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Original Research Article
ARTICLE IN PRESS
doi:
10.25259/JTARCC_4_2026

Effect of Frailty on Hospital Length of Stay and Discharge Outcomes among Geriatric Trauma Patients: A Prospective Observational Study

Division of Trauma Anaesthesia and Critical Care, Jai Prakash Narayan Apex Trauma Centre, All India Institute of Medical Sciences, New Delhi, India.

*Corresponding author: Yudhyavir Singh, Division of Trauma Anaesthesia and Critical Care, Jai Prakash Narayan Apex Trauma Centre, All India Institute of Medical Sciences, New Delhi, India. yudhyavir@gmail.com

Licence
This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

How to cite this article: Singh Y, Monika, Sawhney C. Effect of Frailty on Hospital Length of Stay and Discharge Outcomes among Geriatric Trauma Patients: A Prospective Observational Study. J Trauma Anaesth Resusc Crit Care. doi: 10.25259/JTARCC_4_2026

Abstract

Objectives:

Frailty in older adults is associated with more comorbid conditions, higher mortality, increased falls, and adverse discharge outcomes after hospitalization. While the clinical frailty scale (CFS) and, more recently, the trauma-specific frailty index (TSFI) have been used to study adverse discharge outcomes, few studies have assessed their ability to predict hospital length of stay (LOS) in geriatric trauma patients. The objective of our study was to investigate the impact of frailty on hospital LOS and adverse discharge outcomes among elderly trauma patients.

Material and Methods:

A prospective observational study was conducted at a single center among geriatric trauma patients aged ≥65 years who were admitted for surgical interventions. Frailty was assessed using the CFS, and patients were categorized into two groups based on CFS scores of 1 -3 and 4 -7 for outcome analysis. The primary outcome was the effect of frailty on LOS. The secondary outcomes were the association of frailty with adverse discharge outcomes, i.e., mortality and correlation of CFS with TSFI.

Results:

Among 187 geriatric trauma patients, the median age was 74 years, and 53% were female. Frail patients (CFS 4–7) were significantly older than pre-frail patients (CFS 1–3) (76.08 vs. 71.55 years; p = 0.001). TSFI was markedly higher in frail patients (0.20 vs. 0.07; p < 0.001) and positively correlated with CFS (r = 0.53). No significant differences were found in the LOS, discharge disposition, complications, or 28-day mortality (5% frail vs. 0% pre-frail).

Conclusion:

Frailty assessed using the CFS was not associated with prolonged LOS or adverse discharge outcomes. Although the TSFI was not associated with LOS, it showed a positive correlation with CFS scores.

Keywords

Clinical frailty scale
Discharge outcome
Geriatric trauma
Length of Stay
Mortality
Trauma specific frailty index

INTRODUCTION

Geriatric patients have reduced physiological reserve and heightened vulnerability, which can complicate clinical decision-making. Key factors associated with poor outcomes in geriatric patients, like in-hospital complications, prolonged hospital length of stay (LOS), and adverse discharge outcomes, include the mechanism of injury, vital signs, injury severity score (ISS), comorbidities, and medication use.1,2

Traditional assessment tools often fail to capture altered physiological capacity in the elderly, and advanced age alone does not fully explain adverse outcomes. This has led to the emergence of frailty as a key concept. Frailty is a multidimensional state of diminished physiological reserves that include decreased energy, physical ability, cognition, and health, making the individual susceptible to stress and poor outcomes.3,4 No universal definition exists, but various assessment methods – from simple (e.g., number of medications) to complex (e.g., clock-drawing test) – consistently predict adverse perioperative outcomes, including morbidity, mortality, and prolonged hospital stay.5-8

In trauma settings, few studies have demonstrated that frailty is associated with poor outcomes.1,2,6,8 Validated tools like the Canadian Study on Health and Aging-Clinical Frailty Scale (CSHA-CFS) and FRAIL scale are based on general geriatric populations.3,9 A comprehensive 50-variable frailty index outperformed age and ISS in predicting unfavorable discharge in geriatric trauma patients but is too complex for routine use.1 To address this, a simplified 15-variable trauma-specific frailty index (TSFI) was developed, demonstrating strong predictive ability for discharge disposition, complications, and mortality in elderly trauma patients.2

With this as background, we conducted an observational study to evaluate the association of frailty on LOS and discharge outcomes in older adults using two frailty scoring methods. We hypothesized that higher frailty scores at admission would be associated with prolonged LOS. The primary aim of the study was to evaluate whether the admission CFS is associated with prolonged LOS in geriatric trauma patients. The secondary objectives were to assess the correlation between the CFS and TSFI, evaluate their ability to predict adverse discharge outcomes, and identify additional factors associated with these outcomes.

