ORIGINAL RESEARCH article

Front. Med., 17 April 2025

Sec. Pulmonary Medicine

Volume 12 - 2025 | https://doi.org/10.3389/fmed.2025.1565098

Dexmedetomidine administration reduced mortality in patients with acute respiratory distress syndrome: a propensity score-matched cohort analysis

Conglin Ye,
Conglin Ye1,2*Yang YuYang Yu2Yi LiuYi Liu2
  • 1Department of Critical Care Medicine, The First Affiliated Hospital of Gannan Medical University, Ganzhou, Jiangxi, China
  • 2The First Clinical Medical College of Gannan Medical University, Ganzhou, Jiangxi, China

Background: Acute respiratory distress syndrome (ARDS) continues to pose significant difficulties due to the scarcity of successful preventative and therapeutic measures. Recent clinical trials and experimental research have confirmed the lung-protective and anti-inflammatory properties of dexmedetomidine. The objective of this study was to examine the relationship between the use of dexmedetomidine and mortality outcomes in ICU patients with ARDS.

Methods: This study retrospectively examined data from the Medical Information Mart for Intensive Care (MIMIC) IV, focusing on individuals diagnosed with ARDS. The primary endpoint was the occurrence of death within 28 days after entering the ICU. To ensure a balanced cohort, we applied propensity score matching at a 1:1 ratio. Additionally, multivariable analysis was performed to mitigate the effects of confounding factors.

Results: In this study, a cohort comprising 612 patients diagnosed with ARDS was investigated. Analysis using both univariate and multivariate Cox regression indicated significantly reduced 28-day and 90-day mortality rates in patients administered dexmedetomidine compared to those who were not given this treatment. Following adjustments for potential confounders using propensity score matching, these results were confirmed to be robust.

Conclusion: The results indicate an association between the administration of dexmedetomidine and lower mortality rates among severely ill ARDS patients. However, this result should be interpreted with cause because of a lot of missing data of potential risk factors for clinical outcomes. Nonetheless, it is imperative to perform further randomized controlled trials to corroborate this finding.

1 Introduction

ARDS is identified as an advanced stage of respiratory failure, prominently featuring marked hypoxemia alongside clearly visible bilateral infiltrates on radiographic scans (14). Annually, around three million individuals worldwide receive a diagnosis of ARDS, representing nearly 10% of admissions to Intensive Care Units (ICUs) (57). Notwithstanding significant therapeutic progress, the mortality rates linked to ARDS have largely persisted since the late 1990s (8, 9). Current research estimates in-hospital mortality rates for ARDS to be between 34.9 and 46.1% (5). The pathophysiology of ARDS is intricate, encompassing the activation and dysregulation of various injury response pathways, alongside inflammatory and coagulation processes that influence both pulmonary and systemic circulation (10). These complexities highlight the pressing necessity for innovative and efficacious therapeutic approaches to enhance clinical outcomes and alleviate the health burden linked to ARDS.

Dexmedetomidine (DEX), extensively used as a sedative in intensive care units, has drawn rising attention because of its anti-inflammatory, immunomodulatory, antioxidant and organ protective properties. According to research in animal models, DEX reduces lung injury because of its multiple protective properties (11, 12). In addition, DEX has also been demonstrated to have protective effects against renal and cardiac ischemia and reperfusion injuries (13, 14). Clinical trials show that DEX decreases inflammation and assists in retaining renal and pulmonary functions during surgery (15). Despite the growing evidence of DEX’s efficacy in reducing inflammation and protecting organs, there remains a noticeable lack of specific clinical trials assessing its effectiveness in improving outcomes for patients with severe ARDS. To fill this gap, a thorough retrospective cohort study was started to examine the effect of DEX treatment on the mortality rates of patients who suffered this type of respiratory failure.

