OCD is a potentially devastating illness that can result in considerable social and economic disability for both afflicted patients and for their family members. OCD is usually treated with a combination of specific behavioral therapies, called exposure and response prevention, and medications. It is important to note that many psychoactive medications are not likely to help OCD symptoms, but that a number of partially effective drugs have now been carefully evaluated. The treatment, however, for most OCD patients should involve the combination of behavior therapy with medications. This pamphlet will focus on medications, but that is not meant to diminish the importance of behavior therapy. The topics covered in this pamphlet are based upon questions that I am frequently asked. Some were suggested by Jim Broatch, and others came from Chris Vertullo's list.
The majority of the drugs that help OCD are classified as antidepressants. It is important to note that depression commonly results from the disability produced by OCD, and that doctors can treat both the OCD and depression with the same medication. There are also a number of disorders that are possibly related to OCD, such as compulsive gambling and sexual behaviors, trichotillomania, body dysmorphic disorder, compulsive eating, nail biting, and compulsive spending. There is some evidence that the medications and behavior therapies discussed in this pamphlet will help some of these patients also, but more research is needed in this area to give firm recommendations.
No! Some commonly used antidepressants have no effect whatsoever on OCD symptoms. Drugs, such as imipramine (Tofranil) or amitriptyline (Elavil), that are good antidepressants, only rarely improve OCD symptoms.
There are six drugs that have been shown to be useful in very good double-blind (both physician and patient unaware of whether patient is receiving drug or placebo [inert sugar pill]) placebo-controlled (about half of the patients receive drug and the other half placebo or inactive pill) studies. This is a very good way to evaluate drugs since improvements can be evaluated in an unbiased manner and drug effectiveness can be accurately determined.
The six drugs that have been shown to be effective in such studies include: fluvoxamine (Luvox), fluoxetine (Prozac), sertraline (Zoloft), paroxetine (Paxil), citalopram (Celexa*), and clomipramine (Anafranil). Anafranil has been around the longest and is the best studied throughout the world, but there is growing evidence that the other drugs are as effective.
In addition to these carefully studied drugs, there are hundreds of case reports of other drugs occasionally being helpful. There are small series of patients reported that suggest that venlafaxine (Effexor) may also be somewhat effective, but large scale controlled trials are lacking.
It remains unclear as to why these particular drugs help OCD while similar drugs do not. Each has potent effects on a particular neurotransmitter, or chemical messenger, in the brain called serotonin. It appears that potent effects on brain serotonin are necessary (but not sufficient) to produce improvement in OCD. Serotonin is one of several neurotransmitter chemicals that nerve cells in the brain use in communicating with one another. Unlike some other neurotransmitters, its receptors are not localized in a few specific areas of the brain; hence, its uptake and release affects much of our mental life, including OCD and depression.
Neurotransmitters such as serotonin are active when they are present in the gap (referring to the synaptic cleft) between nerve cells. Transmission is ended by a process by which the chemicals are taken back up into the transmitting cell. The anti-obsessional drugs are called serotonin reuptake inhibitors or SRIs; they work by slowing the reuptake of serotonin, thus making it more available to the receiving cell and prolonging its effect on the brain. We think that this increased serotonin produces changes, over a period of a few weeks, in receptors (areas where serotonin attaches) in some of the membranes of the nerves. We also believe that these receptors may be abnormal in patients with OCD, and that the changes that occur in them due to these medications at least partly reverse the OCD symptoms. This is only part of how drugs work; it is very likely that other brain chemicals in addition to serotonin are involved. In fact, when activity in the brain's serotonergic system is altered, this changes the activity of other brain systems.
Experiments have been done with drugs that directly stimulate components of the serotonin system in the brain, and it was found that such so-called serotonergic agonists actually make OCD symptoms worse. However, after patients are successfully treated for OCD, these agonists do not worsen OCD symptoms, thus suggesting that there may be some changes in the brain's serotonergic system with effective drug treatment that somehow result in improvement in symptoms.
