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<front>
<journal-meta>
<journal-id journal-id-type="publisher-id">Front. Med.</journal-id>
<journal-title>Frontiers in Medicine</journal-title>
<abbrev-journal-title abbrev-type="pubmed">Front. Med.</abbrev-journal-title>
<issn pub-type="epub">2296-858X</issn>
<publisher>
<publisher-name>Frontiers Media S.A.</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.3389/fmed.2025.1643181</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Medicine</subject>
<subj-group>
<subject>Original Research</subject>
</subj-group>
</subj-group>
</article-categories>
<title-group>
<article-title>The Clinical Frailty Scale and incidence of adverse outcomes in older patients with hip fractures in Qatar</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author" corresp="yes">
<name><surname>Syamala</surname> <given-names>Shirmila</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<xref ref-type="corresp" rid="c001"><sup>&#x002A;</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/3093607/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Tarazona-Santabalbina</surname> <given-names>Francisco Jos&#x00E9;</given-names></name>
<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Passarelli</surname> <given-names>Jorge Luis</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Sathian</surname> <given-names>Brijesh</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<uri xlink:href="https://loop.frontiersin.org/people/1004200/overview"/>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Nadukkandiyil</surname> <given-names>Navas</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
</contrib>
<contrib contrib-type="author">
<name><surname>Al Hamad</surname> <given-names>Hanadi</given-names></name>
<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/"/>
<role content-type="https://credit.niso.org/contributor-roles/supervision/"/>
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</contrib-group>
<aff id="aff1"><sup>1</sup><institution>Department of Geriatrics and Long-Term Care, Hamad Medical Corporation</institution>, <addr-line>Doha</addr-line>, <country>Qatar</country></aff>
<aff id="aff2"><sup>2</sup><institution>Geriatric Medicine Department, Hospital Universitario de la Ribera</institution>, <addr-line>Alzira</addr-line>, <country>Spain</country></aff>
<aff id="aff3"><sup>3</sup><institution>Medical School, Universitat Cat&#x00F2;lica de Val&#x00E8;ncia Sant Vicent M&#x00E0;rtir</institution>, <addr-line>Valencia</addr-line>, <country>Spain</country></aff>
<author-notes>
<fn fn-type="edited-by" id="fn0001">
<p>Edited by: Sawsan A. Zaitone, University of Tabuk, Saudi Arabia</p>
</fn>
<fn fn-type="edited-by" id="fn0002">
<p>Reviewed by: Dina Khodeer, Suez Canal University, Egypt</p>
<p>Suguru Yokoo, Fukuyama City Hospital, Japan</p>
</fn>
<corresp id="c001">&#x002A;Correspondence: Shirmila Syamala, <email>ssyamala@hamad.qa</email></corresp>
</author-notes>
<pub-date pub-type="epub">
<day>29</day>
<month>07</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="ecorrected">
<day>19</day>
<month>08</month>
<year>2025</year>
</pub-date>
<pub-date pub-type="collection">
<year>2025</year>
</pub-date>
<volume>12</volume>
<elocation-id>1643181</elocation-id>
<history>
<date date-type="received">
<day>08</day>
<month>06</month>
<year>2025</year>
</date>
<date date-type="accepted">
<day>09</day>
<month>07</month>
<year>2025</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2025 Syamala, Tarazona-Santabalbina, Passarelli, Sathian, Nadukkandiyil and Al Hamad.</copyright-statement>
<copyright-year>2025</copyright-year>
<copyright-holder>Syamala, Tarazona-Santabalbina, Passarelli, Sathian, Nadukkandiyil and Al Hamad</copyright-holder>
<license xlink:href="http://creativecommons.org/licenses/by/4.0/">
<p>This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.</p>
</license>
</permissions>
<abstract>
<sec id="sec1">
<title>Background</title>
<p>Studies conducted on Western populations have shown that the Clinical Frailty Scale (CFS) is a major predictor of adverse outcomes in older patients with hip fractures; however, there are no data on Middle Eastern populations, who may be culturally and ethnically different. We examined the association between the preoperative Clinical Frailty Scale and multiple adverse outcomes in a cohort of patients with hip fractures (aged 60&#x2013;96&#x202F;years) in Qatar.</p>
</sec>
<sec id="sec2">
<title>Methods</title>
<p>This prospective, single-center observational cohort study included 155 patients aged &#x2265; 60&#x202F;years with hip fractures from Qatar. These patients underwent a Clinical Frailty Scale assessment at baseline and were followed to evaluate four outcomes of interest: incident delirium, postoperative complications, all-cause mortality within a year, and increased length of stay (LoS) (LoS&#x202F;&#x2265;&#x202F;14&#x202F;days).</p>
</sec>
<sec id="sec3">
<title>Results</title>
<p>A total of 155 patients with hip fractures (average age 74.6&#x202F;years, 46.5% women) were included in the study. At baseline, 72.2% had a Clinical Frailty Scale score of &#x003C;5, 12.3% had a score of 5, and 15.5% had a score &#x003E; 5. Higher baseline scores on the Clinical Frailty Scale were strongly and positively associated with delirium, postoperative complications, and all-cause mortality, but there was no association with length of hospital stay. Compared to the patients with Clinical Frailty Scale scores &#x003C; 5, those with scores &#x003E; 5 had significantly higher multivariable risk ratios (RR) (with 95% confidence interval [CI]) for various outcomes. Specifically, the RR for delirium was 7.76 (3.17&#x2013;18.97), for postoperative complications, it was 3.59 (1.20&#x2013;10.77), for all-cause mortality, it was 6.39 (1.45&#x2013;28.20), and for length of stay &#x2265;14&#x202F;days, it was 1.43 (0.75&#x2013;2.73).</p>
</sec>
<sec id="sec4">
<title>Conclusion</title>
<p>The Clinical Frailty Scale was positively associated with delirium, postoperative complications, and all-cause mortality but not with length of hospital stay in patients with hip fractures from Qatar.</p>
</sec>
</abstract>
<kwd-group>
<kwd>frailty</kwd>
<kwd>Clinical Frailty Scale</kwd>
<kwd>delirium</kwd>
<kwd>mortality</kwd>
<kwd>Qatar</kwd>
<kwd>Middle East</kwd>
<kwd>hip fracture</kwd>
<kwd>length of stay</kwd>
