for patients
|
Sodium oxybate is the only agent FDA-approved for treating cataplexy—muscle weakness common among patients with narcolepsy.
HOW IT WORKS
Developed as an anesthetic, sodium oxybate induces deep sleep and at higher doses causes amnesia.
Derived from gamma-aminobutyric acid (GABA), sodium oxybate’s mechanism of action is unknown. Some believe it binds to the GABA B receptor and partially inhibits the NMDA and AMPA receptor-mediated excitatory neurons in the hippocampus.2
Food alters its bioavailability, so sodium oxybate should be taken several hours after meals to prevent delays in absorption and effect. Patients taking it should not eat at bedtime.
The agent’s pharmacokinetics are nonlinear, meaning that if the dose is doubled, the medication effect is tripled or quadrupled. For this reason, dosage increases must be small (no more than 0.75 grams for each dose) and gradual (at intervals of at least 2 weeks). The medication reaches peak plasma concentration within 30 to 75 minutes, so patients should not take the medication until they are in bed. Its 1-hour half-life explains its brief duration of action and need for repeat dosing overnight (Table 2).
Sodium oxybate does not modify the activity of any cytochrome P-450 enzymes. The medication is high in sodium (0.5 grams in a 3-gram dose) and has a salty taste. Use caution when considering the agent for patients with hypertension or on low-sodium diets.
Sodium oxybate’s safety has not been adequately tested in patients younger than 18 or older than 65 or in those with dementia and other disease processes. Because the drug is metabolized by the liver, the manufacturer recommends prescribing one-half the starting dosage to patients with significant hepatic impairment.
EFFICACY
Sodium oxybate has been shown to indirectly reduce frequency of cataplexy by improving nocturnal sleep:
- In a placebo-controlled, 4-week trial, 136 patients received either placebo or sodium oxybate at bedtime and again overnight in two equally divided doses of 3, 6, or 9 grams each. Patients who received the medication experienced less-frequent cataplexy, reduced daytime sleepiness, and fewer unplanned daytime naps and nocturnal awakenings.3
- A placebo-controlled trial that followed 55 patients for more than 3 years demonstrated long-term efficacy based on the patients’ cataplexy diaries (mean duration of treatment 21 months). Cataplexy returned after abrupt discontinuation.4
Unlike patients with most other disorders, those with narcolepsy generally are willing to repeat a medication overnight. They awaken easily at night—often without an alarm. Patients taking the medication report that they fall asleep again more readily and experience dramatically improved sleep quality and duration.
TOLERABILITY
Sodium oxybate has been well tolerated in relatively small clinical trials.
In the 4-week, placebo-controlled trial,3 nausea, headache, dizziness, and enuresis were most frequently reported. Out of 136 participants, 1 withdrew because of acute confusion and 9 others left because of mild to moderate adverse events. Twelve others experienced one episode of enuresis—probably because they did not fully awaken from deep sleep when developing urinary urgency. Advise patients taking sodium oxybate to urinate before going to bed.
The medication’s propensity to increase slow-wave sleep may cause sleepwalking. Sleepwalking was reported in 32% of patients in one long-term, uncontrolled study.5 If a patient with a history of sleepwalking needs sodium oxybate, advise against sleeping in upper bunks and other dangerous settings, and recommend precautions such as locking doors.
Because of sodium oxybate’s sedating properties, concomitant use of alcohol, barbiturates, and benzodiazepines should be discouraged.
ABUSE POTENTIAL
As discussed, GHB has a high abuse potential with effects such as euphoria, relaxation, and heightened sexual feelings.
Tolerance and dependence has not been reported with sodium oxybate when used as prescribed. A withdrawal state—similar to alcohol and sedative/hypnotic withdrawal and marked by anxiety, tremor, agitation, and delirium—has been reported with GHB abuse (although other chemicals often are used simultaneously in such cases). Narcolepsy patients in clinical trials have abruptly discontinued sodium oxybate after months of use without significant withdrawal.4
Related resources
- Narcolepsy Network Inc. www.narcolepsynetwork.org
Disclosure
Dr. Krahn reports no financial relationship with Orphan Medical or with manufacturers of competing products.
1. Galloway GP, Frederick SL, Staggers FE, Jr, et al. Gamma-hydroxybutyrate: an emerging drug of abuse that causes physical dependence. Addiction 1997;92(1):89-96.
2. Cammalleri M, Brancucci A, Berton F, et al. Gamma-hydroxybutyrate reduces GABA(A)-mediated inhibitory postsynaptic potentials in the CA1 region of hippocampus. Neuropsychopharmacology. 2002;27(9):960-9.
