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Schizophrenia Research and Treatment
Volume 2012 (2012), Article ID 407171, 12 pages
http://dx.doi.org/10.1155/2012/407171
Review Article

Oral versus Long-Acting Injectable Antipsychotics in the Treatment of Schizophrenia and Special Populations at Risk for Treatment Nonadherence: A Systematic Review

Département de Psychiatrie, Université de Montréal, Montréal, Québec, Canada 2900

Received 23 October 2011; Accepted 21 November 2011

Academic Editor: Robin A. Emsley

Copyright © 2012 Simon Zhornitsky and Emmanuel Stip. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Long-acting injectable antipsychotics (LAIs) should offer better efficacy and tolerability, compared to oral antipsychotics due to improved adherence and more stable pharmacokinetics. However, data on LAIs has been mixed, with some studies finding that they are more effective and tolerable than oral antipsychotics, and others finding the contrary. One possibility for the disparate results may be that some studies administered different antipsychotics in the oral and injectable form. The present systematic review examined the efficacy and tolerability of LAIs versus their oral equivalents in randomized and naturalistic studies. In addition, it examined the impact of LAIs on special populations such as patients with first-episode psychosis, substance use disorders, and a history of violence or on involuntary outpatient commitment. Randomized studies suggest that not all LAIs are the same; for example, long-acting risperidone may be associated with equal or less side effects than oral risperidone, whereas fluphenazine decanoate and enanthate may be associated with equal or more side effects than oral fluphenazine. They also suggest that LAIs reduce risk of relapse versus oral antipsychotics in schizophrenia outpatients when combined with quality psychosocial interventions. For their part, naturalistic studies point to a larger magnitude of benefit for LAIs, relative to their oral equivalents particularly among first-episode patients.

1. Introduction

Schizophrenia is a severely disabling psychiatric disorder that often includes hallucinations, delusions, cognitive deficits, poor insight, and comorbid substance use disorder (SUD) [13]. The first decade of illness in schizophrenia patients is often characterized by repeated episodes of psychosis with varying levels of remission between episodes and increased disability following each episode [35]. Moreover, the bulk of functional deterioration tends to occur in the first five years after onset of schizophrenia, after which the illness typically progresses into a stable phase, wherein positive symptoms are decreased and negative, and cognitive symptoms become predominant [3].

Antipsychotics—drugs that block dopamine D2 receptors—attenuate positive symptoms in schizophrenia and help improve outcomes, especially in the early stages of illness [4, 68]. For example, a pivotal study by May [8] revealed that treatment with antipsychotics or electroconvulsive therapy increased the rate of release from the hospital, reduced the length of hospital stay, and decreased the need for sedatives and hydrotherapy in newly admitted first-episode psychosis (FEP) patients, relative to psychotherapy or milieu therapy. Another study by Crow et al. [6] showed that 46% of 120 FEP patients maintained on antipsychotics relapsed within two years, compared to 62% of patients on placebo. Importantly, the chance of subsequent relapse was significantly increased in patients with a longer duration of untreated psychosis. Overall, multiple reviews found that that early antipsychotic treatment is crucial for improving outcomes in FEP patients and may prevent some functional deterioration and development of a chronic course [4, 5].

Despite the benefits of compliance with antipsychotic therapy during the early stage of illness, data from 2,588 FEP patients revealed that only 58% collected their prescription during the first 30 days of hospital discharge, and only 46% continued their initial treatment for 30 days or longer [9]. Indeed, studies have consistently shown that more than 40% of patients with FEP are nonadherent and discontinue medication during the first nine months of treatment, at which point the chances of relapse increase dramatically [10, 11]. The high rate of noncompliance can be explained by poor insight into illness, cognitive deficits, and elevated substance abuse associated with schizophrenia and by side effects associated with antipsychotics such as anhedonia and extrapyramidal symptoms (EPS) [3]. Clearly, the goal of treatment of FEP patients should be to increase compliance with antipsychotic therapy, thereby decreasing the negative effects of untreated psychosis and—at the same time—to minimize the amount of antipsychotic-induced side effects. This goal may, in part, be achieved by the use of long-acting or depot antipsychotics (LAIs) [1214].

LAIs have a number of advantages over oral antipsychotics. First, they should decrease noncompliance due to forgetfulness and loss of insight (e.g., due to psychotic relapse or substance abuse) because patients are followed up if they miss an appointment for their injection [15]. Moreover, LAIs should maximize pharmacokinetic coverage and minimize antipsychotic withdrawal symptoms resulting from partial compliance [16]. In addition, LAIs are not influenced by first-pass metabolism, decreasing the potential for drug-drug interactions. Finally, some have argued that because the slow rate of absorption associated with LAIs leads to reductions in differences between (peak) and (trough) plasma levels [17], they should induce less side effects (an important predictor of poor treatment compliance), relative to oral antipsychotics [18].

Older (typical) LAIs were made by forming an ester with a fatty acid such as decanoic acid and injecting it in an oily solution such as sesame seed oil or low viscosity vegetable oil, thereby maximizing its lipophilicity and affinity for fatty tissue [19]. Moreover, the resulting highly lipophilic compounds possess more complicated, multicompartment tissue binding [28]. Oil-based formulations must be injected slowly and are commonly associated with acute injection site pain, and skin reactions that can last for up to three months [20, 22]. They may induce “breakthrough EPS” on the day of the injection, which is caused by a small amount of free drug released immediately into the patient’s system [2933]. They may also be detectable in plasma for as long as six months following an injection, increasing the possibility of interaction with other drugs [3436]. By contrast, some of these phenomena should be minimized with the atypical, water-based LAIs, including risperidone microspheres, and olanzapine pamoate (Table 1) [24, 31, 37, 38].

tab1
Table 1: Characteristics of some older and newer LAIs [12, 17, 19].

Interestingly, studies on efficacy of LAIs versus oral antipsychotics have produced conflicting results. For example, a 2-year study by Rosenheck et al. [39] revealed that risperidone LAI did not significantly decrease relapse over mixed oral antipsychotics, but it produced more EPS in unstable schizophrenia patients. Our own 2-year, randomized trial among FEP in/outpatients did not find any efficacy or tolerability differences between risperidone LAI and mixed oral atypical antipsychotics; however, the former medication was associated with a reduction in noncompliance [40]. Altogether, a meta-analysis by Adams et al. [41] did not find major efficacy differences between LAIs and oral antipsychotics in randomized studies of schizophrenia inpatients and outpatients. However, in these studies, the combination of inpatients with outpatients may have biased results towards oral antipsychotics, since medication compliance should be more strictly controlled in an inpatient setting [42]). More recently, Leucht et al. [43] showed LAIs to be superior to oral antipsychotics for preventing relapse among schizophrenia outpatients only.

Although the limitation of including both inpatients and outpatients was addressed by Leucht et al. [43], there is still the confound of comparing different molecules in the oral and injectable forms—an effect that may have confounded results due to the fact that not all antipsychotics possess an equal efficacy and tolerability profile [4446]. The present systematic review will examine the efficacy and tolerability of oral and injectable forms of the same antipsychotic in randomized studies. However, since noncompliant patients are unlikely to participate in randomized studies, we will also include naturalistic studies administering LAIs to a general population of schizophrenia patients and to special populations at risk for treatment nonadherence such as patients with FEP, SUDs, and those with a history of violence or on involuntary outpatient commitment.

