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A comparative evaluation of DECAF and modified DECAF scores for predicting outcomes in COPD exacerbations: A cross-sectional study
*Corresponding authors: E-mail addresses: athar80@gmail.com (M Athar), sunilkumarmed@gmail.com (S Kumar)
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Received: ,
Accepted: ,
Abstract
Chronic obstructive pulmonary disease (COPD) continues to pose a major global health burden, leading to high rates of illness and death across the world. The Dyspnoea, eosinopenia, consolidation, acidemia, atrial fibrillation (DECAF) score is an established prognostic tool in patients hospitalized for COPD. But a modified DECAF (mDECAF) score, in which atrial fibrillation is replaced by frequency of hospitalizations, has recently emerged as potentially more practical, especially in low-resource environments. This study aimed to evaluate the DECAF score as a prognostic indicator and compare its performance with the mDECAF score in predicting mortality, ventilatory support requirements, and hospital length of stay in patients with acute exacerbation of COPD.
A prospective hospital-based observational cross-sectional study was conducted over two years in the Department of Medicine at a tertiary care hospital in Wardha, Maharashtra, India. A total of 100 diagnosed COPD patients meeting inclusion criteria were enrolled. Detailed clinical evaluation, investigations, and application of DECAF and mDECAF scores were performed. Outcomes were recorded and analyzed.
Of the 100 patients, 72% were aged >60 years, and 61% were male. The mean±SD DECAF and mDECAF scores were 2.59 ± 1.66 and 2.71 ± 1.81, respectively. Overall mortality was 26%, 51% required ventilatory support, and the mean hospital stay was 4.47 ± 4.02 days. Patients who improved had significantly lower scores than those who died (DECAF: 1.97 ± 1.28 vs. 4.35 ± 1.35; mDECAF: 2.04 ± 1.44 vs. 4.62 ± 1.33; p < 0.001). Similarly, ventilated patients had higher scores than non-ventilated patients (DECAF: 3.59 ± 1.54 vs. 1.55 ± 1.04; mDECAF: 3.84 ± 1.67 vs. 1.53 ± 1.02; p < 0.001). Both DECAF and mDECAF showed strong correlations with hospital stay (r = 0.6 and 0.7, respectively; p < 0.001) and were strongly intercorrelated (rho = 0.96; p < 0.001). The area under the receiver operating characteristic curve (AUROC) for predicting mortality was 0.882 (95% CI: 0.800–0.964) for DECAF and 0.888 (95% CI: 0.819–0.957) for mDECAF (both p < 0.001). At a cutoff ≥4, DECAF predicted mortality with 81% sensitivity and 89% specificity, while mDECAF showed 77% sensitivity and 86% specificity.
Higher DECAF and mDECAF scores were significantly associated with increased mortality, need for ventilatory support, and longer hospital stay in patients with acute exacerbations of COPD, with both scores demonstrating excellent and comparable prognostic performance.
Keywords
COPD
DECAF
Modified DECAF
Mortality
Prognostic score
1. Introduction
Chronic obstructive pulmonary disease (COPD) is one of the most common causes of chronic morbidity and mortality, and is particularly devastating in India (WHO, 2024). The Global burden of disease (GBD) estimates indicate that COPD is the second leading cause of death in India, as well as being age-dependent, with rising prevalence with age. It also causes an excessive share of disability-adjusted life years (DALYs), with Indian COPDs suffering a 1.7-fold higher DALY burden per case compared to world averages (Verma et al., 2021).
Although tobacco smoke is still the most widely known risk factor for this disease, non-smoking-related COPD is gaining more relevance as a result of exposure to biomass fuels and indoor air pollution, particularly in rural contexts (Salvi et al., 2009). However, COPD is still underdiagnosed due mainly to low spirometry and other diagnostic capabilities, as well as an overall under-recognition of symptoms by both patients and doctors (Yu et al., 2013; Wheatley et al., 2017).
