You are on page 1of 12

The American Journal on Addictions 12:S41^S52, 2003 Published by Brunner-Routledge

# 2003 American Academy of Addiction Psychiatry 1055-0496/03 $12.00 + .00


DOI: 10.1080/10550490390202406

The Role of Psychosocial


Treatments in
Pharmacotherapy for
Alcoholism
Mary E. McCaul, Ph.D., Nancy M. Petry, Ph.D.

Medication treatment for alcohol use disorders often includes a psychotherapy


component. The most appropriate psychotherapy to use may depend upon
characteristics of the patient, the medication, the setting, and the experiences
of the provider. To date, little empirical research has investigated these
issues with respect to outcomes in clinical trials that combine
pharmacotherapy and psychotherapy. This paper reviews seven major
types of psychotherapy for treatment of alcohol use disorders: brief
interventions, motivational enhancement therapy, cognitive-behavioral
therapy, cue exposure therapy, behavioral treatments, behavioral marital
therapy, and twelve-step therapy. The theoretical basis for and empirical
evidence supporting the efficacy of the therapies are reviewed, with an empha-
sis on studies that provided pharmacotherapy in conjunction with
psychotherapy. Directions for future research in this area are also suggested.
(Am J Addict 2003;12[Suppl1]:S41^S52)

P harmacotherapy trials for alcohol


use disorders typically incorporate
psychosocial therapy into the overall treat-
developed and empirically validated for
treating alcohol use disorders. The most
typical pharmacotherapy research design
ment regimen of study patients. This pro- incorporates one such e‘mpirically
cedure is based on the assumption that validated psychosocial treatment and then
medication alone will not be sufficient for varies the type or dosage of the medication.
patients to acquire the new knowledge, Very few studies have manipulated both
skills, and motivations often needed to suc- the psychosocial treatment and the pharma-
cessfully address their alcohol problems. cotherapy, examining the potential interac-
A variety of psychotherapies have been tions of the two interventions. However, a

Received August 15, 2002; accepted December 30, 2002.


From the Johns Hopkins University School of Medicine, Baltimore, Md. (Dr. McCaul); and the University of
Connecticut School of Medicine, Farmington, Conn. (Dr. Petry). Address correspondence to Dr. McCaul,
Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, 911 N.
Broadway, Baltimore, MD 21205. E-mail: betsymc@jhmi.edu.

S41
Psychosocial Treatments in Alcohol Pharmacotherapy

recent meta-analysis of naltrexone and Typically, the interventions demonstrate


acamprosate research1 suggests that efficacy for at least a twelve-month
structured psychosocial treatment is a pre- period,2 with some studies showing longer-
dictor of medication efficacy. This finding term positive effects.6,7Studies in comm-
highlights the need to better understand unity-based primary care clinics present
the types and intensities of psychotherapies compelling evidence for the use of brief
that will be most efficacious in combi- interventions in general medical settings.
nation with alcohol treatment medications. The beneficial effects may not be limited to
This paper briefly reviews the theoretical reductions in alcohol use, but may also
basis and evidence supporting the efficacy extend to decreases in alcohol-related
of common types of psychotherapies. The health problems.6,7 These interventions
review focuses on research in which the typically require little training8 and appear
psychosocial treatments have been com- to be cost-effective.6,7
bined with pharmacotherapy. Of particular Brief interventions have been used in
interest are studies in which the interactions several pharmacotherapy trials.9^12 In a
of psychotherapy and pharmacotherapy are preliminary, open-label study of naltrexone
investigated. treatment by primary care providers,
O’Connor and colleagues10 combined stan-
dard naltrexone treatment of 50 mg/day
PSYCHOSOCIAL TREATMENTS FOR with a brief intervention consisting of an
ALCOHOL USE DISORDERS extended new patient visit followed by
seven follow-up visits over a ten-week
Brief Interventions trial. They observed moderately high rates
of treatment completion (72%) and a sig-
Brief interventions are time-limited, nificant improvement in drinking outcomes,
patient-centered counseling strategies that including percent days abstinent (37%
focus on changing behavior. These vs. 89%), percent days without heavy
interventions can be as brief as five minutes drinking (49% vs. 97%), mean number
or last for up to four, sixty-minute sessions. of drinks/ occasion (9.5 vs. 2.5), and dec-
Five general steps2 are included: reased gamma-glutamyl transferase levels
(GGT:67.1 vs. 45.3 U/L) from baseline
1. provide assessment and direct feedback to end-of-treatment. In a subsequent
2. negotiate and set a goal, typically within randomized clinical trial,13,14 brief inter-
the NIAAA safe-drinking guidelines vention subjects were equally likely
3. invoke behavior modification tech- to respond to naltrexone treatment as
niques, such as identifying high risk those receiving more intensive cognitive-
situations and pros and cons of drinking behavioral therapy during an initial 10-week
4. provide bibliotherapy using infor- open-label medication period; however,
mational materials on alcohol use and those brief intervention responders who
its consequences were subsequently randomized to placebo
5. ensure follow-up and reinforcement to treatment during a six-month double-blind
check on progress. naltrexone trial did not maintain the initial
Over 20 clinical trials have demon- treatment gains. Most recently, Kranzler
strated the efficacy of brief techniques in a and colleagues11 used a brief, four-session
variety of settings. Meta-analyses3^5 all coping skills training intervention that tar-
report beneficial effects of brief inter- geted nonhazardous drinking goals and
ventions in reducing alcohol use in heavy management of high-risk drinking situa-
drinkers who are not alcohol dependent. tions in combination with either daily or