2. Methods

A systematic search was carried out in the electronic databases, PubMed and EMBASE, using the keywords “antipsychotic” and “depot” or “injectable” and “randomized” or “naturalistic” or “first-episode” or “noncompliance” or “substance abuse” or “substance use disorder,” or “alcohol” or “drug” or “cannabis,” or “cocaine” or “heroin” or “amphetamine” or “violence” or “involuntary outpatient commitment” or “community treatment order.” This search looked for studies published between 1 January 1960 and 1 July 2011. In addition, studies and published abstracts were identified by cross-referencing of review articles. Unpublished studies were identified using clinicaltrials.gov.

For our analyses of randomized (open-label and double-blind) and naturalistic studies in the general population of schizophrenia patients, we included only trials comparing an LAI with its oral equivalent. However, due to a lack of studies, we included any comparative pharmacological trial in our examination of LAI-treatment of individuals with FEP, SUDs, and those on involuntary outpatient commitment. Mirror-image studies were excluded. Due to the fact that there were no studies investigating paliperidone LAI versus oral paliperidone, it was not included in the analyses.

3. LAIs Versus Oral Equivalent—Randomized Studies

Studies comparing an LAI with its oral equivalent in hospitalized patients are conducted to show the “non-inferior” efficacy and/or to study differences in tolerability and pharmacokinetics of the formulations. Hospitalized patients are useful for these purposes because compliance with oral antipsychotics should be maximized in an inpatient setting, limiting the potential confounding effect of noncompliance. By contrast, studies of LAIs versus oral antipsychotics conducted in outpatients are designed to mimic the “real world” setting where compliance is a problem.

3.1. Haloperidol Decanoate

One four-month study among schizophrenia inpatients revealed that haloperidol decanoate was associated with marginally better efficacy and more EPS, relative to oral haloperidol (Table 2) [47].

tab2
Table 2: Randomized and naturalistic studies comparing LAIs with their oral equivalents.
3.2. Fluphenazine Enanthate and Decanoate

Four short-term studies compared the efficacy and tolerability of fluphenazine enanthate versus oral fluphenazine among inpatients. All of the studies found that fluphenazine enanthate was equivalent to oral fluphenazine for schizophrenia symptoms [4851]; however, two of the studies also showed that the former produced more EPS than the latter [50, 51]. Interestingly, in the Van Praag et al. [51] study, a marked increase in EPS was witnessed on the week of each injection, and it decreased somewhat the following week, which may be evidence of “breakthrough EPS.” Pharmacokinetic studies have shown that fluphenazine plasma levels spike after administration of the decanoate and enanthate formulations [29, 30]. However, plasma levels of the latter decline much more slowly than that of the former, which may be another reason why two of the aforementioned studies found that fluphenazine enanthate was associated with more EPS overall.

Four pivotal, long-term studies compared fluphenazine enanthate and decanoate with their oral equivalent in stabilized outpatients [5255]. A 21-month study by Del Giudice et al. [52] showed that fluphenazine enanthate was superior to the oral fluphenazine in reducing relapse among 82 schizophrenia outpatients. Analysis of tolerability outcomes revealed that 6 patients on fluphenazine enanthate experienced EPS, whereas none experienced EPS on oral fluphenazine. The design of this study was unique because a nurse was available to administer injections on home visits, which may have increased compliance with injections and reduced relapse. On the other hand, the short length of her visits may have led to underreporting of side effects, since fluphenazine levels may take days to peak following administration of the enanthate [29, 30, 52]. Accordingly, comparisons between the two esters showed that the decanoate produces the majority of EPS up to nine hours after the injection, whereas the enanthate produces it 12–48 hours after the injection [62].

Fluphenazine decanoate was compared to its oral equivalent in a study by Rifkin et al. [53]. The authors found that both treatments were equally superior to placebo in decreasing 1 year relapse rates among 73 outpatients. However, there were significantly more terminations due to toxicity in the fluphenazine decanoate compared with the oral group, and this was attributed to the fact that 35% of patients receiving the former treatment developed severe akinesia. Akinesia was measured by the BPRS and included such items as emotional withdrawal, depressed mood, blunted effect as well as motor retardation [63]. Importantly, the authors noted that patients on oral fluphenazine were relatively reliable pill takers (as defined by pill counting and urine tests)—a fact that renders the efficacy results fairly meaningless.

Hogarty et al. [54] conducted an important two-year study in 105 schizophrenia outpatients. The authors demonstrated that fluphenazine decanoate decreased relapse, but only when combined with intensive individual and family social therapy. In fact, no patient relapsed in the group treated with fluphenazine decanoate and social therapy after month eight, until the end of the study. Interestingly, there was no impact of social therapy in patients treated with oral fluphenazine. Moreover, analyses revealed that fluphenazine decanoate was associated with significantly more symptoms of depression and anxiety, whereas fluphenazine hydrochloride was associated with more positive symptoms [54]. A larger study by Schooler et al. [55] among 214 schizophrenia outpatients did not find a difference in relapse or side effects between fluphenazine decanoate and oral fluphenazine in schizophrenia outpatients over a period of 1 year. However, the oral equivalent mean dose was higher (25 mg/d), and the decanoate dose was lower (34 mg/3 w) than in some previous studies, which makes interpretation difficult [55]. Taken together, the aforementioned studies suggest that fluphenazine decanoate and enanthate may be associated with similar or more side effects than oral fluphenazine. This finding could be explained by the initial spikes in plasma levels as well as decreased conversion of fluphenazine to its clinically inactive sulfoxide metabolite [30, 64]. Additionally, the results may be explained by the fact that more patients are assumed to be noncompliant in the oral fluphenazine group, and thus to experience less side effects (but see [53]). Concerning efficacy, the studies suggest that there is a benefit of injectable fluphenazine preparations in reducing time to relapse among schizophrenia outpatients when combined with additional interventions such as intensive social therapy and/or a nurse available for home visits.

3.3. Zuclopenthixol Decanoate

The only study involving zuclopenthixol was a 1-year study in 46 schizophrenia outpatients with previous violence [56]. The study demonstrated that schizophrenia patients on zuclopenthixol decanoate reduced the number of violent episodes per month of the study and increased the number of months of adherence to medication. Moreover, the authors found that PANSS positive scores were nonsignificantly lower in decanoate-treated patients. However, it is possible that the lack of difference in symptoms may be a type-II error since these patients also had significantly higher PANSS-positive scores at baseline, relative to patients treated with the oral formulation (despite randomization) [56].

