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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">2691</journal-id>
      <journal-title-group>
        <journal-title>Delirium Communications</journal-title>
        <abbrev-journal-title>Delirium Communications</abbrev-journal-title>
      </journal-title-group>
      <issn pub-type="epub">2959-104X</issn>
      <publisher>
        <publisher-name>European Delirium Association</publisher-name>
      </publisher>
      <self-uri xlink:href="https://deliriumjournal.com/">Website: Delirium</self-uri>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="publisher-id">84092</article-id>
      <article-id pub-id-type="doi">10.56392/001c.84092</article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
          <subject>Brief Report</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Low Dose Risperidone Prophylaxis for The Prevention of Delirium in The Intensive Care Unit: A Randomized, Placebo Controlled Trial</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid" authenticated="false">https://orcid.org/0000-0002-0813-8771</contrib-id>
          <name>
            <surname>Jacob</surname>
            <given-names>Amita</given-names>
          </name>
          <xref ref-type="aff" rid="author-aff-1">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid" authenticated="false">https://orcid.org/0000-0002-1609-2208</contrib-id>
          <name>
            <surname>Chacko</surname>
            <given-names>Binila</given-names>
          </name>
          <xref ref-type="aff" rid="author-aff-2">
            <sup>2</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid" authenticated="false">https://orcid.org/0000-0002-9443-0022</contrib-id>
          <name>
            <surname>Sathyendra</surname>
            <given-names>Sowmya</given-names>
          </name>
          <xref ref-type="aff" rid="author-aff-1">
            <sup>1</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid" authenticated="false">https://orcid.org/0000-0002-3423-1830</contrib-id>
          <name>
            <surname>Peter</surname>
            <given-names>J.V.</given-names>
          </name>
          <xref ref-type="aff" rid="author-aff-2">
            <sup>2</sup>
          </xref>
        </contrib>
        <contrib contrib-type="author">
          <contrib-id contrib-id-type="orcid" authenticated="false">https://orcid.org/0000-0002-3934-1756</contrib-id>
          <name>
            <surname>Abraham</surname>
            <given-names>O.C.</given-names>
          </name>
          <xref ref-type="aff" rid="author-aff-1">
            <sup>1</sup>
          </xref>
        </contrib>
      </contrib-group>
      <aff id="author-aff-1">
        <label>1</label>
        <institution-wrap>
          <institution content-type="dept">Department of Medicine</institution>
        </institution-wrap>
        <institution-wrap>
          <institution content-type="edu">Christian Medical College</institution>
        </institution-wrap>
        <institution-wrap>
          <institution-id institution-id-type="ROR">https://ror.org/01vj9qy35</institution-id>
        </institution-wrap>
      </aff>
      <aff id="author-aff-2">
        <label>2</label>
        <institution-wrap>
          <institution content-type="dept">Department of Critical Care</institution>
        </institution-wrap>
        <institution-wrap>
          <institution content-type="edu">Christian Medical College</institution>
        </institution-wrap>
        <institution-wrap>
          <institution-id institution-id-type="ROR">https://ror.org/01vj9qy35</institution-id>
        </institution-wrap>
      </aff>
      <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2023-11-06">
        <day>6</day>
        <month>11</month>
        <year>2023</year>
      </pub-date>
      <elocation-id>84092</elocation-id>
      <history>
        <date date-type="received" iso-8601-date="2023-06-08">
          <day>8</day>
          <month>6</month>
          <year>2023</year>
        </date>
        <date date-type="accepted" iso-8601-date="2023-07-07">
          <day>7</day>
          <month>7</month>
          <year>2023</year>