S42 VOLUME 12  SUPPLEMENT 1  2003


McCaul & Petry

targeted naltrexone/placebo administration outcomes and appeared to be more effec-


in heavy drinkers. Patients randomized to tive with angry subjects.18
targeted medication administration reduced MET has been adapted for use in
their drinking as long as medication (nal- several recent pharmacotherapy trials, in
trexone or placebo) was available at least part because of the potential to move this
three days per week. Among patients relatively brief therapy out of specialized
randomized to daily medication admin- alcoholism treatment programs and into a
istration, drinking was reduced only among broader array of health care settings that
those patients receiving active naltrexone would be conducive to medication use.
therapy. Based on these findings, brief The multi-site, six-month, double-blind,
interventions may offer an effective treat- placebo-controlled U.S. acamprosate study19
ment option for use with alcohol pharma- employed a four-session, manual-guided
cotherapies, particularly in alternative care brief intervention that incorporated a moti-
settings, with heavy drinkers and possibly vational enhancement approach as well as
in combination with medication strategies an emphasis on medication compliance,
aimed at targeted, high-risk situations. feedback from drinking assessments, edu-
cational handouts, and a psychoeducational
approach. Medication efficacy was observed
Motivational Enhancement Therapy in those subjects motivated to have absti-
nence as their treatment objective, sug-
Motivation enhancement therapy gesting an important role for motivational
(MET) is based on the Transtheoretical therapies in combination with acamprosate.
Stages of Change Theory,15 which states
that individuals pass through a series of Cognitive-Behavioral Therapies (Coping
stages of thought, planning, and action in Skills, Relapse Prevention)
the course of modifying behaviors. The
MET intervention is designed to bolster Cognitive-behavioral therapy is
the person’s motivation and commitment grounded in the principles of social
to change, activate the individual’s own learning theory, which views drinking as
resources (including natural helping functionally related to problems and
relationships), and move the person along situations in the individual’s life. The
the readiness-to-change continuum. This focus of the cognitive-behavioral model is
approach is built on motivational inter- training clients in intra- and interpersonal
viewing techniques incorporating feedback skills that reduce relapse risk, maintain
on problems/strengths and clear, directive abstinence, and enhance self-efficacy. Clients
advice from the therapist. Ideally, this are taught to identify triggers that set the
includes a menu of change options, the use occasion for drinking or drug use. Such
of an empathetic and nonconfrontational triggers may be external (drinking or
therapeutic style, and enhancement of the drug-using friends; high-risk places) or
patient’s own responsibility and self-efficacy internal (feeling lonely, angry, or sad;
for change.16 ruminating about past problems or argu-
MET was manualized for inclusion in ments). Coping and problem-solving skills
Project MATCH as a four-session inter- are taught to help the client deal more
vention.17 In comparison to twelve-session effectively with drinking or drug urges
interventions using either cognitive-beha- when these triggers are present.
vioral or twelve-step facilitation therapy, Cognitive-behavioral therapy models
this relatively brief therapy was equally have been widely evaluated and have gen-
efficacious in improving drinking-related erally received strong empirical support for

THE AMERICAN JOURNAL ON ADDICTIONS S43


Psychosocial Treatments in Alcohol Pharmacotherapy

their effectiveness with substance abuse first and second relapse occasions. Foll-
patients. Randomized clinical trials comp- owing the twelve-week active treatment
aring CBT to no-treatment controls have phase, naltrexone-treated subjects continued
consistently found CBT superior to mini- to report reduced drinking, though group
mal or no treatment.20 When CBT is differences between naltrexone-treated and
compared with other active therapeutic placebo subjects were no longer signi-
interventions, results are more mixed. ficant.30 As Anton et al.30 noted, there is a
Some studies have supported the greater sound theoretical basis for predicting
effectiveness of CBT, while others have positive, complementary effects of nal-
found it comparable in effectiveness to trexone and cognitive-behavioral therapy
other treatment approaches.20 For example, in that naltrexone should provide an
in Project MATCH, CBT was found to be improved opportunity for patients to prac-
comparable to Motivational Enhancement tice their relapse prevention strategies
Therapy and 12-Step Facilitation Therapy during a drinking lapse.
for decreasing alcohol use and alcohol-
related problems. All three outpatient Cue Exposure Therapy
therapies resulted in profound improvement
in participants during the twelve-week Through repeated stimulus-response
intervention period.18 pairing in an associative learning paradigm,
Several studies21,22 suggest that CBT alcohol-related cues can come to elicit
produces delayed, positive effects that subjective (eg, craving and urges to drink)
emerge after treatment completion. Speci- and, to a lesser extent, physiological (eg,
fically, patients who received CBT con- increased heart rate and salivation)
tinue to improve relative to responses.31 Importantly, the strength of
end-of-treatment, whereas patients receiv- these cue-induced responses appears to pre-
ing other therapies are stable or gradually dict post-treatment outcomes in recently
return to baseline substance use levels. treated alcohol-dependent patients32,33 Cue
These effects are in line with the principles exposure therapy (CET) teaches coping
of CBT to teach patients coping and relapse skills for dealing with urges and other
prevention skills that they will continue to responses induced by such cues as the sight
use throughout their recovery. and smell of alcohol. It then systematically
The use of CBT has been popular in exposes the patient to these alcohol-related
pharmacotherapy trials using a variety of cues in order to extinguish these triggered
medications with alcohol-dependent pa- responses and give the patient an oppor-
tients.23^28 In a randomized, placebo- tunity to practice alternative, pro-recovery
controlled clinical trial of naltrexone,29 all responses in the presence of these cues.
alcohol-dependent patients received twelve- Although research is limited, several
session, manual-guided cognitive-beha- studies have supported the efficacy of
vioral therapy. Both placebo- and nal- CET with alcohol-dependent patients.
trexone-treated patients had high rates of Monti et al.34 used the combination of
treatment completion and high attendance cue exposure and coping skills training
at therapy sessions (X ¼ 10, SD ¼ 3), to improve six-month post-treatment
suggesting the effectiveness of the psycho- drinking outcomes compared with stan-
social treatment for engaging patients in dard treatment. Similarly, Rohsenow and
treatment. Naltrexone- compared with place- colleagues35 found that CET in combi-
bo-treated subjects reported fewer drinking nation with intensive alcoholism treat-
days and fewer drinks per drinking day; ment reduced heavy drinking days when
they also had a longer time between the compared with intensive treatment alone.