Don't worry if this does not make sense to you. Researchers do not know how the drugs work, and that is why this is all so confusing. The good news is that we do know, after decades of research, how to treat patients, even though we do not know exactly why our treatments work.
As a general rule, it appears that for most people high dosages of these drugs are required to obtain anti-obsessional effects. The studies done to date suggest that the following dosages may be necessary: Luvox (up to 300 mg/day), Prozac (40-80 mg/day), Zoloft (up to 200 mg/day), Paxil (40-60 mg/day), Celexa (up to 60 mg/day), and Anafranil (up to 250 mg/day). Where a lower dosage was listed, at least some of the studies have suggested that a dose lower than the minimum was not significantly better than placebo. I have also seen a very small number of patients who have not responded to large dosages of these medications, but who improved on extremely low doses, such as 5-10 mg/day of Prozac or 25 mg/day of Anafranil. These patients have not been carefully studied and, to my knowledge, these low-dosage responders are not reported in the psychiatric literature. If patients fail to improve with high dosages of the above medications, it is probably worth a trial of a very low dose.
Each of these drugs has side effects, and it is quite unusual for an individual patient not to have one or more side effects. As with all drugs, the patient and physician must weigh the benefits of the drug against the side effects. It is important for the patient to be open and forceful about problems that may be caused by the medication. Sometimes just an adjustment in dosage or switch in the time of day that one takes the medication is all that is required.
Luvox, Prozac, Paxil, Celexa, and Zoloft are called SSRIs or selective serotonin reuptake inhibitors, while Anafranil is an older tricyclic antidepressant or SRI (serotonin reuptake inhibitor) that has effects on other chemical messengers besides serotonin and is thus not selective for serotonin. All of these drugs commonly produce sexual side effects in both sexes that may range from lowering of sexual drive to delayed ability to have an orgasm to complete inability to have an erection or orgasm. Interestingly, there is an uncommon side effect that has been reported where patients have spontaneous orgasms while yawning. This must be quite uncommon since no patient has ever told me of such a symptom, and when patients yawn in my office, they always look bored, not excited. Occasional patients report increased interest in sexual activity.
Although it may seem embarrassing, you should tell your physician about sexual difficulties so that he or she can help you figure out how best to deal with them. These side effects are so common that your psychiatrist will not be surprised. There have recently been a few reports of patients who were having sexual difficulties on these drugs who stopped taking them on Fridays and Saturdays and were able to at least enjoy successful sexual activity on the weekends. It appears so far, that this approach has not produced a relapse in symptoms, but this may be reported as people try this more often. Also, with Prozac this approach has not been as effective since it is such a long acting compound.
There is some evidence that Celexa does not cause as many sexual side effects or weight gain, but it is new to the United States market so the final word on this remains to be determined.
The SSRIs also commonly cause nausea, inability to sit still, sleepiness in some individuals, insomnia in others, and a heightened sense of energy. The tricyclic Anafranil may cause pronounced effects like drowsiness, dry mouth, racing heart, memory problems, concentration difficulties, and problems with urination (mostly in men). Sometimes weight gain is a problem and a strict diet may be needed if appetite is increased. There are many other less common side effects with these drugs that your physician may discuss with you. As a general rule, these drugs are very safe, even with long term use, and all of the side effects completely reverse when the drugs are stopped; thus there is no evidence that they do permanent damage to the body.
Occasional patients are very sensitive to medications and cannot tolerate even the lowest dosage that comes in pills. Many of the pills can be broken in half to allow for lower dosages. There is also a liquid form of Prozac that has allowed many patients to gradually increase the dosage to therapeutic levels. Often, if patients can start at very low dosages (e.g., 1-2 mg/day) and very slowly increase the dose, they will eventually be able to tolerate the medication. This technique has proven so successful for many people that there is now a "fan club" of those helped by this approach. Many patients have been able to use liquid Prozac. For example, one woman who was started on Prozac at 20 mg/day complained of very bothersome side effects such as increased anxiety, shakiness, and terrible insomnia. She also felt it had made her OCD worse. In addition, she had horrible side effects from even 12.5 mg of Anafranil, and later with low dosages of Paxil and Zoloft. She then started 1-2 mg/day of liquid Prozac that she had heard was good from other patients whom she met over a computer bulletin board. She felt no side effects, and over a period of a few weeks, she again got up to 20 mg/day without the previous side effects that she had felt on this dose in the past. She continued to increase the Prozac to 60 mg/day over a couple of months, and her OCD gradually improved quite dramatically. Thus, careful and gradual increases in dosage with liquid medication may allow some medication-sensitive patients to reach therapeutic levels.