        </date>
      </history>
      <permissions>
        <license license-type="open-access">
          <ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">
              http://creativecommons.org/licenses/by/4.0
            </ali:license_ref>
          <license-p>
              This is an open access article distributed under the terms of the <ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/4.0">Creative Commons Attribution License (4.0)</ext-link>, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
            </license-p>
        </license>
      </permissions>
      <self-uri content-type="pdf" xlink:href="https://deliriumjournal.com/article/84092.pdf"/>
      <self-uri content-type="xml" xlink:href="https://deliriumjournal.com/article/84092.xml"/>
      <self-uri content-type="json" xlink:href="https://deliriumjournal.com/article/84092.json"/>
      <self-uri content-type="html" xlink:href="https://deliriumjournal.com/article/84092"/>
      <abstract>
        <sec>
          <title>Background</title>
          <p>Delirium is common among patients in intensive care units. Antipsychotics have been shown to reduce the incidence of delirium in post-operative patients. We set out to compare the efficacy of risperidone to placebo in preventing delirium in critically ill patients admitted to a medical ICU.</p>
        </sec>
        <sec>
          <title>Methods</title>
          <p>This double-blind, randomised controlled trial compared prophylactic low-dose risperidone to placebo in critically ill patients. Patients were screened daily for delirium using a validated screening tool (CAM-ICU), and the incidence of delirium was compared between groups.</p>
        </sec>
        <sec>
          <title>Results</title>
          <p>Forty-five patients were recruited. Baseline demographic characteristics, diagnosis and severity of illness were not statistically significantly different between groups. There was no significant difference in the incidence of delirium, adverse events or complications.</p>
        </sec>
        <sec>
          <title>Conclusion</title>
          <p>In this study, low-dose risperidone did not prevent the incidence of delirium. As delirium is a heterogeneous syndrome, a single intervention may not be effective across subtypes and aetiologies (ISRCTN17375500)</p>
        </sec>
        <sec>
          <title>Key Message</title>
          <p>Prophylactic risperidone did not reduce the incidence of delirium in ICU patients in this small study. As delirium is a heterogeneous syndrome, a single intervention may not be effective across subtypes and aetiologies.</p>
        </sec>
      </abstract>
      <kwd-group>
        <kwd>Intensive care</kwd>
        <kwd>Delirium</kwd>
        <kwd>antipsychotic</kwd>
        <kwd>risperidone</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec>
      <title>Introduction</title>
      <p>Delirium is common in intensive care unit (ICU) patients. In Indian ICUs, the prevalence of delirium is 31-68%.<xref ref-type="bibr" rid="ref-229701 ref-229702"><sup>1,2</sup></xref> It is associated with increased morbidity and mortality.<xref ref-type="bibr" rid="ref-229703"><sup>3</sup></xref> There is some evidence that prophylactic antipsychotic medications reduce the incidence of delirium in high-risk surgical trauma ICU patients.<xref ref-type="bibr" rid="ref-229704"><sup>4</sup></xref> This study examined the efficacy of risperidone in preventing delirium in patients admitted to a medical ICU.</p>
    </sec>
    <sec>
      <title>Methods</title>
      <sec>
        <title>Study design</title>
        <p>This study is a parallel arm, double-blind, placebo-controlled, randomised trial.</p>
      </sec>
      <sec>
        <title>Setting</title>
        <p>The study was conducted in a 24-bed medical ICU of a tertiary-care hospital.</p>
      </sec>
      <sec>
        <title>Participants</title>