Risk stratification is particularly a challenge in the management of COPD, and more so during an exacerbation, and should be done as early and accurately as possible. Prognostic scoring systems are essential for important clinical decisions of hospitalization, ventilator support, and palliative care. Among the various scoring systems created, the DECAF score (Dyspnea, eosinopenia, consolidation, acidemia, atrial fibrillation) is a promising bedside tool used to predict in-hospital mortality of patients admitted due to acute exacerbations of COPD (Steer et al., 2012; Allena et al., 2023; Huang et al., 2020). Several trials, e.g., Steer et al., (2012), have evidenced DECAF to have better discriminative power than triage scores such as CURB-65 (Confusion, Urea, Respiratory rate, Blood pressure, and age ≥ 65 years) and BAP-65 (Blood urea nitrogen, Altered mental status, Pulse, and age ≥ 65 years), with an AUC (Area under the curve) of 0.86. Its chief virtue is that it is a user-friendly score based on typical admission data and is therefore practical in daily practice. Of note, utilization of stable-state dyspnea through the eMRCD (extended Medical Research Council Dyspnoea) score enhances its prognostic power.
However, DECAF has some limitations. Atrial fibrillation may not be detected in all patients, particularly in resource-limited settings where electrocardiogram (ECG) access is limited, and eosinopenia has reduced specificity due to the influence of steroids, infections, or comorbidities (Silva et al., 2020). Besides, the majority of validation studies were performed among Western populations; thus, their applicability in the Indian population (of which a large proportion develop COPD from biomass smoke exposure) is questioned (Verma et al., 2021). To overcome these limitations, the modified DECAF (mDECAF) score was developed, and atrial fibrillation was replaced by previous hospitalizations to enhance applicability in low-resource settings (Zidan et al., 2020). Preliminary results suggest mDECAF to be a good clinical predictor, but few comparative data are available.
Notably, very few validated studies are conducted in India, a population whose environmental exposures, healthcare access, and clinical presentation differ significantly from those in developed countries. Comparatively few have compared DECAF and mDECAF scores in a single population, and a majority that exist are retrospective in design, have inconsistently defined outcome measures, and have poor comorbidity adjustment. These limitations, along with dependency on ECGs by DECAF, underscore a need for more adaptable and context-transmissible measures of risk of COPD.
Although numerous studies have examined the development, validation, and clinical application of the DECAF score in different contexts, further research is required to confirm its predictive accuracy and assess its applicability across diverse patient populations. Therefore, this study aimed to evaluate the prognostic accuracy of the DECAF and modified DECAF scores in predicting mortality, ventilatory support, and hospital stay among COPD patients admitted with acute exacerbations. The outcome could influence triage practice, inform treatment planning, and optimize resource allocation in COPD care.
2. Materials and Methods
This prospective hospital-based observational cross-sectional study was conducted in the Department of Medicine at Acharya Vinobha Bhave Rural Hospital, a tertiary healthcare center attached to Jawaharlal Nehru Medical College, Wardha, Maharashtra, India. The study period extended from July 2022 to June 2024.
2.1 Study population
All consecutive patients aged >18 years, diagnosed with COPD by pulmonary function testing based on GOLD criteria, irrespective of gender or ethnicity, and admitted to the Medicine or respiratory medicine departments were enrolled. Patients with concomitant diseases - coronary artery disease as a cause of atrial fibrillation, congestive cardiac failure, interstitial lung disease exacerbation, lung malignancy, pneumothorax, acute on chronic decompensated liver disease, psychiatric illness, or those unwilling to consent were excluded. All patients fulfilling the selection criteria were informed about the nature of the study, and written informed consent was obtained prior to enrollment.
2.2 Ethics
The study protocol was approved by the Institutional Ethical Committee (ID: DMIMS(DU)/IEC/2022/1081). All procedures followed institutional and national ethical guidelines in line with the Helsinki Declaration (1975, revised 1983).