As far as we know, there are no irreversible side effects caused by the standard anti-obsessional drugs. Many patients have used them for years without difficulties. Some of the drugs that are occasionally used such as the antipsychotic (or sometimes called neuroleptic) drugs like haloperidol (Haldol), chlorpromazine (Thorazine), thioridazine (Mellaril), and trifluoperazine (Stelazine) can produce irreversible neurologic problems, such as persistent tremor or tongue thrusting. These drugs are best avoided in patients with the usual forms of OCD; if they are used, it should generally be for only a few weeks. Occasionally, patients need to remain on these potentially troublesome drugs for longer periods of time.
For example, in OCD patients who also have tics (brief muscle jerks, such as repetitive eye blinks, nervous cough, or shoulder shrugs), there is now evidence that very low doses of these neuroleptic drugs added to ongoing SRI medication helps OCD symptoms. In OCD patient s without tics, there is no evidence that neuroleptics are helpful, and they are best avoided. There are newer neuroleptic agents, like clozapine (Clozaril) and risperidone (Risperdal), that may have fewer of these types of neurologic problems, and that may be helpful when added to SRI treatment. These new drugs should not be used alone since they have been associated with worsening of OCD symptoms when not taken in combination with a SRI.
In general, we try not to give anti-obsessional medications to women who are pregnant or who are breast-feeding. Since we do not clearly understand the long-term effects of these drugs on a fetus or infant, this is the most prudent course of action. If severe OCD cannot be controlled any other way, however, these medications seem to be safe, and many pregnant women have taken them without difficulty. If there were risk to the fetus, it is likely that most of the risk would be during the first three months of pregnancy when the baby's brain is developing. Some OCD patients are able to use the behavioral techniques of exposure and response prevention to avoid medications at least during the initial three months of pregnancy. If your OCD is very severe, you may need to take a medication throughout the course of pregnancy. In very elderly patients, it is best to avoid Anafranil as the initial drug since it has side effects that can interfere with thinking and cause or worsen confusion in the elderly. Some of the other anti-obsessional drugs like Prozac, Zoloft, Luvox, and Paxil can be used in the elderly, but greatly reduced dosages are usually needed. Although these drugs can be taken by patients with heart disorders, special caution is required, and close monitoring with frequent cardiograms (ECGs) may be necessary.
No. This is a common mistake. These medications are meant to be taken on a regular daily basis to maintain a constant level in your blood stream. They are not taken like the typical anti-anxiety agents, when you feel upset or anxious. It is best not to miss dosages if possible. Having said this, it is unlikely that any adverse effect on OCD will occur if a daily dose is missed occasionally, and sometimes missed dosages are prescribed by your doctor to help manage troublesome side effects, such as sexual dysfunction (see earlier section).
Although any licensed physician can legally prescribe these drugs, it is probably best to deal directly with a board-certified psychiatrist who understands OCD. A list of psychiatrists with special interest in OCD can be obtained from the OC Foundation. Keep in mind, however, that these are physicians who have expressed an interest in OCD and whom the Foundation has not evaluated in any way. (Legally, OCF is obligated to list any psychiatrist who expresses an interest in the disorder; a Treatment Providers List is available upon request.) It is also important to find a psychiatrist who is a psychopharmacologist; that is, one who has special knowledge about the use of drugs to treat psychiatric disorders.