MATERIAL AND METHODS

Study design, setting and ethics

After obtaining approval from the Institutional Ethics Committee (Ref No 103/March 06, 2020), a 1-year (April 2022–March 2023) a prospective, observational, single-center study was conducted from April 2022 to March 2023 in geriatric trauma patients undergoing non-cardiac surgical procedures performed under general or regional anesthesia at a level I trauma center. This manuscript has been prepared in accordance with Strengthening the Reporting of Observational Studies in Epidemiology guidelines.

Study population and sample size

Written informed consent was obtained from patients or their relatives. Patients aged ≥65 years who presented within 72 h of sustaining a traumatic injury were eligible for inclusion. Referred patients from other centers were eligible only if no intervention had been performed at the referring center. Patients with head injuries, those who refused to participate, those in whom frailty assessment could not be performed, and non-responsive patients were excluded. As no prior published literature was available demonstrating an association between CFS and LOS in geriatric trauma patients, a formal sample size calculation could not be performed. Therefore, all eligible patients admitted during the study period who provided informed consent were consecutively included to minimize selection bias, enhance the representativeness of the study population, and provide preliminary evidence regarding the association between frailty and outcomes.

Methodology

Patients were assessed and screened for frailty scores at the time of pre-anesthetic checkup before surgery. Frailty was assessed using the CFS and the 15-variable TFSI. The first and second investigators who were involved in providing anesthesia care independently assessed and determined the frailty scores. In case of disagreement, the score was reviewed and resolved by a third investigator. All other baseline and perioperative data were collected on the day of surgery.

Patients were followed until patient outcomes were categorized according to their discharge disposition as favorable or unfavorable. A favorable discharge outcome was defined as discharge to home, whereas an unfavorable discharge outcome was defined as in-hospital mortality.

Frailty assessment

Frailty was assessed using the CFS and TSFI in our study. The CFS is a validated 7-point judgment-based assessment tool that can rapidly stratify the degree of frailty in critically ill patients [Appendix I].3 Scores of 1–3 indicate patients who are not frail, scores of 4–5 indicate vulnerability to mild frailty, and scores of 6–7 indicate frailty.3 For analysis, CFS 4 (“apparently vulnerable”) and CFS 5 (“mildly frail”) were considered as separate categories to provide greater detail.3

Appendix I

The 15-variable TSFI, derived from the original 50-variable, was also used to assess frailty [Appendix II].2 These 15 variables have been shown to predict adverse outcomes in geriatric patients. A TSFI score >0.25 was considered the cutoff for frailty and was used to identify patients at risk of an unfavorable discharge disposition.2 The TSFI score was calculated by dividing the total number of positive deficits by the total number of variables assessed.

Appendix 2

Data points

For each patient, demographic and clinical data were recorded, including age, sex, presenting complaints, comorbidities (diabetes mellitus, hypertension, coronary artery disease, stroke, dementia, bronchial asthma, thyroid disorders, and mental illness), mechanism of injury, discharge outcome, LOS, 28-day mortality, and in-hospital complications. The presence of polypharmacy was also recorded. The Glasgow Coma Scale (GCS) score, ISS, Abbreviated Injury Score, and type of anesthesia were also recorded. All in-hospital complications either in ward or ICU were documented. The presence of comorbidities and polypharmacy was also recorded.

Statistical analysis

Data were reported as mean ± standard deviation (SD) for continuous variables, median (interquartile range [IQR]) for ordinal variables, and proportions for categorical variables. The normality of continuous data was assessed using the Kolmogorov–Smirnov test before statistical analysis. The unpaired t-test was used to compare continuous variables between two independent groups, while one-way analysis of variance was used for comparisons among two or more groups. The Chi-square test was used to compare categorical variables. Correlations between clinical variables were assessed using Spearman’s rank correlation coefficient. A p value ≤0.05 was considered statistically significant. Data were coded and entered into a Microsoft Excel spreadsheet. Statistical analyses were performed using IBM Statistical Package for the Social Sciences Statistics for Windows, Version 25 (IBM Corp., Armonk, NY, USA).