2.3 Sample size calculation
To achieve the stated objectives of this study, the required sample size was calculated using the formula: N = Z2 × P (1 − P)/d2 where Z is the standard normal variate corresponding to a 95% confidence level (Z = 1.96), P is the expected prevalence of COPD (5% or 0.0512), and d is the absolute precision or allowable margin of error (4.5% or 0.045). Using this formula, the calculated minimum sample size is N = 90.1. To enhance statistical power and ensure better representation, 100 patients will be included in the study.
2.4 Clinical evaluation and investigations
Each patient underwent detailed history taking, including comorbidities and previous hospitalizations within the past year, followed by a general and systemic examination. Disease severity was classified using GOLD criteria. Laboratory and imaging investigations included complete blood count with eosinophil count, arterial blood gas analysis, chest radiography, and electrocardiography at admission. Blood samples were collected aseptically in dipotassium ethylenediaminetetraacetic acid (EDTA) tubes at admission, kept at room temperature for one hour, and refrigerated if processing was delayed. Hemoglobin, total platelet count, and total leukocyte count were measured using an automated hematology analyzer (Beckman coulter unicel DxH 800, Beckman coulter Inc., Brea, CA, USA). Absolute eosinophil count (AEC) was calculated as: AEC = total leukocyte count per cumm × eosinophil percentage. Chest radiographs were evaluated by the treating physician for new consolidation, and the presence of atrial fibrillation was confirmed by ECG and 2D echocardiography. All patients were monitored throughout hospitalization, with individualized treatment provided by the attending physician.
2.5 Scoring and outcomes
Patients were scored according to the DECAF and modified DECAF (mDECAF) scoring systems (Tables 1 and 2). Clinical outcomes were recorded in terms of in-hospital mortality, requirement of ventilatory support, and duration of hospital stay.
| Criteria | Score |
|---|---|
|
1. Extended MRC dyspnoea scale (eMRCD) - Not too dyspnoeic to leave the house (eMRCD 1-4) - Too dyspnoeic to leave the house but independent with washing/dressing (eMRCD 5a) - Too dyspnoeic to leave the house and wash/dress (eMRCD 5b) |
0 1 2 |
|
2. Eosinopenia (eosinophils <0.05x109/L) - No - Yes |
0 1 |
|
3. Consolidation on chest X-ray - No - Yes |
0 1 |
|
4. Acidaemia (pH <7.30) -No - Yes |
0 1 |
|
5. Atrial fibrillation (including a history of paroxysmal atrial fibrillation) - No - Yes |
0 1 |
| MAXIMUM DECAF SCORE | 6 |
eMRCD: Extended medical research council dysnpoea score
| Criteria | Score |
|---|---|
|
1. Extended MRC dyspnoea scale (eMRCD) - Not too dyspnoeic to leave the house (eMRCD 1-4) - Too dyspnoeic to leave the house but independent with washing/dressing (eMRCD 5a) - Too dyspnoeic to leave the house and wash/dress (eMRCD 5b) |
0 1 2 |
|
2. Eosinopenia (eosinophils <0.05x109/L) - No - Yes |
0 1 |
|
3. Consolidation on chest X-ray - No - Yes |
0 1 |
|
4. Acidaemia (pH <7.30) - No - Yes |
0 1 |
|
5. Frequency of hospitalization in the last one year (more than or equal to 2) - No - Yes |
0 1 |
| Maximum mDECAF score | 6 |
2.6 Statistical analysis
Data were entered in Microsoft Excel, cross-checked, and cleaned for discrepancies. Statistical analyses were performed using SPSS version 24.0 (IBM Inc., Chicago, USA) and Jamovi software. Statistical package for the social sciences (SPSS) was used for primary analyses, while Jamovi was used for supplementary and graphical analyses. Descriptive statistics were performed, with categorical variables presented as frequencies and proportions, and continuous variables reported as mean ± standard deviation (SD).
