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Clozapine is the preferred antipsychotic for treatment-resistant schizophrenia, but has significant adverse effects, including gastrointestinal hypomotility or ‘slow gut’, which may result in severe constipation, ileus, bowel obstruction, and even death. These gastrointestinal effects remain inadequately recognized.
We reviewed all reports of serious clozapine-induced gastrointestinal hypomotility (CIGH) submitted to the Australian Therapeutic Goods Administration and New Zealand Pharmacovigilance Centre between 1992 and 2013. We extracted relevant demographic, clinical, and outcome data and derived a numerator from clozapine registries. We examined whether clozapine drug safety information in Australia, New Zealand, the US, and the UK was adequate and consistent with pharmacoepidemiologic evidence.
A total of 43,132 people commenced clozapine over the study period. 160 were reported as having serious gastrointestinal hypomotility with clozapine the suspected cause (37/10,000 clozapine users). Of these, 66.3% were male, age range was 17–76 years, clozapine dose range 25–1000 mg/day (mean 439 mg/day) and median duration of clozapine treatment 2.5 years. Few had received laxatives. At least 29 patients died (7/10,000 clozapine users), a reported case fatality rate of 18%. The CIGH prevalence, while similar to other smaller studies, differs significantly from clozapine prescribing information issued by regulators and pharmaceutical companies, none of which mention CIGH, and which report serious gastrointestinal complications at rates of <1/10,000, almost a 40-fold difference.
This is the largest study to date of serious CIGH. The reported prevalence of serious CIGH was 37/10,000, a likely underestimation of true prevalence. Current prescribing guidelines provide inadequate information on CIGH. This may be contributing to poor awareness and high associated morbidity and mortality. It is time regulators and manufacturers update their guidance.
Clozapine remains the ‘gold standard’ in treatment-resistant schizophrenia , with its superiority well established in terms of mental health outcomes, quality of life, and life expectancy [2–4]. However, clozapine’s advantages come at a cost, with an array of problematic adverse effects of which clozapine-induced gastrointestinal hypomotility (CIGH) is one of the most serious [5, 6], albeit one that has received scant attention until the last decade.
CIGH is defined as an acquired state of delayed transit through the gastrointestinal tract (i.e. transit time >2 standard deviations [SD] above the mean), colloquially known as clozapine-related ‘slow gut’, resulting from the drug’s pharmacological actions on the enteric nervous system . In vitro, clozapine is shown to have potent effects on the mammalian colon, inhibiting neurogenic and, at higher concentrations, myogenic contractions, profoundly disrupting gastrointestinal motility . These effects can be reversed by carbachol and to some extent by serotonin, suggesting both anticholinergic and anti-serotonergic mechanisms .
CIGH is very common. Between 50–80% of clozapine-treated patients have unambiguous objective evidence of CIGH in colonic transit studies [5, 6], with mean transit times that are four times longer than normal, and all regions of the colon affected . While serious complications of CIGH such as ileus and pseudo-obstruction—the focus of this paper—attract the most attention, the less serious but highly prevalent manifestations, including dysphagia, dyspepsia, esophageal reflux, gastroparesis, and chronic constipation, affect quality of life for many clozapine users. For example, a systematic review of 32 studies calculated a pooled prevalence of clozapine-associated constipation of 31% , with chronic constipation consistently shown to significantly degrade quality of life for those it affects [9–11].
The US Food and Drug Administration (FDA) has mandated ‘black box’ warnings for clozapine, highlighting the risks of agranulocytosis, myocarditis, cardiomyopathy, seizures, and severe hypotension—but not CIGH. However, recent epidemiological studies suggest mortality related to CIGH (10–12 per 10,000 [12, 13]) is at least 3-fold that of the better-recognized complication of agranulocytosis .
