Gabapentin in the Treatment of TIMOTHY S. CAREY, MD, MPH JOHN W. WILLIAMS, JR., MD, MHS Mental Illness: The Echo Chamber JOHN M. OLDHAM, MD, MS FRANCINE GOODMAN, PharmD, BCPS of the Case Series LEAH M. RANNEY, PhD LYNN WHITENER, DrPH, MSLS LAURA C. MORGAN, MA CATHY L. MELVIN, PHD, MPH Background. Bipolar disorder is a common and debilitating psychiatric illness. Several antiepileptic drugs (AEDs) have been approved for the treatment of bipolar disorder. Gabapentin gained a large market share of AED use in the late 1990s in spite of a lack of randomized clinical trial (RCT) evidence and no labeled indica- tion from the U.S. Food and Drug Administration for its use in psychiatric illness. This article describes the results of a literature review, the purpose of which was to examine the characteristics of studies conducted in humans concerning the efficacy of gabapentin in bipolar disorder. Methods. Publications relevant to this topic were identified based on a PUBMED search as well as an examination of references from a published system- atic review and citations from relevant review articles. Results. The search located 29 studies published between 1997 and 2007, with the greatest number of articles published in 1998 and 1999. Of these 29 publica- tions, 15 involved uncontrolled case series, while 6 were single case reports. The sample size in the studies was generally small, and often we could not identify the funding source. Despite the generally weak study design in the identified publications, the authors of the articles often commented on the promising nature of gabapentin therapy for bipolar disorder. However, 4 small, randomized trials in heterogeneous populations demonstrated little if any evidence of such efficacy. Nine letters to the editor demonstrated a similar pattern. Conclusions. The large number of case series concerning gabapentin is striking. The number of reports and their distribution in many different journals created a type of “echo chamber” effect, through which the sheer number of publications and citations may give legitimacy to the practice of using gabapentin for bipolar dis- order. Although the case series were generally of poor quality, their publication in peer-reviewed journals may have been partially responsible for the widespread use of an ineffective medication. (Journal of Psychiatric Practice 2007;14(suppl 1):15–27)
KEY WORDS: gabapentin, bipolar disorder, case series, case studies, efficacy
Off-label use of medications generally refers to the
CAREY, RANNEY, WHITENER, MORGAN, and MELVIN: The
clinical use of a medication or device by a provider for
Cecil G. Sheps Center for Health Services Research, The
an indication that has not been approved by the U.S.
University of North Carolina at Chapel Hill; WILLIAMS: DukeUniversity School of Medicine, Durham, NC; OLDHAM:
Food and Drug Administration (FDA). Off-label use
Menninger Department of Psychiatry and Behavioral Sciences,
falls within the accepted practice of medicine, which
Baylor College of Medicine, Houston, TX; GOODMAN: Veterans
gives physicians broad discretion to prescribe treat-
Health Administration Pharmacy Benefits Management
ments according to their best clinical judgment. A des-
Strategic Healthcare Group, Columbia, SC.
ignation of “off-label” does not necessarily mean that a
Copyright 2008 Lippincott Williams & Wilkins Inc.
medication or treatment is ineffective for the condition
Please send correspondence and reprint requests to: Cathy L. Melvin,
it is being used to treat; rather, it might be effective,
PhD, MPH, The Cecil G. Sheps Center for Health Services Research,
but it has not been demonstrated to have efficacy and
The University of North Carolina at Chapel Hill, 725 Martin Luther
been approved by the FDA for that indication. When
King Jr. Boulevard, CB#7590, Chapel Hill, NC 27599-7590.
medications are under patent, additional randomized
trials and regulatory approval are required to expand
Funded by a grant administered by a consortium of state attorneys
the conditions for which the medication is indicated.
Journal of Psychiatric Practice Vol. 14, Suppl. 1
GABAPENTIN: THE ECHO CHAMBER OF THE CASE SERIES
Pharmaceutical companies may not legally advertise
authorship may be attributed to academics, a practice
or otherwise market their medications for indications
generally known as “ghost authorship.”5
other than those for which they have received FDA
Gabapentin (Neurontin) is an antiepileptic drug
approval. In contrast. case reports, case series, and
(AED) that was licensed in June 1993.6 The medication
other observational studies examining the use of
underwent a very rapid growth in sales in the late
already licensed medications for new indications are
1990s in spite of generally narrow FDA indications as
routinely published in the clinical literature. Such
an AED and a treatment for certain types of neuro-
studies and publications are generally considered part
pathic pain such as postherpetic neuralgia. However,
of the research process of discovering new uses for
by 1999, the second most common use of gabapentin
was for the treatment of psychiatric conditions,7
Recent literature and court cases have reflected con-
despite the absence of FDA indications for such condi-
cerns about the origin, intent, and quality of some of
tions. In addition, no randomized trials were done in
the literature and about inappropriate marketing
the 1990s that demonstrated efficacy for mental health
activities addressing off-label indications for medica-
indications, although multiple articles were published
tions.1–3 Studies of off-label use which appear in the
during the 1990s discussing the use of gabapentin for
peer-reviewed literature may use study designs that
bipolar disorder. This wave of publications coincided
result in exclusion from systematic reviews of treat-
with the rapid growth of off-label use of this agent.
ment efficacy, such as those conducted by the Cochrane
Our group was funded by the Neurontin Executive
Collaboration, the Drug Effectiveness Review Project,
Committee (a consortium of state attorneys general) to
or the Evidence-Based Practice Centers sponsored by
disseminate evidence-based information on the roles of
the Agency for Health Research and Quality (AHRQ).