3. Results
A total of 100 patients with COPD were enrolled in the study, with a mean age of 66.36 ± 11.44 years; the majority (72%) were above 60 years, 26% were between 41–60 years, and only 2% were in the 20–40 years group. Males constituted 61% of the population, while females accounted for 39%. Among lifestyle factors, 40% of patients were smokers, 32% consumed alcohol, and 19% reported both smoking and alcohol use. Co-morbidities were present in 63% of participants, with systemic hypertension (25%) and pulmonary tuberculosis sequelae (24%) being the most common, followed by diabetes mellitus (11%), chronic kidney disease (11%), bronchial asthma (5%), and other conditions (2%). The baseline demographic and clinical characteristics of the study population are summarized in Table 3.
| Basic details | Mean ± SD (%) |
|---|---|
| Age (Years) | 66.36 ± 11.44 |
| Age | |
| 20-40 Years | 2 (2.0%) |
| 41-60 Years | 26 (26.0%) |
| >60 Years | 72 (72.0%) |
| Gender | |
|
Male Female |
61 (61.0%) 39 (39.0%) |
| Smoking (Yes) | 40 (40.0%) |
| Alcohol (Yes) | 32 (32.0%) |
| Smoking and alcohol (Yes) | 19 (19.0%) |
| Co-Morbidity | |
| Any | 63 (63.0%) |
| Systemic hypertension | 25 (25.0%) |
| Diabetes mellitus | 11 (11.0%) |
| PTB sequalae | 24 (24.0%) |
| Chronic kidney disease | 11 (11.0%) |
| Bronchial asthma | 5 (5.0%) |
| Other | 2 (2.0%) |
| Mean (SD) of DECAF score | 2.59 (1.66) |
| Mean (SD) of modified DECAF score | 2.71 (1.81) |
| Mortality | 26.0% |
| Use of ventilator | 51.0% |
| Hospital stay | 4.47 (4.02) |
PTB: Pulmonary tuberculosis
The mean (±SD) DECAF and modified DECAF (mDECAF) scores were 2.59 ± 1.66 and 2.71 ± 1.81, respectively. The overall mortality rate was 26%, more than half of the patients (51%) required ventilatory support, and the mean (±SD) hospital stay was 4.47 ± 4.02 days (Table 3).
Among the study participants, patients who showed clinical improvement (Improved) had lower mean DECAF and mDECAF scores (1.97 ± 1.28 and 2.04 ± 1.44, respectively), whereas those who died (Mortality) had significantly higher scores (4.35 ± 1.35 and 4.62 ± 1.33, respectively). Similarly, patients requiring ventilatory support demonstrated higher mean DECAF and mDECAF scores (3.59 ± 1.54 and 3.84 ± 1.67, respectively) compared to those who did not require ventilatory support (1.55 ± 1.04 and 1.53 ± 1.02, respectively). These differences were statistically significant, with a p-value of <0.001, indicating a strong correlation between higher DECAF/mDECAF scores and adverse outcomes. Table 4 summarizes the outcome of study participants with respect to DECAF and mDECAF scores.
| Parameter | DECAF score mean (±SD) | Modified DECAF mean (±SD) |
|---|---|---|
| Improved | 1.97 (1.28) | 2.04 (1.44) |
| Mortality | 4.35 (1.35) | 4.62 (1.33) |
| Use of ventilator-YES | 3.59 (1.54) | 3.84 (1.67) |
| Use of ventilator-NO | 1.55 (1.04) | 1.53 (1.02) |
| p-value | <0.001 | <0.001 |
Table 5 shows a strong positive correlation between hospital stay and DECAF score (Spearman’s r = 0.6, p < 0.001), while an even stronger correlation was observed with the modified DECAF score (Spearman’s r = 0.7, p < 0.001). Table 6 further demonstrated that for every one-unit increase in hospital stay, the DECAF score increased by 0.26 units. Conversely, for every one-unit increase in DECAF score, the hospital stay increased by 1.55 units. Similarly, for the modified DECAF score, each one-unit increase in hospital stay corresponded to a 0.30-unit rise in the score. Conversely, a one-unit increase in the score was associated with a 1.51-day increase in hospital stay. These findings indicate that higher DECAF and modified DECAF scores were significantly associated with longer hospital stay.