3.4. Risperidone Microspheres

Long-acting risperidone was compared with its oral equivalent in two randomized trials. A 12-week study among 541 inpatients and outpatients found no efficacy difference, but risperidone LAI (25 mg, 50 mg or 75 mg/2 w) produced significantly less prolactin elevation than oral risperidone (2 mg, 4 mg, or 6 mg/d) [26]. Similarly, a 48-week study by Bai et al. [57] in 50 inpatients revealed no significant differences in overall efficacy; however, long-acting risperidone (25 mg, 37.5 mg, or 50 mg/2 w) produced significantly less EPS and prolactin elevation and lower serum concentrations of 9-hydroxy-risperidone (9-OH risperidone, paliperidone), relative to oral risperidone (4 mg, 5-6 mg, or 7+ mg/d) [57]. However, subanalyses revealed that patients who received the two lowest doses showed increased PANSS scores and an increased tendency to relapse. Taken together, these data reveal that risperidone LAI may produce equal or less side effects, compared to oral risperidone. The data may be explained by the fact that treatment with long-acting risperidone leads to significantly lower serum concentrations of risperidone and 9-OH risperidone [65, 66]—the latter which also displays high affinity for D2 receptors [67]. They may also be explained by the lack of “breakthrough EPS” and depressive symptoms associated with long-acting risperidone, in contrast to fluphenazine LAIs. Finally, the differences may be explained by the difficulty in finding equivalent doses between LAIs and oral antipsychotics. Interestingly, Bai et al. [57] found that 25 mg and 37.5 mg/2 w provided insufficient efficacy when switching from 4 mg and 5-6 mg/d oral risperidone, respectively. Based on their results, the authors recommended that the threshold for switching should be reduced to oral risperidone 3 mg/d for risperidone LAI 37.5 mg/2 w, and oral risperidone 5 mg/d for risperidone LAI 50 mg/2 w.

3.5. Olanzapine Pamoate

An unpublished, open-label, 2-year study among 524 outpatients evidenced that those treated with olanzapine pamoate required significantly fewer hospitalizations; however, there were no other major differences in efficacy or side effects [58]. Moreover, a recent 24-week study has found similar efficacy between a high and a medium of olanzapine pamoate (300 mg/2 w; 405 mg/4 w) and oral olanzapine (10, 15, and 20 mg/d) in 1065 schizophrenia outpatients [25]. Patients treated with a low dosing regimen (150 mg/2 w) evidenced significantly more psychotic exacerbation, compared to those treated with the high dose. Olanzapine plasma levels in patients treated with the 405 mg/4 w dose were lower than that of patients maintained on the oral equivalent of 15 mg/d, and they evidenced (nonsignificantly) less weight gain (15%; criteria ≥ 7% of baseline) than patients treated with 300 mg/2 w (21%) and patients on 15 mg/d oral olanzapine (21%) [25], suggesting that this may be the optimal dosing to maintain high efficacy, without compromising tolerability, especially given the risk of inadvertent intravascular injections [24].

It is important to note that in most of the aforementioned randomized studies patients were selected on the basis of having been stabilized on (and likely adherent to) the oral equivalent prior to the study, resulting in a potential bias in favor of oral formulations [25]. This interpretation is consistent with results of Rifkin et al. [53], which found that patients on oral fluphenazine were, in fact, reliable pilltakers.

4. LAIs versus Oral Equivalent—Naturalistic Studies in Schizophrenia and FEP Patients

Naturalistic studies are an important indicator of the value of LAIs because they include patients for whom these agents are typically prescribed. Four naturalistic studies all found that LAIs were superior to their oral equivalents. Among the general population of schizophrenia patients, there is evidence that patients treated with haloperidol or fluphenazine LAI had a significantly longer mean time to all-cause medication discontinuation and were twice as likely to stay on medication, compared to patients treated with oral haloperidol or fluphenazine [59]. Among FEP patients, a 2-year study showed that risperidone LAI significantly reduced relapse and improved compliance, relative to oral risperidone [60]. Similarly, a cohort study of 2,234-consecutive FEP patients showed that perphenazine depot was associated with the lowest relative risk of rehospitalization, compared to oral perphenazine and other typical and atypical antipsychotics [61]. A more recent study by the same authors examined the risk of rehospitalization and drug discontinuation in 2,588 FEP patients [9]. The authors found that the risk of rehospitalization for FEP patients receiving LAIs was two thirds lower than for patients receiving the oral equivalent. These data support the notion that randomized studies in outpatients may underestimate the efficacy benefits of LAI therapy because they underrepresent noncompliant schizophrenia patients.

5. LAIs for SUDs

The lifetime prevalence of comorbid SUDs in schizophrenia patients is estimated to be nearly 50% [68]. Among FEP patients, a recent 2-year followup study found that 24% of individuals abused either alcohol or drugs at baseline and 72% of substance abusers, and 31% of nonabusers had experienced at least one occasion of involuntary hospitalization [69]. In general, studies suggest that compared to nonabusing patients, dual diagnosis schizophrenia patients have more psychiatric symptoms and EPS [70], they are more frequently hospitalized, suicidal, impulsive and violent, homeless, and unemployed, and they have more legal and health problems [71, 72]. Moreover, substance use is commonly associated with poor adherence to antipsychotic treatment, and, naturally, LAIs are commonly recommended as for improving adherence in psychosis patients with comorbid SUDs [14, 31, 73]. In order to better elucidate the potential implications of prescribing LAIs to SUD patients, we examined the literature for comparative studies in dual diagnosis patients. Due to the lack of LAI trials in this group, we also included randomized studies administering LAIs in nonpsychosis substance abusers.

Only one published study exists, which randomized dual diagnosis patients to treatment with an LAI. It was a 6-month, open-label trial that compared long-acting risperidone with zuclopenthixol decanoate in outpatients with mixed SUDs [74]. The authors found that schizophrenia patients treated with risperidone LAI evidenced significantly diminished substance use (measured by urine screens), less PANSS-negative symptoms, less EPS, and better compliance with a substance abuse treatment program. Unfortunately, however, all patients relapsed in both treatment groups [74]. In addition, a retrospective study compared the effectiveness of oral olanzapine, risperidone, ziprasidone, and typical LAIs in tobacco-dependant inpatients with mixed SUDs, undergoing a 90-day substance abuse treatment program [75]. Results revealed that significantly fewer patients treated with olanzapine and typical LAIs completed the program, relative to those treated with risperidone. Moreover, patients treated with oral olanzapine and typical LAIs stayed for a shorter time in treatment, and all claimed that they planned to smoke immediately after discharge, compared to only 56% for risperidone and 50% for ziprasidone [75]. Knowing that cigarette smoke induces the enzyme (CYP1A2) responsible for the metabolism of olanzapine and most typicals [76, 77], and that patients were forbidden to smoke during the program, it was hypothesized that individuals on olanzapine and typicals were noncompliant with treatment because they were experiencing more side effects due to rising plasma levels of the antipsychotics. Indeed, the authors noted subtle effects such as mild sedation that affected cognitive ability or motivation and led the patients to be recorded as being “sleepy” or “inattentive” [75].