2 Method

2.1 Data source

All research data we used were from the MIMIC-IV database, release version 3.1 (16). MIMIC-IV is a complete collection of patient information from electronic health records within Beth Israel Deaconess Medical Center at Boston, Massachusetts, USA. It consists of rich demographic profiles, vast laboratory test results, complex treatment regimens, and subtle intensive care monitoring records (17). Only researchers who have successfully participated in specialized training courses concerning ethical considerations and protection of human subjects in research have access to this repository. Prior to engaging in data analysis, the investigator CLY was granted the requisite permissions to utilize these resources (certification number: 36,937,255).

2.2 Study population and data extraction

The dataset for this study was sourced from the MIMIC-IV database, which provided comprehensive hospital admission records. The identification of patients suffering from ARDS was accomplished through specific ICD-9 codes: J80 and R0603. The criteria for exclusion included any patient whose ICU duration was less than 72 h or who was younger than 18 years of age at the time of admission. In instances where a patient had multiple ICU admissions, the analysis was restricted to only the first ICU stay. Within the cohort, patients who were administered dexmedetomidine (DEX) during their ICU admission were grouped as the DEX cohort, and those who did not receive DEX were designated as the non-DEX cohort.

2.3 Outcomes

The principal outcome of this study was mortality within 28 days following ICU admission. The secondary outcome evaluated was the mortality rates at 90 days after the admission to the ICU.

2.4 Data analysis

Continuous variables are described using the median alongside the interquartile range (IQR), while categorical variables are summarized as counts and percentages. The Kolmogorov–Smirnov test was applied to examine the distribution of continuous data for normality. For non-normally distributed continuous variables, the Wilcoxon rank-sum test was used. The Pearson’s chi-square test was performed for comparing categorical data.

The association between DEX administration and mortality risk was analyzed using Cox proportional hazards regression models, generating hazard ratios (HRs) with 95% confidence intervals (CIs). Kaplan–Meier survival analysis was utilized to evaluate survival distributions, and comparisons were made using the log-rank test. A multivariable Cox proportional hazards regression model was further applied to assess the relationship between DEX use and mortality outcomes. To address potential confounders, baseline characteristics of patients treated with DEX and those who were not were balanced using Propensity Score Matching (PSM). A 1:1 nearest-neighbor matching approach with a caliper of 0.02, performed without replacement, was utilized for this purpose. The variables included in Table 1 were used to estimate propensity scores. Both the primary and secondary outcomes were re-evaluated within the matched cohort. Statistical analyses were carried out using SPSS software (version 27.0, IBM, USA), and statistical significance was defined as p < 0.05.

Table 1
www.frontiersin.org

Table 1. Baseline characteristics of ARDS patient cohorts pre- and post-matching.

3 Results

3.1 Patient characteristics

Data were extracted from the MIMIC-IV database, comprising a cohort of 612 patients, as depicted in Figure 1. Within this cohort, 380 patients (approximately 62.1%) received dexmedetomidine (DEX) during their ICU stay. A detailed breakdown of baseline characteristics for both the DEX-treated group and the non-DEX group is systematically presented in Table 1. It was observed that the DEX-treated patients generally presented with a younger demographic profile and had higher instances of sepsis and mechanical ventilation usage compared to their counterparts. Further analysis through propensity score matching (PSM), as also detailed in Table 1, allowed for a balanced comparison between the two groups. After the application of PSM, 174 patients who were administered DEX were effectively matched with 174 patients from the non-DEX group, ensuring comparability. This matching process confirmed that patient characteristics were evenly distributed between the groups, as all p values were found to be above the 0.05 threshold, indicating no significant differences statistically.

Figure 1
www.frontiersin.org

Figure 1. A flowchart illustrating the criteria for inclusion and exclusion.