S44 VOLUME 12  SUPPLEMENT 1  2003


McCaul & Petry

Additionally, CET-treated patients reported patients in more traditional treatments. A


greater reductions in the urge to drink in manual for this approach is available.42
simulated high-risk situations and an CM treatments are based on the same
increase in the use of coping strategies behavioral principles as CRA, but CM
during the one-year follow-up period. extends the use of non-drinking positive
Encouraged by laboratory-based evidence reinforcements to include tangible rewards.
that naltrexone dampened cue-induced For example, every time the patient pro-
craving in recently abstinent alcoholics,36 vides a substance-negative specimen or
a recent study has combined CET with consumes medication, s/he earns a reward,
naltrexone treatment for alcohol-dependent such as a voucher exchangeable for retail
patients.37 Among compliant patients who goods and services.43 Although there is an
ingested at least 70% of prescribed doses, extensive literature on the use of CM for
CET and naltrexone independently reduced treatment of drug use disorders, few
self-reported urges to drink, heavy drinking studies have evaluated the efficacy of CM
days, and drinks per drinking day com- in alcoholism treatment.44 Petry et al.45
pared with standard treatment or placebo; found that among alcohol-dependent
however, no interaction of medication veterans who received CM for providing
and psychosocial treatment was observed. negative breathalyzer readings in addition
to standard psychosocial therapy, there
Behavioral Treatments: Community was a significantly greater time to first
Reinforcement Approach (CRA) and drinking episode and first heavy drinking
Contingency Management (CM) episode compared with veterans who
received standard treatment alone.
Behavioral treatments are based on Studies show that patients can be
the principle that alcohol induces positive reinforced for compliance with medicat-
subjective and physiological effects that ions as well.46 Liebson et al.47 found that
reinforce continued alcohol use. To methadone-maintained, alcohol-dependent
reduce alcohol consumption, reinforce- patients significantly reduced alcohol use
ment from alcohol use is decreased while when methadone treatment was contin-
reinforcement from other sources is gent upon disulfiram consumption. To
increased. In CRA, the therapist rearranges date, the most common application of con-
the patient’s environment so that drinking tingency management techniques to phar-
is less reinforcing than abstinence, and re- macotherapy has been the provision of
inforcing disulfiram compliance is one of vouchers or cash, contingent upon nal-
the primary components of CRA. Positive trexone consumption in recently detoxi-
reinforcement for not drinking comes in fied opioid-dependent patients.48^50 These
the form of scheduling other recreational studies have generally reported significant
activities and reorganizing daily life by increases in treatment retention and
breaking down practical barriers. For reductions in opioid use among CM-
example, the therapist may assist the enhanced patients as compared to standard
patient in obtaining a telephone line, a treatment patients.
place to live, or transportation. Strong
evidence exists for the efficacy of CRA.38 Behavioral Marital Therapy
In controlled studies conducted on an
inpatient39 or outpatient basis,40,41 patients Behaviorally-based couples therapy
receiving CRA evidenced substantial (BCT) has been the most often investi-
improvements in abstinence rates and gated form of family therapy for alcohol
psychosocial functioning compared with dependence.51 BCT is grounded in social