</kwd-group>
<counts>
<fig-count count="1"/>
<table-count count="5"/>
<equation-count count="0"/>
<ref-count count="46"/>
<page-count count="8"/>
<word-count count="6325"/>
</counts>
<custom-meta-wrap>
<custom-meta>
<meta-name>section-at-acceptance</meta-name>
<meta-value>Geriatric Medicine</meta-value>
</custom-meta>
</custom-meta-wrap>
</article-meta>
</front>
<body>
<sec sec-type="intro" id="sec5">
<title>Introduction</title>
<p>Frailty is a well-recognized syndrome characterized by a decline in physiological and functional reserves in older adults, causing increased vulnerability to adverse health outcomes, even with minor stressors (<xref ref-type="bibr" rid="ref1">1</xref>). As the global population is aging and increasingly requires complex medical and surgical care, the importance of screening for and addressing frailty in medical and surgical patients assumes great significance.</p>
<p>Frailty assessment is recommended in several pre-operative risk assessment guidelines (<xref ref-type="bibr" rid="ref2">2</xref>), and various tools for the assessment of frailty have been utilized and show a strong correlation with outcomes (<xref ref-type="bibr" rid="ref3">3</xref>). The Clinical Frailty Scale (CFS), a nine-point global assessment tool for frailty based on clinical assessments, was developed from extensive Canadian studies on frailty (<xref ref-type="bibr" rid="ref4">4</xref>). The CFS is an accurate, reliable, and feasible instrument for preoperative frailty assessment (<xref ref-type="bibr" rid="ref3">3</xref>). It can be completed in an average of 45&#x202F;s after a preoperative clinical assessment and is logistically easy to perform (<xref ref-type="bibr" rid="ref5">5</xref>). However, despite the availability of effective and feasible frailty assessment tools, their incorporation in the preoperative evaluation of older patients remains suboptimal (<xref ref-type="bibr" rid="ref6">6</xref>, <xref ref-type="bibr" rid="ref7">7</xref>).</p>
<p>Hip fracture is an increasing public health challenge. According to the International Osteoporosis Foundation, there were 1.6 million patients with hip fractures globally in 2000, and this number is projected to increase up to 6.3 million by 2050 (<xref ref-type="bibr" rid="ref8">8</xref>, <xref ref-type="bibr" rid="ref9">9</xref>). The incidence rate of osteoporotic hip fractures in Qatar has been reported as 141.7 per 100,000 for the population aged 50&#x202F;years and older (<xref ref-type="bibr" rid="ref10">10</xref>). Preoperative frailty has been associated with poor outcomes after hip fracture (<xref ref-type="bibr" rid="ref11">11</xref>, <xref ref-type="bibr" rid="ref12">12</xref>). A higher Clinical Frailty Scale score has been found to be associated with adverse outcomes such as delirium, postoperative complications, mortality, and increased length of hospital stay in surgical patients (<xref ref-type="bibr" rid="ref3">3</xref>, <xref ref-type="bibr" rid="ref13">13</xref>, <xref ref-type="bibr" rid="ref14">14</xref>). However, the majority of these studies were conducted on Western populations. Despite an estimated pooled frailty prevalence of 35% among older adults in the Middle East (<xref ref-type="bibr" rid="ref15">15</xref>), no studies have examined the association between Clinical Frailty Scale scores and hip fracture outcomes in this region. In this context, we examined the association between the Clinical Frailty Scale and several adverse outcomes, including incident delirium during hospitalization, postoperative complications, all-cause mortality, and increased length of hospital stay, in a prospective sample of older adult patients with hip fractures from the largest healthcare facility in Qatar.</p>
</sec>
<sec sec-type="methods" id="sec6">
<title>Methods</title>
<p>This study was designed as a prospective, single-center observational cohort study. Consecutive inpatients aged &#x2265;60&#x202F;years who were residents of Qatar and admitted with neck of femur fractures between 2022 and 2024 at Hamad Medical Corporation&#x2014;the largest acute tertiary care academic public sector hospital in Qatar&#x2014;were included. Patients who refused to consent, were temporary visitors, had fractures resulting from high-impact trauma (e.g., traffic accidents), suffered from periprosthetic fractures, or were terminally ill were excluded. Informed consent was obtained from all patients (or their legally authorized representatives), and ethical approval for the study was obtained from the Hamad Medical Corporation Institutional Review Board (Reference number IRGC 05-JI-18-297; approved June 22, 2020).</p>
<p>Eligible patients were screened for inclusion in the study when they were admitted to the emergency department. Informed written consent was obtained to assess and follow up on patient outcomes, including electronic healthcare record reviews. Data collectors, including the study research assistant, pathway coordinator, and physical therapists, received training prior to the start of the study. Of the 252 patients with hip fractures screened during the study period, 42 were non-residents of Qatar on temporary visits, 45 refused to give consent, 2 had terminal illnesses, and 8 had high-impact trauma or periprosthetic fractures. A total of 155 patients with hip fractures who provided informed consent were included in the current study.</p>
<sec id="sec7">
<title>Measures</title>
<p>All patients were assessed using the Clinical Frailty Scale (CFS), which is scored from 1 to 9, with 1 indicating &#x2018;very fit&#x2019; and 9 indicating &#x2018;terminally ill&#x2019; (<xref ref-type="bibr" rid="ref4">4</xref>). Information was also collected on demographic variables, comorbidities, medications, length of stay (LoS), postoperative complications, and mortality up to 1&#x202F;year. All patients underwent a comprehensive geriatric assessment conducted by the orthogeriatric team. Demographic and clinical variables, including diagnoses of diabetes, chronic kidney disease, and polypharmacy, were collected from hospital records.</p>