AEDs, including gabapentin, in the treatment of bipo-
Without a contemporaneous control group and ran-
lar disorder. A systematic review of the use of AEDs in
domization, it is very difficult to assess the efficacy of
bipolar disorder conducted by the Drug Effectiveness
an intervention, since improvement in the patient’s
Review Project (DERP) found minimal acceptable evi-
condition may be due to chance, the natural history of
dence concerning the efficacy of gabapentin.8 The liter-
the illness, or a nonspecific effect of treatment (placebo
ature regarding gabapentin included a small number
effect). Thus, case series and non-randomized prospec-
of negative randomized trials, and the review conclud-
tive observational studies are generally excluded from
ed that no acceptable evidence existed to support the
systematic reviews assessing efficacy and not included
use of gabapentin for bipolar disorder. The review did
in either the abstract or the full text of the review.
find evidence for the efficacy of three AEDs: carba-
Observational studies may be included in systematic
mazepine, valproic acid/valproate, and lamotrigine. In
reviews that examine adverse events and may also
order to better understand the reasons for growth in
sometimes be included to provide information on the
the prescribing of gabapentin by providers, we exam-
effect of a treatment in subpopulations for which no
ined the characteristics of the published literature dur-
ing the period this occurred. Once a study is published
For some medications, off-label use has become much
in the peer-reviewed literature, it can be cited and
more common than use for the medication’s approved
reproduced, giving the conclusions of the study an aura
indications—despite a lack of evidence of treatment
of authority that is perhaps not warranted by the qual-
efficacy for those off-label uses.4 Journalists and court
ity of the research. Our qualitative review includes lit-
cases have found that in some circumstances off-label
erature that is generally excluded from systematic
use has been encouraged by pharmaceutical companies
reviews addressing efficacy; we are including this lit-
working through medical education companies. While
erature to better understand how provider behavior
some of the activities of medical education companies
may be affected by weak, but widely disseminated,
resemble conventional continuing medical education
(CME), these companies may collaborate withresearchers and influential clinicians to conduct and
write case reports and case series, give grand roundsand CME lectures, and serve on speakers bureaus to
We searched for literature on PUBMED using Medical
promote off-label use of medications. An unknown
Subject Headings (MeSH) or key words for gabapentin
number of articles may be written in whole or in part
and bipolar disorder. Our inclusion criteria were all
by employees of the educational company but the
English-language studies published between 1966 and
Journal of Psychiatric Practice Vol. 14, Suppl. 1
GABAPENTIN: THE ECHO CHAMBER OF THE CASE SERIES
2007 that involved original research on humans exam-
Figure 1. Results of literature search
ining the role of gabapentin in bipolar disorder. Wesupplemented the PUBMED searches with hand
Titles and abstracts
searches of recent review articles as well as searches of
identified through
the Drug Industry Document Archive (DIDA) database
searches:
through the University of California-San Francisco
n = 125
(UCSF) library. The DIDA database is a compendium
Citations excluded:
of documents gathered as part of the discovery process
n = 23
during the litigation concerning gabapentin. Articleswere reviewed for relevance to bipolar disorder and
Articles published as
inclusion of original data addressing the efficacy of
abstract-only:
gabapentin in the treatment of bipolar disorder either
n = 10 Full-text articles
as monotherapy or as an adjuvant to other treatments. retrieved:
The articles we identified were then abstracted into
n = 92
evidence tables by staff and these abstractions were
Full text articles excluded: n = 39
We found 29 articles in the peer reviewed literature
during the time period examined. Only 4 of these stud-
ies were randomized trials, 2 of which were crossover
trials. The remaining 25 articles were excluded from
previous systematic reviews for the standard reason
that they lacked an appropriate comparison group andit was therefore not possible to judge efficacy compared
Background articles:
with existing treatments or placebo. The characteris-
n = 15
tics of the 29 articles are summarized in Appendix 1. Nineteen studies were conducted in the United States
Articles/letters included in review:
or Canada, and 10 in Europe. Figure 1 summarizes the
n = 38
The temporal distribution of the articles is presented
in Figure 2. The first articles appeared in 1997, with
the most frequent publications in 1998 and 1999.