THE AMERICAN JOURNAL ON ADDICTIONS S45


Psychosocial Treatments in Alcohol Pharmacotherapy

learning theory and family systems considerable difficulty in engaging family


models. The model assumes a reciprocal members and significant others in care.
connection between alcohol use and Among these treatment-exposed subjects,
relationship functioning: alcohol use family counseling appeared to increase
impacts the quality and nature of a treatment retention and rates of opioid-free
couple’s relationship, and the functioning urine toxicology screens in comparison to
of the relationship in turn impacts alcohol standard treatment or CM-enhanced treat-
use. The therapy focuses on improving ment. Further, there was strong evidence
interactional behaviors, such as communi- of treatment-specific effects, with subjects
cation and problem-solving skills and in the family counseling group reporting
enhancing social support. significant reductions in family problems
Several studies show that BCT is over the twelve-week trial as compared
associated with positive outcomes in with subjects in the other two treatment
relationship adjustment and reductions groups.
in alcohol use.52,53 Moreover, compared to
individual or group counseling, BCT is Twelve-Step Therapies
more cost-effective.54 However, little is
known about necessary or sufficient com- Alcoholics Anonymous (AA) is an
ponents of BCT, and most studies have independent organization that promotes a
limited its use to homogenous populations fellowship of people whose common
with little psychiatric comorbidity. Of goal is recovery from the disease of
course, this treatment is only applicable to alcoholism. It is the most widely accessed
patients who have cooperative significant resource for individuals with alcohol
others. problems.56 The AA philosophy is based
A number of studies have examined on alcoholism as a chronic, progressive,
the impact of the involvement of a spouse spiritual, and medical disease. Because
or significant other in observing medi- alcoholics are believed to have lost the
cation ingestion. In a six-month study of ability to control drinking, they can
disulfiram treatment supervised by a only be effectively treated through long-
significant other elected by the patient,55 term abstinence from alcohol. Over the
disulfiram 200 mg/day significantly in- years, AA has set forth principles and
creased abstinent days and decreased total steps to help guide persons in recovery.
drinks consumed compared with placebo. The ‘‘twelve steps’’ describe a series of
To date, there are very few published actions and beliefs that persons can follow
pharmacotherapy studies that have to achieve long-term recovery. Twelve-
included BCT or other styles of family Step Facilitation, a manualized intervention
counseling in the psychotherapeutic inter- to promote AA participation,57 was equally
vention. Carroll et al.48 incorporated family efficacious with cognitive-behavioral and
counseling into naltrexone treatment for motivational enhancement therapies in
opioid dependence. Subjects (N ¼ 127) Project MATCH.18
were randomized to one of three con- It is often thought that AA discourages
ditions: 1) standard thrice-weekly nal- the use of medications, which they consider
trexone treatment, 2) naltrexone treatment ‘‘crutches.’’ However, in an anonymous
plus CM, and 3) naltrexone treatment, survey of a large sample of active AA
CM, and family counseling. Importantly, participants, Rychtarik and colleagues58
only 62% of subjects assigned to the found that over half the members reported
family counseling group attended at that the use of relapse-preventing medicat-
least one counseling session, suggesting ion either was a good idea or might be a

S46 VOLUME 12  SUPPLEMENT 1  2003


McCaul & Petry

good idea, and only 12 percent would tell across sites in a multi-site trial can permit a
another member to stop taking it. Given crude analysis of psychotherapy by
the positive outcomes of twelve-step facili- medication interactions. In several large-
tation observed in Project MATCH and scale studies of acamprosate,61^63 treatment
the apparent tolerance of medication sites have been allowed to retain routine
among the majority of AA members, counseling practices. For example, one
the use of this treatment approach in com- twelve-site German study was conducted
bination with pharmacotherapy seems in the context of usual care resulting in a
appropriate. variety of therapeutic services across
In a large, multi-site, placebo-con- sites, although some general similarities
trolled study of naltrexone conducted by (behavioral rather than interpersonal
the U.S. Veterans Administration,59 parti- emphasis, mean frequency of once per
cipants received twelve-step facilitation week and mean duration of one hour
counseling for twelve months, with further per session) were noted. The emergence
encouragement to attend AA meetings. of a medication effect despite inter-site
The intervention was adapted to also variability suggests that acamprosate out-
promote acceptance of pharmacotherapy, comes are not highly sensitive to psycho-
introduce basic relapse-prevention infor- therapy effects.
mation, and reinforce abstinence and A more elegant but less frequent
continuedtreatmentparticipation.Although experimental approach has been to
no treatment outcome differences were manipulate the type of psychosocial
observed between naltrexone- and placebo- therapy in order to explicitly examine the
treated patients, overall results for the interaction with medication. In one of the
thirteen-week initial treatment phase first published studies of naltrexone treat-
suggest moderately high rates of medi- ment for alcohol dependence, O’Malley
cation and counseling compliance, high et al.64 randomized subjects to receive either
rates of alcohol abstinence, and a relatively individual cognitive-behavioral coping
low proportion of drinking days across skills treatment or supportive therapy in
the two treatment groups. A recent trial combination with either 50 mg of nal-
of sertraline treatment for alcohol trexone daily or placebo. An interesting
dependence60 also incorporated manual- interaction of medication and psycho-
guided twelve-step facilitation therapy and therapy was observed. Subjects who received
community-based support group atten- naltrexone and supportive therapy evi-
dance, supplemented by brief physician denced greater continuous abstinence in
visits to monitor medication compliance comparison with the other treatment
and any adverse effects. This research groups. In contrast, those subjects who
suggests that AA-oriented interventions received naltrexone and coping skills
can be successfully combined with pharma- therapy reported greater reductions in
cotherapy to engage and retain patients craving and evidenced reduced relapse risk
in care. if they consumed alcohol.
More recent studies have examined the
effectiveness of more intensive, highly
INTERACTIONS OF PSYCHOSOCIAL structured psychotherapies vs. brief inter-
AND PHARMACOLOGICAL ventions with alcoholism pharmaco-
TREATMENTS therapies. O’Malley and colleagues13,14
explored the interaction of cognitive-beha-
At times, the decision to allow variability vioral therapy vs. brief medical manage-
in the delivery of psychosocial treatments ment with naltrexone therapy. During an