Four studies randomized nonpsychosis SUD patients to treatment with an LAI, relative to placebo. A large 6-month trial in nonpsychosis alcoholics found that flupenthixol decanoate (10 mg) aggravated relapse to alcohol use, relative to placebo, possibly due to increased craving for alcohol [78]. Another study reported that long-acting risperidone had no effect on cocaine use or craving but significantly aggravated depressive symptoms, compared to placebo [79]. Two other studies evidenced high rates of EPS following the administration of flupenthixol decanoate in cocaine abusers [8082]. Specifically, a pilot trial found that a large portion of individuals treated with flupenthixol decanoate (12 mg) experienced severely disturbing akathisia, dysarthria, myalgia, and dystonia that required medical intervention after they smoked crack cocaine [80, 81]. More recently, an experimental study by Evans et al. [82] has showed that flupenthixol decanoate (10 and 20 mg) dose dependently increased the desire for cocaine, drug liking, drug potency and good drug effects in cocaine abusers given intravenous injections of cocaine. The study was terminated by the sponsor after the second of seven subjects experienced a dystonic reaction in the high-dose flupenthixol group. Intriguingly, the latter two studies provide clinical evidence for the existence of dopaminergic supersensitivity to psychostimulant challenge—a consequence of repeated antipsychotic treatment in preclinical models [83].

Altogether, the preliminary studies on LAIs in psychosis and nonpsychosis substance abusers show the potential for these agents to aggravate of substance abuse, possibly through increased incidence of adverse events (anhedonia, EPS, sedation) and drug liking/craving. In comparison to typical LAIs, long-acting risperidone seems to produce better outcomes and may be helpful, especially when relapse and rehospitalization due to noncompliance is a concern. In addition, oil-based vehicle should be avoided for SUD patients because they are cleared from the system more slowly. Oil-based vehicles such as sesame seed oil and viscoleo may extend the half-life of antipsychotics by accumulating in tissue and prolonging absorption [84]. For example, there is evidence that six months after discontinuation of treatment with low-dose haloperidol decanoate (30–50 mg/4 weeks), D2 receptor occupancy reached 24%, 32% and 34% in three of four patients [85]. Likewise, other studies have reported persistently elevated plasma fluphenazine and prolactin levels for up to six months following administration of the decanoate ester [3335]. The aforementioned findings suggest that risperidone LAI should be preferred to typical LAIs when the goal is to minimize side effects, whilst combating relapse due to that noncompliance, in psychosis patients with comorbid SUDs. Further research is required to make conclusions about other atypical LAIs for schizophrenia patients with SUDs.

6. LAIs for Involuntary Outpatient Commitment

Despite the potential benefits, prescription of LAIs is not a guarantee of compliance. For example, a study by Olfson et al. [86] in California MEDICAID patients prescribed an LAI for poor compliance found that less than 10% of patients continued treatment after the six-month follow-up. This suggests that a legal framing in the form of involuntary outpatient commitment—in conjunction with the help of an interdisciplinary team—can be necessary to ensure the observance of LAIs. In Québec, the order for involuntary outpatient commitment is obtained within via the Supreme Court of Québec for the patients whose capacity to take care of themselves is deteriorated by lack of awareness of illness and difficulty of evaluating the advantages/disadvantages of agreement or refusal of treatment. The purpose of it is to help the patients to control their disease and possibly, to regain control of their life. Even if it appears paradoxical, this coercive step aims at as well as possible guaranteeing the autonomy of the person, especially because lack of insight is an integral symptom of the disease [3]. Moreover, despite obvious concerns that outpatient commitment may negatively affect the therapeutic alliance, our data among 39 schizophrenia patients who explicitly refused treatment revealed that the therapeutic alliance remained unchanged, even after the legal procedure [87]. Recently, an expert consensus panel from the association des médecins psychiatres du Québec (AMPQ) has recommended more widespread prescription of LAIs and involuntary outpatient commitment—with the goal of increasing treatment compliance among FEP patients (Figure 1) [12]. In the countries where the regulation of LAIs is more frequent, it is generally less difficult enforce outpatient commitment than in Québec. In Australia, for example, a one-page report of health signed by only one psychiatrist, the “community treatment order”, is enough to obtain authorization to treat a patient without his consent, with the aim of avoiding future deterioration and preventing it when it occurs [88, 89].

407171.fig.001
Figure 1

In this context, three studies compared oral to depot antipsychotics for schizophrenia patients on involuntary outpatient commitment/community treatment orders [8890]. One retrospective study found significantly less medication adherence and more rehospitalization among 123 patients on community treatment orders who were receiving oral antipsychotics, compared to those receiving LAIs [88]. Another retrospective study among 94 community treatment orders patients revealed that LAIs were associated with fewer crisis team referrals and other episodes of relapse [89]. In addition, a prospective study found that patients undergoing sustained periods of involuntary outpatient commitment (six months or more) were more likely to remain compliant with medication and other treatment, relative to those who underwent only brief outpatient commitment or none [90]. In that study, administration of depot antipsychotics significantly improved treatment adherence independently of the effect of sustained outpatient commitment. As a whole, these preliminary case-control trials reveal that LAIs may be an important tool to improve outcomes in patients on involuntary outpatient commitment and they highlight the need for better controlled trials to confirm the superior efficacy of LAIs in this population.

7. Conclusion

The present systematic review compared LAIs with their oral equivalents in order to avoid bias associated with comparing different molecules in the oral and injectable forms. Randomized studies suggest that not all LAIs are the same; for example, long-acting risperidone may be associated with equal or less side effects than oral risperidone, whereas fluphenazine enanthate and decanoate may be associated with equal or more side effects than oral fluphenazine. These differences may be the result of more predictable drug delivery via the use of microspheres [17, 31]. However, these conclusions are limited because of the difficulty in finding appropriate equivalent doses from oral antipsychotics to LAIs and the wide ranges of equivalent doses noted in different studies [9193]. In addition, randomized studies suggest that LAIs reduce risk of relapse when combined with additional interventions such as individual and family social therapy and/or a nurse available for home visits. On the other hand, randomized studies may have underestimated the benefits of LAIs because of underrepresentation of the nonadherent patient population. Indeed, large-scale naturalistic studies show major benefits of LAIs versus oral antipsychotics, especially among FEP patients [9, 61]. Among SUD patients, preliminary studies indicate that risperidone LAI may be the preferred compound, possibly due to a lower rate of side effects and interactions with drugs of abuse. Nonetheless, clinicians must be aware of the potential for antipsychotics to interact with psychostimulants, resulting in increased EPS and, in some cases, enhanced drug liking/craving and drug relapse, especially at high doses [7577]. Preliminary studies also suggest that LAIs may reduce violence in patients with a history of violence and decrease relapse and rehospitalization in schizophrenia patients on involuntary outpatient commitment, relative to oral antipsychotics [56, 8890].

Despite the potential advantages of LAIs, their use in the United States, Canada, and Germany remains the lowest among developed countries [94]. We feel that the evidence in favor of more widespread use of LAIs in schizophrenia (especially among FEP patients) is mounting, having been boosted by the advent of newer molecules and better methods of delivery. Nevertheless, we acknowledge that the efficacy benefits of LAIs may be constrained by the limitations of antipsychotics themselves. For example, at the end of the Del Giudice et al. [52] study, the chance of experiencing a relapse in patients treated with fluphenazine enanthate returned to the level of those treated with oral fluphenazine. These data indicate that LAIs do not prevent a patient from relapsing, but they may increase the time between relapses by improving adherence. Indeed, it is crucial that the only patients that evidenced sustained improvement on LAIs for over two years was the group who received intensive individual and family social therapy [54]. This finding is a testament to the importance of psychotherapy and quality followup services to maintain the benefits of LAIs [95, 96]. Further research is required to elucidate which special populations may benefit most from LAI therapy and which psychosocial interventions work best when paired with LAIs.