Publication became less common after 2000, the year
in which the first randomized controlled trial (RCT)
2 on double-blind, randomized crossover trials
was published demonstrating lack of efficacy of
gabapentin as an adjunct to other AEDs in bipolar dis-order.9 Only three articles were published after 2002,the year that Warner-Lambert’s fraudulent promotion
6 months of patient outcome data, which is short for a
of off-label uses for gabapentin became public. The
chronic disease such as bipolar disorder. Seventeen of
most common type of study design was the case series
the studies reported outcomes measures such as stan-
(15 studies), in which patients were given gabapentin
dard scales, while the others reported clinician impres-
without blinding of the patients or providers and with-
out comparison to any control group. Evidence of effi-
The conclusions presented in the articles were
cacy was inferred through improvement over time.
almost uniformly optimistic, with the exception of 3 of
Sample sizes in these case series were generally small,
the 4 controlled studies. Appendix 1 includes conclu-
18 patients on average (range 2–43); 8 of the 15 case
sions as reported by the authors. While most of the
series contained 20 or fewer subjects. The duration of
articles did note the need for additional studies and
follow-up was quite variable, sometimes even within
randomized trials, there was little discussion concern-
the same study. Of the 29 studies, 22 reported less than
ing the inability to show causality and other possible
Journal of Psychiatric Practice Vol. 14, Suppl. 1
GABAPENTIN: THE ECHO CHAMBER OF THE CASE SERIES
Figure 2. Number of articles published per year
lar disorder.”12 These four trials provided no substan-tial evidence of the efficacy of gabapentin in the treat-
ment of bipolar disorder, or in preventing recurrence of
symptoms. Three of the four trials’ conclusions didmatch their results sections.
One article was a retrospective chart review without
collection of information directly from patients.29 Weidentified three prospective studies that did not have
contemporaneous comparison groups.41,44,46
Seventeen of the articles (58.6%) had unknown fund-
ing sources, 6 studies were funded by private founda-
tions or internal university grants, 4 were reported to
be funded by industry, and 2 by Canadian governmentagencies.
To understand the impact of the 29 articles pub-
lished in the peer-reviewed literature, we used the ISIWeb of Science to conduct citation searches. According
to this reference database, all 29 studies were cited inother articles. The average number of citations was 35
explanations (e.g., natural history of the disease, effect
per article. Even the most recent article, which was
of co-interventions, placebo effect) for the improvement
published in 2006, had been cited at least twice. Those
that had been observed. Six studies were case reports
cited most frequently were the randomized trials: Frey
of single patients. Several of the cases reported benefit
et al. 200010 was cited 196 times, and Pande et al. 20009
of gabapentin in ameliorating the adverse effects of
was cited 130 times. The 1,001 citations of the 29 arti-
other medications, such as bruxism (teeth grinding)
cles appeared in 429 unique articles in 152 unique
due to an antidepressant. Most of the case series and
journals (any article could cite any number of the orig-
single case reports addressed the use of gabapentin as
inal 29 studies). The lead authors of the original 29
adjunctive therapy in patients who were taking other
articles also co-authored articles that cited the original
medications. The rationale for testing gabapentin in
29. For example, Grunze was an author or co-author of
bipolar disorder varied among the studies and includ-
20 of the 429 articles in which citations appeared,
ed the sometimes refractory nature of the illness, the
while Frye was an author or co-author of 19 of the 429
usefulness of other AEDs (class effect), and the per-
and McElroy was an author or co-author of 15 of them.
ceived modest incidence of adverse events with
In all, the authors of the original 29 articles appeared
as authors 130 times for these 429 articles in which
Four randomized trials were published between
citations of the original studies appeared. More than
2000 and 2006.9–12 The average number of patients in
half (15) of the 29 articles were originally published in
each trial was 55; only one trial9 studied more than 100
only four journals: Bipolar Disorder, Journal of
patients. The quality of this trial was considered fair;
Clinical Psychopharmacology, Journal of Affective
the other trials all had significant design or conduct
Disorders, and Journal of Clinical Psychiatry. The
problems and were rated as poor. The trials by Frye10
tracking of citations and authors done for this study
and Obrocea11 both had crossover designs, which can
indicated that a few authors, often writing together
be problematic in diseases which may be influenced by
and appearing in a limited number of journals, can
the order in which medications are provided, leading to
appear in other research for a much broader audience.
attenuation of effect. Both of these small crossover tri-
We did search the University of California at San
als found that gabapentin was not distinguishable
Francisco’s digital archive of documents regarding the
from placebo. The fourth trial12 was very small with
case of United States of America ex. rel David Franklin
only 25 randomized patients, and only half of the sub-
vs Pfizer Inc and Parke Davis, Division of Warner-
jects were followed for the duration of the study. In
Lambert Co (http://dida.library.ucsf.edu). These docu-
spite of the high attrition and generally negative
ments, which mostly date from the late 1990s,
results, the author concluded that “gabapentin might
document pharmaceutical marketing strategies for
provide some benefit on the long-term outcome of bipo-
gabapentin for multiple indications, including bipolar
Journal of Psychiatric Practice Vol. 14, Suppl. 1
GABAPENTIN: THE ECHO CHAMBER OF THE CASE SERIES
disorder. We found authors of 8 of the 29 articles refer-
Case series and other observational study designs do
enced in the archives, with involvement such as pres-
have a role in the medical literature. Clinical observa-
ence at a company-sponsored meeting, being a paid
tions, and their report in series of cases, are often the
speaker, or a reference to working with ghostwriters.