<p>To account for pre-existing diseases and medical conditions present at the time of admission, the Charlson Comorbidity Index was calculated. Patients were classified based on the scores calculated using the weighted categories of the CCI. Myocardial infarction, peripheral vascular disease, congestive heart failure, cerebrovascular disease, dementia, chronic obstructive pulmonary disease, peptic ulcer disease, mild liver disease, and uncomplicated diabetes mellitus were each assigned a score of one. Diabetes mellitus with end-organ damage, severe chronic kidney disease (on dialysis, status post-kidney transplant), solid tumors without metastasis, leukemia, and lymphoma were each assigned a score of two points. Moderate and severe liver diseases were assigned a score of three. Solid tumors with metastasis and AIDS were each assigned a score of six (<xref ref-type="bibr" rid="ref16">16</xref>). Polypharmacy was defined as the use of five or more concurrent systemic medications (<xref ref-type="bibr" rid="ref17">17</xref>).</p>
<p>Delirium was defined as an acute disturbance in attention and cognition that cannot be better explained by a pre-existing neurocognitive disorder, according to the DSM-V criteria. Screening for delirium was performed by the study team using the validated 4 AT score (<xref ref-type="bibr" rid="ref18">18</xref>) and confirmed clinically by the team geriatrician. Our outcome measure was the new onset of delirium during hospitalization among study participants who were delirium-free at baseline.</p>
<p>The research team monitored the patients during their inpatient stay for postoperative complications. Post-operative complications included chest infection, surgical site infection, deep vein thrombosis and/or pulmonary embolism, bleeding, renal insufficiency, and pressure ulcers. Electronic medical records and death records were reviewed to identify mortality data for up to 1&#x202F;year. An increased length of stay (LoS) was defined as a hospital stay of &#x2265;14&#x202F;days.</p>
</sec>
<sec id="sec8">
<title>Statistical analysis</title>
<p>We reported continuous data as means and standard deviations (SDs) and categorical data as counts with relative frequencies. A chi-squared test was performed to compare categorical variables between the groups. We categorized the CFS scores at baseline into three groups based on clinical relevance and available sample size: &#x003C;5 (no frailty or vulnerable), 5 (mild frailty), and &#x003E;5 (moderate, severe, or very severe frailty) (<xref ref-type="bibr" rid="ref4">4</xref>). We also examined the Clinical Frailty Scale as a continuous variable. We calculated risk ratios (RRs) and 95% confidence intervals (CIs) for the association between Clinical Frailty Scale categories and our four outcomes of interest (incident delirium, in-hospital postoperative complications, all-cause mortality, and length of hospital stay &#x2265;14&#x202F;days), employing log-binomial regression models (<xref ref-type="bibr" rid="ref19">19</xref>, <xref ref-type="bibr" rid="ref20">20</xref>) due to the short and relatively uniform duration of follow-up. We used an age-and sex-adjusted model and a multivariable-adjusted regression model, adjusting for age (years), sex (male, female), diabetes mellitus (yes, no), chronic kidney disease (yes, no), serum hemoglobin levels (mg/dL), polypharmacy (yes, no), and the Charlson Comorbidity Index (score). All analyses were conducted using R version 4.0.2.</p>
</sec>
</sec>
<sec sec-type="results" id="sec9">
<title>Results</title>
<p><xref ref-type="table" rid="tab1">Table 1</xref> shows the baseline characteristics of the elderly study population. A total of 155 patients with hip fractures were included in our study, with an average age of 74.6&#x202F;years (ranging between 60 and 96&#x202F;years). Of these, 28.4% were aged 60&#x2013;69&#x202F;years, 44.5% were 70&#x2013;79&#x202F;years, and 27.1% were 80&#x202F;years or older; 53.5% of the participants were men. At baseline, 69.7% had a clinical diagnosis of diabetes mellitus, 27.1% had chronic kidney disease, and 77.4% were on polypharmacy. The mean serum hemoglobin level was 11.8&#x202F;mg/dL, and the mean Charlson Comorbidity Index score was 4.6. Regarding the Clinical Frailty Scale score distribution at baseline, 72.2% had a score of &#x003C;5, 12.3% had a score of 5, and 15.5% had a score of &#x003E;5.</p>
<table-wrap position="float" id="tab1">
<label>Table 1</label>
<caption>
<p>Characteristics of the study population.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Baseline characteristics</th>
<th align="center" valign="top">Number</th>
<th align="center" valign="top">Mean (SD) or %</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">Age, years</td>
<td align="center" valign="top">155</td>
<td align="center" valign="top">74.6 (7.6)</td>
</tr>
<tr>
<td align="left" valign="top">Age groups, %</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">60&#x2013;69&#x202F;years</td>
<td align="center" valign="top">44</td>
<td align="center" valign="top">28.4%</td>
</tr>
<tr>
<td align="left" valign="top">70&#x2013;79&#x202F;years</td>
<td align="center" valign="top">69</td>
<td align="center" valign="top">44.5%</td>
</tr>
<tr>
<td align="left" valign="top">&#x2265;80&#x202F;years</td>
<td align="center" valign="top">42</td>
<td align="center" valign="top">27.1%</td>
</tr>
<tr>
<td align="left" valign="top">Sex, %</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Male</td>
<td align="center" valign="top">83</td>
<td align="center" valign="top">53.5%</td>
</tr>
<tr>
<td align="left" valign="top">Female</td>
<td align="center" valign="top">72</td>
<td align="center" valign="top">46.5%</td>
</tr>
<tr>
<td align="left" valign="top">Diabetes mellitus, %</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Yes</td>
<td align="center" valign="top">108</td>
<td align="center" valign="top">69.7%</td>
</tr>
<tr>
<td align="left" valign="top">No</td>
<td align="center" valign="top">47</td>
<td align="center" valign="top">30.3%</td>
</tr>
<tr>
<td align="left" valign="top">Chronic kidney disease, %</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Yes</td>
<td align="center" valign="top">42</td>
<td align="center" valign="top">27.1%</td>
</tr>
<tr>
<td align="left" valign="top">No</td>
<td align="center" valign="top">113</td>
<td align="center" valign="top">72.9%</td>
</tr>
<tr>
<td align="left" valign="top">Serum hemoglobin, mg/dL</td>
<td align="center" valign="top">155</td>
<td align="center" valign="top">11.8 (1.9)</td>
</tr>
<tr>
<td align="left" valign="top">Polypharmacy, %</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Yes</td>