        <p>Consecutive adult patients admitted to the ICU, who were expected to stay for at least two days, were screened for inclusion. Exclusion criteria were anticipated survival &lt;2 days, severe hemodynamic instability, drug overdose causing coma, prolonged QTc interval &gt;450 msec, neurodegenerative disorders, prior delirium, dementia, alcohol dependence, use of antipsychotic drugs, pregnancy or breastfeeding, difficulty in assessment (e.g., serious auditory or visual disorders) using the Confusion Assessment Method for the ICU (CAM-ICU), known allergy to risperidone, liver failure and renal failure.</p>
      </sec>
      <sec>
        <title>Randomisation</title>
        <p>Eligible patients were randomly assigned in blocks of 4 using a computer-generated randomisation sequence with a 1:1 allocation ratio to oral/naso-enteral risperidone 1-mg twice daily or identical oral placebo for the duration of ICU stay or until delirium developed.</p>
      </sec>
      <sec>
        <title>Blinding and allocation concealment</title>
        <p>The study drugs were prepared by a pharmacist according to the randomisation sequence and stored in sequentially labelled containers, thereby concealing allocation. Patients, healthcare providers and investigators were blinded to the treatment.</p>
      </sec>
      <sec>
        <title>Assessments</title>
        <p>CAM-ICU, the validated diagnostic tool for delirium assessment in the ICU,<xref ref-type="bibr" rid="ref-229705 ref-229706"><sup>5,6</sup></xref> was used in English or two local languages (Tamil, Hindi) as appropriate, by the primary investigator, to identify delirium. Patients were followed up for 28-days post-enrolment. The primary outcome was the incidence of delirium. Secondary outcomes included ventilator-free days (VFD),<xref ref-type="bibr" rid="ref-229707"><sup>7</sup></xref> duration of ICU and hospital stay, mortality and adverse events due to risperidone. Factors predisposing to delirium, such as electrolyte imbalance and infection, were screened for and treated.</p>
      </sec>
      <sec>
        <title>Sample size calculation</title>
        <p>For this study, assuming an incidence of delirium of 70% in the control arm<xref ref-type="bibr" rid="ref-229701"><sup>1</sup></xref> and a reduction in the incidence of delirium to 30% in the risperidone-treated arm, with 80% power and 95% confidence, a sample size of 46 was calculated. Continuous and categorical variables were compared between the treatment and control groups using mean (standard deviation, SD) or median (interquartile range, IQR) as appropriate. Student t-test and the Mann-Whitney U test were used for continuous variables. Categorical variables were analysed using frequencies and the chi-squared test. We used an intention-to-treat analysis. Statistical analysis was performed using SPSS version 16.0</p>
      </sec>
      <sec>
        <title>Ethical considerations</title>
        <p>The study was approved by the Institutional Review Board (IRB) and the institution’s ethics committee (IRB no.10226). We obtained written informed consent from the patient or the next of kin. This trial was registered at ISRCTN (ISRCTN17375500). The study was funded by an institutional research grant.</p>
      </sec>
    </sec>
    <sec>
      <title>Results</title>
      <p>During the study period from February 2017 to October 2018, of the 368 patients screened, 304 were excluded. An additional 19 patients did not consent to participate (<xref ref-type="fig" rid="attachment-173303">Figure 1</xref>). The mean (SD) age of the recruited patients (n=45) was 41.0 (17.3) years; 62% were men. Most were admitted due to an infection or poisoning; the APACHE-II score was 13.0 (5.8). Baseline characteristics were similar in both arms (<xref ref-type="table" rid="attachment-173304">Table 1</xref>).</p>
      <fig id="attachment-173303">
        <object-id pub-id-type="publisher-id">173303</object-id>
        <label>Figure 1.</label>
        <caption>
          <title>Details of recruitment into the trial, assessment and follow up</title>
        </caption>
        <graphic xlink:href="assets/delirium_2023_84092_173303.png"/>
      </fig>
      <table-wrap id="attachment-173304">
        <object-id pub-id-type="publisher-id">173304</object-id>
        <label>Table 1.</label>
        <caption>
          <title>Baseline Characteristics and Outcomes</title>
        </caption>
        <table>