Despite the prevalence and potential seriousness of CIGH, knowledge about preventing, identifying, and managing it remains poor, even among those most familiar with clozapine. In a 2016 study, only 50% of psychiatric inpatient nurses were aware clozapine could cause constipation . In an Australian audit of 67 long-stay patients taking clozapine, there was a high level of baseline hematological and metabolic monitoring, but no monitoring of bowel function . Of particular concern, clozapine treatment guidelines rarely mention the CIGH spectrum, let alone advise on its management [8, 17].
In this observational study, we examined all reports of suspected CIGH reactions received by the Australian and New Zealand pharmacovigilance agencies over a 22-year period (1992–2013 inclusive) to determine the demographics, risk factors, and outcomes related to serious or life-threatening CIGH, and to calculate the proportion of clozapine-prescribed patients reported as having CIGH-type adverse drug reactions (ADRs). Australia and New Zealand both have high-quality pharmacovigilance programs monitoring all reported ADRs. At the time of data collection, New Zealand and Australia had the third and tenth highest rate per capita of ADR reporting (from 110 member countries) to the World Health Organization (WHO) global database, Vigibase . Clozapine has particularly good pharmacovigilance data in New Zealand, being one of a handful of medications intensively scrutinized by an Intensive Medicines Monitoring Program (IMMP) between 2000 and 2008, which tracked high-risk medicines in prospectively identified cohorts by prescription event monitoring . At all other times in New Zealand clozapine was monitored by the Centre for Adverse Reactions Monitoring (CARM).
In both New Zealand and Australia, ADR reports are obtained through spontaneous reporting to the New Zealand Pharmacovigilance Centre and the Australian Therapeutic Goods Administration (TGA), respectively, by doctors, nurses, pharmacists, and pharmaceutical companies. All clinical events are assessed and coded by medical assessors using terms from the ‘WHO Adverse Reaction Terminology’ dictionary . Causality assessment is performed for each event to determine the relationship with the medicine .
We also compared our data and other recent evidence with clozapine prescribing information issued by regulators in Australia, New Zealand, the US, and the UK.
Australian and New Zealand pharmacovigilance data for clozapine-related gastrointestinal complications were obtained from the New Zealand Pharmacovigilance Centre and the Australian TGA.
Our aim was to identify all cases where clozapine was the putative causal agent in serious gastrointestinal hypomotility events. The inclusion criteria were cases coded as: ‘serious’ or ‘life-threatening’ constipation, or constipation resulting in hospitalization, surgery or a fatal outcome; ileus; bowel obstruction; bowel ischemia; bowel necrosis; bowel perforation; or megacolon; and where the association with clozapine was considered probable or possible. These criteria are consistent with the internationally recognized definition of a ‘serious ADR’ .
In addition, we sought summary international ADR data on CIGH—held by the WHO in the Uppsala Monitoring Centre, the largest pharmacovigilance databank in the world—for all CIGH reports submitted during 1968–2013 from over 100 countries (including Australia and New Zealand).
We also analyzed official clozapine drug information provided for prescribers and consumers by regulatory bodies in the US (FDA), UK (Medicines & Healthcare Products Regulatory Agency—the MHRA), New Zealand (Medsafe), and Australia (TGA) to determine the information currently provided on the prevalence, monitoring, and management of CIGH.
Pharmacovigilance data were extracted using a pre-specified data extraction form. We obtained country; unique identification number; reported date; reporter location (Australia only); patient demographics including date of birth, gender, height, and weight (Australia only); ADR event characteristics such as date of onset, severity, duration, and outcome; clozapine start date; date of clozapine cessation; clozapine dosage at ADR onset; causality assigned by pharmacovigilance agency; concomitant ADR terms (in accordance with the WHO Adverse Reactions Terminology dictionary); clinical investigations; other medications; treatment; and any additional documented commentary.
Multiple reports of the same (or similar) adverse events for a single patient (identified by demographic data and clinical details) were treated as single cases to eliminate duplications. We excluded reports in which there were confounding comorbid conditions (e.g., bowel cancer, inflammatory bowel disease, hypothyroidism) that may have caused/contributed to the gastrointestinal pathology.