Disclosure

E. Stip is holder of the Eli Lilly Chair of Schizophrenia from the University of Montreal.

References

  1. S. M. Stahl, Essential Psychopharmacology, Cambridge University Press, New York, NY, USA, 2nd edition, 2005.
  2. W. W. Eaton, S. S. Martins, G. Nestadt, O. J. Bienvenu, D. Clarke, and P. Alexandre, “The burden of mental disorders,” Epidemiologic Reviews, vol. 30, no. 1, pp. 1–14, 2008. View at Publisher · View at Google Scholar · View at Scopus
  3. R. Tandon, H. A. Nasrallah, and M. S. Keshavan, “Schizophrenia, “just the facts” 4. Clinical features and conceptualization,” Schizophrenia Research, vol. 110, no. 1–3, pp. 1–23, 2009. View at Publisher · View at Google Scholar · View at Scopus
  4. R. J. Wyat, “Neuroleptics and the natural course of schizophrenia,” Schizophrenia Bulletin, vol. 17, no. 2, pp. 325–351, 1991. View at Scopus
  5. R. de Bont, “Schizophrenia, evolution and the borders of biology: on Huxley et al.'s 1964 paper in Nature,” History of Psychiatry, vol. 21, no. 2, pp. 144–159, 2010. View at Publisher · View at Google Scholar · View at Scopus
  6. T. J. Crow, J. F. MacMillan, A. L. Johnson, and E. C. Johnstone, “II. A randomized controlled trial of prophylactic neuroleptic treatment,” British Journal of Psychiatry, vol. 148, pp. 120–127, 1986. View at Scopus
  7. M. Harrow, T. H. Jobe, L. S. Grossman, V. Ghogari, and R. N. Faull, “Lifetime antipsychotic treatment for all schizophrenia patients? A 26-year evidence-based approach,” Schizophrenia Bulletin, vol. 37, no. s1, pp. 1–342, 2011.
  8. P. R. May, Treatment of Schizophrenia: A Comparative Study of Five Treatment Methods, Science House, New York, NY, USA, 1968.
  9. J. Tiihonen, J. Haukka, M. Taylor, P. M. Haddad, M. X. Patel, and P. Korhonen, “A nationwide cohort study of oral and depot antipsychotics after first hospitalization for schizophrenia,” American Journal of Psychiatry, vol. 168, no. 6, pp. 603–609, 2011. View at Publisher · View at Google Scholar
  10. B. J. Miller, “A review of second-generation antipsychotic discontinuation in first-episode psychosis,” Journal of Psychiatric Practice, vol. 14, no. 5, pp. 289–300, 2008. View at Publisher · View at Google Scholar · View at Scopus
  11. C. Guevremont, J. Sablier, P. Vincent et al., “DoPill, an electronic pill dispenser, helping control medication adherence in patients with schizophrenia,” International Clinical Psychopharmacology, vol. 26, p. e83, 2011. View at Publisher · View at Google Scholar
  12. E. Stip, A. Abdel-Baki, D. Bloom, S. Grignon, and M.-A. Roy, “An expert opinion from the Association des médecins psychiatres du Québec,” Canadian Journal of Psychiatry, vol. 56, no. 6, pp. 367–376, 2011.
  13. E. Stip, “Expert opinion on APAP (prolonged action atypical antipsychotic agents). Position of Canadian psychiatry,” Encephale, supplement 3, pp. S115–S118, 2009.
  14. J. M. Kane and C. Garcia-Ribera, “Clinical guideline recommendations for antipsychotic long-acting injections,” British Journal of Psychiatry, vol. 195, no. 52, pp. s63–s67, 2009. View at Publisher · View at Google Scholar · View at Scopus
  15. D. A. Johnson and H. Freeman, “Drug defaulting by patients on long-acting phenothiazines,” Psychological Medicine, vol. 3, no. 1, pp. 115–119, 1973. View at Scopus
  16. D. A. Hughes, “Estimation of the impact of noncompliance on pharmacokinetics: an analysis of the influence of dosing regimens,” British Journal of Clinical Pharmacology, vol. 65, no. 6, pp. 871–878, 2008. View at Publisher · View at Google Scholar · View at Scopus
  17. L. Ereshefsky and C. A. Mascarenas, “Comparison of the effects of different routes of antipsychotic administration on pharmacokinetics and pharmacodynamics,” Journal of Clinical Psychiatry, vol. 64, no. 16, pp. 18–23, 2003. View at Scopus
  18. W. W. Fleischhacker, U. Meise, V. Gunther, and M. Kurz, “Compliance with antipsychotic drug treatment: influence of side effects,” Acta Psychiatrica Scandinavica, vol. 89, no. 382, pp. 11–15, 1994. View at Scopus
  19. J. M. Davis, L. Metalon, M. D. Watanabe, and L. Blake, “Depot antipsychotic drugs. Place in therapy,” Drugs, vol. 47, no. 5, pp. 741–773, 1994. View at Scopus
  20. Y. Bloch, S. Mendlovic, S. Strupinsky, A. Altshuler, S. Fennig, and G. Ratzoni, “Injections of depot antipsychotic medications in patients suffering from schizophrenia: do they hurt?” Journal of Clinical Psychiatry, vol. 62, no. 11, pp. 855–859, 2001. View at Scopus
  21. J. Hay, “Complications at site of injection of depot neuroleptics,” British Medical Journal, vol. 311, no. 7002, p. 421, 1995. View at Scopus
  22. G. L. Hamann, T. M. Egan, B. G. Wells, and J. E. Grimmig, “Injection site reactions after intramuscular administration of haloperidol decanoate 100 mg/mL,” Journal of Clinical Psychiatry, vol. 51, no. 12, pp. 502–504, 1990. View at Scopus
  23. H. Li, Q. Rui, X. Ning, H. Xu, and N. Gu, “A comparative study of paliperidone palmitate and risperidone long-acting injectable therapy in schizophrenia,” Progress in Neuro-Psychopharmacology and Biological Psychiatry, vol. 35, no. 4, pp. 1002–1008, 2011. View at Publisher · View at Google Scholar
  24. J. P. Lindenmayer, “Long-acting injectable antipsychotics: focus on olanzapine pamoate,” Journal of Neuropsychiatric Disease and Treatment, vol. 24, pp. 261–267, 2010.
  25. J. M. Kane, H. C. Detke, D. Naber et al., “Olanzapine long-acting injection: a 24-week, randomized, double-blind trial of maintenance treatment in patients with schizophrenia,” American Journal of Psychiatry, vol. 167, no. 2, pp. 181–189, 2010. View at Publisher · View at Google Scholar · View at Scopus
  26. P. Chue, M. Eerdekens, I. Augustyns et al., “Comparative efficacy and safety of long-acting risperidone and risperidone oral tablets,” European Neuropsychopharmacology, vol. 15, no. 1, pp. 111–117, 2005. View at Publisher · View at Google Scholar · View at Scopus