3.2 Primary outcome

In this investigation, data from the MIMIC-IV database revealed that within a cohort of patients, 56.9% (132 out of 232) of those not treated with dexmedetomidine (non-DEX) experienced mortality within 28 days, a rate significantly higher than the 22.6% (86 out of 380) observed in patients who received DEX treatment during their ICU stay. Statistical tests demonstrated a significant discrepancy with a p-value below 0.001. Upon applying propensity score matching techniques, the revised 28-day mortality rate for the cohort administered DEX markedly decreased to 30.5%. This reduction contrasts profoundly with the mortality rate of 60.3% observed in the cohort not receiving DEX treatment. Such findings prominently suggest the potential effectiveness of the therapy (p < 0.001), as elaborated in Table 2.

Table 2
www.frontiersin.org

Table 2. Primary and secondary outcomes of the study.

Cox proportional hazards models were used to further quantify the relationship between DEX administration and survival over the 28-day period in the ICU. The findings, as summarized in Table 3, showed that DEX usage significantly reduced the risk of 28-day mortality (univariate model: hazard ratio [HR] = 0.286, 95% Confidence Interval [CI]: 0.218–0.376, p < 0.001). The reduction in risk persisted even after adjusting for potential confounding variables (multivariate model: HR = 0.286, 95% CI: 0.214–0.383, p < 0.001). A rigorous approach involving 1:1 propensity score matching was undertaken, involving a total of 348 ARDS patients, to confirm these initial results. The beneficial association of DEX with reduced 28-day mortality continued to hold true after this matching, as evidenced by a HR of 0.331 (multivariate model: 95% CI: 0.236–0.463, p < 0.001), further detailed in Table 3.

Table 3
www.frontiersin.org

Table 3. Association between dexmedetomidine use and in-ICU mortality.

A Kaplan–Meier survival analysis was executed to further elucidate differences in mortality rates between patient groups. At the conclusion of the 28-day period, the analysis revealed a significantly reduced mortality rate in patients treated with DEX compared to those who did not receive DEX (log-rank test: p < 0.001; Figure 2). This analysis visually reinforced the statistical findings, illustrating a clear survival advantage for patients treated with DEX during their ICU admission.

Figure 2
www.frontiersin.org

Figure 2. Kaplan–Meier survival curves for 28-day and 90-day in-ICU mortality in ARDS patients from the DEX group and the non-DEX group, both prior to (A,B) and subsequent to (C,D) PSM.

3.3 Secondary outcome

The 90-day mortality rate in the DEX cohort was 28.7% (109 of 380), indicating a substantial reduction relative to the 62.9% (146 of 232) recorded in the non-DEX cohort (p < 0.001).

Similarly, the results of the univariate Cox regression analysis demonstrated that DEX usage correlated with a reduced risk of 90-day mortality relative to non-use (univariate model: HR = 0.314, 95% CI: 0.244–0.402, p < 0.001). The association maintained its statistical significance after adjusting for potential confounding variables (multivariate model: HR = 0.316, 95% CI: 0.242–0.412, p < 0.001). The association between DEX administration and 90-day mortality persisted as significant after PSM (multivariate model: HR = 0.366, 95% CI: 0.269–0.498, p < 0.001) (Table 3).

A Kaplan–Meier survival analysis demonstrated that the DEX group exhibited a markedly reduced mortality rate relative to the non-DEX group at the 90-day interval (log-rank test: p < 0.001; Figure 2).

4 Discussion

This retrospective cohort study revealed that patients administered DEX had markedly reduced 28-day and 90-day mortality rates in comparison to those who were not given DEX. Following the adjustment for baseline disparities via propensity score matching (PSM), DEX utilization was consistently linked to diminished mortality rates. Multivariate Cox regression analysis further corroborated the protective effect of DEX on 28-day and 90-day mortality in ARDS patients admitted to the ICU. The Kaplan–Meier survival curves corroborated these findings, indicating extended survival in the DEX group.