          <thead>
            <tr>
              <th>
                <bold>Characteristic</bold>
              </th>
              <th>
                <bold>Overall</bold>
                <break/>
                <bold>(n=45)</bold>
              </th>
              <th>
                <bold>Risperidone</bold>
                <break/>
                <bold>(n=24)</bold>
              </th>
              <th>
                <bold>Control</bold>
                <break/>
                <bold>(n=21)</bold>
              </th>
              <th>
                <bold>P value</bold>
              </th>
            </tr>
          </thead>
          <tbody>
            <tr>
              <td>Age, mean (SD) years</td>
              <td>41.0 (17.3)</td>
              <td>40.9 (18.4)</td>
              <td>41.1 (16.5)</td>
              <td>0.97</td>
            </tr>
            <tr>
              <td>Gender, male, n (%)</td>
              <td>28 (62.2)</td>
              <td>15 (62.5)</td>
              <td>13 (61.9)</td>
              <td>0.97</td>
            </tr>
            <tr>
              <td>Admission APACHE-II, mean (SD)</td>
              <td>13.0 (5.8)</td>
              <td>11.8 (5.6)</td>
              <td>14.0 (5.9)</td>
              <td>0.27</td>
            </tr>
            <tr>
              <td>Admission SOFA score, mean (SD)</td>
              <td>5.0 (2.9)</td>
              <td>5.2 (3.0)</td>
              <td>4.7 (2.8)</td>
              <td>0.62</td>
            </tr>
            <tr>
              <td colspan="5">
                <bold>Primary Diagnosis</bold>
              </td>
            </tr>
            <tr>
              <td>Infection</td>
              <td>20 (44.4)</td>
              <td>11 (45.8)</td>
              <td>9 (42.9)</td>
              <td rowspan="6">0.84</td>
            </tr>
            <tr>
              <td>Poisoning/Toxin related disease</td>
              <td>17 (37.8)</td>
              <td>8 (33.3)</td>
              <td>9 (42.9)</td>
            </tr>
            <tr>
              <td>Autoimmune disease</td>
              <td>2 (4.4)</td>
              <td>1 (4.2)</td>
              <td>1 (4.8)</td>
            </tr>
            <tr>
              <td>Malignancy</td>
              <td>2 (4.4)</td>
              <td>2 (8.3)</td>
              <td>0 (0)</td>
            </tr>
            <tr>
              <td>Respiratory disease</td>
              <td>2 (4.4)</td>
              <td>1 (4.2)</td>
              <td>1 (4.8)</td>
            </tr>
            <tr>
              <td>Other</td>
              <td>2 (4.4)</td>
              <td>1 (4.2)</td>
              <td>1 (4.8)</td>
            </tr>
            <tr>
              <td colspan="5">
                <bold>Laboratory parameters at admission</bold>
              </td>
            </tr>
            <tr>
              <td>Urea (mg/dl), mean (SD)</td>
              <td>39.8 (24.9)</td>
              <td>40.1 (22.3)</td>
              <td>39.4 (28.4)</td>
              <td>0.92</td>
            </tr>
            <tr>
              <td>Albumin(g/dL), mean (SD)</td>
              <td>3.2 (0.9)</td>
              <td>3.0 (0.8)</td>
              <td>3.5 (0.9)</td>
              <td>0.07</td>
            </tr>
            <tr>
              <td>Sodium (mmol/L), mean (SD)</td>
              <td>134.9 (5.7)</td>
              <td>133.6 (4.5)</td>
              <td>136.3 (6.6)</td>
              <td>0.17</td>
            </tr>
            <tr>
              <td>Bicarbonate (mmol/L), mean (SD)</td>
              <td>16.3 (5.2)</td>
              <td>17.01 (6.0)</td>
              <td>15.5 (4.1)</td>
              <td>0.39</td>
            </tr>
            <tr>
              <td colspan="5">
                <bold>Treatment Details</bold>
              </td>
            </tr>
            <tr>
              <td>Non-invasive ventilation</td>
              <td>16 (35.6)</td>
              <td>8 (33.3)</td>
              <td>8(38.1)</td>
              <td>0.74</td>
            </tr>
            <tr>
              <td>Invasive Ventilation</td>
              <td>22 (48.9)</td>
              <td>12 (50)</td>
              <td>10 (47.6)</td>