  27. J. P. Lindenmayer, K. Jarboe, C. A. Bossie, Y. Zhu, A. Mehnert, and R. Lasser, “Minimal injection site pain and high patient satisfaction during treatment with long-acting risperidone,” International Clinical Psychopharmacology, vol. 20, no. 4, pp. 213–221, 2005. View at Publisher · View at Google Scholar · View at Scopus
  28. L. Ereshefsky, S. R. Saklad, and M. W. Jann, “Future of depot neuroleptic therapy: pharmacokinetic and pharmacodynamic approaches,” Journal of Clinical Psychiatry, vol. 45, no. 5 II, pp. 50–59, 1984.
  29. M. W. Jann, L. Ereshefsky, and S. R. Saklad, “Clinical pharmacokinetics of the depot antipsychotics,” Clinical Pharmacokinetics, vol. 10, no. 4, pp. 315–333, 1985. View at Scopus
  30. F. Jouen, P. Verite, D. Andre, L. Colonna, and P. Boucly, “Plasma fluphenazine levels measured by high-performance liquid chromatography in patients treated with depot injections,” Arzneimittel-Forschung/Drug Research, vol. 43, no. 5, pp. 509–511, 1993. View at Scopus
  31. S. J. Keith, J. M. Kane, M. Turner, R. R. Conley, and H. A. Nasrallah, “Guidelines for the use of long-acting injectable atypical antipsychotics,” Journal of Clinical Psychiatry, vol. 65, no. 1, pp. 120–130, 2004. View at Publisher · View at Google Scholar
  32. D. A. W. Johnson, “The side effects of fluphenazine decanoate,” British Journal of Psychiatry, vol. 122, no. 576, pp. 519–522, 1973. View at Scopus
  33. S. H. Curry, A. C. Altamura, and S. Montgomery, “Unwanted effects of fluphenazine enanthate and decanoate,” The Lancet, vol. 1, no. 8111, pp. 331–332, 1979. View at Scopus
  34. M. J. Gitlin, K. H. Nuechterlein, J. Mintz et al., “Fluphenazine levels during maintenance treatment of recent-onset schizophrenia: relation to side effects, psychosocial function and depression,” Psychopharmacology, vol. 148, no. 4, pp. 350–354, 2000. View at Scopus
  35. T. L. Purvis, R. N. Hieber, T. Dellenbaugh, and R. W. Sommi, “Pharmacokinetics of the long-acting, first-generation antipsychotic fluphenazine,” Pharmacotherapy, vol. 31, no. 4, article 438, pp. 71e–75e, 2011. View at Publisher · View at Google Scholar
  36. B. Wistedt, D. Wiles, and T. Kolakowska, “Slow decline of plasma drug and prolactin levels after discontinuation of chronic treatment with depot neuroleptics,” The Lancet, vol. 1, no. 8230, p. 1163, 1981. View at Scopus
  37. R. C. Love and R. J. Conley, “Long-acting risperidone injection,” American Journal of Health-System Pharmacy, vol. 61, no. 17, pp. 1792–1800, 2004. View at Scopus
  38. R. T. Owen, “Paliperidone palmitate injection: its efficacy, safety and tolerability in schizophrenia,” Drugs of Today, vol. 46, no. 7, pp. 463–471, 2010. View at Publisher · View at Google Scholar · View at Scopus
  39. R. A. Rosenheck, J. H. Krystal, R. Lew et al., “Long-acting risperidone and oral antipsychotics in unstable schizophrenia,” New England Journal of Medicine, vol. 364, no. 9, pp. 842–851, 2011. View at Publisher · View at Google Scholar
  40. Ortho Janssen, “An open-label randomized trial comparing Risperdal Consta with oral antipsychotic care in the treatment of early psychosis,” CR005959, http://download.veritasmedicine.com/PDF/CR005959_CSR_synopsis.pdf.
  41. C. E. Adams, M. K. P. Fenton, S. Quraishi, and A. S. David, “Systematic meta-review of depot antipsychotic drugs for people with schizophrenia,” British Journal of Psychiatry, vol. 179, pp. 290–299, 2001. View at Publisher · View at Google Scholar · View at Scopus
  42. J. R. Vittengl, “Temporal regularities in physical control at a state psychiatric hospital,” Archives of Psychiatric Nursing, vol. 16, no. 2, pp. 80–85, 2002. View at Publisher · View at Google Scholar · View at Scopus
  43. C. Leucht, S. Heres, J. M. Kane, W. Kissling, J. M. Davis, and S. Leucht, “Oral versus depot antipsychotic drugs for schizophrenia-A critical systematic review and meta-analysis of randomised long-term trials,” Schizophrenia Research, vol. 127, no. 1–3, pp. 83–92, 2011. View at Publisher · View at Google Scholar
  44. R. S. Kahn, W. W. Fleischhacker, H. Boter et al., “Effectiveness of antipsychotic drugs in first-episode schizophrenia and schizophreniform disorder: an open randomised clinical trial,” The Lancet, vol. 371, no. 9618, pp. 1085–1097, 2008. View at Publisher · View at Google Scholar · View at Scopus
  45. K. Komossa, C. Rummel-Kluge, F. Schmid et al., “Quetiapine versus other atypical antipsychotics for schizophrenia,” Cochrane Database of Systematic Reviews, vol. 20, no. 1, article CD006625, 2010. View at Scopus
  46. S. Zhornitsky, S. Potvin, H. Moteshafi, S. Dubreucq, P.-P. Rompré, and E. Stip, “Dose-response and comparative efficacy and tolerability of quetiapine across psychiatric disorders: a systematic review of the placebo-controlled monotherapy and add-on trials,” International Clinical Psychopharmacology, vol. 26, no. 4, pp. 183–192, 2011. View at Publisher · View at Google Scholar
  47. A. W. Zuardi, A. C. Giampietro, and E. R. Grassi, “Double-blind comparison between two forms of haloperidol: an oral preparation and a new depot decanoate in the maintenance of schizophrenic inpatients,” Current Therapeutic Research, vol. 34, no. 2 I, pp. 253–261, 1983.
  48. J. Kinross-Wright and K. D. Charalampous, “A controlled study of a very long-acting phenothiazine preparation,” International Journal of Neuropsychiatry, vol. 1, pp. 66–70, 1964.
  49. C. L. Ravaris, L. A. Weaver, and G. W. Brooks, “A controlled study of fluphenazine enanthate in chronic schizophrenic patients,” Diseases of the Nervous System, vol. 26, pp. 33–39, 1965. View at Scopus
  50. I. Haider, “A controlled trial of fluphenazine enanthate in hospitalized chronic schizophrenics,” British Journal of Psychiatry, vol. 114, no. 512, pp. 837–841, 1968. View at Scopus
  51. H. M. van Praag, J. Breetveld, H. van Mesdag-Etty, R. Westerhuis, A. Pen, and T. Schut, “A controlled comparative study of fluphenazine and fluphenazine enanthate in acute and chronic psychotic patients,” Psychiatria, Neurologia, Neurochirurgia, vol. 73, no. 3, pp. 165–175, 1970. View at Scopus
