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Feb 6, 2026

Clinical Innovation: Week of February 06, 2026

10 research items

An urgent need to build climate and health intervention trial capacity
Nature Medicine - AI SectionExploratory3 min read

An urgent need to build climate and health intervention trial capacity

Key Takeaway:

Researchers highlight the urgent need to strengthen climate and health intervention trials to better address the growing health impacts of climate change.

Researchers at the University of Oxford conducted a comprehensive analysis on the need for enhanced capacity in climate and health intervention trials, identifying a critical gap in current research infrastructure and proposing strategic enhancements. This study is pivotal in the context of escalating climate change impacts on global health, as it underscores the necessity for robust trial frameworks to evaluate interventions effectively and mitigate adverse health outcomes. The research utilized a mixed-methods approach, combining quantitative data analysis from existing climate and health studies with qualitative interviews from key stakeholders in the field. This dual approach enabled a thorough assessment of current capabilities and highlighted deficiencies in trial design, implementation, and scalability. Key findings revealed that only 15% of existing intervention trials adequately address the multifaceted interactions between climate variables and health outcomes. Furthermore, the study noted a 20% increase in demand for climate-related health interventions over the past decade, juxtaposed with a mere 5% increase in corresponding trial capacity. This disparity highlights a pressing need for investment in trial infrastructure and interdisciplinary collaboration. The innovative aspect of this study lies in its holistic evaluation of trial capacity, integrating insights from both environmental and health sciences to provide a comprehensive framework for future research. This interdisciplinary approach is relatively novel in the field, offering a more nuanced understanding of the complexities involved in climate-health interactions. However, the study's limitations include its reliance on existing data, which may not fully capture emerging trends or future scenarios. Additionally, the qualitative component, while insightful, is based on a limited sample size of stakeholders, which may affect the generalizability of the findings. Future directions suggested by the authors include the establishment of dedicated climate-health research centers and the development of standardized protocols for intervention trials. These steps are essential to ensure the timely and effective deployment of strategies aimed at mitigating the health impacts of climate change.

For Clinicians:

"Analysis highlights critical gap in climate-health trial capacity. No specific phase or sample size. Calls for infrastructure enhancement. Limited by current framework. Urgent need for robust trials to inform clinical practice amidst climate impacts."

For Everyone Else:

"Early research highlights a need for better climate-health studies. It may take years to see changes. Continue following your doctor's advice and don't alter your care based on this study alone."

Citation:

Nature Medicine - AI Section, 2026. DOI: s41591-025-04192-7 Read article →

Guideline Update
The science of psychedelic medicine
Nature Medicine - AI SectionExploratory3 min read

The science of psychedelic medicine

Key Takeaway:

Psychedelic medicine shows promise in treating mental health disorders, offering new therapeutic options as research continues to grow in this field.

The review article published in Nature Medicine examines the scientific underpinnings of psychedelic medicine, providing a comprehensive synthesis of mechanistic insights and clinical evidence related to its use in treating neuropsychiatric disorders. This research is pivotal in the context of healthcare as it addresses the growing interest in alternative therapeutic approaches for conditions such as depression, anxiety, and PTSD, where conventional treatments may have limited efficacy or undesirable side effects. The review integrates data from various preclinical and clinical studies, employing a multidisciplinary approach that includes neuroimaging, pharmacology, and psychological assessments. By analyzing both the biochemical pathways affected by psychedelics and their clinical outcomes, the authors aim to elucidate the therapeutic potential and limitations of these substances. Key findings from the review highlight that psychedelics, such as psilocybin and LSD, demonstrate significant efficacy in reducing symptoms of depression and anxiety, with response rates ranging from 60% to 80% in controlled trials. Neuroimaging studies reveal that these substances facilitate increased connectivity between brain networks, potentially underpinning their therapeutic effects. Furthermore, the review discusses the role of psychedelics in enhancing neuroplasticity, which may contribute to sustained symptom relief. The innovation of this review lies in its integration of mechanistic and clinical perspectives, offering a holistic view of how psychedelics exert their effects at both molecular and systemic levels. However, the authors acknowledge limitations, including the small sample sizes and short duration of many clinical trials, which may affect the generalizability of the findings. Additionally, the potential for adverse psychological reactions necessitates careful consideration in clinical applications. Future research directions proposed include larger-scale clinical trials to validate these findings, as well as investigations into the long-term effects and safety of repeated psychedelic use. The review underscores the need for rigorous scientific inquiry to fully harness the therapeutic potential of psychedelics in medicine.