<td align="center" valign="top">120</td>
<td align="center" valign="top">77.4%</td>
</tr>
<tr>
<td align="left" valign="top">No</td>
<td align="center" valign="top">35</td>
<td align="center" valign="top">22.6%</td>
</tr>
<tr>
<td align="left" valign="top">Charlson Comorbidity Index, score</td>
<td align="center" valign="top">155</td>
<td align="center" valign="top">4.6 (1.6)</td>
</tr>
<tr>
<td align="left" valign="top">Clinical frailty scale categories, %</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">&#x003C;5</td>
<td align="center" valign="top">112</td>
<td align="center" valign="top">72.2%</td>
</tr>
<tr>
<td align="left" valign="top">5</td>
<td align="center" valign="top">19</td>
<td align="center" valign="top">12.3%</td>
</tr>
<tr>
<td align="left" valign="top">&#x003E;5</td>
<td align="center" valign="top">24</td>
<td align="center" valign="top">15.5%</td>
</tr>
</tbody>
</table>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Incidence of adverse outcomes</th>
<th align="center" valign="top">Number</th>
<th align="center" valign="top">%</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">Delirium, %</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Yes</td>
<td align="center" valign="top">26</td>
<td align="center" valign="top">16.8%</td>
</tr>
<tr>
<td align="left" valign="top">No</td>
<td align="center" valign="top">129</td>
<td align="center" valign="top">83.2%</td>
</tr>
<tr>
<td align="left" valign="top">In-hospital postoperative complications, %<sup>&#x002A;</sup></td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Yes</td>
<td align="center" valign="top">17</td>
<td align="center" valign="top">11.3%</td>
</tr>
<tr>
<td align="left" valign="top">No</td>
<td align="center" valign="top">133</td>
<td align="center" valign="top">88.7%</td>
</tr>
<tr>
<td align="left" valign="top">All-cause deaths, %</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Yes</td>
<td align="center" valign="top">9</td>
<td align="center" valign="top">5.8%</td>
</tr>
<tr>
<td align="left" valign="top">No</td>
<td align="center" valign="top">146</td>
<td align="center" valign="top">94.2%</td>
</tr>
<tr>
<td align="left" valign="top">Length of stay &#x2265;14&#x202F;days, %</td>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">Yes</td>
<td align="center" valign="top">46</td>
<td align="center" valign="top">30%</td>
</tr>
<tr>
<td align="left" valign="top">No</td>
<td align="center" valign="top">109</td>
<td align="center" valign="top">70%</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p><sup>&#x002A;</sup>Analysis confined to <italic>n</italic>&#x202F;=&#x202F;150 out of the 155 patients who underwent hip fracture surgery.</p>
</table-wrap-foot>
</table-wrap>
<p><xref ref-type="table" rid="tab1">Table 1</xref> also shows the four outcomes of interest: incident delirium during hospital stay occurred in 16.8% of the patients; in-hospital postoperative complications occurred in 11.3%; all-cause mortality occurred in 5.8% during the follow-up period of up to 1&#x202F;year; and the length of hospital stay was &#x2265;14&#x202F;days in 30% of patients. The length of hospital stay in this study ranged from 3 to 163&#x202F;days, with a median value of 9&#x202F;days. The cutoff of &#x2265;14&#x202F;days to define a prolonged hospital stay was determined by dividing the length of stay variable into tertiles and selecting the highest third as the outcome.</p>
<p><xref ref-type="fig" rid="fig1">Figure 1</xref> shows the incidence of outcomes of interest by categories of the Clinical Frailty Scale at baseline divided into three groups: &#x003C;5, 5, and &#x003E;5. In separate analysis for each outcome, there was a clear pattern of statistically significantly higher incidence of delirium (<italic>p&#x202F;&#x003C;</italic> 0.0001), in-hospital postoperative complications (<italic>p</italic>&#x202F;=&#x202F;0.003), and all-cause mortality (<italic>p</italic>&#x202F;=&#x202F;0.02) with increasing CFS groups. For example, compared to the participants with a Clinical Frailty Scale score &#x003C; 5 (incidence&#x202F;=&#x202F;5.4%), the incidence of delirium was almost 4 times higher in those with a Clinical Frailty Scale score of 5 (incidence&#x202F;=&#x202F;21.1%) and more than 12 times higher in those with a Clinical Frailty Scale score of &#x003E;5 (incidence&#x202F;=&#x202F;66.7%). A similar pattern was observed in the analyses of postoperative complications (e.g., incidence of 6.3% vs. 29.2% comparing Clinical Frailty Scale categories &#x003C;5 vs. &#x003E;5) and all-cause mortality (incidence of 2.7% vs. 16.7% comparing Clinical Frailty Scale categories &#x003C;5 vs. &#x003E;5) as outcomes (see <xref ref-type="fig" rid="fig1">Figure 1</xref>).</p>
<fig position="float" id="fig1">
<label>Figure 1</label>
<caption>
<p>Clinical Frailty Scale and adverse outcomes among the older patients with hip fractures in Qatar.</p>
</caption>
<graphic xlink:href="fmed-12-1643181-g001.tif">
<alt-text content-type="machine-generated">Bar charts compare elderly hip fracture patients in Qatar across Clinical Frailty Scale categories. Delirium rates are 5.4% (&#x003C;5), 21.1% (5), 66.7% (&#x003E;5). Postoperative complications: 6.4% (&#x003C;5), 16.7% (5), 30.4% (&#x003E;5). One year mortality: 2.7% (&#x003C;5), 10.5% (5), 16.7% (&#x003E;5). Length of stay &#x2265;14 days: 27.7% (&#x003C;5), 31.6% (5), 37.5% (&#x003E;5).</alt-text>
</graphic>
</fig>
<p>However, as shown in <xref ref-type="fig" rid="fig1">Figure 1</xref>, there was no significant association between increasing Clinical Frailty Scale categories and longer hospital stay, which was defined as length of hospital stay &#x2265;14&#x202F;days (<italic>p</italic>&#x202F;=&#x202F;0.62). In a supplementary analysis (data not presented in tables), first, we examined the mean length of stay by the Clinical Frailty Scale categories (&#x003C;5, 5, and &#x003E;5); the mean length of stay for these respective categories was 12.1&#x202F;days, 19.7&#x202F;days, and 17.9&#x202F;days, and there was no statistically significant difference (<italic>p</italic>&#x202F;=&#x202F;0.1367). Second, when we examined both length of stay (dependent variable) and the Clinical Frailty Scale score (independent variable) as continuous variables in a multivariable linear regression model, the association remained statistically non-significant (beta coefficient for Clinical Frailty Scale&#x202F;=&#x202F;0.009; <italic>p</italic>&#x202F;=&#x202F;0.7).</p>