THE AMERICAN JOURNAL ON ADDICTIONS S47


Psychosocial Treatments in Alcohol Pharmacotherapy

initial open-label naltrexone treatment FUTURE DIRECTIONS


phase, comparable effects were obtained
with the brief and more intensive inter- There has been considerable progress in the
ventions; however, when treatment respon- design and conduct of pharmacotherapy
ders were subsequently randomized to trials for substance use disorders; however,
naltrexone or placebo during an extended much of the emphasis to date has been
treatment phase, placebo-treated subjects placed on methodological enhancements
who had received the brief intervention related to medication delivery, compliance
deteriorated, whereas placebo-treated monitoring, and other aspects of drug
subjects who had CBT continued to evi- therapy. Comparable attention is now
dence improved drinking outcomes. In a needed for the rigorous delivery of
multisite trial, DeWildt and colleagues65 psychosocial treatments that may enhance
compared the effectiveness of acamprosate and extend medication effects. For
across three psychosocial treatment con- example, existing manualized therapies
ditions: none; three-session brief moti- might benefit from adaptation for use in
vational enhancement therapy; and pharmacotherapy studies, adding content
seven-session cognitive-behavioral therapy. to directly address issues such as
Drinking outcomes at the end of acam- compliance, side effects, and participation
prosate administration and at six-month in self-help programs. Research also is
follow-up were comparable across the three needed that systematically manipulates the
psychosocial treatment groups, and the intensity, duration, format (ie, group vs.
groups did not differ in medication individual), and providers of the
compliance, dropout rates, or psychologi- psychosocial therapy used in conjunction
cal distress. These findings suggest that with pharmacotherapy. Recent research has
psychotherapy does not enhance acam- tended to minimize exposure to psycho-
prosate effectiveness; however, results therapy to avoid the perceived risk of a
should be interpreted with caution due to ceiling on drinking improvements that
high overall dropout rates and differential could limit the ability to detect medication
therapy effects across study sites. effects. As noted earlier, however, the
This research strategy of examining recent meta-analysis by Hopkins1 suggests
the interactions of psychosocial and phar- that such an approach may in fact be
macological treatments is epitomized by counterproductive and interfere with the
the COMBINE Study, a multi-site, emergence of pharmacotherapy effects.
NIAAA-sponsored project. Study medi- Thus, we may learn that the nonspecific
cations include naltrexone and acamprosate effects of psychotherapy that help to main-
alone and in combination. Subjects also tain patient engagement also bolster patient
receive either low-intensity psychosocial adherence to the medication procedures, a
care that incorporates medication adher- factor that has been repeatedly shown to
ence and side-effects monitoring with brief impact drinking outcomes.66,67 Greater
intervention or high-intensity treatment attention should also be focused on the level
that includes the medication management of adherence to the selected psychotherapy.
plus elements of cognitive-behavioral, It is critical to distinguish between a failure
motivational, and twelve-step therapies. At to maintain the validity of two separate
its completion, this project should provide therapies and no real difference in their
invaluable data on the complex ways in effects.
which different medications interact with Greater attention is needed for the
different intensities and types of therapy in potential emergence of psychosocial therapy
different patient subgroups. effects during the post-medication follow-up

S48 VOLUME 12  SUPPLEMENT 1  2003


McCaul & Petry

period. To date, most studies have shown estingly, similar findings have been observed
diminishing medication effects over time in cocaine-dependent subjects treated with
following drug discontinuation. It may be fluoxetine and relapse prevention therapy.69
that this period is key to demonstrating Given the recent observations of differential
important interactions of pharmacotherapy medication effects as a function of subject
and psychosocial treatments. For example, typology,25,70 further interactions with
it might be expected that subjects receiving psychosocial treatments might be expected.
more intensive, cognitive- There has been surprisingly little research
behavioral therapies will sustain their beha- on pharmacotherapy for alcohol depen-
vioral changes more successfully in the dence in patients with a comorbid psychia-
absence of medication than subjects receiv- tricdisorder,andnonespecificallyaddressing
ing brief interventions. the interaction of pharmaco- and psycho-
Another potentially fruitful area of social therapies in this large and clinically
research focuses on patient characteristics important population. Given the potential
(eg, alcoholism typology, severity, family need for more intensive psychosocial
history, and other psychiatric comorbidity) intervention in these more complicated
as they interact with psychosocial and phar- patients, research in this area is needed.
macological therapies. For example, limited Finally, additional research is needed
evidence has emerged for a potential inter- to directly examine the interaction of differ-
action of cognitive-behavioral therapy with ent types of psychotherapy with different
medication effects as a function of the alco- medications. While the complexity and size
holic subtype of the patient. In a study of of these studies may limit opportunity, it is
fluoxetine for alcoholism treatment,68 Type only through these more sophisticated
B alcoholicswho are characterized by designs that we will better understand the
early onset of alcoholism, high levels of potential interplay of these different treat-
premorbid psychopathology, and high ment components.
severity of alcohol-related problemshad Supported in part by grants AA11855 and
poorer outcomes when cognitive-beha- AA12837 (Dr. McCaul) from the National
vioral therapy was combined with active Institute on Alcohol Abuse and Alcoholism,
fluoxetine compared with placebo. Inter- Rockville, Md.