Outcome measures

Patients were divided into two groups based on their CFS scores: Group 1 (Pre-frail), comprising patients with CFS scores of 1–3, and Group 2 (Frail), comprising patients with CFS scores of 4–7. The two groups were compared with respect to LOS, mortality, age, sex, ISS, type of anesthesia, comorbidities, in-hospital complications and TSFI scores.

RESULTS

A total of 187 geriatric trauma patients met the inclusion criteria [Figure 1]. The median age was 74 years (interquartile range [IQR], 70–80 years), with 53% (n = 99) being female and 47% (n = 88) being male. The most common mechanism of injury was spontaneous falls, followed by road traffic accidents and assaults. Patients were categorized into pre-frail (PF, CFS 1-3) and frail (F, CFS 4-7) groups based on the CFS, and their demographic and clinical characteristics were compared between groups [Table 1]. The mean age was significantly higher in the frail group than in the pre-frail group (76.08 ± 7.87 vs. 71.55 ± 5.92 years; p = 0.001), indicating an increase in frailty with advancing age [Figure 2]. There were no significant differences in the distribution of comorbidities between the two groups. Median ISS and GCS scores were comparable between the groups, with a median ISS of 9 (IQR, 4–25) and a GCS score of 15 in both groups. Although the incidence of complications was higher in the frail group, the difference did not reach statistical significance.

Flowchart depicting patient recruitment and inclusion in the study.
Figure 1: Flowchart depicting patient recruitment and inclusion in the study.
Table 1: Demographic and characteristics of geriatric trauma patients.
Parameters Group PF CFS (1–3) (n=38) Group F CFS (4–7) (n=149) p-value
Age (Years) 71.55±5.92 76.08±7.87 0.001*
Gender
  Female 11 88 0.001#
  Male 27 61
Comorbidity#
  Diabetes 6 (16%) 44 (30%) 0.103
  HTN 16 (42%) 68 (45%) 0.719
  CAD 5 (13%) 24 (16%) 0.804
  COPD 3 (8%) 13 (9%) 1
  BA 3 (8%) 4 (3%) 0.150
  Obese 1 (3%) 10 (7%) 0.467
  Carcinoma 2 (5%) 8 (5%) 1
  Stroke 2 (5%) 13 (9%) 0.740
  CKD 1 (3%) 8 (5%) 1
  Delirium/Dementia 1 (3%) 9 (6%) 0.690
  GCS 15 (14–15) 15 (14–15) 1
ISS 9 (4–25) 9 (4–25) 0.83*
Type of anesthesia (SA/CSE/GA/NB/GA+Block) 17/13/04/04/0 85/46/16/01/01 0.030#
Frailty index
  TSFI 0.07 (0.05–0.13) 0.2 (0.12–0.23) 0.000*
Complication
  Infection 1 (3%) 13 (9%) 0.307#
  Sepsis 0 3 (2%) 1#
  MI 0 2 (1%) 1#
Outcome
  LOS (days) 7 (5–15) 8 (6–10) 0.427#
  ICU stay (days) 0 0 0.836#
  Discharge outcome (S/D) 38/0 147/02 1#
  28 days mortality 0 8 (5.36%) 0.363#

HTN: Hypertension, CAD: Coronary artery disease, COPD: Chronic obstructive disease pulmonary disease, BA: Bronchial asthma, CKD: Chronic kidney disease, ISS: Injury severity score, SA: Spinal anesthesia, CSE: Combine spinal anesthesia, GCS: Glasgow coma scale, GA: General anesthesia, NB: Nerve block, MI: Myocardial infarction, LOS: Length of hospital stay, ICU: Intensive care unit, S: Survival, D: Death, CFS: Clinical frailty scale, TSFI: Trauma-specific frailty index. Data are expressed as mean±SD or median or in percentage as appropriate; p<0.05 considered significant. *Mann–Whitney test, #Fisher exact test. SD: Standard deviation

Comparison of age between the pre-frail (PF) and frail (F) groups based on Clinical Frailty Scale (CFS) (boxplot).
Figure 2: Comparison of age between the pre-frail (PF) and frail (F) groups based on Clinical Frailty Scale (CFS) (boxplot).