<p><xref ref-type="table" rid="tab2">Tables 2</xref>&#x2013;<xref ref-type="table" rid="tab5">5</xref> show the association between baseline Clinical Frailty Scale categories and incident delirium (<xref ref-type="table" rid="tab2">Table 2</xref>), in-hospital postoperative complications (<xref ref-type="table" rid="tab3">Table 3</xref>), all-cause mortality (<xref ref-type="table" rid="tab4">Table 4</xref>), and length of stay &#x2265;14&#x202F;days (<xref ref-type="table" rid="tab5">Table 5</xref>). For all outcomes, we examined the Clinical Frailty Scale at baseline as a 3-level variable (&#x003C;5, 5, and &#x003E;5) and a binary variable defined as the presence of clinical frailty at baseline (&#x003C;5, &#x2265;5). In the age-and sex-adjusted models and the multivariable-adjusted model, we found that higher baseline Clinical Frailty Scale categories and the binary clinical frailty variable were strongly and positively associated with delirium (<xref ref-type="table" rid="tab2">Table 2</xref>), postoperative complications (<xref ref-type="table" rid="tab3">Table 3</xref>), and all-cause mortality (<xref ref-type="table" rid="tab4">Table 4</xref>). The overall pattern and direction of association for these outcomes were consistent and statistically significant. In contrast, there was no significant association between the baseline Clinical Frailty Scale categories or the binary clinical frailty variable and prolonged hospital stay, defined as length of stay &#x2265;14&#x202F;days (<xref ref-type="table" rid="tab5">Table 5</xref>).</p>
<table-wrap position="float" id="tab2">
<label>Table 2</label>
<caption>
<p>Clinical Frailty Scale categories and incidence of delirium in the older patients with hip fractures.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Clinical Frailty Scale (CFS)</th>
<th align="center" valign="top">No. of participants (no. of delirium cases)</th>
<th align="center" valign="top">Percentage (%)</th>
<th align="center" valign="top">Age-and sex-adjusted risk ratio (95% confidence interval) of incident delirium</th>
<th align="center" valign="top">Multivariable-adjusted risk ratio (95% confidence interval) of incident delirium&#x2020;</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">CFS categories<sup>&#x002A;</sup></td>
<td/>
<td/>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">&#x003C;5</td>
<td align="center" valign="top">112 (6)</td>
<td align="center" valign="top">5.4%</td>
<td align="center" valign="top">1 (Referent)</td>
<td align="center" valign="top">1 (Referent)</td>
</tr>
<tr>
<td align="left" valign="top">5</td>
<td align="center" valign="top">19 (4)</td>
<td align="center" valign="top">21.1%</td>
<td align="center" valign="top">3.53 (1.17&#x2013;10.67)</td>
<td align="center" valign="top">3.45 (1.25&#x2013;9.58)</td>
</tr>
<tr>
<td align="left" valign="top">&#x003E;5</td>
<td align="center" valign="top">24 (16)</td>
<td align="center" valign="top">66.7%</td>
<td align="center" valign="top">10.15 (4.22&#x2013;24.40)</td>
<td align="center" valign="top">7.76 (3.17&#x2013;18.97)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic>-trend</td>
<td/>
<td/>
<td align="center" valign="top">&#x003C;0.0001</td>
<td align="center" valign="top">&#x003C;0.0001</td>
</tr>
<tr>
<td align="left" valign="top">CFS continuous variable<sup>&#x002A;</sup></td>
<td align="center" valign="top">155 (26)</td>
<td align="center" valign="top">16.8%</td>
<td align="center" valign="top">2.19 (1.66&#x2013;2.88)</td>
<td align="center" valign="top">1.98 (1.48&#x2013;2.64)</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p><sup>&#x002A;</sup>Clinical Frailty Scale based on Rockwood et al. (<xref ref-type="bibr" rid="ref4">4</xref>). <sup>&#x2020;</sup>Multivariable log-binomial regression model adjusted for age (years), sex (male, female), diabetes mellitus (yes, no), chronic kidney disease (yes, no), serum hemoglobin levels (mg/dL), polypharmacy (yes, no), and the Charlson Comorbidity Index (score).</p>
</table-wrap-foot>
</table-wrap>
<table-wrap position="float" id="tab3">
<label>Table 3</label>
<caption>
<p>Clinical Frailty Scale categories and incidence of postoperative complications in older patients with hip fractures.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Clinical Frailty Scale (CFS)</th>
<th align="center" valign="top">No. of participants (no of postoperative complication cases)</th>
<th align="center" valign="top">Percentage (%)</th>
<th align="center" valign="top">Age-and sex-adjusted risk ratio (95% confidence interval) of in-hospital postoperative complications</th>
<th align="center" valign="top">Multivariable-adjusted risk ratio (95% confidence interval) of in-hospital postoperative complications&#x2020;</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">CFS categories<sup>&#x002A;</sup></td>
<td/>
<td/>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">&#x003C;5</td>
<td align="center" valign="top">109 (7)</td>
<td align="center" valign="top">6.4%</td>
<td align="center" valign="top">1 (Referent)</td>
<td align="center" valign="top">1 (Referent)</td>
</tr>
<tr>
<td align="left" valign="top">5</td>
<td align="center" valign="top">18 (3)</td>
<td align="center" valign="top">16.7%</td>
<td align="center" valign="top">2.25 (0.69&#x2013;7.34)</td>
<td align="center" valign="top">2.34 (0.69&#x2013;7.90)</td>
</tr>
<tr>
<td align="left" valign="top">&#x003E;5</td>
<td align="center" valign="top">23 (7)</td>
<td align="center" valign="top">30.4%</td>
<td align="center" valign="top">3.40 (1.21&#x2013;9.60)</td>
<td align="center" valign="top">3.59 (1.20&#x2013;10.77)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic>-trend</td>
<td/>
<td/>
<td align="center" valign="top">0.02</td>
<td align="center" valign="top">0.02</td>
</tr>
<tr>
<td align="left" valign="top">CFS continuous variable<sup>&#x002A;</sup></td>
<td align="center" valign="top">150 (17)</td>
<td align="center" valign="top">11.3%</td>
<td align="center" valign="top">1.40 (1.02&#x2013;1.94)</td>