  52. J. Del Giudice, W. G. Clark, and E. F. Gocka, “Prevention of recidivism of schizophrenics treated with fluphenazine enanthate,” Psychosomatics, vol. 16, no. 1, pp. 32–36, 1975. View at Scopus
  53. A. Rifkin, F. Quitkin, C. J. Rabiner, and D. F. Klein, “Fluphenazine decanoate, fluphenazine hydrochloride given orally, and placebo in remitted schizophrenics. I. Relapse rates after one year,” Archives of General Psychiatry, vol. 34, no. 1, pp. 43–47, 1977. View at Scopus
  54. G. E. Hogarty, N. R. Schooler, and R. Ulrich, “Fluphenazine and social therapy in the aftercare of schizophrenic patients. Relapse analyses of a two-year controlled study of fluphenazine decanoate and fluphenazine hydrochloride,” Archives of General Psychiatry, vol. 36, no. 12, pp. 1283–1294, 1979.
  55. N. R. Schooler, J. Levine, and J. B. Severe, “Prevention of relapse in schizophrenia. An evaluation of fluphenazine decanoate,” Archives of General Psychiatry, vol. 37, no. 1, pp. 16–24, 1980.
  56. C. Arango, I. Bombín, T. González-Salvador, I. García-Cabeza, and J. Bobes, “Randomised clinical trial comparing oral versus depot formulations of zuclopenthixol in patients with schizophrenia and previous violence,” European Psychiatry, vol. 21, no. 1, pp. 34–40, 2006. View at Publisher · View at Google Scholar · View at Scopus
  57. Y. M. Bai, T. T. Chen, J. Y. Chen et al., “Equivalent switching dose from oral risperidone to risperidone long-acting injection: a 48-week randomized, prospective, single-blind pharmacokinetic study,” Journal of Clinical Psychiatry, vol. 68, no. 8, pp. 1218–1225, 2007. View at Scopus
  58. E. Lily and Company, “Olanzapine pamoate depot versus oral olanzapine on treatment outcomes in outpatients with schizophrenia,” NCT00320489, 2010.
  59. B. Zhu, H. Ascher-Svanum, L. Shi, D. Faries, W. Montgomery, and S. R. Marder, “Time to discontinuation of depot and oral first-generation antipsychotics in the usual care of schizophrenia,” Psychiatric Services, vol. 59, no. 3, pp. 315–317, 2008. View at Publisher · View at Google Scholar · View at Scopus
  60. B. Kim, S. H. Lee, T. K. Choi et al., “Effectiveness of risperidone long-acting injection in first-episode schizophrenia: in naturalistic setting,” Progress in Neuro-Psychopharmacology and Biological Psychiatry, vol. 32, no. 5, pp. 1231–1235, 2008. View at Publisher · View at Google Scholar · View at Scopus
  61. J. Tiihonen, K. Wahlbeck, J. Lönnqvist et al., “Effectiveness of antipsychotic treatments in a nationwide cohort of patients in community care after first hospitalisation due to schizophrenia and schizoaffective disorder: observational follow-up study,” British Medical Journal, vol. 333, no. 7561, pp. 224–227, 2006. View at Publisher · View at Google Scholar · View at Scopus
  62. A. C. Altamura, S. H. Curry, S. Montgomery, and D. H. Wiles, “Early unwanted effects of fluphenazine esters related to plasma fluphenazine concentrations in schizophrenic patients,” Psychopharmacology, vol. 87, no. 1, pp. 30–33, 1985. View at Scopus
  63. A. Rifkin, F. Quitkin, and D. F. Klein, “Fluphenazine decanoate, oral fluphenazine, and placebo in treatment of remitted schizophrenics. II. Rating scale data,” Archives of General Psychiatry, vol. 34, no. 10, pp. 1215–1219, 1977. View at Scopus
  64. K. K. Midha, J. W. Hubbard, S. R. Marder, B. D. Marshall, and T. Van Putten, “Impact of clinical pharmacokinetics on neuroleptic therapy in patients with schizophrenia,” Journal of Psychiatry and Neuroscience, vol. 19, no. 4, pp. 254–264, 1994. View at Scopus
  65. R. Nesvåg, M. Hendset, H. Refsum, and L. Tanum, “Serum concentrations of risperidone and 9-OH risperidone following intramuscular injection of long-acting risperidone compared with oral risperidone medication,” Acta Psychiatrica Scandinavica, vol. 114, no. 1, pp. 21–26, 2006. View at Publisher · View at Google Scholar · View at Scopus
  66. I. Castberg and O. Spigset, “Serum concentrations of risperidone and 9-hydroxyrisperidone after administration of the long-acting injectable form of risperidone: evidence from a routine therapeutic drug monitoring service,” Therapeutic Drug Monitoring, vol. 27, no. 1, pp. 103–106, 2005. View at Publisher · View at Google Scholar · View at Scopus
  67. J. E. Leysen, P. M. F. Janssen, A. A. H. P. Megens, and A. Schotte, “Risperidone: a novel antipsychotic with balanced serotonin-dopamine antagonism, receptor occupancy profile, and pharmacologic activity,” Journal of Clinical Psychiatry, vol. 55, no. 5, pp. 5–12, 1994. View at Scopus
  68. D. A. Regier, M. E. Farmer, D. S. Rae et al., “Comorbidity of mental disorders with alcohol and other drug abuse. Results from the epidemiologic catchment area (ECA) study,” Journal of the American Medical Association, vol. 264, no. 19, pp. 2511–2518, 1990. View at Publisher · View at Google Scholar · View at Scopus
  69. A. Opsal, T. Clausen, O. Kristensen, I. Elvik, I. Joa, and T. K. Larsen, “Involuntary hospitalization of first-episode psychosis with substance abuse during a 2-year follow-up,” Acta Psychiatrica Scandinavica, vol. 124, no. 3, pp. 198–204, 2011. View at Publisher · View at Google Scholar
  70. S. Zhornitsky, E. Stip, T. Pampoulova et al., “Extrapyramidal symptoms in substance abusers with and without schizophrenia and in nonabusing patients with schizophrenia,” Movement Disorders, vol. 25, no. 13, pp. 2188–2194, 2010. View at Publisher · View at Google Scholar · View at Scopus
  71. K. T. Mueser, R. E. Drake, and M. A. Wallach, “Dual diagnosis: a review of etiological theories,” Addictive Behaviors, vol. 23, no. 6, pp. 717–734, 1998. View at Publisher · View at Google Scholar · View at Scopus
  72. J. C. Negrete, “Clinical aspects of substance abuse in persons with schizophrenia,” Canadian Journal of Psychiatry, vol. 48, no. 1, pp. 14–21, 2003. View at Scopus
  73. M. Valenstein, D. Ganoczy, J. F. McCarthy, H. M. Kim, T. A. Lee, and F. C. Blow, “Antipsychotic adherence over time among patients receiving treatment for schizophrenia: a retrospective review,” Journal of Clinical Psychiatry, vol. 67, no. 10, pp. 1542–1550, 2006. View at Scopus