              <td>0.87</td>
            </tr>
            <tr>
              <td>Shock requiring vasopressors</td>
              <td>19 (42.2)</td>
              <td>9 (37.5)</td>
              <td>10 (47.6)</td>
              <td>0.49</td>
            </tr>
            <tr>
              <td>Any Opioid use</td>
              <td>25 (56.8)</td>
              <td>13 (56.5)</td>
              <td>12 (57.1)</td>
              <td>0.97</td>
            </tr>
            <tr>
              <td>Any Benzodiazepine use</td>
              <td>28 (62.2)</td>
              <td>13 (54.2)</td>
              <td>15 (71.4)</td>
              <td>0.23</td>
            </tr>
            <tr>
              <td colspan="5">
                <bold>Outcomes</bold>
              </td>
            </tr>
            <tr>
              <td>Delirium</td>
              <td>22 (48.9)</td>
              <td>10 (41.7)</td>
              <td>12(57.1)</td>
              <td>0.30</td>
            </tr>
            <tr>
              <td>In-hospital mortality</td>
              <td>5 (11.1)</td>
              <td>3 (12.5)</td>
              <td>2 (9.5)</td>
              <td>0.75</td>
            </tr>
            <tr>
              <td>Day of onset of delirium, Median, IQR</td>
              <td>1 (1-2)</td>
              <td>1 (1-2.3)</td>
              <td>1(1-3)</td>
              <td>0.65</td>
            </tr>
            <tr>
              <td>ICU length of stay, Median, IQR</td>
              <td>5 (4-8)</td>
              <td>4.5 (3.3-8.5)</td>
              <td>5 (4-8)</td>
              <td>0.99</td>
            </tr>
            <tr>
              <td>Ventilator-free days, Median, IQR</td>
              <td>25 (20.5-27.3)</td>
              <td>25 (20.3-27)</td>
              <td>25 (18-28)</td>
              <td>0.93</td>
            </tr>
            <tr>
              <td>Hospital length of stay, Median, IQR</td>
              <td>11.5 (8-21.3)</td>
              <td>13 (8.5-17.5)</td>
              <td>11 (8-34)</td>
              <td>0.10</td>
            </tr>
            <tr>
              <td colspan="5">
                <bold>Safety Outcomes</bold>
              </td>
            </tr>
            <tr>
              <td>Any adverse effect†</td>
              <td>4 (8.9)</td>
              <td>1 (4.3)</td>
              <td>3 (14.3)</td>
              <td>0.25</td>
            </tr>
            <tr>
              <td>QTc Prolongation</td>
              <td>3 (6.7)</td>
              <td>1 (4.3)</td>
              <td>2 (9.5)</td>
              <td>0.50</td>
            </tr>
            <tr>
              <td>Neurological complications</td>
              <td>1 (2.2)</td>
              <td>0 (0)</td>
              <td>1 (4.8)</td>
              <td>0.29</td>
            </tr>
            <tr>
              <td>Other complications†</td>
              <td>9 (20.0)</td>
              <td>4 (17.4)</td>
              <td>5 (23.8)</td>
              <td>0.60</td>
            </tr>
          </tbody>
        </table>
        <table-wrap-foot>
          <p>APACHE – Acute Physiology and Chronic Health Evaluation; All values are number (n) and percentage (%) unless specified; SD (Standard Deviation); SOFA – Sequential Organ Failure Assessment score; IQR – Interquartile range; † includes nosocomial infections, bed sores, failed extubation attempts and acute kidney injury</p>
        </table-wrap-foot>
      </table-wrap>
      <p>The incidence of delirium was 49% (22/45). Of the 5 patients who died, 3 had documented delirium. The other two were intubated and too sedated to be assessed; they were considered to have developed delirium in the intention-to-treat analysis. The median time to onset of delirium was 1 day (IQR 1-2) from ICU admission, similar in both groups (p=0.65). The proportion of patients who developed delirium was lower in the risperidone group (42%) when compared with placebo (57%), though this was not statistically significant (p=0.3).</p>