The adrenergic system exhibits a significant interrelationship with the immune system (18). Innate and adaptive immune cells express adrenergic receptors, allowing direct responses to signal from the sympathetic nervous system (19, 20). Postganglionic sympathetic nerve fibers, primarily secreting norepinephrine, modulate primary and secondary lymphoid tissues (21). The interplay between the adrenergic and immune systems has garnered heightened interest in recent years. DEX selectively binds with high affinity to α2 adrenergic receptor subtypes α2A and α2C, as indicated in references (22, 23). DEX regulates norepinephrine release by activating α2 receptors on the presynaptic membrane, which supports its immunomodulatory effects. Studies confirm the critical role of DEX in modulating cellular immunity, dampening inflammatory activity within the tissues, and obviously boosting the immune function of patients who are being treated (24, 25). Also, a growing body of research strongly validates that DEX possesses comprehensive protective benefits to a variety of organ systems. The utility of DEX in protection of multiple organs during acute organ injury and the perioperative period, owing to its anti-inflammatory and immunoregulatory properties, has been well investigated (2628). DEX has also shown its protective properties against diverse organ injuries in several animal models (2931). In addition, DEX protects against damage to vital organs by blocking ferroptosis in both in vitro and in vivo experiments (32).

ARDS continues to be a challenge in medical management because of its persistently high mortality. Treatment modalities now place substantial emphasis on supportive care directed to slowing the rate of lung function deterioration and improving survival of the patients. Therapeutic strategies for ARDS include implementing mechanical ventilation to promote breathing, positioning a patient in the prone position for better oxygenation, using neuromuscular blockers to facilitate easier ventilation and applying extracorporeal life support for maintenance of vital functions when other measures do not work (33, 34). Despite these interventions, mortality of ARDS remains at an unacceptable 35% and there is a dearth of effective pharmacologic intervention (35). The complicated pathophysiology of ARDS consists of multiple mechanisms of injury, inflammation, and coagulation in lung and the systemic circulation (1). Therefore, pharmacological interventions suggest a potential strategy for the treatment of ARDS (34, 36). However, the therapeutic function of DEX as a drug rather than a sedation has not been sufficiently investigated in patients with ARDS.

To the best of our knowledge, this is the first investigation of the relationship between DEX administration and in-ICU mortality in patients with ARDS. The results help inform the strategies and clinical management of ARDS therapy. Additionally, through application of multivariate Cox regression and PSM, confounding factors were controlled, and the reliability of the study was strengthened. Yet some limitations exist. First, population data were gleaned from a single center retrospective cohort study which is prone to selection bias, decreasing the generalizability of the results to other ARDS populations. Second, detailed timing and criteria of DEX administration were not available within the MIMIC-IV database, which could have introduced bias into assessing the effect of DEX on reducing mortality. Third, outcomes may have been influenced by unmeasured variables. Fourth, more potential confounders should be included in propensity score matching, such as the etiology of ARDS, the severity of ARDS, variations in treatment strategies, and the duration of mechanical ventilation, PaO2/FiO2 ratio, the mode and settings of invasive ventilator, the use of prone position and ECMO, and the use of other sedatives, analgesics, and neuromuscular blockades, which are demonstrated to influence the clinical outcomes of ARDS (37, 38). However, a large proportion of these factors are missing in MIMIC-IV database, which may cause inaccuracy in statistical results. Thus, we did not include all the confounding factors in propensity score matching. Moreover, because data from the MIMIC-IV database include data from 2008 to 2022, the results may not fully reflect the most recent ARDS management. In the case of this study, patients who developed ARDS early in the ICU stay were excluded, making the applicability of the results to this specific group of patients uncertain. Additionally, changes in dexmedetomidine usage over time, potentially linked to the adoption of other ARDS therapies, represent a potential source of bias. These limitations highlight the need for well-designed, prospective randomized controlled trials to definitively establish the efficacy of dexmedetomidine in ARDS and to address these potential confounding factors. In summary, the findings indicate an association of DEX administration with the better prognosis in ARDS patients. However, the standard therapy for ARDS is still limited to low tidal volume ventilation (LTVV), prone position and neuromuscular blockade. It is crucial to recognize the inherent limitations of a retrospective study design. These findings should be validated by further prospective trials and DEX’s full therapeutic potential in ARDS should be explored.