| Correlation | Spearman correlation coefficient | P value |
|---|---|---|
| Hospital stay vs DECAF score | 0.6 | <0.001 |
| Hospital stay vs modified DECAF score | 0.7 | <0.001 |
| Score type | Effect per 1 unit ↑ in hospital Stay | Effect per 1 unit ↑ in score | p-value |
|---|---|---|---|
| DECAF | Score ↑ by 0.26 units | Hospital stay ↑ by 1.55 units | <0.001 |
| Modified DECAF | Score ↑ by 0.30 units | Hospital stay ↑ by 1.51 units | <0.001 |
Fig. 1 illustrates the correlation between the DECAF and mDECAF scores, showing a very strong positive correlation (rho = 0.96, p < 0.001). The blue trendline depicts the relationship between the two scores, while the shaded grey area indicates the 95% confidence interval. The diagnostic performance of the DECAF score for predicting mortality versus improvement is presented in Fig. 2. The area under the receiver operating characteristic curve (AUROC) was 0.882 (95% CI: 0.800–0.964; p < 0.001), indicating good discriminative ability. At a cutoff of ≥4, the DECAF score predicted mortality with a sensitivity of 81% and specificity of 89%. Similarly, the mDECAF score demonstrated comparable performance (Fig. 3), with an AUROC of 0.888 (95% CI: 0.819–0.957; p < 0.001). Using a cutoff of ≥4, it predicted mortality with a sensitivity of 77% and specificity of 86%.



4. Discussion
The COPD is a leading global health concern and continues to contribute significantly to morbidity, mortality, and healthcare burden, particularly in low- and middle-income countries. India, in particular, faces one of the highest COPD burdens worldwide (WHO, 2024). Early identification of patients at risk of poor outcomes during acute exacerbations is vital for guiding clinical decision-making, prioritizing high-risk cases for advanced care, and facilitating safe and timely discharges. The DECAF score and its modified version (mDECAF) are increasingly recognized as simple yet effective tools for risk stratification in patients with acute exacerbations of COPD (AECOPD), drawing on readily available clinical, serological, and radiological parameters (Memon et al., 2019).
In our study, the mean age of participants was 66.36 ± 11.44 years with a male predominance (61%), consistent with findings by Memon et al., 2019 and Sharma et al., 2020. The predominance of elderly males among COPD patients is likely due to the combined effect of smoking habits being more common among men and advanced age being an established risk factor for COPD progression. Similar demographic trends have been reported internationally, including in European cohorts studied by Steer et al. and Trethewey et al., suggesting that these findings are broadly generalizable across populations (Steer et al., 2012; Trethewey et al., 2018). Co-morbidities were highly prevalent (63%), with systemic hypertension and sequelae of pulmonary tuberculosis being the most common, underlining the multifactorial burden of disease in Indian patients (Table 3).
The overall mortality rate in our cohort was 26%, underscoring the substantial severity of illness among hospitalized COPD patients. Both DECAF and mDECAF scores demonstrated strong discriminatory ability for predicting mortality. Patients who died had significantly higher DECAF and mDECAF scores compared with survivors (4.35 vs. 1.97 and 4.62 vs. 2.04, respectively). These findings are consistent with previous studies, which demonstrated that the DECAF score provides superior predictive accuracy compared with conventional triage tools (Steer et al., 2012; Bansal et al., 2020; VD et al., 2025).