A useful way of thinking about the use of medication for OCD is to compare your illness with a common medical disorder such as diabetes. There is growing evidence that OCD is, in fact, a neurologic or medical illness and not simply a result of some problem in the environment or of improper upbringing. As with the diabetic who needs insulin to live a normal life, some OCD patients need anti-compulsive medication to function normally (diabetics, like Obsessive-Compulsives, often feel angry and up set about having to take medication). There is no evidence that OCD is a result of anything that the patient has done, and it is best to consider it a chemical or neurologic disorder affecting a part of the brain.
Usually, with reassurance from a doctor that you trust, your fears can be overcome. If you still refuse to take medication, behavior therapy can be started first, and part of the therapy can focus on your reluctance to take medication. Our experience indicates that the combination of medication and behavior therapy will maximize your chances for improvement.
Unfortunately, these drugs are very expensive and can cost the patient up to $6 or $7 per day for larger doses. When the patent expires on each of these drugs, other companies can make generic forms of each drug, and then the prices will fall. However, this will not happen for many years with the drugs currently available.
One can think of all sorts of sinister reasons why pharmaceutical companies charge so much for these medications, but we must keep in mind that it costs many millions of dollars to bring just a single drug to market in the United States. Most drugs do not make it to the market and represent a lost investment. But, if the pharmaceutical companies do not try out new agents, no progress in this area is likely. These companies spend millions in research trying to identify new compounds that may have therapeutic value. Without pharmaceutical companies, there would likely be few, if any, advances in clinical pharmacology in the United States, and we would not have new drugs available to us.
Pharmaceutical companies are also heavily involved in promoting awareness of the various diseases, including OCD, for which they have a medication. These promotions (television, radio, print) benefit patients as they often are the means by which patients discover that they have OCD, that it has a name , and that it can be treated. Pharmaceutical companies have even been active in promoting non-drug treatments, such as behavior therapy, when they have nothing financially to gain. They also sponsor educational programs to physicians, and have been instrumental in spreading the knowledge base about OCD to both physicians and patients. They have been financial backers of organizations like the national Obsessive-Compulsive Foundation.
It is important not to give up on a medication until you have been taking it at a therapeutic dose for 10 to 12 weeks. Many patients feel no positive effects for the first few weeks of treatment, but then they may improve greatly. Unfortunately during the early part of treatment, patients may only have side effects and no positive results, and sometimes physicians forget to tell patients about this lag in response. We do not know why the medications take so long to work for OCD. Keep in mind that even many psychiatrists give up on the medications after four to six weeks, since this is the time it takes for depressed patients to improve. Thus, you may have to remind your psychiatrist to keep you on the medication longer.
In the large studies that have been done, each medication helps about 75% to 85% of the patients at least a little. About 50% to 60% of patients in each trial had at least a moderate response to medication. We know that some patients have no response at all. If you do not respond to the first medication, then it is important to go on to the next. I have seen patients who have had no response to three of the above medications, then have a wonderful response to the next one. There are also techniques of combining medications that may increase the response magnitude and rate (see next section). One patient wrote this to me: "Seeking an effective medication for OCD is a lot like dating to find a mate; don't be afraid to shop around and try different meds till you find one that works for you!"
The best augmenting technique is to add behavior therapy to ongoing drug treatment. However, to boost a drug's effect, we sometimes combine two or more medications together. For example, some people respond to combining Luvox or Prozac with Anafranil. It is important for the physician to keep in mind that Anafranil's blood level can be dramatically increased by adding one of the other drugs, so it is important to keep Anafranil's dose low, at least during the initial stages of treatment. Some times, blood levels are helpful, but most of the time, a good clinician can just follow side effects and symptom reduction to find the correct dosage.
Other drugs are sometimes combined with ongoing SRI medications. Some that have commonly been used include the following: buspirone (Buspar), lithium carbonate (Eskalith), clonazepam (Klonopin), methylphenidate (Ritalin), fenfluramine (Pondamin), and other antidepressants (e.g., trazodone, bupropion, desipramine, etc.). The controlled trials that have been done with these augmenting agents have been largely disappointing, but since occasional patients respond to the addition of a second drug, clinicians frequently try this technique.