5 Conclusion

In summary, the current research demonstrates that dexmedetomidine administration correlates with reduced 28-day and 90-day mortality rates in ICU patients with ARDS. The potential of dexmedetomidine as a treatment for individuals with ARDS is significant and requires further investigation.

Data availability statement

The original contributions presented in the study are included in the article/Supplementary material, further inquiries can be directed to the corresponding author.

Ethics statement

Ethical review and approval was not required for the study on human participants in accordance with the local legislation and institutional requirements. Written informed consent from the [patients/ participants or patients/participants legal guardian/next of kin] was not required to participate in this study in accordance with the national legislation and the institutional requirements.

Author contributions

CY: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Project administration, Validation, Visualization, Writing – original draft, Writing – review & editing. YY: Methodology, Writing – original draft. YL: Methodology, Writing – original draft.

Funding

The author(s) declare that no financial support was received for the research and/or publication of this article.

Acknowledgments

The authors wish to convey their sincere appreciation to all the researchers involved in the development and maintenance of the MIMIC-IV database.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Generative AI statement

The authors declare that no Gen AI was used in the creation of this manuscript.

Publisher’s note

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.

Supplementary material

The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmed.2025.1565098/full#supplementary-material

References

1. Bos, LDJ, and Ware, LB. Acute respiratory distress syndrome: causes, pathophysiology, and phenotypes. Lancet. (2022) 400:1145–56. doi: 10.1016/S0140-6736(22)01485-4

PubMed Abstract | Crossref Full Text | Google Scholar

2. Ferguson, ND, Fan, E, Camporota, L, Antonelli, M, Anzueto, A, Beale, R, et al. The Berlin definition of ARDS: an expanded rationale, justification, and supplementary material. Intensive Care Med. (2012) 38:1573–82. doi: 10.1007/s00134-012-2682-1

PubMed Abstract | Crossref Full Text | Google Scholar

3. Thompson, BT, Chambers, RC, and Liu, KD. Acute respiratory distress syndrome. N Engl J Med. (2017) 377:1904–5. doi: 10.1056/NEJMc1711824

PubMed Abstract | Crossref Full Text | Google Scholar

4. Ware, LB, and Matthay, MA. The acute respiratory distress syndrome. N Engl J Med. (2000) 342:1334–49. doi: 10.1056/NEJM200005043421806

PubMed Abstract | Crossref Full Text | Google Scholar

5. Bellani, G, Laffey, JG, Pham, T, Fan, E, Brochard, L, Esteban, A, et al. Epidemiology, patterns of care, and mortality for patients with acute respiratory distress syndrome in intensive care units in 50 countries. JAMA. (2016) 315:788–800. doi: 10.1001/jama.2016.0291

PubMed Abstract | Crossref Full Text | Google Scholar

6. Fan, E, Brodie, D, and Slutsky, AS. Acute respiratory distress syndrome: advances in diagnosis and treatment. JAMA. (2018) 319:698–710. doi: 10.1001/jama.2017.21907

PubMed Abstract | Crossref Full Text | Google Scholar

7. Rubenfeld, GD, Caldwell, E, Peabody, E, Weaver, J, Martin, DP, Neff, M, et al. Incidence and outcomes of acute lung injury. N Engl J Med. (2005) 353:1685–93. doi: 10.1056/NEJMoa050333

Crossref Full Text | Google Scholar

8. Herridge, MS, Tansey, CM, Matté, A, Tomlinson, G, Diaz-Granados, N, Cooper, A, et al. Functional disability 5 years after acute respiratory distress syndrome. N Engl J Med. (2011) 364:1293–304. doi: 10.1056/NEJMoa1011802