REFERENCES

1. Hopkins JS, Garbutt JC, Poole CL, West SL, addressing brief interventions in heavy alcohol
Carey TS. Naltrexone and acamprosate: drinkers. J Gen Intern Med. 1997;12:274^283.
meta-analysis of two medical treatments for 5. Poikolainen K. Effectiveness of brief inter-
alcoholism. Alcohol Clin Exp Res. 2002; 26 ventions to reduce alcohol intake in primary
(suppl): 130A. health care populations: a meta-analysis. Prev
2. Fleming M, Manwell LB. Brief intervention in Med. 1999;28:503^509.
primary care settings: a primary treatment 6. Fleming MF, Barry KL, Manwell LB, Johnson
method for at-risk, problem, and dependent K, London R. Brief physician advice for prob-
drinkers. Alcohol Res Health. 1999;23:128^137. lem alcohol drinkers: a randomized controlled
3. Bien TH, Miller WR, Tonigan JS. Brief trial in community-based primary care practices.
interventions for alcohol problems: a review. JAMA. 1997;277:1029^1045.
Addiction. 1993;88:315^335. 7. Kristenson H, Ohlin H, Hulten-Nousslin M,
4. Wilk AI, Jensen NM, Havighurst TC. Trell E, Hood B. Identification and
Meta-analysis of randomized control trials intervention of heavy drinking in middle-aged

THE AMERICAN JOURNAL ON ADDICTIONS S49


Psychosocial Treatments in Alcohol Pharmacotherapy

men: results and follow-up of 24^60 months of U.S. multicenter study. Biol Psychiatry. 2001;
long-term study with randomized controls. 49(8 suppl):14S.
Alcohol Clin Exp Res. 1983;7:203^209. 20. Carroll KM. Relapse prevention as a
8. Ockene JK, Adams A, Hurley TG, Wheeler psychosocial treatment: a review of controlled
EV, Hebert JR. Brief physician- and nurse clinical trials. Exp Clin Psychopharmacol.
practitioner-delivered counseling for high-risk 1996;4:46^54.
drinkers: does it work? Arch Intern Med. 21. Carroll KM, Rounsaville BJ, Nich C, Gordon
1999;11:2198^2205. LT, Wirtz PW, Gawin F. One-year follow-up
9. Bohn MJ, Kranzler HR, Beazoglou D, Staehler of psychotherapy and pharmacotherapy for
BA. Naltrexone and brief counseling to reduce cocaine dependence: delayed emergence of
heavy drinking: results of a small clinical psychotherapy effects. Arch Gen Psychiatry.
trial. Am J Addict. 1994;3:91^99. 1994;51:989^997.
10. O’Connor PG, Farren CK, Rounsaville BJ, 22. O’Malley SS, Jaffe AJ, Chang G, Rode S,
O’Malley SS. A preliminary investigation of Schottenfeld RS, Meyer RE, Rounsaville B.
the management of alcohol dependence with Six-month follow-up of naltrexone and psycho-
naltrexone by primary care providers. Am J therapy for alcohol dependence. Arch Gen
Med. 1997;103:477^482. Psychiatry. 1996;53:217^224.
11. Kranzler HR, Armeli S, Tennen H, Blomqvist 23. Angelone SM, Bellini L, DiBella D, Catalano
O, Oncken C, Petry NM, Feinn R. Targeted M. Effects of fluvoxamine and citalopram in
naltrexone for early problem drinkers. J Clin maintaining abstinence in a sample of Italian
Psychopharmacol. In press. detoxified alcoholics. Alcohol Alcohol.
12. Naranjo CA, Bremner KE, Lanctot KL. Effects 1998;33:151^156.
of citalopram and a brief psychosocial 24. Johnson A, Jasinski DR, Galloway GP,
intervention on alcohol intake, dependence, Kranzler H, Weinreib R, Anton RF, Mason
and problems. Addiction. 1995;90:87^99. BJ, Bohn MJ, Pettinati HM, Rawson R,
13. O’Malley SS, O’Connor PG, Farren C, Clyde C. Ritanserin in the treatment of alcohol
Rounsaville BJ. Comparison of naltrexone in dependence: a multi-center clinical trial.
combination with either CB therapy or medical Psychopharmacology. 1996;128:206^215.
model counseling. J Addict Dis. 1998;17:160 25. Johnson BA, Roache JD, Javors MA,
(abstract). DiClemente CC, Cloninger CR, Prihoda TJ,
14. O’Malley SS, O’Connor PG, Farren C, Bordnick PS, Ait-Daoud N, Hensler J.
Namkoong K, Wu R, Rounsaville BJ. Ondansetron for reduction of drinking
Naltrexone in the treatment of alcoholism: among biologically predisposed alcoholic
new research. Biol Psychiatry. 2001;49(8 suppl): patients: a randomized controlled trial.
14s (abstract). JAMA. 2000;284:963^971.
15. Prochaska JO, DiClemente CC. Toward a com- 26. Kiefer F. Randomized controlled trial of
prehensive model of change. In Miller WR, naltrexone, acamprosate, and the combination
Heather N, eds. Treating Addictive Behaviors: Pro- in the treatment of alcoholism. Paper presented
cesses of Change. New York: Plenum Press; at: the 25th annual meeting of the Research
1986:3^27. Society on Alcoholism, San Francisco, CA,
16. Miller WR, Rollnick S. Motivational Interviewing: June 29^July 3, 2002.
Preparing People to Change Addictive Behavior. New 27. Kranzler HR, Burleson JA, Korner P, DelBoca
York: Guilford Press; 1991. FK, Bohn MJ, Brown J, Liebowitz N.
17. Miller WR, Zweben A, DiClemente CC, Placebo-controlled trial of fluoxetine as an
Rychtarik RG. Motivational Enhancement Therapy adjunct to relapse prevention in alcoholics.
Manual: A Clinical Research Guide for Therapists Am J Psychiatry. 1995;152:391^397.
Treating Individuals with Alcohol Abuse and 28. Mason BJ, Salvato FR, Williams LD, Ritvo
Dependence. Vol. 2: Rockville, MD: National EC, Cutler RB. Double-blind, placebo-
Institute on Alcohol Abuse and Alcoholism; controlled study of oral nalmefene for alcohol
1994. Project MATCH Monograph Series, dependence. Arch Gen Psychiatry. 1999;56:
NIH Publication No. 94-3723. 719^724.
18. Project MATCH Research Group. Matching 29. Anton RF, Moak DH, Waid LR, Latham PK,
alcoholism treatments to client heterogeneity: Malcolm RJ, Dias JK. Naltrexone and
Project MATCH posttreatment drinking out- cognitive behavioral therapy for the treatment
comes. J Stud Alcohol. 1997;58:7^29. of outpatient alcoholics: results of a
19. Mason BJ, Goodman AM. Acamprosate treat- placebo-controlled trial. Am J Psychiatry.
ment of alcohol dependence: results of the 1999;156:1758^1764.