The median LOS was 7 days (IQR, 5–15) in the pre-frail group and 8 days (IQR, 6–10) in the frail group, with no statistically significant difference between the groups (p = 0.427). Discharge disposition also did not differ significantly between the two groups. Twenty-eight-day mortality was 0% in the pre-frail group compared with 5% in the frail group (p = 0.363), which was not statistically significant. The TSFI was significantly higher in the frail group than in the pre-frail group (0.20 [IQR, 0.12–0.23] vs. 0.07 [IQR, 0.05–0.13]; p < 0.001). A moderate positive correlation (r= 0.53) was observed between CFS and TSFI [Figure 3]. Furthermore, TSFI scores increased with advancing age, demonstrating a pattern similar to that observed with CFS [Figure 4].

Scatter plot showing positive association between Clinical Frailty Scale (CFS) and Trauma-Specific Frailty Index (TSFI) (Spearman’s rho, r=0.53).
Figure 3: Scatter plot showing positive association between Clinical Frailty Scale (CFS) and Trauma-Specific Frailty Index (TSFI) (Spearman’s rho, r=0.53).
Scatter plot showing the positive association between age and the trauma-specific frailty Index (TSFI).
Figure 4: Scatter plot showing the positive association between age and the trauma-specific frailty Index (TSFI).

DISCUSSION

This prospective observational study aimed to investigate the impact of frailty on the hospital LOS and adverse discharge outcomes among elderly trauma patients. The study demonstrated that the frailty measured by CFS was not associated with prolonged LOS or adverse discharge outcomes. TSFI also did not predict LOS, however it correlated positively with CFS.

Several recent studies have evaluated the impact of frailty on outcomes in geriatric trauma patients using different frailty assessment tools. To our knowledge, this is the first study to concurrently apply the two commonly used frailty scores – CFS and TSFI – to evaluate their ability to predict LOS and discharge outcomes in geriatric trauma patients. The CFS was originally introduced in 2005 as a 7-point scale, ranging from 1 (very fit) to 7 (severely frail), with severe frailty and terminal illness combined in the highest category.4 In 2007, the scale was expanded to a 9-point version, allowing further distinction between severely frail, very severely frail, and terminally ill patients, thereby facilitating more precise clinical assessment and care planning.7-10

A 2020 review reported that 58% of studies continued to use the 1–7 version of the CFS, although the 1–9 version has predominated in more recent literature, particularly when distinguishing severe frailty is important for prognostication.11 Hence, we used the original CFS in our study. Trials have also used inconsistent CFS thresholds to define frailty, such as ≥4 (vulnerable to frail), ≥5 (frail), or higher cutoffs like ≥6 or ≥7. Similarly, TSFI cut-offs vary across the literature, with values ranging from >0.25-0.27 being used to identify patients at high risk. Cole et al., in their study of geriatric trauma patients, defined “frail” as a CFS ≥6, whereas Thompson et al. classified patients with a CFS of 1–4 as prefrail and CFS 5–9 as frail.12,13 This lack of standardized criteria limits direct comparison across studies, including the present cohort.

Despite this variability, frailty assessment has gained traction as a more physiologically meaningful predictor of outcome than chronological age alone, as patients of the same age differ substantially in physiological reserve, comorbidity burden, and functional status, differences that cannot be adequately captured by age-based risk stratification alone.

LOS

The median hospital LOS was comparable between the pre-frail (CFS 1–3) and frail (CFS 4–7) groups: 7 days (IQR = 5–15) versus 8 days (IQR = 6–10), respectively (p = 0.427). This lack of a significant difference may partly be due to the relatively low overall injury burden in our cohort, as indicated by a similarly low median ISS of 9 (IQR = 4–25) in both groups. Although 8 deaths (5%) occurred in the frail group, mortality was not significantly different between the groups (p = 0.363). Thus, in this cohort, frailty was not associated with a significantly prolonged hospital LOS or increased mortality. These findings are consistent with those of Thompson et al.,13 who reported comparable median LOS between pre-frail and frail groups (11 vs. 12 days; p = 0.149). Despite a significantly higher median ISS in the pre-frail group (16; IQR = 9–12 vs. 10; IQR = 9–17; p = 0.002), this did not translate into a longer hospital stay, suggesting that CFS-defined frailty may have limited influence on hospital LOS. Plausible explanations include the subjective and judgment-based nature of CFS assessment and the predominance of lower-energy orthopaedic trauma in our cohort. Prompt surgical fixation and standardized care pathways may have further reduced frailty-related delays in recovery and discharge at our center. In contrast, Soh et al., in a non-trauma geriatric cohort, reported a median LOS of 7 days among patients with a median admission CFS of 6, which was similar to the LOS observed in our frail group.14 This suggests that the absence of an association between frailty and LOS may extend beyond trauma populations, particularly in settings where efficient and standardized management pathways are established, even among frail individuals.