PubMed Abstract | Crossref Full Text | Google Scholar

9. Phua, J, Badia, JR, Adhikari, NK, Friedrich, JO, Fowler, RA, Singh, JM, et al. Has mortality from acute respiratory distress syndrome decreased over time?: a systematic review. Am J Respir Crit Care Med. (2009) 179:220–7. doi: 10.1164/rccm.200805-722OC

PubMed Abstract | Crossref Full Text | Google Scholar

10. Matthay, MA, Zemans, RL, Zimmerman, GA, Arabi, YM, Beitler, JR, Mercat, A, et al. Acute respiratory distress syndrome. Nat Rev Dis Primers. (2019) 5:18. doi: 10.1038/s41572-019-0069-0

Crossref Full Text | Google Scholar

11. Li, J, Chen, Q, He, X, Alam, A, Ning, J, Yi, B, et al. Dexmedetomidine attenuates lung apoptosis induced by renal ischemia-reperfusion injury through α(2)AR/PI3K/Akt pathway. J Transl Med. (2018) 16:78. doi: 10.1186/s12967-018-1455-1

Crossref Full Text | Google Scholar

12. Zhang, H, Sha, J, Feng, X, Hu, X, Chen, Y, Li, B, et al. Dexmedetomidine ameliorates LPS induced acute lung injury via GSK-3β/STAT3-NF-κB signaling pathway in rats. Int Immunopharmacol. (2019) 74:105717. doi: 10.1016/j.intimp.2019.105717

PubMed Abstract | Crossref Full Text | Google Scholar

13. He, H, Liu, P, and Li, P. Dexmedetomidine ameliorates cardiac ischemia/reperfusion injury by enhancing autophagy through activation of the AMPK/SIRT3 pathway. Drug Des Devel Ther. (2023) 17:3205–18. doi: 10.2147/DDDT.S428024

PubMed Abstract | Crossref Full Text | Google Scholar

14. Tao, WH, Shan, XS, Zhang, JX, Liu, HY, Wang, BY, Wei, X, et al. Dexmedetomidine attenuates Ferroptosis-mediated renal ischemia/reperfusion injury and inflammation by inhibiting ACSL4 via α2-AR. Front Pharmacol. (2022) 13:782466. doi: 10.3389/fphar.2022.782466

Crossref Full Text | Google Scholar

15. Chen, X, Chen, Q, Qin, Z, Alam, A, Zhao, H, West, R, et al. Dexmedetomidine attenuates inflammation in elderly patients following major hepatobiliary and pancreatic surgery: a randomized clinical trial. Clin Interv Aging. (2024) 19:981–91. doi: 10.2147/CIA.S455987

PubMed Abstract | Crossref Full Text | Google Scholar

16. Gorman, EA, O'kane, CM, and Mcauley, DF. Acute respiratory distress syndrome in adults: diagnosis, outcomes, long-term sequelae, and management. Lancet. (2022) 400:1157–70. doi: 10.1016/S0140-6736(22)01439-8

PubMed Abstract | Crossref Full Text | Google Scholar

17. Peng, S, Huang, J, Liu, X, Deng, J, Sun, C, Tang, J, et al. Interpretable machine learning for 28-day all-cause in-hospital mortality prediction in critically ill patients with heart failure combined with hypertension: a retrospective cohort study based on medical information mart for intensive care database-IV and eICU databases. Front Cardiovasc Med. (2022) 9:994359. doi: 10.3389/fcvm.2022.994359

Crossref Full Text | Google Scholar

18. Keating, GM. Dexmedetomidine: a review of its use for sedation in the intensive care setting. Drugs. (2015) 75:1119–30. doi: 10.1007/s40265-015-0419-5