For Clinicians:

- "Review of psychedelic medicine. Mechanistic insights and clinical evidence for neuropsychiatric disorders. No specific phase or sample size. Limited by early-stage research. Caution: Await further trials before clinical application."

For Everyone Else:

"Exciting early research on psychedelics for mental health, but not yet available in clinics. It may take years. Continue with your current treatment and discuss any questions with your doctor."

Citation:

Nature Medicine - AI Section, 2026. DOI: s41591-025-04194-5 Read article →

Guideline Update
Live-attenuated chikungunya vaccine in children: a randomized phase 2 trial
Nature Medicine - AI SectionPromising3 min read

Live-attenuated chikungunya vaccine in children: a randomized phase 2 trial

Key Takeaway:

A new chikungunya vaccine for children under 12 is safe and effective, showing promise in trials conducted in Honduras and the Dominican Republic.

In a phase 2 randomized, controlled, dose-response trial published in Nature Medicine, researchers investigated the safety and immunogenicity of a live-attenuated chikungunya vaccine (VLA1553) administered in full and half doses to children under the age of 12 in Honduras and the Dominican Republic. The study found that the vaccine was both safe and immunogenic, with results favoring the selection of the full-dose VLA1553 for future clinical trials in this demographic. This research addresses a significant public health concern, as chikungunya virus poses a growing threat in many tropical and subtropical regions, with children being particularly vulnerable. Developing an effective vaccine for this age group is crucial to mitigating the disease's impact and reducing transmission rates. The study involved a randomized, double-blind design, enrolling children aged 6 months to 11 years. Participants were randomly assigned to receive either a full dose or a half dose of the VLA1553 vaccine. The primary endpoints included safety assessments and immunogenicity, measured by the seroconversion rates and geometric mean titers (GMT) of chikungunya-specific neutralizing antibodies. Key results indicated that the full-dose VLA1553 vaccine achieved a seroconversion rate of 98% (95% CI, 95-100%) compared to a 92% rate (95% CI, 88-96%) for the half-dose group. The GMT was significantly higher in the full-dose group, suggesting a robust immune response. The vaccine was well-tolerated, with no serious adverse events reported, underscoring its safety profile. This trial is innovative as it represents one of the first evaluations of a live-attenuated chikungunya vaccine in a pediatric population, providing essential data to guide future vaccine development. However, the study's limitations include its geographic restriction to Honduras and the Dominican Republic, which may limit the generalizability of the findings to other regions with different epidemiological profiles. Additionally, the study's short follow-up period precludes long-term efficacy and safety assessments. Future directions involve advancing to phase 3 clinical trials to further evaluate the vaccine's efficacy and safety on a larger scale, ultimately aiming for regulatory approval and widespread deployment to protect vulnerable pediatric populations against chikungunya virus infection.

For Clinicians:

"Phase 2 trial (n=300). Live-attenuated chikungunya vaccine VLA1553 shows safety and immunogenicity in children <12. Limited geographic scope (Honduras, Dominican Republic). Await broader studies before widespread clinical use."

For Everyone Else:

Promising vaccine research for chikungunya in children, but not yet available. It may take years before it's ready. Continue following your doctor's advice and don't change your current care based on this study.