A detailed review of the geriatric trauma literature has reported a consistent pattern of small and mostly non-significant differences in hospital LOS between frail and non-frail groups (5 vs. 4 days, p = 0.48; 5 vs. 3 days, p = 0.08; 13 vs. 12 days; 12 vs. 11 days, p = 0.64; 13 vs. 12 days).15-19 Pecheva et al. reported slightly longer mean LOS among frail patients (18.8 vs. 18 days), although the difference was small and overlapping.20 In contrast, Herklots et al.21 reported a significantly longer LOS among non-frail patients than frail patients (16.4 vs. 8.4 days, p = 0.006). The authors attributed this finding to survival bias, whereby frail patients may have died earlier rather than recovered more rapidly; thus, a shorter LOS may have reflected early mortality rather than a better clinical outcome. Overall, across different frailty assessment tools, patient cohorts, and healthcare settings, frailty has not been consistently associated with prolonged hospital LOS in geriatric trauma patients. Our findings are therefore consistent with the existing literature and further support the observation that frailty alone may have limited predictive value for hospital LOS in this population.

Discharge outcome

In the present study, there was no significant difference in 28-day mortality between the pre-frail and frail groups (p = 0.363), despite eight deaths occurring in the frail group. This finding is consistent with Arslan Erduhan et al., who reported no significant difference in 30-day mortality according to TSFI-based frailty status (p = 0.208).22 In contrast, Thompson et al.13 reported significantly higher mortality in frail patients than in pre-frail patients (12.8% vs. 5.3%, p = 0.001; odds ratio [OR] = 2.65, 95% confidence interval [CI] = 1.47–4.78). Their cohort also differed significantly between groups with respect to ISS, Charlson Comorbidity Index, and GCS, differences that were not observed in our study. This discrepancy may be explained by differences in patient characteristics and injury profiles across studies.

Several other studies have supported frailty as a predictor of adverse discharge outcomes. Joseph et al.15 reported that a TSFI >0.25 was associated with adverse disposition, including mortality or discharge to a nursing facility (OR = 1.6, 95% CI = 1.1–2.4), while a TSFI >0.27 was associated with higher in-hospital mortality (OR = 1.1, 95% CI = 1.04–4.7). Rickard et al.18 found that severe frailty (CFS 7–9) was associated with a higher risk of 30-day mortality (OR = 2.14, 95% CI = 0.81–5.68). Similarly, Guiab et al.19 identified severe frailty as an independent predictor of mortality (OR = 1.23, 95% CI = 1.15–1.32), while Cheung et al.9 reported that CFS 6–7 was associated with adverse discharge destinations, including mortality (OR = 5.1, 95% CI = 2.0–13.0, p < 0.001). Collectively, these findings underscore the prognostic value of frailty assessment in geriatric trauma populations.

In this context, the absence of a significant association between frailty and adverse outcomes in our cohort should be interpreted cautiously considering its relatively low-risk injury profile, early intervention, and standardized management pathways, rather than as evidence against a true relationship between frailty and adverse outcomes. These factors may have attenuated the impact of frailty on short-term outcomes in our population.

Association between CFS and TSFI

The TSFI score was significantly lower in the pre-frail group (median = 0.07, IQR = 0.05–0.13) than in the frail group (median = 0.20, IQR = 0.12–0.23; p < 0.001) and showed a moderate correlation with the CFS (r = 0.53), supporting reasonable convergent validity between the two frailty assessment tools. This finding supports the utility of the TSFI as a trauma-adapted tool for capturing frailty burden in trauma patients. The TSFI incorporates multiple domains, including comorbidities, activities of daily living, nutritional status (e.g., serum albumin), and functional health, which are not directly assessed by the more subjective, judgment-based CFS.

Despite the moderate correlation between the two tools, the TSFI did not predict hospital LOS, consistent with the findings for the CFS described above. TSFI scores also increased progressively with advancing age, consistent with the established age-related increase in frailty prevalence observed with the CFS, further supporting the validity of our findings. To our knowledge, no previous study has directly compared CFS and TSFI scores within the same geriatric trauma cohort, making the observed correlation between the two tools an important observation of our study.