Yes, there are drugs that are occasionally helpful in individual patients besides the ones already mentioned. For example, some patients may be helped by drugs called monoamine oxidase inhibitors (e.g., Nardil [phenelzine] and Parnate [tranylcypromine]) that work in a different way than the previously mentioned drugs.
These drugs inhibit one of the enzymes that degrades the chemical messengers in the nerve gaps, thereby lengthening the time that the messenger can be active. There is some anecdotal evidence that OCD patients who also have panic attacks or prominent concerns with symmetry may be more likely to improve with monoamine oxidase inhibitors. With these drugs, certain foods and medications cannot be taken or potentially fatal reactions can occur. They are particularly dangerous in combination with the SRI medications, so these must be stopped for at least two weeks (five weeks for Prozac, which is longer lasting) prior to starting monoamine oxidase inhibitors.
The other antidepressants occasionally help, but chances of this are quite small.
No one knows how long patients should take these medications once they have been effective. Some patients are able to discontinue medications after a six- to twelve-month treatment period. However, it does appear that more than half of OCD patients (and maybe many more) will need to be on at least a low dosage of medication for years, perhaps even for life. It seems likely that the risk of relapse will be lower if patients learn to use behavior-therapy techniques while they are doing well on medication that is tapered very slowly (even over several months).
The behavioral techniques may enable patients to control any symptoms that return when they stop taking medication. Typically, after medications are stopped, symptoms do not return immediately, but they may start to return within a few weeks to a few months. When one of these drugs is working and then discontinued and symptoms return, the vast majority of patients have a good response upon reinstitution of the medication. However, I have now seen a few patients who did not respond when the discontinued drug was restarted.
Many patients drink alcohol while on these medications and tolerate it well. It is important to keep in mind that alcohol may have a greater effect on individuals who are taking medication; that is, one drink could affect an individual as if it were two drinks, etc. Also, it is not known if alcohol can counteract some of the therapeutic effects of the medication, so it may be worth trying not to drink alcohol during the first couple of months after starting medication.
As noted earlier, most psychiatrists and behavior therapists today believe that combining behavior therapy, consisting of exposure and response prevention, with medication is the most effective approach.
Traditional psychotherapy, aimed at helping the patient develop insight into his or her problem, is generally not helpful specifically for OCD symptoms themselves. However, traditional psychotherapy may be of benefit as part of a treatment package for patients who have been ill and isolated for many years or for those whose illness started at an early age. On the other hand, behavior therapy consisting of techniques called exposure and response prevention is effective for many people with OCD.
In this approach, the patient is deliberately and voluntarily exposed to feared objects or ideas, either directly or by imagination (the exposure component), and then is discouraged or prevented (with the patient's permission) from carrying out the usual compulsive response (the response-prevention component). For example, a compulsive hand washer may be urged to touch an object believed to be contaminated, and then may be denied the opportunity to wash for several hours. When the treatment works well, the patient gradually experiences less anxiety from the obsessive thoughts and becomes able to do without the compulsive actions for extended periods of time.
Studies of behavior therapy for OCD have found it to produce lasting benefits. To achieve the best results, a combination of factors is necessary: The therapist should be well-trained in the specific method developed, the patient must be highly motivated, and the patient's family must be cooperative. In addition to visits to the therapist, the patient must be faithful in fulfilling homework assignments. For those patients who complete the course of treatment, the improvements can be significant.
With a combination of drug and behavioral therapy, the majority of OCD patients will be able to function well in both their work and social lives. The ongoing search for causes, together with research on treatment, promises to yield even more hope for people with OCD and their families.
Approximately two-thirds of OCD patients have also suffered at least one major depression at some point in their life. About one-third are depressed when they present to us for treatment. Some schools of thought feel that the OCD causes the depression while others believe the OCD and depression simply tend to coexist. Most patients tell me that their OCD symptoms came first, and then depression began when they were unable to handle the OCD.
It sometimes happens that OCD
improves and depression persists. Occasionally, a second drug is added to combat
the depression. Sometimes, your doctor can assist you in finding other reasons
why depression persists.
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