When examining the individual components of the DECAF score, significant differences were observed between survivors and non-survivors for dyspnoea severity (eMRCD 5b), eosinopenia, consolidation, acidemia, and atrial fibrillation. These results closely align with those of Steer et al., who demonstrated that each DECAF component independently predicted mortality, with dyspnoea severity and consolidation being the strongest predictors (Steer et al., 2012). The consistent replication of these findings across studies strengthens the evidence base for DECAF as a reliable prognostic marker.
As shown in Table 7, the prognostic performance of individual DECAF components in our cohort aligns closely with previous studies, particularly for dyspnoea severity, eosinopenia, and consolidation (Sangwan et al., 2017; Mathialagan et al., 2024). Minor variations in effect sizes across reports may be explained by differences in study design, patient characteristics, and healthcare settings. This consistency across independent cohorts underscores the robustness of DECAF as a prognostic tool. Notably, no prior studies have compared individual components of the modified DECAF score with the original DECAF, highlighting an important gap for future investigation.
| Components | Current study (%) | Sangwan and colleagues [17] (%) | Zidan et al. [11] (%) | Mathialagan et al. [18] (%) |
|---|---|---|---|---|
| Dyspnoea eMRCD 5b | 37.8 | 0 | 0 | 37.5 |
| Eosinopenia | 56.2 | 77.8 | 14 | 20 |
| Consolidation | 41.7 | 89.9 | 25 | 30.5 |
| Acidemia | 48.9 | 100 | 24 | 30.8 |
| Atrial fibrillation | 56.5 | 33 | 5 | 37.5 |
The association between higher DECAF/mDECAF scores and the need for ventilatory support was also a significant finding of this study. More than half (51%) of our participants required ventilator use, and their DECAF and mDECAF scores were markedly higher than those who did not. Comparable outcomes were reported by Mathialagan et al., Trethewey et al., and Steer et al., who all observed worse prognoses among ventilated patients, particularly those requiring invasive ventilation (Steer et al., 2012; Trethewey et al., 2018; Mathialagan et al., 2024). Indeed, Steer et al. noted that all patients requiring invasive ventilation expired, highlighting the prognostic significance of ventilation status in acute exacerbations of chronic obstructive pulmonary disease (AECOPD). Our results reaffirm that DECAF and mDECAF can serve as early indicators of patients likely to require ventilatory support, allowing clinicians to prepare and escalate care accordingly.
Hospital stay was another significant factor associated with DECAF and mDECAF scores in our cohort. Patients with higher scores tended to remain hospitalized for longer durations, reflecting more severe disease and delayed recovery. For every one-unit increase in DECAF or mDECAF score, hospital stay increased by 1.55 and 1.51 days, respectively. These findings are supported by earlier work, which also observed a positive correlation between higher DECAF scores and prolonged hospitalization (Memon et al., 2019; Sharma et al., 2020). From a clinical standpoint, these results are important because they suggest that DECAF and mDECAF scores may help predict not only mortality but also resource utilization, which is a critical consideration in healthcare systems with limited capacity.
The diagnostic accuracy of DECAF and mDECAF in predicting mortality was confirmed through receiver operating characteristic (ROC) curve analysis. Both scores demonstrated excellent discriminative performance, with AUROC values of 0.882 and 0.888, respectively (Figs. 2 and 3). At a cutoff of ≥4, DECAF predicted mortality with 81% sensitivity and 89% specificity, while mDECAF showed slightly lower sensitivity (77%) but comparable specificity (86%). Sangwan et al. reported similar findings, noting high sensitivity and specificity for DECAF in predicting mortality (Sangwan et al., 2017). Zidan et al. further demonstrated that while both DECAF and mDECAF achieved 100% sensitivity, mDECAF offered better specificity, suggesting a potential advantage in avoiding risk overestimation in lower-severity cases. Importantly, beyond diagnostic metrics, the clinical advantage of mDECAF lies in its practical applicability and feasibility in low-resource settings, as it avoids dependence on electrocardiography for atrial fibrillation detection while retaining robust prognostic performance.