S50 VOLUME 12  SUPPLEMENT 1  2003


McCaul & Petry

30. Anton RF, Moak DH, Latham PK, Waid LR, 41. Smith JE, Meyers RJ, Delaney HD. Com-
Malcolm RJ, Dias JK, Roberts JS. Post- munity reinforcement approach with homeless
treatment results of combining naltrexone alcohol-dependent individuals. J Consult Clin
with cognitive-behavior therapy for the treat- Psychol. 1998;66:541^548.
ment of alcoholism. J Clin Psychopharm. 2001; 42. Meyers RJ, Smith JE. Clinical Guide to Alcohol
21:72^77. Treatment: The Community Reinforcement
31. Carter BL, Tiffany ST. Meta-analysis of Approach. New York: Guilford Press; 1995.
cue-reactivity in addiction research. Addiction. 43. Higgins ST, Budney AJ, Bickel WK, Foerg FE,
1999;94:327^340. Donham R, Badger GJ. Incentives improve
32. Cooney NL, Litt MD, Morse PA, Bauer LO, outcome in outpatient behavioral treatment
Gaupp L. Alcohol cue reactivity, negative- of cocaine dependence. Arch Gen Psychiatry.
mood reactivity, and relapse in treated alcoholic 1994;568^576.
men. J Abnormal Psych. 1997;106:243^250. 44. Higgins ST, Petry NM. Contingency
33. Rohsenow DJ, Monti PM, Rubonis AV, Sirota management: incentives for sobriety. Alcohol
AD, Niaura RS, Colby SM, Wunschel SM, Res Health. 1999;23:122^127.
Abrams DB. Cue reactivity as a predictor of 45. Petry NM, Martin B, Cooney JL, Kranzler, HR.
drinking among male alcoholics. J Consult Give them prizes, and they will come: contin-
Clin Psychol. 1994;62:620^626. gency management for treatment of alcohol
34. Monti PM, Rohsenow DJ, Rubonis AV, Niaura dependence. J Consult Clin Psychol. 2000;68:
RS, Sirota AD, Colby SM, Goddard P, Abrams 250^257.
DB. Cue exposure with coping skills treatment 46. Petry NM. A comprehensive guide to the appli-
for male alcoholics: a preliminary investigation. cation of contingency management procedures
J Consult Clin Psychol. 1993;61:1011^1019. in clinical settings. Drug Alcohol Depend.
35. Rohsenow DJ, Monti PM, Rubonis AV, 2000;58:9^25.
Gulliver SB, Colby SM, Binkoff JA, Abrams 47. Liebson IA, Tommasello A, Bigelow GE. A
DB. Cue exposure with coping skills training behavioral treatment of alcoholic methadone
and communication skills training for alcohol patients. Ann Intern Med. 1978;89:342^344.
dependence: 6- and 12-month outcomes. 48. Carroll KM, Ball SA, Nich C, O’Connor PG,
Addiction. 2001;96:1161^1174. Eagan DA, Frankforter TL, Triffleman EG,
36. Monti PM, Rohsenow DJ, Hutchison KE, Shi J, Rounsaville BJ. Targeting behavioral
Swift RM, Mueller TI, Colby SM, Brown therapies to enhance naltrexone treatment of
RA, Gulliver SB, Gordon A, Abrams DB. opioid dependence: efficacy of contingency
Naltrexone’s effect on cue-elicited craving management and significant other involvement.
among alcoholics in treatment. Alcohol Clin Arch Gen Psychiatry. 2001;58:755^761.
Exp Res. 1999;23(8):1386^1394. 49. Carroll KM, Sinha R, Nich C, Babuscio T,
37. Monti PM, Rohsenow DJ, Swift RM, Gulliver Rounsaville BJ. Contingency management to
SB, Colby SM, Mueller TI, Brown RA, Gordon enhance naltrexone treatment of opioid
A, Abrams DB, Niaura RS, Asher MK. dependence: a randomized clinical trial of
Naltrexone and cue exposure with coping reinforcement magnitude. Exp Clin
and communication skills training for Psychopharmacol. 2002;10:54^63.
alcoholics: treatment process and 1-year out- 50. Preston KL, Silverman K, Umbricht A,
comes. Alcohol Clin Exp Res. 2001;25(11): DeJesus A, Montoya ID, Schuster CR.
1634^1647. Improvement in naltrexone treatment com-
38. Miller WR, Brown JM, Simpson TL, pliance with contingency management. Drug
Handmaker NS, et al. A methodological analy- Alcohol Depend. 1999;54:127^135.
sis of the alcohol treatment outcome literature. 51. Epstein EE, McCrady BS. Behavioral couples
In: Hester RK, Miller WR, eds. Handbook of treatment of alcohol and drug use disorders:
Alcoholism Treatment Approaches. Boston: current status and innovations. Clin Psychol
Allyn and Bacon; 1995:12^44. Rev. 1998;18:689^711.
39. Azrin NH. Improvements in the community 52. McCrady BS, Stout N, Noel N, Abrams D,
reinforcement approach to alcoholism. Behav Nelson, HF. Effectiveness of three types of
Res Ther. 1976;14:339^348. spouse-involved behavioral alcoholism
40. Azrin NH, Sisson RW, Meyers R, Godley M. treatments. Br J Addiction. 1991;86:1415^1424.
Alcoholism treatment by disulfiram and com- 53. O’Farrell TJ, Cutter HSG, Choquette KA,
munity reinforcement therapy. J Behav Ther Floyd FJ, Bayog R. Behavioral marital therapy
Exp Psychiatry. 1982;13:105^112. for male alcoholics: marital and drinking adjust-