      <p>Overall mortality was 11% and similar in both groups (<xref ref-type="table" rid="attachment-173304">Table 1</xref>). There was no significant difference between the two groups with respect to VFD (p=0.93) or length of ICU (p=0.99), or hospital stay (p=0.1). The medication was discontinued in four patients. One patient in the control group developed neurological symptoms; in three patients, the treating physicians requested withdrawal from the study due to the worsening clinical condition.</p>
    </sec>
    <sec>
      <title>Discussion</title>
      <p>Delirium is a significant problem in the ICU. In this study, 49% of patients developed delirium at a median time of 1 day (IQR 1-2 days) following ICU admission. Compared with placebo, risperidone did not reduce the incidence of delirium in patients admitted to the medical ICU.</p>
      <p>Previous small trials reported reduced delirium with antipsychotic prophylaxis in peri-operative and critically-ill surgical patients.<xref ref-type="bibr" rid="ref-229704 ref-229708"><sup>4,8</sup></xref> However, a large randomised trial of 1789 patients that compared two doses of haloperidol (1-mg, 2-mg) with placebo in a mixed cohort of medical, surgical and trauma patients showed that haloperidol did not prevent delirium.<xref ref-type="bibr" rid="ref-229709"><sup>9</sup></xref> A recent meta-analysis that examined the role of pharmacological prophylaxis for delirium in the ICU found insufficient evidence of benefit.<xref ref-type="bibr" rid="ref-229710"><sup>10</sup></xref> However, the review noted that multiple trials were ongoing and a definite recommendation could not be made. Current guidelines provide the option for short-term use of haloperidol and atypical antipsychotic medications, along with non-pharmacological measures for delirium treatment and prevention.<xref ref-type="bibr" rid="ref-229711"><sup>11</sup></xref></p>
      <p>The lack of a consistent effect of pharmacological prophylaxis on the incidence of delirium in the current and previous studies is likely due to several factors. The early onset of delirium in our study (1 day) and another study,<xref ref-type="bibr" rid="ref-229704"><sup>4</sup></xref> which reported a mean onset time of 1.4 days in the placebo arm, suggests insufficient time for the full efficacy of the drug. Likely, complex pathologies and multiple aetiologies of delirium and the heterogeneous nature of the disease makes it less likely for a single intervention to be effective across multiple aetiologies and subtypes of delirium (hypoactive, hyperactive). The study’s limitations were the small sample size and the exclusion of a large number of patients. Nevertheless, this study adds to the body of literature on the role of pharmacological prophylaxis for delirium in ICU patients.</p>
      <p>A review of delirium in India showed that the prevalence of ICU delirium is between 16.1 and 68.2%.<xref ref-type="bibr" rid="ref-229712"><sup>12</sup></xref> The majority of studies reported a hypoactive or a mixed delirium as the most common subtypes.<xref ref-type="bibr" rid="ref-229712"><sup>12</sup></xref> Multiple scales including the ICDSC, MAS and CAM-ICU have been validated in Indian ICUs for the diagnosis of delirium.<xref ref-type="bibr" rid="ref-229712"><sup>12</sup></xref> Patients with delirium were found to have longer ICU stays and a higher mortality rate.<xref ref-type="bibr" rid="ref-229712"><sup>12</sup></xref> Studies assessing ICU clinicians showed that most did not routinely screen for delirium and underestimated its prevalence in ICUs.<xref ref-type="bibr" rid="ref-229712"><sup>12</sup></xref> Although ICU staff were aware of some preventive practices such as early mobilization, many did not implement these for logistic reasons.<xref ref-type="bibr" rid="ref-229712"><sup>12</sup></xref> The only study assessing the treatment of delirium in ICU showed that melatonin reduced the duration of delirium in ICU patients with organophosphate poisoning.<xref ref-type="bibr" rid="ref-229712"><sup>12</sup></xref></p>
    </sec>
    <sec>
      <title>Conclusion</title>
      <p>Prophylactic use of risperidone did not reduce the incidence of delirium among patients admitted to the medical ICU. Further trials are required for a definitive recommendation.</p>
    </sec>
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