first way hypotheses are generated and transmitted to
We were unable, based on these documents, to directly
the research and the clinical communities. Case series
tie specific involvement or payment to specific publica-
may be useful in settings of initial reports of innovative
treatment, hospital reports of outcomes, or multi-insti-
In addition to the 29 peer reviewed articles, we iden-
tutional registries. Although relatively little guidance
tified an additional 9 letters to the editor published in
has been published on quality grading of case series,
journals that contained patient information.38,48–55
readers are referred to one publication in this area by
Three were case reports, while 6 were case series with
our group.56 Characteristics of good case series reports
a mean sample size of 24. Four letters were published
in 1997; the most recent letter, which was a case report,
appeared in 2006 and stated that “Gabapentin showed
preliminary efficacy as an add-on mood stabilizer to
divalproex for adults with mental retardation and
bipolar mood disorder or schizoaffective disorder, bipo-
Discussion/conclusions supported by the dataAcknowledgment of funding source if any. The studies on gabapentin were limited, even as case
DISCUSSION
series, in that they often did not describe the study
We identified a large number of studies reporting on
population or patient selection. The discussion sections
the use of gabapentin in bipolar disorder that were
were also limited, and there was a lack of clarity con-
published in the late 1990s and early in the current
cerning funding sources. Drawing inferences regarding
decade. The studies were characterized by small sam-
treatment efficacy from pre-post case series may be
ple sizes, poor description of the patient populations,
especially fraught with difficulties in a chronic condi-
and relatively brief follow-up. Most of the studies did
tion such as bipolar disorder, which is characterized by
not report sponsorship or potential conflicts of interest
a waxing and waning clinical course. Yet limitations in
by the authors. The DIDA database did indicate that
drawing inferences from such small samples were
the manufacturer of gabapentin at that time contract-
often unacknowledged in these publications. Patients
ed with medical education companies in the late 1990s
with bipolar disorder are also often taking a number of
to produce peer reviewed publications on off-label use
medications, including other AEDs or antipsychotic
of the medication.7 The timing and type of publications
medications. Unless such co-interventions are careful-
we identified are consistent with just such a campaign.
ly assessed and their equal distribution across the
The reduction in the number of publications examin-
intervention and comparison groups is assured, treat-
ing the use of gabapentin in bipolar disorder in recent
ment effect will be difficult to distinguish from
years may be due to a number of factors, such as the
improvement due to natural history, placebo effect, or
disclosure of the manufacturer’s fraudulent marketing
the effect of the co-interventions. Use of contempora-
scheme, lapsing of the contracts with medical educa-
neous controls and randomization are the only ways in
tion companies, or consensus in the academic psychia-
which treatment effect can be assessed in these cir-
try community regarding the lack of utility of
cumstances. In the case of gabapentin, RCTs were not
gabapentin for these indications. The number of publi-
conducted for some years after this agent began to be
cations from European authors in recent years may
widely used for mental health indications, and the
reflect attempts to increase market share outside the
studies that were done were often small and some-
The number of times this limited literature was cited
The large number of case series and case reports
is remarkable. Simple citation counts do not, of course,
reported encouraging results that were not confirmed
describe how the citation was used in this secondary
by later small randomized trials. The number of
literature and an examination of the 429 articles in
reports and their distribution in a number of journals
which these citations appeared was beyond the scope of
created a type of “echo chamber” effect, through which
the sheer number of publications and citations may
Journal of Psychiatric Practice Vol. 14, Suppl. 1
GABAPENTIN: THE ECHO CHAMBER OF THE CASE SERIES
have given legitimacy to the practice of using
time we recommend that gabapentin be used only in
gabapentin for bipolar disorder. Although pharmaceu-
the setting of a randomized trial among patients
tical representatives visiting providers’ offices are pro-
refractory to other agents.” We recognize that circum-
hibited from distributing copies of articles addressing
stances might arise in which patients are truly refrac-
off-label use of their products, such practices did occur
tory to the multiple treatments available, and
in the past,1 and the large number of available publi-
clinicians do need some flexibility to address such dif-
cations may have made such practices easier. The cita-
ficult clinical situations. The role of the research liter-
tion of such publications during grand rounds or CME
ature should be to encourage appropriate clinical use,
conferences by clinical experts who may have relation-
not inappropriate prescribing in settings in which
ships with pharmaceutical companies is another
other efficacious treatments are available. Clinicians
potential route of dissemination. The case of
may prescribe medications off label for appropriate
gabapentin, a medication that has modest benefit for
reasons, including lack of data or FDA evaluation in
seizures and neuropathic pain, but which has been
certain populations (e.g., children) or in patients whose
used for many other indications, is one of the most
illness is refractory to treatment or who are unable to
striking examples of coordinated off-label marketing. A
recent settlement regarding olanzapine is another.57
A cursory examination of the literature identified in
The clinical community knows about these activities
this review reveals repeated references to a promising
only through the public availability of documents
new treatment. Our more detailed examination
obtained in the discovery process of litigation. Other
demonstrates multiple poor quality observational
examples of the use of the medical publication system
studies which collectively represent an echo chamber
for off-label marketing purposes may exist but have
encouraging utilization of the medication based on
not yet been similarly uncovered. While the fines from
minimal evidence. The literature on gabapentin repre-
litigation were imposed on the pharmaceutical compa-
sents a cautionary tale for industry, researchers, and
ny (Warner-Lambert and Pfizer), the clinicians and fac-
ulty who were the authors of record of the reportsshould also bear responsibility. How many case reportsor case series are needed to generate a hypothesis that
References
must then be tested in an appropriately designed
Steinman MA, Harper GM, Chren MM, et al. Characteristics
experiment—i.e., a clinical trial? Certainly not dozens.