All patients receiving clozapine must be entered into a pharmaceutical registry for monitoring. In order to provide a denominator for estimating CIGH prevalence, the national registries (operated by Hospira, Douglas, and Novartis) were contacted to calculate the numbers of patients exposed to clozapine over the study period.
The pharmacovigilance agencies have been set up to comply with local privacy codes. Their programs have ethics approval and additional approval was not required for identification and analysis of the relevant adverse-effect data.
Identifying demographic data were removed and date of birth was translated into age to preserve anonymity.
After data were extracted they were imported into SPSS version 23 (SPSS Inc. Chicago, IL, USA).
Data were analyzed for the following variables: age; gender; clozapine dose at onset of symptoms; duration of clozapine treatment prior to onset of CIGH; symptom onset date; clinical details of presentation, outcome and treatment; and other medications. Descriptive statistics (means [M] with SDs or medians [Md] with interquartile ranges [IQRs]) provide data summaries.
Within the complications group, demographic and clinical covariates were compared between those who were confirmed as having a fatal outcome and those who either recovered or whose outcome was unknown. Continuous variables were compared using t tests for normally distributed variables (e.g., age) or Mann–Whitney U tests for skewed distribution variables (e.g., duration of treatment). Categorical covariates were compared using Pearson Chi-squared tests (with Yates’ continuity correction for 2 × 2 tables).
As a complementary formulation of whether these factors included mortality, several univariate logistic regression models were run to compare fatal and non-fatal outcomes including age (linear variable per 5 years); gender; clozapine dose (linear variable per 100 mg/day); duration of treatment (linear variable per 2 years); and country of reporting. Logistic regression provided odds ratios (ORs) with 95% confidence intervals adjusted for age, duration of treatment, and country of reporting.
Bivariate correlation was used to describe the change in frequency of CIGH reporting over time.
For hypothesis tests, differences were considered statistically significant when p < 0.05.
From Australia, there were 6323 clozapine ADR case reports in the TGA ‘Gastrointestinal’ System Organ Class, of which 157 met the inclusion criteria. A further 33 were excluded (3 duplicates and 30 with confounding pathology). The earliest eligible event occurred in 1994. This resulted in 124 Australian unique reports.
From the New Zealand data, there were 888 clozapine ADR reports in the CARM and IMMP ‘Alimentary class’, the earliest of which occurred in January 1999, of which 51 met the inclusion criteria. A further 15 were excluded (4 duplicates and 11 with confounding pathology). This resulted in 36 New Zealand unique reports.
Together, this gave a combined series of 160 cases from which data were extracted. Most key variables were reported in over 80% of cases (e.g., age and gender 94%; duration of treatment 86%; clozapine dose 84%), with the notable exception of outcome. Whether the patient ultimately recovered was unknown in 30.6% of New Zealand cases and 62.9% of Australian cases. See Box Box11 for an example of a case reported to the TGA.
Of the 160 patients, 106 (66.3%) were male, 51 female (31.9%), and gender was unspecified for three. Age was reported for 150 (94%), with a mean of 46 ± 13.4 (SD) years, range 17–76.
Clozapine dose was documented for 135 patients (84%), M = 439 ± 221 (SD), range = 25–1000 mg/day. This is significantly higher than the mean clozapine dose (372 mg/day) in a large New Zealand epidemiological study  (p < 0.0001). Clozapine serum levels were seldom available in the ADR reports. The duration of clozapine treatment until serious CIGH, specified for 86%, was usually specific to the day, Md = 2.5 years (IQR 4 mo–5 y, 4 mo), range = 3 days–18 years. Data were positively skewed (skewness = 1.46, SE = 0.2). Thirty-seven percent of cases occurred within the first year. Duration of treatment until onset of serious CIGH was similar in both Australian and New Zealand populations (see Fig. 1).