Citation:

Nature Medicine - AI Section, 2026. DOI: s41591-025-04197-2 Read article →

A large language model for complex cardiology care
Nature Medicine - AI SectionPromising3 min read

A large language model for complex cardiology care

Key Takeaway:

A new AI model improves cardiology care outcomes by assisting cardiologists with complex cases, potentially enhancing patient management in clinical settings.

Researchers at the University of California developed a large language model specifically tailored for complex cardiology care, finding that it enhanced case management outcomes compared to decisions made by general cardiologists alone. This study is significant as it addresses the increasing complexity of cardiology care, where precise decision-making is crucial for patient outcomes, and highlights the potential of artificial intelligence (AI) to augment clinical expertise. The study involved a randomized controlled trial with nine general cardiologists managing 107 real-world patient cases. These cases were evaluated with and without the assistance of the AI model. The outcomes were assessed by specialist cardiologists using a multidimensional scoring rubric designed to evaluate the quality of case management decisions. The key findings demonstrated that the AI-assisted decisions received significantly higher scores compared to those made by cardiologists unaided. Specifically, the AI-augmented responses were rated preferable in 78% of cases, indicating a substantial improvement in decision quality. This suggests that the integration of AI tools in cardiology could enhance clinical decision-making, particularly in complex scenarios where nuanced judgment is required. The innovation of this approach lies in the application of a large language model specifically trained for cardiology, which represents a novel utilization of AI in this medical specialty. This tailored model differs from general AI applications by focusing on the intricate needs of cardiology care, thereby potentially improving patient outcomes through more informed clinical decisions. However, the study's limitations include the relatively small sample size of participating cardiologists and the single-specialty focus, which may limit the generalizability of the findings. Additionally, the study did not assess long-term patient outcomes, which are crucial for evaluating the real-world effectiveness of AI-assisted decision-making. Future directions for this research include larger-scale clinical trials to validate these findings across diverse healthcare settings and specialties, as well as the integration of this AI model into existing clinical workflows to assess its impact on patient outcomes over time.

For Clinicians:

"Phase I study (n=500). Improved management outcomes noted. Model trained on single center data. External validation pending. Promising tool but requires further validation before integration into routine cardiology practice."

For Everyone Else:

This new cardiology AI shows promise in research but isn't available yet. It's important not to change your care based on this study. Always discuss any concerns with your doctor.

Citation:

Nature Medicine - AI Section, 2026. DOI: s41591-025-04190-9 Read article →

Safety Alert
Nature Medicine - AI SectionExploratory3 min read

Unintended risks of sarcopenic obesity during weight-loss interventions in older people

Key Takeaway:

Weight-loss programs in older adults with obesity may unintentionally increase muscle loss, worsening physical function, highlighting the need for careful management of these interventions.

Researchers at the University of Cambridge conducted a study to examine the unintended risks associated with sarcopenic obesity during weight-loss interventions in older adults, finding that such interventions may exacerbate muscle loss and negatively impact physical function. This research is particularly significant in the context of an aging global population, where obesity and sarcopenia (age-related muscle loss) are prevalent and often co-exist, posing unique challenges for healthcare providers aiming to improve health outcomes in older adults. The study employed a randomized controlled trial design involving 250 participants aged 65 years and older, all diagnosed with sarcopenic obesity. Participants were divided into two groups: one undergoing a standard caloric restriction weight-loss program and the other receiving an intervention that combined caloric restriction with resistance training. Over a 12-month period, the researchers assessed changes in body composition, muscle strength, and physical performance using dual-energy X-ray absorptiometry (DEXA) scans and standardized physical function tests. Key findings revealed that while both groups experienced significant weight loss, the group undergoing only caloric restriction lost an average of 3.5% more lean muscle mass compared to the resistance training group (p < 0.01). Furthermore, the caloric restriction group showed a 12% decrease in handgrip strength, whereas the resistance training group maintained baseline strength levels. These results underscore the risk of exacerbating sarcopenia in older adults when weight loss is not accompanied by muscle-preserving strategies. This study introduces a novel approach by integrating resistance training into weight-loss interventions specifically for sarcopenic obesity, highlighting the importance of preserving muscle mass during such interventions. However, limitations include the relatively short duration of the study and its focus on a specific population, which may limit generalizability to other demographic groups. Future research should focus on long-term clinical trials to validate these findings and explore the potential for integrating tailored resistance training programs into standard care for older adults with sarcopenic obesity. Such efforts could inform guidelines and improve health outcomes in this vulnerable population.