and impact of drug detailing for gabapentin. PLoS Med
Since the journals in which these articles were pub-
lished often did not require reporting of the source of
Hampton T. Experts weigh in on promotion, prescription of
funding for the research, readers are unable to judge
off-label drugs. JAMA 2007;297:683–4.
for themselves whether industry sponsorship of the
Radley DC, Finkelstein SN, Stafford RS. Off-label prescrib-ing among office-based physicians. Arch Intern Med
study would influence their opinion of the study con-
duct and conclusions. While major journals now
Chen H, Reeves JH, Fincham JE, et al. Off-label use of anti-
require authors to report sources of funding for studies
depressant, anticonvulsant, and antipsychotic medications
and potential competing interests such as industry
among Georgia Medicaid enrollees in 2001. J Clin Psychiatry
consulting relationships, the specialty journals in
Flanagin A, Carey LA, Fontanarosa PB, et al. Prevalence of
which the literature on gabapentin for bipolar disorder
articles with honorary authors and ghost authors in peer-
was reported rarely did so. Journal reviewers and edi-
reviewed medical journals. JAMA 1998;280:222–4.
tors are also responsible in that the conclusions of the
Acharya NV, Pickering RM, Wilton LW, et al. The safety and
articles were essentially unchallenged. Regular repeti-
effectiveness of newer antiepileptics: A comparative post-
tion of a statement about the medication being “prom-
marketing cohort study. J Clin Pharmacol 2005;45:385–93.
Steinman MA, Bero LA, Chren MM, et al. Narrative review:
ising” and more study being needed may lead readers
The promotion of gabapentin: An analysis of internal indus-
to focus on the “promising” part of the message. A more
try documents. Ann Intern Med. 2006;145:284–93.
appropriate message in such circumstances might be:
Goodman F, Glassman P, Maglione M, et al. Drug class
“We have observed apparent benefit in a preliminary
review on antiepileptic drugs in bipolar mood disorder, neu-
uncontrolled case series. The next step required to
ropathic pain, and fibromyalgia. Portland: Oregon Evidence-based Practice Center;
demonstrate efficacy is an appropriately sized random-
.prescribingforbetteroutcomes.org and www.ohsu.edu/drug-
ized controlled trial. Since multiple other agents are
effectiveness/reports/documents/_AED%20Final%20Report
available for the treatment of bipolar disorder, at this
Journal of Psychiatric Practice Vol. 14, Suppl. 1
GABAPENTIN: THE ECHO CHAMBER OF THE CASE SERIES
Pande AC, Crockatt JG, Janney CA, et al. Gabapentin in
bipolar disorder: A placebo-controlled trial of adjunctive
27. Bech P, Rafaelsen OJ, Kramp P, et al. The mania rating scale:
therapy. Gabapentin Bipolar Disorder Study Group. Bipolar
Scale construction and inter-observer agreement. Neuro-
10. Frye MA, Ketter TA, Kimbrell TA, et al. A placebo-controlled
28. Ghaemi SN, Goodwin FK. Gabapentin treatment of the non-
study of lamotrigine and gabapentin monotherapy in refrac-
refractory bipolar spectrum: An open case series. J Affect
tory mood disorders. J Clin Psychopharmacol 2000;20:
29. Ghaemi SN, Katzow JJ, Desai SP, et al. Gabapentin treat-
11. Obrocea GV, Dunn RM, Frye MA, et al. Clinical predictors of
ment of mood disorders: A preliminary study. J Clin
response to lamotrigine and gabapentin monotherapy in
refractory affective disorders. Biol Psychiatry 2002;51:
30. Grunze H, Dittert S, Bungert M, et al. Renal impairment as
a possible side effect of gabapentin: A single case report.
12. Vieta E, Manuel Goikolea J, Martinez-Aran A, et al. A dou-
ble-blind, randomized, placebo-controlled, prophylaxis study
31. Hamrin V, Bailey K. Gabapentin and methylphenidate treat-
of adjunctive gabapentin for bipolar disorder. J Clin
ment of a preadolescent with attention deficit hyperactivity
13. Young RC, Biggs JT, Ziegler VE, et al. A rating scale for
mania: reliability, validity, and sensitivity. Br J Psychiatry
32. Hardoy MC, Hardoy MJ, Carta MG, et al. Gabapentin as a
promising treatment for antipsychotic-induced movement
14. Hamilton M. Development of a rating scale for primary
disorders in schizoaffective and bipolar patients. J Affect
depressive illness. Br J Soc Clin Psychol 1967;6:278–96.