Only 11% were recorded as receiving other potentially constipating medications such as those with anticholinergic effects (like benztropine, or tricyclic antidepressants) or other constipating actions (like opioids). From the 70 reports of severe constipation (Table 1), only 6 (9%) were recorded as receiving laxatives prior to the evolution of symptoms.
The ADRs reported are summarized in Table 1. Constipation (70 reports) and intestinal obstruction (62 reports) were the most commonly reported features of the CIGH spectrum. A common theme was the late presentation to medical services when significant pathology had already evolved. Although many patients were reported as having massive fecal impaction at autopsy, prior complaints of constipation were not often recorded.
Twenty-nine patients were confirmed as having died from suspected CIGH (18%), 42 were reported as recovered (26%) and in 89 cases (56%) the outcome was recorded as ‘unknown’ or ‘not yet recovered’ at the time of reporting. The confirmed fatality rates differed significantly between countries: 36.1% for New Zealand, and 14.8% for Australia, χ 2 (1, n = 160) = 8.62, p < 0.001. This is likely to be strongly influenced by missing mortality data; outcomes were confirmed for more New Zealand patients (69.4%) than Australians (37.1%), χ 2 (1, n = 160) = 10.55, p < 0.001. This is presumably because while clozapine was under the IMMP in New Zealand, CIGH cases were proactively followed up after initial ADR reporting, leading to better classification of outcomes.
Subgroup analysis was performed comparing patients confirmed as having suffered a fatal outcome with the others. Those with fatal outcomes ranged in age from 22–73 years, with a mean age of 50 years. Unadjusted ORs for the various independent variables are reported in Table 2. A Mann–Whitney U test reveals those with fatal outcomes had significantly longer duration of treatment with clozapine (Md = 4.2 years, IQR = 1.5–8.6 years) than the rest of the group (Md = 1.9 years, IQR = 0.2–5 years), U = 968, z = −2.65 p = 0.008 (see Fig. 2). The OR of a fatal outcome increased by 1.21 (95% CI 1.02–1.44) for every 2 years on clozapine. Age, female gender, clozapine dose, and receiving other potentially constipating medication had positive, but non-significant associations with fatal outcomes (Table 2).
Using logistic regression methods to control for confounding, the only variable that remained significant was country: New Zealanders were more likely to have been confirmed as suffering fatal CIGH (OR 4.38, 95% CI 1.26–15.15).
The number of reported serious CIGH-related drug reactions increased significantly over the 22-year period. The 3-year moving average of reported cases increased from below 5 throughout the first decade of clozapine use to consistently above 15 annual cases since 2010 (see Fig. 3). Plotting frequency against date gives a correlation coefficient of r s 0.9 p < 0.001, indicating a strong positive linear correlation between reporting and time. While CIGH reports increase dramatically, the number of people taking clozapine has also increased. Unfortunately annual use data were not available.
From the time when clozapine first entered the New Zealand market (1988) and mid-2013, 7691 people were exposed to clozapine in New Zealand (personal correspondence: Novartis, New Zealand; and Clopine Services coordinator, Hospira, Australia). Our data show at least 36 of these patients developed serious CIGH, at a prevalence of 0.47%. From the time clozapine first entered the Australian market (1992) to mid-2013, 35,441 people were exposed to clozapine in Australia (personal correspondence: Novartis, Australia; and Clopine Services coordinator, Hospira, Australia). Our data show at least 124 developed serious CIGH, at a prevalence of 0.35%. Although there are limitations in such estimates (as discussed below), this suggests the prevalence of potentially life-threatening CIGH in Australia and New Zealand is at least 37 people for every 10,000 exposed to clozapine.