<td align="center" valign="top">1.42 (1.01&#x2013;2.00)</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p><sup>&#x002A;</sup>Clinical Frailty Scale based on Rockwood et al. (<xref ref-type="bibr" rid="ref4">4</xref>). <sup>&#x2020;</sup>Multivariable log-binomial regression model adjusted for age (years), sex (male, female), diabetes mellitus (yes, no), chronic kidney disease (yes, no), serum hemoglobin levels (mg/dL), polypharmacy (yes, no), and the Charlson Comorbidity Index (score).</p>
</table-wrap-foot>
</table-wrap>
<table-wrap position="float" id="tab4">
<label>Table 4</label>
<caption>
<p>Clinical Frailty Scale categories and all-cause mortality up to 1-year follow-up in older patients with hip fractures.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Clinical Frailty Scale</th>
<th align="center" valign="top">No. of participants (no. of deaths)</th>
<th align="center" valign="top">Percentage (%)</th>
<th align="center" valign="top">Age-and sex-adjusted risk ratio (95% confidence interval) of all-cause mortality</th>
<th align="center" valign="top">Multivariable-adjusted risk ratio (95% confidence interval) of all-cause mortality&#x2020;</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">CFS categories<sup>&#x002A;</sup></td>
<td/>
<td/>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">&#x003C;5</td>
<td align="center" valign="top">112 (3)</td>
<td align="center" valign="top">2.7%</td>
<td align="center" valign="top">1 (Referent)</td>
<td align="center" valign="top">1 (Referent)</td>
</tr>
<tr>
<td align="left" valign="top">5</td>
<td align="center" valign="top">19 (2)</td>
<td align="center" valign="top">10.5%</td>
<td align="center" valign="top">2.64 (0.45&#x2013;15.43)</td>
<td align="center" valign="top">3.06 (0.54&#x2013;17.51)</td>
</tr>
<tr>
<td align="left" valign="top">&#x003E;5</td>
<td align="center" valign="top">24 (4)</td>
<td align="center" valign="top">16.7%</td>
<td align="center" valign="top">6.01 (1.44&#x2013;25.03)</td>
<td align="center" valign="top">6.39 (1.45&#x2013;28.20)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic>-trend</td>
<td/>
<td/>
<td align="center" valign="top">0.01</td>
<td align="center" valign="top">0.01</td>
</tr>
<tr>
<td align="left" valign="top">CFS continuous variable<sup>&#x002A;</sup></td>
<td align="center" valign="top">155 (9)</td>
<td align="center" valign="top">5.8%</td>
<td align="center" valign="top">1.77 (1.03&#x2013;3.03)</td>
<td align="center" valign="top">1.83 (1.07&#x2013;3.13)</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p><sup>&#x002A;</sup>Clinical Frailty Scale based on Rockwood et al. (<xref ref-type="bibr" rid="ref4">4</xref>). <sup>&#x2020;</sup>Multivariable log-binomial regression model adjusted for age (years), sex (male, female), diabetes mellitus (yes, no), chronic kidney disease (yes, no), serum hemoglobin levels (mg/dL), polypharmacy (yes, no), and the Charlson Comorbidity Index (score).</p>
</table-wrap-foot>
</table-wrap>
<table-wrap position="float" id="tab5">
<label>Table 5</label>
<caption>
<p>Clinical Frailty Scale categories and length of stay &#x2265; 14&#x202F;days in the older patients with hip fractures.</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th align="left" valign="top">Clinical Frailty Scale (CFS)</th>
<th align="center" valign="top">No. of participants (length of stay &#x2265; 14&#x202F;days)</th>
<th align="center" valign="top">Percentage (%)</th>
<th align="center" valign="top">Age-and sex-adjusted risk ratio (95% confidence interval) of length of stay &#x2265; 14&#x202F;days</th>
<th align="center" valign="top">Multivariable-adjusted risk ratio (95% confidence interval) of length of stay &#x2265; 14&#x202F;days&#x2020;</th>
</tr>
</thead>
<tbody>
<tr>
<td align="left" valign="top">CFS categories<sup>&#x002A;</sup></td>
<td/>
<td/>
<td/>
<td/>
</tr>
<tr>
<td align="left" valign="top">&#x003C;5</td>
<td align="center" valign="top">112 (31)</td>
<td align="center" valign="top">27.7%</td>
<td align="center" valign="top">1 (Referent)</td>
<td align="center" valign="top">1 (Referent)</td>
</tr>
<tr>
<td align="left" valign="top">5</td>
<td align="center" valign="top">19 (6)</td>
<td align="center" valign="top">31.6%</td>
<td align="center" valign="top">1.02 (0.49&#x2013;2.12)</td>
<td align="center" valign="top">1.13 (0.51&#x2013;2.50)</td>
</tr>
<tr>
<td align="left" valign="top">&#x003E;5</td>
<td align="center" valign="top">24 (9)</td>
<td align="center" valign="top">37.5%</td>
<td align="center" valign="top">1.28 (0.69&#x2013;2.37)</td>
<td align="center" valign="top">1.43 (0.75&#x2013;2.73)</td>
</tr>
<tr>
<td align="left" valign="top"><italic>P</italic>-trend</td>
<td/>
<td/>
<td align="center" valign="top">0.47</td>
<td align="center" valign="top">0.32</td>
</tr>
<tr>
<td align="left" valign="top">CFS continuous variable<sup>&#x002A;</sup></td>
<td align="center" valign="top">155 (46)</td>
<td align="center" valign="top">29.7%</td>
<td align="center" valign="top">1.02 (0.83&#x2013;1.24)</td>
<td align="center" valign="top">1.04 (0.84&#x2013;1.29)</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<p><sup>&#x002A;</sup>Clinical Frailty Scale based on Rockwood et al. (<xref ref-type="bibr" rid="ref4">4</xref>). <sup>&#x2020;</sup>Multivariable log-binomial regression model adjusted for age (years), sex (male, female), diabetes mellitus (yes, no), chronic kidney disease (yes, no), serum hemoglobin levels (mg/dL), polypharmacy (yes, no), and the Charlson Comorbidity Index (score).</p>
</table-wrap-foot>
</table-wrap>
<p>In a second supplementary analysis (data not presented in tables) to study the relation between Clinical Frailty Scale categories and age, we performed a cross-tabulation of age categories (&#x003C;80&#x202F;years, &#x2265;80&#x202F;years) by Clinical Frailty Scale groups (&#x003C;5, 5, &#x003E;5). There was a statistically significant association between increasing Clinical Frailty Scale categories and older age. The percentage of participants aged &#x2265;80&#x202F;years was 20.5% among those with a score of &#x003C;5, 42.1% among those with a score of 5, and 45.8% among those with a score of &#x003E;5 (<italic>p</italic>&#x202F;=&#x202F;0.01).</p>
</sec>
<sec sec-type="discussion" id="sec10">
<title>Discussion</title>