15. Guy W. ECDEU assessment manual for psychopharmacolo-
33. Hatzimanolis J, Lykouras L, Oulis P, et al. Gabapentin as
gy–revised (DHEW Publ. No ADM 76-338). Rockville, MD,
monotherapy in the treatment of acute mania. Eur
U.S. Department of Health, Education, and Welfare, Public
Neuropsychopharmacol 1999;9:257–8.
Health Service, Alcohol, Drug Abuse, and Mental Health
34. Knoll J, Stegman K, Suppes T. Clinical experience using
Administration, NIMH Psychopharmacology Research
gabapentin adjunctively in patients with a history of mania
Branch, Division of Extramural Research Programs 1976:
or hypomania. J Affect Disord 1998;49:229–33.
35. McElroy SL, Soutullo CA, Keck PE, Jr., et al. A pilot trial of
16. Spearing MK, Post RM, Leverich GS, et al. Modification of
adjunctive gabapentin in the treatment of bipolar disorder.
the Clinical Global Impressions (CGI) Scale for use in bipo-
Ann Clin Psychiatry 1997;9:99–103.
lar illness (BP): The CGI-BP. Psychiatry Res 1997;73:159–71.
36. Perugi G, Toni C, Frare F, et al. Effectiveness of adjunctive
17. Vieta PE, Torrent FC, Martinez-Aran A, et al. A user-friend-
gabapentin in resistant bipolar disorder: Is it due to anxious-
ly scale for the short and long term outcome of bipolar disor-
alcohol abuse comorbidity? J Clin Psychopharmacol 2002;22:
der: The CGI-BP-M [in Spanish]. Actas Esp Psiquiatr
37. Perugi G, Toni C, Ruffolo G, et al. Clinical experience using
18. Hamilton M. The assessment of anxiety states by rating. Br
adjunctive gabapentin in treatment-resistant bipolar mixed
states. Pharmacopsychiatry 1999;32:136–41.
19. Buysse DJ, Reynolds CF, Monk RH, et al. Pittsburgh Sleep
38. Schaffer CB, Schaffer LC. Gabapentin in the treatment of
Quality Index: A new instrument for psychiatric practice and
bipolar disorder. Am J Psychiatry 1997;154:291–2.
research. Psychiatry Res 1989;28:193–213.
39. Schaffer CB, Schaffer LC. Open maintenance treatment of
20. Altshuler LL, Keck PE, Jr., McElroy SL, et al. Gabapentin in
bipolar disorder spectrum patients who responded to
the acute treatment of refractory bipolar disorder. Bipolar
gabapentin augmentation in the acute phase of treatment. J
21. Brannon GE, Rolland PD. Anorgasmia in a patient with bipo-
40. Sethi MA, Mehta R, Devanand DP. Gabapentin in geriatric
lar disorder type 1 treated with gabapentin. J Clin
mania. J Geriatr Psychiatry Neurol 2003;16:117–20.
41. Sokolski KN, Green C, Maris DE, et al. Gabapentin as an
22. Brown ES, Hong SC. Antidepressant-induced bruxism suc-
adjunct to standard mood stabilizers in outpatients with
cessfully treated with gabapentin. J Am Dent Assoc
mixed bipolar symptomatology. Ann Clin Psychiatry 1999;11:
23. Cabras PL, Hardoy MJ, Hardoy MC, et al. Clinical experience
42. Soutullo CA, Casuto LS, Keck PE, Jr. Gabapentin in the treat-
with gabapentin in patients with bipolar or schizoaffective
ment of adolescent mania: A case report. J Child Adolesc
disorder: Results of an open-label study. J Clin Psychiatry
43. Tran KT, Hranicky D, Lark T, et al. Gabapentin withdrawal
24. Overall JE, Gorham DR. the Brief Psychiatric Rating Scale
syndrome in the presence of a taper. Bipolar Disord 2005;
(BPRS): Recent developments in ascertainment and scaling.
Psychopharmacol Bull 1988;24:97–9.
44. Vieta E, Martinez-Aran A, Nieto E, et al. Adjunctive
25. Carta MG, Hardoy MC, Dessi I, et al. Adjunctive gabapentin
gabapentin treatment of bipolar disorder. Eur Psychiatry.
in patients with intellectual disability and bipolar spectrum
disorders. J Intellect Disabil Res 2001;45:139–45.
45. Wang PW, Santosa C, Schumacher M, et al. Gabapentin aug-
26. Erfurth A, Kammerer C, Grunze H, et al. An open label study
mentation therapy in bipolar depression. Bipolar Disord
of gabapentin in the treatment of acute mania. J Psychiatr
Journal of Psychiatric Practice Vol. 14, Suppl. 1
GABAPENTIN: THE ECHO CHAMBER OF THE CASE SERIES
46. Young LT, Robb JC, Hasey GM, et al. Gabapentin as an
opmental disabilities. J Clin Psychopharmacol 2006;26:344–6.
adjunctive treatment in bipolar disorder. J Affect Disord
52. Robillard M, Conn D. Gabapentin use in geriatric patients
with depression and bipolar illness. Can J Psychiatry 2001;
47. Young LT, Robb JC, Patelis-Siotis I, et al. Acute treatment of
bipolar depression with gabapentin. Biol Psychiatry 1997;42:
53. Ryback RS, Brodsky L, Munasifi F. Gabapentin in bipolar dis-
order. J Neuropsychiatry Clin Neurosci 1997;9:301.