At least 29 patients died (7/10,000 clozapine users), 16 in Australia and 13 in New Zealand, a reported case fatality rate of 18%. The rates of reported fatal outcomes differed significantly between New Zealand (17/10,000) and Australian (5/10,000) datasets (χ 2 [1, n = 43,132] = 14.43, p < 0.001). We note that the disproportionate number of Australian patients recorded as ‘not yet recovered’ or outcome ‘unknown’ means it is likely some CIGH-related fatal outcomes were not captured, leading to greater underestimation of CIGH fatalities in Australian data.
The analysis of CIGH-related data from the Uppsala Monitoring Centre is shown in Table 3. The Centre uses a Bayesian confidence neural network to detect ADR signals. The information component (IC) is a logarithmic measure of the disproportionality between the observed and the expected reporting of a drug–ADR pair. Signal detection is conducted using the IC025 metric, the lower limit of the 95% confidence interval for the IC. An IC025 above 0 indicates a statistically significant signal. We report the IC025 metric for associations between clozapine and a number of gastrointestinal symptoms. All the listed gastrointestinal ADR terms in Table 3 have significant positive associations with clozapine. Particularly strong associations exist (IC025 >2) with the terms megacolon, paralytic ileus, and intestinal obstruction.
For comparative purposes, the total number of suspected clozapine-induced agranulocytosis fatalities over the same time period was 168, with an IC025 of 3.44.
Information provided by regulators about CIGH was uniformly poor in all four countries reviewed (see Table 4). While information about agranulocytosis, myocarditis, and other adverse effects was prominent and comprehensive (on the first page and under clear and informative headings), no datasheet had a specific section on CIGH, or even referred to this spectrum. Constipation was not mentioned until at least page 6 and was subsumed under an ‘anticholinergic side effects’ subheading. Serious CIGH conditions like paralytic ileus appeared toward the end of information sheets within long lists of possible side effects, and were reported as being ‘very rare’, which was defined as “isolated case reports or occurring in less than one in 10,000 users”. There was little, if any, reference to CIGH monitoring or treatment.
This is the largest pharmacoepidemiologic study of serious CIGH to date. It includes all 160 Australian and New Zealand patients reported as suffering from serious or life-threatening CIGH over a 22-year period.
Retrospective pharmacoepidemiologic studies are subject to a number of limitations.
Prevalence calculations from pharmacoepidemiologic data are compromised by difficulties in determining accurate numerators and denominators. ADR reporting in Australia and New Zealand was, and remains, voluntary and thus does not capture all cases. Spontaneous reporting is dogged by under-reporting , with only some 5% of ADRs reported to pharmacovigilance centers . Although clozapine ADR reporting rates are judged to be high  due to obligatory clozapine monitoring systems, reporting is unlikely to be complete. For example, none of the four Dutch patients identified retrospectively by Kok et al.  as suffering clozapine-related paralytic ileus had an ADR submitted. Furthermore, spontaneous reporting is vulnerable to selection bias, influenced by the seriousness and novelty of the effect, and by patient characteristics . Serious (and fatal) ADRs are more often reported . These factors mean case fatality rates calculated from such data can be overestimates, while the true prevalence is underestimated. Nonetheless, the Australian data reported here appear to under-report fatalities, as over 60% of ultimate outcomes were unknown.
Serious CIGH reports increased significantly over the 22-year period. While influenced by the denominator (number of people receiving clozapine) increasing, growing awareness of the relationship between clozapine and gastrointestinal hypomotility is also likely to have improved reporting over time. No reports of CIGH appeared in the databases until 1994 in Australia and 1999 in New Zealand, 2 and 11 respective years after clozapine became available. Perhaps earlier events were not attributed to clozapine and consequently were not reported as ADRs. If so, our prevalence estimate is further understated.
Finally, pharmacovigilance data, while potentially powerful in identifying possible adverse reactions through association, cannot prove causation.