Beyond India, international studies have also validated DECAF as a practical prognostic tool. Steer et al. in the UK and other investigators have consistently demonstrated its superiority over traditional scoring systems such as CURB-65, BAP-65, and acute physiology and chronic health evaluation (APACHE II) (Almarshoodi et al., 2024; Bayramoğlu et al, 2013; Echevarria et al., 2019; Huang et al., 2020; Steer et al., 2012; Zidan et al., 2020). The advantage of DECAF lies in its simplicity, requiring only basic clinical evaluation, routine laboratory investigations, and chest radiography, all of which are available in most healthcare settings. This makes it particularly valuable in resource-limited environments such as rural hospitals in India, where access to complex scoring systems or advanced monitoring tools may be restricted. By enabling risk stratification at the triage level, DECAF and mDECAF can guide allocation of scarce resources, reduce unnecessary admissions for low-risk patients, and ensure intensive monitoring for those at high risk.
4.1 Clinical implications
The findings of this study underscore the clinical value of incorporating DECAF and mDECAF scoring into the routine assessment of AECOPD patients. These tools allow for rapid identification of high-risk patients who may benefit from early escalation to intensive care, while also supporting decisions for early discharge in low-risk cases. This dual capacity improves patient outcomes and optimizes the use of healthcare resources. Importantly, in countries like India, where the COPD burden is high and hospital resources are often constrained, such simple yet robust prognostic tools could play a pivotal role in standardizing care pathways and improving survival rates.
4.2 Limitations of the study
This study was conducted at a single tertiary care center with a sample size of 100 patients, which may limit generalizability. Additionally, we did not perform head-to-head comparisons of DECAF/mDECAF with other established scoring systems, such as CURB-65 or BAP-65, in this cohort. Future multicenter studies with larger and more diverse populations are needed to confirm these findings and further refine the predictive thresholds for both DECAF and mDECAF. Long-term outcomes beyond hospital discharge were also not assessed, which could provide additional insights into the prognostic value of these scores.
5. Conclusions
Both DECAF and mDECAF scores are effective predictors of mortality, ventilator requirement, and hospital stay in patients with AECOPD. The two tools demonstrated excellent and comparable diagnostic performance, supporting their utility in clinical risk stratification. Given their simplicity and reliance on routinely available clinical parameters, DECAF and mDECAF can be considered practical and reliable tools in both high-resource and resource-limited settings. Their adoption could improve triage, treatment planning, and discharge decisions, ultimately enhancing outcomes for patients with COPD.
Acknowledgment
The authors gratefully acknowledge the technical and financial support provided by the Deanship of Scientific Research (DSR) at King Abdulaziz University, Jeddah, Saudi Arabia. The authors would also like to gratefully acknowledge the research facility provided by the Special Infectious Agents Unit, King Fahd Medical Research Center, King Abdulaziz University, Jeddah, Saudi Arabia.
CRediT authorship contribution statement
Rinkle Gemnani: Investigation, data curation, writing – original draft; Sunil Kumar: Conceptualization, data curation, project administration and supervision; Anil Wanjari: Investigation, statistical analysis; Meraj Khan: Formal analysis, writing- review and editing; Sayed Sartaj Sohrab: Investigation, methodology, funding acquisition; Sourya Acharya: Formal analysis, resources; Mohammad Athar: Methodology, formal analysis, writing- review and editing.
Declaration of competing interest
The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
Data availability
The authors confirm that the data supporting the findings of this study are available within the article.
Declaration of generative AI and AI-assisted technologies in the writing process
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.
Funding
This Project was funded by the Deanship of Scientific Research (DSR) at King Abdulaziz University, Jeddah, Saudi Arabia under grant no. (IPP: 202-141-2025). The authors, therefore, acknowledge with thanks DSR for technical and financial support.
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