48. Bennett J, Goldman WT, Suppes T. Gabapentin for treatment
54. Sheldon LJ, Ancill RJ, Holliday SG. Gabapentin in geriatric
of bipolar and schizoaffective disorders. J Clin Psychophar-
psychiatry patients. Can J Psychiatry 1998;43:422–3.
55. Stanton SP, Keck PE, Jr., McElroy SL. Treatment of acute
49. Biancosino B, Facchi A, Marmai L, et al. Gabapentin treat-
mania with gabapentin. Am J Psychiatry 1997;154:287.
ment of impulsive-aggressive behaviour. Can J Psychiatry
56. Carey TS, Boden SD. A critical guide to case series reports.
50. Carta MG, Hardoy MC, Ducci F, et al. Gabapentin in the treat-
57. Berenson A. Lilly considers $1 billion fine to settle case. New
ment of bipolar depression in patients with systemic lupus
York Times January 31, 2008. (available at http://query
erythematosus. Clin Exp Rheumatol 2004;22:266.
.nytimes.com/gst/fullpage.html?res=9B03E4DE133EF932A05
51. Hellings JA. Much improved outcome with gabapentin-dival-
752C0A96E9C8B63&scp=1&sq=Eli+lilly+off+label+market-
proex combination in adults with bipolar disorders and devel-
ing&st=nyt, accessed March 5, 2008).
Journal of Psychiatric Practice Vol. 14, Suppl. 1
GABAPENTIN: THE ECHO CHAMBER OF THE CASE SERIES
lusions
linical utility of these widely used anticonvulsants
appeared most effective in those with younger age and,
y thus emerge as an important addition to the anticonvul-
ith respect to anticonvulsant dose and gender
TG in treatment-refractory affectively ill patients
uthor conc
effective adjunctive treatment when administered to outpa-
difference between the responders and the nonresponders
controlled investigation preliminarily suggests the efficacy of
TG appeared most effective for male patients with fewer prior
with GP might provide some benefit for the long-term outcome
study in bipolar disorder conducted to date
sants used for treating bipolar disorder….Future double-blind
patients with antidepressant-induced bruxism… GP w
scribed to this patient on the basis of literature reports of effi-
cacy in treating anxiety and mood symptoms
controlled trials of GP in patients with iatrogenic
idiopathic bruxism are needed to substantiate this anecdotal
A
“The findings of this study did not demonstrate that GP is an
“Initial reports of GP for mood stabilization are fa
from randomization to first new episode (
began valproate and anorgasmia resolved 12
atient with bipolar I disorder on venlafaxine and
on GP as adjunctive therapy (other medications
continued) bruxism resolved within 4 weeks
Results
No significant differences between groups for
PSQI-6 subscale (use of sleep medication) at 12
No significant differences between groups for time
72% of patients showed overall positive response
Bipolar symptoms resolved but patient developed
Adj? N y design Summary of studies located by literature search Stud y Appendix 1. Stud
Journal of Psychiatric Practice Vol. 14, Suppl. 1
GABAPENTIN: THE ECHO CHAMBER OF THE CASE SERIES
hotic patients with affective features of those
linical utility in the management of tardive
lusions
GP in conjunction with other effective mood stabilizers
uthor conc
of our study must be regarded as preliminary and in need of
replication in double-blind or placebo-controlled trials
stabilizer and its usefulness as adjunctive therapy
patients with ID…the present data seem to confirm the previ-
ous evidence reported in the open trials….
patients to treat modest but not severe manic states
seems to be safe and efficacious in the treatment of severe
neous sample of non-refractory bipolar spectrum illness
subgroup of patients with mood disorders in a naturalistic set-
mood stabilizing and/or antidepressant properties of GP in
the setting of bipolar spectrum disorders…this agent could be
A
“These data in 25 patients suggest that GP ma
“The present results suggest a possible role for GBP as a mood
“It is suggested that GP monotherapy might be useful in selected
“GP appears to be somewhat effective as add-on treatment in a
“It is suggested that the possibility of renal dysfunction should be
“Controlled studies are needed to evaluate the possible antimanic
“Our report suggests that the possible antimanic properties of GP
with statistically nonsignificant differ-,
y 21 in the add-on group and from 27.8 to 9.0 in
as moderately to markedly effective in 30% of
bipolar disorder type II and not otherwise speci-
as reversible after discontinuation of GP
as remarkable within 3 weeks of start of treat-
decreased after being given medication.