PubMed Abstract | Crossref Full Text | Google Scholar

19. Lorton, D, and Bellinger, DL. Molecular mechanisms underlying β-adrenergic receptor-mediated cross-talk between sympathetic neurons and immune cells. Int J Mol Sci. (2015) 16:5635–65. doi: 10.3390/ijms16035635

PubMed Abstract | Crossref Full Text | Google Scholar

20. Scanzano, A, and Cosentino, M. Adrenergic regulation of innate immunity: a review. Front Pharmacol. (2015) 6:171. doi: 10.3389/fphar.2015.00171

PubMed Abstract | Crossref Full Text | Google Scholar

21. Sharma, D, and Farrar, JD. Adrenergic regulation of immune cell function and inflammation. Semin Immunopathol. (2020) 42:709–17. doi: 10.1007/s00281-020-00829-6

Crossref Full Text | Google Scholar

22. Berkowitz, DE, Price, DT, Bello, EA, Page, SO, and Schwinn, DA. Localization of messenger RNA for three distinct alpha 2-adrenergic receptor subtypes in human tissues. Evidence for species heterogeneity and implications for human pharmacology. Anesthesiology. (1994) 81:1235–44.

PubMed Abstract | Google Scholar

23. Carnet Le Provost, K, Kepp, O, Kroemer, G, and Bezu, L. Trial watch: dexmedetomidine in cancer therapy. Onco Targets Ther. (2024) 13:2327143. doi: 10.1080/2162402X.2024.2327143

PubMed Abstract | Crossref Full Text | Google Scholar

24. Ferreira, JA, and Bissell, BD. Misdirected sympathy: the role of Sympatholysis in Sepsis and septic shock. J Intensive Care Med. (2018) 33:74–86. doi: 10.1177/0885066616689548

PubMed Abstract | Crossref Full Text | Google Scholar

25. Li, Y, Wang, B, Zhang, LL, He, SF, Hu, XW, Wong, GT, et al. Dexmedetomidine combined with general anesthesia provides similar intraoperative stress response reduction when compared with a combined general and epidural anesthetic technique. Anesth Analg. (2016) 122:1202–10. doi: 10.1213/ANE.0000000000001165

PubMed Abstract | Crossref Full Text | Google Scholar

26. Biccard, BM, Goga, S, and De Beurs, J. Dexmedetomidine and cardiac protection for non-cardiac surgery: a meta-analysis of randomised controlled trials. Anaesthesia. (2008) 63:4–14. doi: 10.1111/j.1365-2044.2007.05306.x

PubMed Abstract | Crossref Full Text | Google Scholar

27. Gong, Z, Ma, L, Zhong, YL, Li, J, Lv, J, and Xie, YB. Myocardial protective effects of dexmedetomidine in patients undergoing cardiac surgery: a meta-analysis and systematic review. Exp Ther Med. (2017) 13:2355–61. doi: 10.3892/etm.2017.4227

PubMed Abstract | Crossref Full Text | Google Scholar

28. Liu, J, Shi, K, Hong, J, Gong, F, Mo, S, Chen, M, et al. Dexmedetomidine protects against acute kidney injury in patients with septic shock. Ann Palliat Med. (2020) 9:224–30. doi: 10.21037/apm.2020.02.08

PubMed Abstract | Crossref Full Text | Google Scholar

29. Hu, G, Shi, Z, Shao, W, and Xu, B. MicroRNA-214-5p involves in the protection effect of Dexmedetomidine against neurological injury in Alzheimer's disease via targeting the suppressor of zest 12. Brain Res Bull. (2022) 178:164–72. doi: 10.1016/j.brainresbull.2021.10.016

PubMed Abstract | Crossref Full Text | Google Scholar

30. Wang, N, Nie, H, Zhang, Y, Han, H, Wang, S, Liu, W, et al. Dexmedetomidine exerts cerebral protective effects against cerebral ischemic injury by promoting the polarization of M2 microglia via the Nrf2/HO-1/NLRP3 pathway. Inflamm Res. (2022) 71:93–106. doi: 10.1007/s00011-021-01515-5