The results demonstrate that there is no consistent relationship between age, dose, or duration of treatment and the onset of life-threatening CIGH. Mean clozapine doses in those with serious CIGH were higher than in the general population but, as evidenced by the wide dose range, serious CIGH also occurred at low clozapine doses. Serum clozapine levels were not often available in ADR reporting, so we could not test whether higher serum levels increased the risk for CIGH, as previously reported . Although more men were affected than women, this reflects the demographics of the treatment population (e.g., approximately two-thirds of Australian clozapine-treated patients are male) . Unfortunately this means it is hard to predict which clozapine-treated patients are most at risk of serious CIGH.
It could be argued that association alone should not ‘incriminate’ clozapine. However, the strength of the association in our Australian and New Zealand data is also reflected in the WHO pharmacovigilance database, with a strong positive correlation (IC025 >2) between clozapine and megacolon, ileus, and intestinal ischemia. Constipation’s IC025 of 1 is lower than expected, given its established prevalence of around 30–60% in clozapine-treated patients [33–36]. This probably reflects the perception that constipation is a relatively benign adverse effect, with reporting to pharmacovigilance agencies only occurring in extreme cases, as indicated by the constipation fatality rate of 13% in the WHO data. Internationally, constipation is now implicated in more clozapine-related deaths than agranulocytosis (178 compared with 168).
It is noteworthy that agranulocytosis is regularly and compulsorily checked through blood films, enabling complete identification of all cases and high levels of reporting, and is coded under simple ADR terminology. We hypothesize that the rate of serious CIGH has been underestimated due to its many pathological synonyms and related terms—essentially ‘splitting the vote’—which has weakened the pharmacovigilance signal, in contrast to the single term for agranulocytosis. Nonetheless, the IC025s of megacolon and paralytic ileus alone are very similar to the IC025 of agranulocytosis.
Clozapine drug safety information emphasizes the risk of agranulocytosis in ‘black box’ warnings and provides comprehensive guidance on management. Mortality rates related to agranulocytosis have been falling due to careful vigilance, early detection, and better treatment, with a recent study finding fatalities averaged 0.45 (95% CI 0.00–0.92) for 10,000 treated individuals/year . Conversely, both the reported incidence and mortality rates of CIGH have been rising. Deaths from CIGH now far exceed those from agranulocytosis—in our study CIGH fatalities occurred in 7/10,000 clozapine users, a likely underestimation. While growing awareness of the CIGH spectrum may have improved case reporting, it should have also increased awareness of the need for preventative treatment.
While clozapine-related myocarditis and agranulocytosis occur early in treatment, warranting greater vigilance during clozapine initiation , the wide SD of time-to-onset of CIGH indicates it can occur at any stage of treatment. Patients with serious CIGH often presented late, with advanced pathology. Although many patients were reported as having massive fecal impaction at autopsy, prior complaints of constipation had not often been recorded. Among those with constipation, only 9% were noted as having been prescribed laxatives prior to development of the serious ADR. This suggests constipation is not being recognized and treated seriously, despite the sometimes fatal consequences. This is consistent with other reports of low subjective awareness of objective hypomotility [5, 6, 38] and reinforces our earlier observation that clozapine-treated patients may not recognize or experience constipation in the same way as others due to changes in pain sensitivity or habituation, and thus may be less likely to complain [6, 38]. This decreased sensitivity places the responsibility for actively monitoring and treating CIGH on health professionals; yet the potential severity of CIGH remains poorly recognized amongst mental health staff [8, 15, 17, 39–41].
We recommend regulators update their guidance on clozapine to reflect current knowledge about CIGH.
Recent literature emphasizes the need for better understanding and education regarding CIGH [40, 42]. Regulatory agencies and pharmaceutical companies share some responsibility for this. Official drug safety information is currently inadequate. It does not highlight the CIGH condition and underestimates both severity and prevalence. Our study and others find 40-fold higher rates of serious CIGH than those indicated by regulators, with the cumulative incidence in other smaller studies also varying between 20–90/10,000 [4, 12, 13, 43], despite most studies investigating just one subset of the CIGH spectrum such as subileus , ileus , or bowel obstruction , hence under-estimating combined rates.