<p>In this prospective cohort study of patients aged 60&#x202F;years and older with hip fractures from Qatar, the Clinical Frailty Scale score at admission was positively associated with incident delirium, postoperative complications, and all-cause mortality, but it did not show an association with length of stay. Our results contribute to the existing literature on frailty and adverse outcomes by providing one of the few data sets on this topic from the Middle East. Our findings are largely consistent with reports from across the world (<xref ref-type="bibr" rid="ref3">3</xref>, <xref ref-type="bibr" rid="ref11">11</xref>, <xref ref-type="bibr" rid="ref12">12</xref>, <xref ref-type="bibr" rid="ref21 ref22 ref23 ref24 ref25">21&#x2013;25</xref>).</p>
<p>Frailty has been consistently associated with delirium in post-surgical and hip fracture patients in several studies (<xref ref-type="bibr" rid="ref3">3</xref>, <xref ref-type="bibr" rid="ref5">5</xref>). In a systematic review of eight studies (n&#x202F;=&#x202F;5,541, mean age 77.8), a 2.2-fold increased risk of delirium in persons with frailty was noted (<xref ref-type="bibr" rid="ref24">24</xref>). Our results showed a similar association between higher Clinical Frailty Scale scores and delirium in patients with hip fractures. Frailty has been shown to be a state of low-grade inflammation, and the concept of &#x201C;inflammaging&#x201D; has been proposed (<xref ref-type="bibr" rid="ref26">26</xref>), with inflammatory biomarkers such as IL-10, soluble TNF-<italic>&#x03B1;</italic> receptors, and ICAM-1 suggested as frailty markers (<xref ref-type="bibr" rid="ref27">27</xref>). Neuroinflammation and cerebral metabolic insufficiency are the likely mechanisms underlying the pathophysiology of delirium in the context of frailty (<xref ref-type="bibr" rid="ref23">23</xref>). Fracture and surgery can trigger an increase in systemic inflammatory mediators (<xref ref-type="bibr" rid="ref28">28</xref>, <xref ref-type="bibr" rid="ref29">29</xref>), which are transported to the brain across the blood&#x2013;brain barrier and through the transporters in the afferent nerves of the vagus nerve. Increased central inflammatory mediators can cause cerebral dysfunction through the suppression of hippocampal plasticity and neurogenesis, neurotoxicity, and neuronal apoptosis, all of which are implicated in the development of delirium (<xref ref-type="bibr" rid="ref30 ref31 ref32">30&#x2013;32</xref>). In addition, metabolic abnormalities such as alterations in the levels of glycolysis products, low serum lipid metabolic phosphatidylinositol, and increased serum neuropeptide galanin levels may predispose individuals with frailty to delirium, and the latter could be a potential biomarker for predicting postoperative delirium (<xref ref-type="bibr" rid="ref23">23</xref>).</p>
<p>An association between frailty and mortality after surgical procedures has been well established (<xref ref-type="bibr" rid="ref3">3</xref>, <xref ref-type="bibr" rid="ref13">13</xref>, <xref ref-type="bibr" rid="ref21">21</xref>, <xref ref-type="bibr" rid="ref33">33</xref>). Furthermore, studies have shown an increased risk of both short-term and long-term mortality in older patients with pre-existing frailty presenting with hip fractures (<xref ref-type="bibr" rid="ref11">11</xref>, <xref ref-type="bibr" rid="ref22">22</xref>). Forssten et al. (<xref ref-type="bibr" rid="ref11">11</xref>), in a Swedish nationwide retrospective study, reported a 4 times higher risk of mortality in patients with frail hip fractures. Narula et al. (<xref ref-type="bibr" rid="ref25">25</xref>) reported on the predictive value of the Clinical Frailty Scale for mortality outcomes following proximal femur fractures. Alterations in innate and adaptive immunity with increased susceptibility to infections, impaired nutritional status, a heightened inflammatory response, and prolonged sympathetic activation with stressors such as fracture and surgery could be the possible mechanisms leading to multiple organ dysfunction and mortality in frail older adults (<xref ref-type="bibr" rid="ref34 ref35 ref36 ref37">34&#x2013;37</xref>).</p>
<p>A wealth of evidence suggests an association between frailty and adverse postoperative complications (<xref ref-type="bibr" rid="ref3">3</xref>, <xref ref-type="bibr" rid="ref5">5</xref>, <xref ref-type="bibr" rid="ref25">25</xref>). In a study from the US, Kistler et al. (<xref ref-type="bibr" rid="ref12">12</xref>) reported higher rates of postoperative complications and prolonged length of stay for patients with hip fractures using a modified frailty index. Frailty is hypothesized to be due to dysregulated stress response systems, including immune, endocrine, and energy response systems (<xref ref-type="bibr" rid="ref38">38</xref>). Traditionally, preoperative risk assessments focused mainly on cardiovascular, anesthesia, and surgical risks; current guidelines recommend including frailty assessment for older individuals (<xref ref-type="bibr" rid="ref2">2</xref>, <xref ref-type="bibr" rid="ref39">39</xref>). While the opportunity exists for prehabilitation to address frailty in elective surgeries, in geriatric patients with hip fractures, the healthcare team should focus on immediate perioperative risk intervention strategies based on orthogeriatric comprehensive care (<xref ref-type="bibr" rid="ref23">23</xref>) and multi-component care bundles (<xref ref-type="bibr" rid="ref40">40</xref>) to prevent postoperative delirium and other adverse outcomes.</p>
<p>Studies have shown both positive (<xref ref-type="bibr" rid="ref13">13</xref>, <xref ref-type="bibr" rid="ref41">41</xref>) and negative (<xref ref-type="bibr" rid="ref42">42</xref>) associations between frailty and length of stay. Vainqueur et al. (<xref ref-type="bibr" rid="ref42">42</xref>) reported that in a retrospective cohort of 158 patients, frailty did not show a significant association with length of stay. Similarly, frailty did not show a significant association with length of stay in our group of Middle Eastern patients either, possibly because of early discharge to rehabilitation or other local cultural or sociodemographic factors affecting length of stay.</p>