  74. G. Rubio, I. Martínez, G. Ponce, M. A. Jiménez-Arriero, F. López-Muñoz, and C. Álamo, “Long-acting injectable risperidone compared with zuclopenthixol in the treatment of schizophrenia with substance abuse comorbidity,” Canadian Journal of Psychiatry, vol. 51, no. 8, pp. 531–539, 2006. View at Scopus
  75. E. B. Stuyt, T. A. Sajbel, and M. H. Allen, “Differing effects of antipsychotic medications on substance abuse treatment patients with co-occurring psychotic and substance abuse disorders,” American Journal on Addictions, vol. 15, no. 2, pp. 166–173, 2006. View at Publisher · View at Google Scholar · View at Scopus
  76. M. L. Dahl, “Cytochrome P450 phenotyping/genotyping in patients receiving antipsychotics: useful aid to prescribing?” Clinical Pharmacokinetics, vol. 41, no. 7, pp. 453–470, 2002. View at Scopus
  77. L. Ereshefsky, S. R. Saklad, M. D. Watanabe, C. M. Davis, and M. W. Jann, “Thiothixene pharmacokinetic interactions: a study of hepatic enzyme inducers, clearance inhibitors, and demographic variables,” Journal of Clinical Psychopharmacology, vol. 11, no. 5, pp. 296–301, 1991. View at Scopus
  78. G. A. Wiesbeck, H. G. Weijers, O. M. Lesch, T. Glaser, P. J. Toennes, and J. Boening, “Flupenthixol decanoate and relapse prevention in alcoholics: results from a placebo-controlled study,” Alcohol and Alcoholism, vol. 36, no. 4, pp. 329–334, 2001. View at Scopus
  79. T. Loebl, G. A. Angarita, G. N. Pachas et al., “A randomized, double-blind, placebo-controlled trial of long-acting risperidone in cocaine-dependent men,” Journal of Clinical Psychiatry, vol. 69, no. 3, pp. 480–486, 2008. View at Scopus
  80. F. H. Gawin, M. E. Khalsa-Denison, and P. Jatlow, “Flupenthixol and desipramine treatment of crack users: double blind results,” European Neuropsychopharmacology, vol. 6, pp. 120–121, 1996.
  81. F. H. Gawin, M. E. Khalsa-Denison, and P. Jatlow, “Flupentixol-induced aversion to crack cocaine,” New England Journal of Medicine, vol. 334, no. 20, pp. 1340–1341, 1996. View at Publisher · View at Google Scholar · View at Scopus
  82. S. M. Evans, S. L. Walsh, F. R. Levin, R. W. Foltin, M. W. Fischman, and G. E. Bigelow, “Effect of flupenthixol on subjective and cardiovascular responses to intravenous cocaine in humans,” Drug and Alcohol Dependence, vol. 64, no. 3, pp. 271–283, 2001. View at Publisher · View at Google Scholar · View at Scopus
  83. A. N. Samaha, P. Seeman, J. Stewart, H. Rajabi, and S. Kapur, “"Breakthrough" dopamine supersensitivity during ongoing antipsychotic treatment leads to treatment failure over time,” Journal of Neuroscience, vol. 27, no. 11, pp. 2979–2986, 2007. View at Publisher · View at Google Scholar · View at Scopus
  84. S. R. Marder, T. V. Putten, M. Aravagiri et al., “Plasma levels of parent drug and metabolites in patients receiving oral and depot fluphenazine,” Psychopharmacology Bulletin, vol. 25, no. 3, pp. 479–482, 1989. View at Scopus
  85. S. Nyberg, L. Farde, and C. Halldin, “Delayed normalization of central D2 dopamine receptor availability after discontinuation of haloperidol decanoate: preliminary findings,” Archives of General Psychiatry, vol. 54, no. 10, pp. 953–958, 1997. View at Scopus
  86. M. Olfson, S. C. Marcus, and H. Ascher-Svanum, “Treatment of schizophrenia with long-acting fluphenazine, haloperidol, or risperidone,” Schizophrenia Bulletin, vol. 33, no. 6, pp. 1379–1387, 2007. View at Publisher · View at Google Scholar · View at Scopus
  87. M. H. Trudeau, M. A. Bruneau, E. Stip, F. Grünberg, and M. Boivin, “Categorical refusal of treatment by psychiatric patients: balance, survey and prospects,” Canadian Journal of Psychiatry, vol. 44, pp. 583–588, 1999.
  88. K. Vaughan, N. McConaghy, C. Wolf, C. Myhr, and T. Black, “Community Treatment Orders: relationship to clinical care, medication compliance, behavioural disturbance and readmission,” Australian and New Zealand Journal of Psychiatry, vol. 34, no. 5, pp. 801–808, 2000. View at Publisher · View at Google Scholar · View at Scopus
  89. D. Muirhead, C. Harvey, and G. Ingram, “Effectiveness of community treatment orders for treatment of schizophrenia with oral or depot antipsychotic medication: clinical outcomes,” Australian and New Zealand Journal of Psychiatry, vol. 40, no. 6-7, pp. 596–605, 2006. View at Publisher · View at Google Scholar · View at Scopus
  90. M. S. Swartz, J. W. Swanson, H. R. Wagner, B. J. Burns, and V. A. Hiday, “Effects of involuntary outpatient commitment and depot antipsychotics on treatment adherence in persons with severe mental illness,” Journal of Nervous and Mental Disease, vol. 189, no. 9, pp. 583–592, 2001. View at Publisher · View at Google Scholar · View at Scopus
  91. J. M. Kane, A. Rifkin, and M. Woerner, “Low-dose neuroleptic treatment of outpatient schizophrenics I. Preliminary results for relapse rates,” Archives of General Psychiatry, vol. 40, no. 8, pp. 893–896, 1983.
  92. S. R. Marder, T. Van Putten, and J. Mintz, “Low- and conventional-dose maintenance therapy with fluphenazine decanoate: two-year outcome,” Archives of General Psychiatry, vol. 44, no. 6, pp. 518–521, 1987.
  93. H. A. McClelland, R. G. Farquharson, and P. Leyburn, “Very high dose fluphenazine decanoate. A controlled trial in chronic schizphrenia,” Archives of General Psychiatry, vol. 33, no. 12, pp. 1435–1439, 1976.
  94. W. Kissling, Guidelines for Neuroleptic Relapse Prevention in Schizophrenia, Springer, 1991.
  95. D. A. W. Johnson, “Historical perspective on antipsychotic long-acting injections,” British Journal of Psychiatry, vol. 195, no. 52, pp. s7–s12, 2009. View at Publisher · View at Google Scholar · View at Scopus
  96. G. E. Hogarty and R. F. Ulrich, “The limitations of antipsychotic medication on schizophrenia relapse and adjustment and the contributions of psychosocial treatment,” Journal of Psychiatric Research, vol. 32, no. 3-4, pp. 243–250, 1998. View at Publisher · View at Google Scholar · View at Scopus