PubMed Abstract | Crossref Full Text | Google Scholar

31. Yu, Q, Zou, L, Yuan, X, Fang, F, and Xu, F. Dexmedetomidine protects against septic liver injury by enhancing autophagy through activation of the AMPK/SIRT1 signaling pathway. Front Pharmacol. (2021) 12:658677. doi: 10.3389/fphar.2021.658677

PubMed Abstract | Crossref Full Text | Google Scholar

32. Tian, L, Liu, Q, Wang, X, Chen, S, and Li, Y. Fighting ferroptosis: protective effects of dexmedetomidine on vital organ injuries. Life Sci. (2024) 354:122949. doi: 10.1016/j.lfs.2024.122949

PubMed Abstract | Crossref Full Text | Google Scholar

33. Grasselli, G, Calfee, CS, Camporota, L, Poole, D, Amato, MBP, Antonelli, M, et al. ESICM guidelines on acute respiratory distress syndrome: definition, phenotyping and respiratory support strategies. Intensive Care Med. (2023) 49:727–59. doi: 10.1007/s00134-023-07050-7

PubMed Abstract | Crossref Full Text | Google Scholar

34. Lin, P, Zhao, Y, Li, X, Jiang, F, and Liang, Z. Decreased mortality in acute respiratory distress syndrome patients treated with corticosteroids: an updated meta-analysis of randomized clinical trials with trial sequential analysis. Crit Care. (2021) 25:122. doi: 10.1186/s13054-021-03546-0

Crossref Full Text | Google Scholar

35. Ahmad, S, Wrennall, JA, Goriounova, AS, Sekhri, M, Iskarpatyoti, JA, Ghosh, A, et al. Specific inhibition of Orai1-mediated calcium Signalling resolves inflammation and clears Bacteria in an acute respiratory distress syndrome model. Am J Respir Crit Care Med. (2024) 209:703–15. doi: 10.1164/rccm.202308-1393OC

PubMed Abstract | Crossref Full Text | Google Scholar

36. Villar, J, Ferrando, C, Martínez, D, Ambrós, A, Muñoz, T, Soler, JA, et al. Dexamethasone treatment for the acute respiratory distress syndrome: a multicentre, randomised controlled trial. Lancet Respir Med. (2020) 8:267–76. doi: 10.1016/S2213-2600(19)30417-5

PubMed Abstract | Crossref Full Text | Google Scholar

37. Hendrickson, KW, Peltan, ID, and Brown, SM. The epidemiology of acute respiratory distress syndrome before and after coronavirus disease 2021. Crit Care Clin. (2021) 37:703–16. doi: 10.1016/j.ccc.2021.05.001

PubMed Abstract | Crossref Full Text | Google Scholar

38. Meyer, NJ, Gattinoni, L, and Calfee, CS. Acute respiratory distress syndrome. Lancet. (2021) 398:622–37. doi: 10.1016/S0140-6736(21)00439-6

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: dexmedetomidine, acute respiratory distress syndrome, mortality, propensity score, MIMIC IV database

Citation: Ye C, Yu Y and Liu Y (2025) Dexmedetomidine administration reduced mortality in patients with acute respiratory distress syndrome: a propensity score-matched cohort analysis. Front. Med. 12:1565098. doi: 10.3389/fmed.2025.1565098

Received: 22 January 2025; Accepted: 07 April 2025;
Published: 17 April 2025.

Edited by:

Verena Tretter, Medical University of Vienna, Austria

Reviewed by:

Jian-Xin Zhou, Capital Medical University, China
Jovana Stanisavljevic, University of Belgrade, Serbia

Copyright © 2025 Ye, Yu and Liu. 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.

*Correspondence: Conglin Ye, MTQyNjc5MDQ2NkBxcS5jb20=

Disclaimer: 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.