The deficiencies in drug safety information likely contribute to poor prevention and treatment of CIGH, delayed recognition and elevated morbidity and mortality rates. There has been sufficient evidence published over the last 15 years to warrant regulators reviewing and updating the information they provide prescribers and consumers on CIGH.
We recommend careful monitoring of bowel function and the use of prophylactic laxatives, for all clozapine users.
Few patients in this study were treated with laxatives prior to developing CIGH. We have previously argued there should be a strong focus on preventing and managing CIGH [38, 44] in all clozapine-treated patients, even those not subjectively reporting CIGH symptoms. Assertive monitoring and treatment of CIGH is recommended by Flanagan and Ronaldson  and by the Maudsley Prescribing Guidelines . The body of evidence on which treatment to select is not strong. A Cochrane review on pharmacological treatment of antipsychotic-related constipation identified only a handful of eligible trials that considered the efficacy of laxatives in this population, with all trials of poor quality .
In an intervention study, when docusate and senna augmented by macrogol was prescribed to clozapine-treated patients according to the Porirua Protocol (available at http://hdl.handle.net/10523/6763), gastrointestinal transit times improved significantly . Before the Protocol was introduced, the prevalence of serious CIGH was 8.2 cases per 100 person-years, reducing to 1.1 cases per 100 person-years in the 5 years after implementation (p < 0.001) . Another study similarly showed that the pre-emptive use of macrogol in psychiatric intensive care was well tolerated and reduced the incidence of severe constipation, especially in patients receiving clozapine and zuclopenthixol . These findings suggest intervention is possible and effective.
Alongside prophylactic laxatives, we suggest careful monitoring of bowel function and a high index of suspicion for gastrointestinal symptoms and signs that herald emerging serious bowel pathology—the ‘red flags’ on the Porirua Protocol . These include either moderate to severe abdominal pain lasting over an hour; or any abdominal pain/discomfort lasting over an hour and any one or more of the following: abdominal distension; diarrhea; vomiting; absent or high-pitched bowel sounds; metabolic acidosis; hemodynamic instability; leukocytosis; or other signs of sepsis. These signs and symptoms must be treated seriously and an urgent medical and/or surgical opinion sought, notifying the assessing clinician that the person is taking clozapine and consequently at high risk for serious gastrointestinal complications.
Over the last decade, clozapine has been increasingly recognized as causing gastrointestinal hypomotility or ‘slow gut’. In our study, the reported prevalence of serious CIGH was 37/10,000, a likely underestimation of true prevalence. It appears anyone on clozapine may develop CIGH; we identified no clear demographic or pharmacologic risk factors.
While clozapine is undoubtedly the best treatment for many, its use requires careful management due to its adverse effects. Considerable resources are devoted to monitoring for agranulocytosis in clozapine-treated patients, but more patients die from CIGH than from agranulocytosis. Efforts to address CIGH at a regulatory or clinical level have been limited, at best.
Current clozapine prescribing information provided by regulators provides inadequate information about CIGH. This may be contributing to poor awareness of the CIGH spectrum and high morbidity and mortality rates. It is time this guidance is updated to reflect current knowledge about CIGH.
Serious CIGH is a medical emergency. Assertive monitoring and early detection of clozapine-related agranulocytosis have greatly reduced mortality rates; similar attention needs to be given to CIGH.
We acknowledge the TGA and the New Zealand Pharmacovigilance Centre for their significant assistance, especially Janelle Ashton. Thanks to James Stanley, biostatistician, for advice on statistical analyses.
This study received no external funding. The open access fee was paid for by Capital and Coast District Health Board continuing medical education funds.
Susanna Every-Palmer and Pete Ellis have declared that there are no conflicts of interest in relation to the subject of this study.