3. U.S. Xyrem Multicenter Study Group. A randomized, double blind, placebo-controlled multicenter trial comparing the effects of three doses of orally administered sodium oxybate with placebo for the treatment of narcolepsy. Sleep 2002;25(1):42-9.
4. U.S. Xyrem Multi-Center Study Group. The abrupt cessation of therapeutically administered sodium oxybate (GHB) does not cause withdrawal symptoms. J Toxicol Clin Toxicol 2003;41:131-5.
5. Physicians’ Desk Reference (57th ed). Montvale, NJ: Thomson Healthcare, 2003.
6. Mitler MM, Hayduk R. Benefits and risks of pharmacotherapy for narcolepsy. Drug Saf. 2002;25(11):791-809.
1. Galloway GP, Frederick SL, Staggers FE, Jr, et al. Gamma-hydroxybutyrate: an emerging drug of abuse that causes physical dependence. Addiction 1997;92(1):89-96.
2. Cammalleri M, Brancucci A, Berton F, et al. Gamma-hydroxybutyrate reduces GABA(A)-mediated inhibitory postsynaptic potentials in the CA1 region of hippocampus. Neuropsychopharmacology. 2002;27(9):960-9.
3. U.S. Xyrem Multicenter Study Group. A randomized, double blind, placebo-controlled multicenter trial comparing the effects of three doses of orally administered sodium oxybate with placebo for the treatment of narcolepsy. Sleep 2002;25(1):42-9.
4. U.S. Xyrem Multi-Center Study Group. The abrupt cessation of therapeutically administered sodium oxybate (GHB) does not cause withdrawal symptoms. J Toxicol Clin Toxicol 2003;41:131-5.
5. Physicians’ Desk Reference (57th ed). Montvale, NJ: Thomson Healthcare, 2003.
6. Mitler MM, Hayduk R. Benefits and risks of pharmacotherapy for narcolepsy. Drug Saf. 2002;25(11):791-809.
Managing Atrial Fibrillation
Supplement Editor:
Roger M. Mills, MD
Contents
Beyond drugs alone: Pacing, ablation, and surgery for atrial fibrillation
R.M. Mills, MD, MPH
Basic mechanisms of atrial fibrillation
D.R. Van Wagoner, PhD
Current clinical issues in atrial fibrillation
M.K. Chung, MD
Approaches to restoring and maintaining normal sinus rhythm
I. Pharmacologic management: Often insufficient, but still first-line
D.O. Martin, MD, MPH
II. Pacing and devices: Progress toward a preventive role
W. Saliba, MD
III. Surgical approaches: At the 'tipping point'
P.M. McCarthy, MD, and A.M. Gillinov, MD
IV. Catheter ablation: A less invasive path to potential cure
W. Belden, MD; N.F. Marrouche, MD; and A. Natale, MD
Managing chronic atrial fibrillation: Strategies to control symptoms and prevent embolism
D.O. Martin, MD, MPH
Supplement Editor:
Roger M. Mills, MD
Contents
Beyond drugs alone: Pacing, ablation, and surgery for atrial fibrillation
R.M. Mills, MD, MPH
Basic mechanisms of atrial fibrillation
D.R. Van Wagoner, PhD
Current clinical issues in atrial fibrillation
M.K. Chung, MD
Approaches to restoring and maintaining normal sinus rhythm
I. Pharmacologic management: Often insufficient, but still first-line
D.O. Martin, MD, MPH
II. Pacing and devices: Progress toward a preventive role
W. Saliba, MD
III. Surgical approaches: At the 'tipping point'
P.M. McCarthy, MD, and A.M. Gillinov, MD
IV. Catheter ablation: A less invasive path to potential cure
W. Belden, MD; N.F. Marrouche, MD; and A. Natale, MD
Managing chronic atrial fibrillation: Strategies to control symptoms and prevent embolism
D.O. Martin, MD, MPH
Supplement Editor:
Roger M. Mills, MD
Contents
Beyond drugs alone: Pacing, ablation, and surgery for atrial fibrillation
R.M. Mills, MD, MPH
Basic mechanisms of atrial fibrillation
D.R. Van Wagoner, PhD
Current clinical issues in atrial fibrillation
M.K. Chung, MD
Approaches to restoring and maintaining normal sinus rhythm
I. Pharmacologic management: Often insufficient, but still first-line
D.O. Martin, MD, MPH
II. Pacing and devices: Progress toward a preventive role
W. Saliba, MD
III. Surgical approaches: At the 'tipping point'
P.M. McCarthy, MD, and A.M. Gillinov, MD
IV. Catheter ablation: A less invasive path to potential cure
W. Belden, MD; N.F. Marrouche, MD; and A. Natale, MD
Managing chronic atrial fibrillation: Strategies to control symptoms and prevent embolism
D.O. Martin, MD, MPH