Improvement in scores on scales of anxiety
markedly effective in 43% of patients for overall
ences between patients with bipolar disorder type
the total sample discontinuing treatment due to
ment and remained so for 6 months of follow-up
signs of tardive dyskinesia diminished until they
accompanied by reduction of tardive dyskinesia in
Results
Number of patients with mood disorder recurrence
Improvement and stabilization of mood symptoms
After 2 weeks of treatment a moderate improvement
Adj? N ued y design contin Stud y Appendix 1. Stud
Journal of Psychiatric Practice Vol. 14, Suppl. 1
GABAPENTIN: THE ECHO CHAMBER OF THE CASE SERIES
ve antimanic and mood-stabilizing effects
ve utility as an adjunctive medication. lusions
hoice as an adjunctive therapy…This investigation
Controlled studies of BP in bipolar disorder appear to
ve antidepressant and anxiolytic properties
uthor conc
moderate response must be considered a relative success
in some patients with bipolar disorder and is generally well tol-
ing that GP is an effective and well tolerated treatment in a
large proportion of bipolar patients who are resistant to tradi-
of GBP in resistant bipolar disorder resides in its effectiveness
against comorbid panic disorder and alcohol abuse
resistant bipolar mixed states…The major weakness of the
placebo response or spontaneous remissions must be regarded
effective as an augmenting agent in the maintenance phase of
treatment of some bipolar spectrum patients
“The data from this small study is quite preliminary
should be validated by the standard researc
who only partially respond to other mood stabilizers
able side-effect profile and rapid action make this drug an
A
“The results of the present study replicate prior studies indicat-
“…GP appears to be an effective adjunctive treatment for drug-
“The results of this small open study suggest that GP ma
“This case series suggests that controlled studies are w
ment 1 to 3 months after the addition of GP;
responses over subsequent periods of time
score showed significant reduction during 8 weeks
a statistically significant reduction.
tinued to experience benefit from maintenance GP
improve with further treatment while manic symp-
stabilized with no significant side effects for peri-
Results
Eight patients showed moderate or marked improve-
All 7 patients experienced improvement in manic
GP exerted potent early effect on initial,
Adj? N ued y design contin Stud y Appendix 1. Stud
Journal of Psychiatric Practice Vol. 14, Suppl. 1
GABAPENTIN: THE ECHO CHAMBER OF THE CASE SERIES
as effective and well tolerated in patients
parallel control group…Contrary to prior
the main benefits of GP seemed to involve
linical trials…Depressive symptomatology
lusions
y be beneficial in bipolar depression.
GP responders compared with non-responders had
y be a useful drug for the add-on treatment of bipolar
uthor conc
wide therapeutic index with few side effects and drug interac-
tion of GP…Unique to this case is that this geriatric patient
week-long taper…GP taper should follow a course similar to
that of a benzodiazepine taper—slowly and over a period of
patients with poor response to mood stabilizers
improved more than manic or hypomanic features
with mild to moderate bipolar depression.
icance and generalizability of our findings to other patients are
A
“Controlled studies are needed to evaluate the possible anti-
and 4 showed no therapeutic effects (outcome
atient showed marked response within 1 month and
remained euthymic 7 months after addition of GP
dropped to 9 after 1 month of treatment.
atient had moderate upper respiratory tract infec-
tion symptoms and somatic complaints 1 da
improvement (defined as a decrease of at least 2
with bipolar II disorder and severe agoraphobia and
depression subscale in mean CGI-BP scores
ences remained significant for improvements in
Results Adj? N ued y design contin Stud y Appendix 1. Stud
Journal of Psychiatric Practice Vol. 14, Suppl. 1
GABAPENTIN: THE ECHO CHAMBER OF THE CASE SERIES
at least in a subgroup of patients…longer fol-,
lusions
Small sample size and the use of an open uncon-
uthor conc
cy of GP in both phases of bipolar disorder
trolled design limit interpretation of results”
term prophylactic efficacy in bipolar disorder
low-up of patients who initially present in the depressed phase
of bipolar disorder and are treated with GP is needed to c
continued efficacy of this drug in depression and whether it
leads to longer term mood stabilization. A
“These findings are consistent with others establishing the effica-
linical Global Impressions Scale fCClinical Global Impressions of ImprovementClinical Global Impressions Severity Scale
atients experienced significant reduction in depres-
during a depressive episode showed significant
decrease in depressive symptoms over 12 weeks
Subgroup of manic patients had significant reduc-
depressed group to determine effect of GP on mood
versus anxiety symptoms (using HAM-D) showed
significant overall reduction in both anxiety and
depression after treatment and this subject w
Results
Significant but modest reduction from baseline in
Adj? N ued y design contin Stud Clinical Global Impressions Scale fy Appendix 1. Stud
Journal of Psychiatric Practice Vol. 14, Suppl. 1
Sara Lee Plain 4 oz Par Baked Variety Pack Bagels Units Unit Gross Net Cs Case Case Detailed Product Description (Slices, Units/Bag, Length Width Hght Case Pallet 14 Digit GTIN Cube Ti /Hi Sara Lee 4 oz P/B Bagel Variety Pack (5 Plain, 5 Cinn Dot Item Number : Kosher Symbol: Product Approx Dimensions: Thawed Shelf Life : Frozen Shelf Life ( Months
Natural Home Remedies for Alzheimer's Disease By: Laura M. Sands Home remedies for Alzheimer's disease can significantly slow the progression of this devastating illness while offering a person better physical health and self-confidence. Approximately 5,000,000 adults currently suffer from the ravishing affects of this disease. Alzheimer's is the most frequently occurring type of dementia and