<p>Our study is a confirmatory study in a new setting (i.e., Middle Eastern population) examining the association between frailty and adverse outcomes in patients with hip fractures. In this group of patients aged 60&#x202F;years and above presenting with hip fractures, 27.9% were assessed to have frailty at admission&#x2014;12.3% were assessed to be living with mild frailty (CFS of 5) and 15.6% with moderate to severe frailty (CFS 6 and above), based on the Clinical Frailty Scale. This is slightly lower than the prevalence of frailty reported in other studies in patients with hip fractures, which ranged between 41 and 53% (<xref ref-type="bibr" rid="ref11">11</xref>, <xref ref-type="bibr" rid="ref33">33</xref>, <xref ref-type="bibr" rid="ref43">43</xref>). This could be attributed to the different frailty assessment tools used and the relatively younger age of our study population, as our cutoff age was 60&#x202F;years and above. Even so, our data further validate and extend the evidence supporting the importance of frailty screening using the Clinical Frailty Scale in this vulnerable population from the Middle Eastern region.</p>
<p>This study has some limitations. First, we would like to acknowledge that our findings may be prone to a certain degree of selection bias due to the exclusion of certain individuals&#x2014;specifically, 21.7% of eligible individuals who refused consent&#x2014;which may have potentially resulted in an overestimation of the findings. Second, the sample size, while reasonable, was underpowered for some outcomes (e.g., only nine deaths), leading to wide confidence intervals, limiting the robustness of the findings&#x2014;particularly for the mortality analysis (<xref ref-type="bibr" rid="ref44">44</xref>). However, the overall pattern and positive direction of the association remained consistent even after adjusting for confounders. Furthermore, a similar strong association between frailty and delirium has been reported in other studies (<xref ref-type="bibr" rid="ref45">45</xref>, <xref ref-type="bibr" rid="ref46">46</xref>). Similarly, the lack of a significant association for length of stay&#x2014;despite a clinically meaningful trend in average length of stay by the Clinical Frailty Scale, could be due to limited statistical power. Therefore, our findings of no associations for length of stay need to be confirmed in larger, well-powered studies from the Middle East. Third, although we adjusted for potential associated factors in the multivariable analysis, the effects of unmeasured confounding factors, such as nutritional status, caregiver support, socioeconomic status, dementia, the American Society of Anesthesiologists (ASA) classification score, time to surgery, and fracture pattern, may have influenced the results. Finally, we did not perform direct comparisons between the Clinical Frailty Scale and other frailty assessment tools, such as the FRAIL scale or frailty phenotype; however, comparing multiple frailty scales was not the primary objective of the current study. An advantage of this study is that our sample is representative of all patients with hip fractures in Qatar, as Hamad Medical Corporation is the major government-funded tertiary care hospital managing orthopedic emergencies nationwide.</p>
<p>In conclusion, frailty as measured by the Clinical Frailty Scale showed a strong positive association with adverse outcomes, including incident delirium during hospitalization, in-hospital postoperative complications, and all-cause mortality, but not with length of hospital stay in a cohort of older patients with hip fractures from Qatar. The Clinical Frailty Scale is a simple and feasible tool that should be incorporated into the preoperative assessment of older adults. Studies with larger sample sizes from the Middle East are needed to confirm and also expand on our findings.</p>
</sec>
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<back>
<sec sec-type="data-availability" id="sec11">
<title>Data availability statement</title>
<p>The datasets presented in this article are not readily available because of patient confidentiality. Further inquiries can be directed to the corresponding authors. Requests to access the datasets should be directed to SS, <email>ssyamala@hamad.qa</email>.</p>
</sec>
<sec sec-type="ethics-statement" id="sec12">
<title>Ethics statement</title>
<p>The studies involving humans were approved by the Institutional Review Board at the Hamad Medical Corporation, Qatar (Ref No. IRGC 05-JI-18-297, approved 22-June-2020). The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.</p>
</sec>
<sec sec-type="author-contributions" id="sec13">
<title>Author contributions</title>
<p>SS: Writing &#x2013; original draft. FT-S: Writing &#x2013; review &#x0026; editing. JP: Writing &#x2013; review &#x0026; editing. BS: Writing &#x2013; review &#x0026; editing. NN: Writing &#x2013; review &#x0026; editing. HA: Writing &#x2013; review &#x0026; editing, Supervision.</p>
</sec>
<sec sec-type="funding-information" id="sec14">
<title>Funding</title>
<p>The author(s) declare that financial support was received for the research and/or publication of this article. This work was funded by Hamad Medical Corporation Medical Research Centre Internal Research Grant Cycle Grant# IRGC 05-JI-18-297. The funder had no role or influence in the contents of the manuscript.</p>
</sec>
<ack>
<p>We would like to acknowledge the support of Mohammad Al Dosari, Director of the Bone and Joint Centre; Amir Abdalla, Consultant Geriatrician; Ahmad Musallam, Pathway Coordinator; Zulfeequer Ottayil, Gopalakrishnan Girish, Mais AlQudah, Santosh Payinkintavida, Aljo Romero, Diana Austria, and Abdul Rasheed Pookkara Valappil, Physiotherapy Specialists; and Jazna Naushad, Maraeh Mancha, and Sarah Abdelazim, Research Assistants, for their contribution to the study.</p>
</ack>
<sec sec-type="COI-statement" id="sec15">
<title>Conflict of interest</title>
<p>SS, FT-S, JP, BS, NN, and HA had no commercial conflicts of interest. The 4th author BS declared that he was an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.</p>
<p>The remaining author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.</p>
<p>The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.</p>
</sec>
<sec id="sec99">
<title>Correction note</title>
<p>This article has been corrected with minor changes. These changes do not impact the scientific content of the article.</p>
</sec>
<sec sec-type="ai-statement" id="sec16">
<title>Generative AI statement</title>
<p>The authors declare that no Gen AI was used in the creation of this manuscript.</p>
</sec>
<sec sec-type="disclaimer" id="sec17">
<title>Publisher&#x2019;s note</title>
<p>All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.</p>
</sec>
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