THE AMERICAN JOURNAL ON ADDICTIONS S51


Psychosocial Treatments in Alcohol Pharmacotherapy

ment during the two years after treatment. Behav 62. Poldrugo F. Acamprosate treatment in a
Ther. 1992;23:529^549. long-term community-based alcohol rehabili-
54. O’Farrell TJ, Choquette KA, Cutter HS, Floyd tation programme. Addiction. 1997;92:
FJ. Cost-benefit and cost-effectiveness analyses 1537^1546.
of behavioral marital therapy as an addition 63. Sass H, Soyka M, Mann D, Zieglgansberger W.
to outpatient alcoholism treatment. J Subst Relapse prevention by acamprosate. Arch Gen
Abuse. 1996;8:145^166. Psychiatry. 1996;53:673^680.
55. Chick J, Gough K, Faldowski W, Kershaw P, 64. O’Malley SS, Jaffe AJ, Chang G, Schottenfeld
Hore B, Mehita B, Ritson B, Ropner R, RS, Meyer RE, Rounsaville B. Naltrexone
Torley D. Disulfiram treatment of alcoholism. and coping skills therapy for alcohol
Br J Psychiatry. 1992;161:84^89. dependence: a controlled study. Arch Gen
56. McCrady BS, Miller WR, eds. Alcoholics Anony- Psychiatry. 1992;49:894^898.
mous: Opportunities and Alternatives. New 65. DeWildt WAJM, Schippers GM, Van den
Brunswick, NJ: Rutgers Center of Alcohol Brink W, Potgieter AS, Deckers F, Bets
Studies; 1993. D. Does psychosocial treatment enhance
57. Nowinski J, Baker S, Carroll K. Twelve-Step the efficacy of acamprosate in patients with
Facilitation Therapy Manual: A Clinical Research alcohol problems? Alcohol Alcohol.
Guide for Therapists Treating Individuals with 2002;37:375^382.
Alcohol Abuse and Dependence. Vol. 1. Bethesda, 66. Chick J, Howlett H, Morgan MY, Ritson B.
MD: National Institute on Alcohol Abuse United Kingdom multicentre acamprosate
and Alcoholism; 1992. Project MATCH study (UKMAS): a 6-month prospective
Monograph Series. DHHS Publication No. study of acamprosate versus placebo in pre-
(ADM)92-1893. venting relaspe after withdrawal from alcohol.
58. Rychtarik RG, Connors GJ, Dermen KH, Alcohol Alcohol. 2000;35:176^187.
Stasiewicz PR. Alcoholics Anonymous and 67. Volpicelli J, Rhines, KC, Rhines JS, Volpicelli
the use of medications to prevent relapse: an LA, Alterman AI, O’Brien CP. Naltrexone
anonymous survey of member attitudes. and alcohol dependence: role of subject
J Stud Alcohol. 2000;61:134^138. compliance. Arch Gen Psychiatry. 1997;54:
59. Krystal JH, Cramer JA, Krol WF, Kirk GF, 737^742.
Rosenheck RA. Naltrexone in the treatment 68. Kranzler HR, Burleson JA, Brown J, Babor
of alcohol dependence. N Engl J Med. 2001; TF. Fluoxetine treatment seems to reduce the
345:1734^1739. beneficial effects of cognitive-behavioral
60. Pettinati HM, Volpicelli JR, Luck G, Kranzler therapy in Type B alcoholics. Alcohol Clin
HR, Rukstalis MR, Cnaan A. Double-blind Exp Res. 1996;20:1534^1541.
clinical trial of sertraline treatment for alcohol 69. Covi L, Hess JM, Dreiter NA, Haertzen CA.
dependence. J Clin Psychopharmacol. 2001; Effects of combined fluoxetine and
21:143^153. counseling in the outpatient treatment of
61. Paille FM, Guelfi JD, Perkins AC, Royer RJ, cocaine abusers. Am J Drug Alcohol Abuse.
Steru L, Parot P. Double-blind randomized 1995;21:327^344.
multicentre trial of acamprosate in maintaining 70. Pettinati HM. The use of selective serotonin
abstinence from alcohol. Alcohol Alcohol. reuptake inhibitors in treating alcoholic
1995;30:239^247. subtypes. J Clin Psychiatry. 2001;62:26^31.

S52 VOLUME 12  SUPPLEMENT 1  2003

You might also like