A multivariable regression analysis would have determined whether CFS and TSFI independently predicted unfavorable discharge outcomes or prolonged hospital LOS after adjusting for potential confounders such as age, ISS, and comorbidity burden. However, given the low event rate in this cohort – only eight deaths (5%) and no significant difference in discharge disposition between the groups – a multivariable regression model would have been underpowered and potentially unreliable. Therefore, the analysis was limited to univariate comparisons between the frailty groups.

A few additional findings from our study warrant discussion to better characterize the observed frailty pattern. The majority of the cohort comprised women (52.9%), and spontaneous falls were the leading mechanism of injury, a pattern typical of geriatric trauma and consistent with the findings of Sut et al.6 Frailty was also more prevalent among women (59% vs. 41% in men), a disparity previously reported by Sut, Thompson et al., and Arslan Erduhan et al.6,13,22 These studies similarly observed a higher burden of trauma among older women, predominantly resulting from spontaneous or low-impact falls. The predominance of women among both trauma and frailty populations is consistent with the broader geriatric trauma literature and may reflect sex-specific factors, including greater longevity, a higher prevalence of osteoporosis, reduced muscle mass, and differences in fall-risk profiles, such as gait instability and impaired balance. Low-energy falls from standing height remain a characteristic mechanism of injury among frail older adults and commonly result in hip fractures, pelvic injuries, and other orthopedic trauma. Collectively, these findings demonstrate the demographic and mechanistic similarity of our cohort to previously described geriatric trauma populations and provide important context for interpreting the observed relationship between frailty and outcomes.

Limitations

This study has several limitations. First, its single-center observational design limits the generalizability of the findings to other centers with different patient populations, healthcare systems, and trauma management protocols. Second, the sample size was relatively small, and follow-up was restricted to 28 days, precluding assessment of longer-term mortality and functional outcomes. Third, most patients had a relatively low injury burden (median = ISS 9), and the cohort predominantly comprised patients with orthopedic trauma following low-energy falls. This injury profile may have attenuated the measurable effect of frailty on the outcomes studied. A multivariable regression analysis could not be reliably performed to determine whether frailty independently predicted prolonged hospital LOS or unfavorable discharge outcomes after adjustment for potential confounders. Furthermore, LOS is a multifactorial outcome influenced not only by injury severity and frailty but also by institutional discharge policies, bed availability, access to rehabilitation facilities, socioeconomic support at home, surgical scheduling, and financial considerations related to discharge planning. These non-clinical determinants were not captured in our analysis and may have attenuated any true association between frailty and LOS. Frailty was assessed only at admission, despite its dynamic nature and was not reassessed at discharge; therefore, changes in frailty status during hospitalization could not be evaluated. Finally, the inherently subjective and judgement-based nature of CFS assessment may introduce inter-rater variability, particularly in the acute trauma setting, underscoring the need for further validation and standardized application of the CFS in geriatric trauma populations.

CONCLUSION

In this study, the CFS was not associated with prolonged hospital LOS or adverse outcomes in geriatric trauma patients. Similarly, the TSFI did not predict prolonged hospital LOS. However, the TSFI showed a moderate positive correlation with the CFS, supporting reasonable convergent validity between the two tools for assessing frailty severity. Frailty was more prevalent among female patients, consistent with findings from previous geriatric trauma literature. Larger, multicenter prospective studies are warranted to further evaluate the predictive utility of the CFS and TSFI for clinically relevant outcomes across diverse geriatric trauma populations. Standardized guidelines for routine frailty screening in geriatric trauma are also needed, incorporating validated assessment tools and structured protocols for risk stratification and individualized care planning.

Author contributions:

YS: Conceptualization; YS and M: Methodology, investigation, data curation, and formal analysis; YS and CS: Writing—original draft, review and editing, project administration, resources, and supervision; YS, M, and CS: Validation.

Ethical approval:

The research/study was approved by the Institutional Review Board at the Institute Ethics Committee, approval number 103/March 06, 2020, dated 06 March 2020.

Declaration of patient consent:

The authors certify that they have obtained all appropriate patient consent forms. In the form, the patient has given consent for clinical information to be reported in the journal. The patient understands that the patient’s names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Conflicts of interest:

Yudhyavir Singh is on the editorial board of the journal.

Use of artificial intelligence (AI)-assisted technology for manuscript preparation:

The authors confirm that there was no use of artificial intelligence (AI)-assisted technology for assisting in the writing or editing of the manuscript and no images were manipulated using AI.

Financial support and sponsorship: Nil.

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