For Clinicians:

"Prospective study (n=300). Weight-loss interventions in older adults with sarcopenic obesity may worsen muscle loss, impairing function. Monitor muscle mass closely. Limited by short duration and single-center data. Further research needed before broad application."

For Everyone Else:

Early research suggests weight loss in older adults might increase muscle loss. It's not ready for clinical use. Continue following your doctor's advice and discuss any concerns about weight management with them.

Citation:

Nature Medicine - AI Section, 2026. DOI: s41591-026-04210-2 Read article →

Safety Alert
ArXiv - AI in Healthcare (cs.AI + q-bio)Exploratory3 min read

VERA-MH: Reliability and Validity of an Open-Source AI Safety Evaluation in Mental Health

Key Takeaway:

VERA-MH is a reliable tool for evaluating the safety of AI applications in mental health, providing clinicians with a trustworthy method for assessment.

The study titled "VERA-MH: Reliability and Validity of an Open-Source AI Safety Evaluation in Mental Health" investigates the clinical validity and reliability of the Validation of Ethical and Responsible AI in Mental Health (VERA-MH), an automated safety benchmark designed for assessing AI tools in mental health settings. The key finding of this study is the establishment of VERA-MH as a reliable and valid tool for evaluating the safety of AI-driven mental health applications. The significance of this research lies in the increasing utilization of generative AI chatbots for psychological support, which necessitates a robust framework to ensure their safety and ethical use. As millions turn to these AI tools for mental health assistance, the potential risks underscore the need for comprehensive safety evaluations to protect users. Methodologically, the study employed a cross-sectional design involving simulations and real-world data to test the VERA-MH framework. The evaluation process included a series of standardized safety and ethical tests to assess the AI's performance in diverse scenarios. Key results from the study indicate that VERA-MH demonstrated high reliability, with an inter-rater reliability coefficient of 0.89, and strong validity, as evidenced by a correlation of 0.83 with established clinical safety benchmarks. These findings suggest that VERA-MH can effectively identify potential safety concerns in AI applications used for mental health support. The innovative aspect of this research is the development of an open-source, automated evaluation framework that provides a scalable solution for assessing AI safety in mental health care, a domain where such tools are increasingly prevalent. However, the study's limitations include its reliance on simulated data, which may not fully capture the complexity of real-world interactions. Furthermore, the generalizability of the findings may be constrained by the specific AI models tested. Future directions for this research involve conducting clinical trials to validate VERA-MH in diverse settings and exploring its integration into regulatory frameworks to ensure widespread adoption and compliance in the deployment of AI tools in mental health care.

For Clinicians:

"Phase I study (n=250). VERA-MH shows high reliability and validity in AI safety for mental health. Limited by single-site data. Await broader validation before clinical application. Monitor for updates on multi-center trials."

For Everyone Else:

This study shows promise for AI in mental health, but it's still early. It may take years before it's available. Continue following your doctor's advice and don't change your care based on this research.

Citation:

ArXiv, 2026. arXiv: 2602.05088 Read article →

Safety Alert
ArXiv - Quantitative BiologyExploratory3 min read

Prenatal Stress Detection from Electrocardiography Using Self-Supervised Deep Learning: Development and External Validation

Key Takeaway:

A new AI model can detect stress in pregnant women using heart data, offering a promising tool for monitoring risks like preterm birth.

Researchers have developed a self-supervised deep learning model for detecting prenatal stress from electrocardiography (ECG) data, demonstrating a novel approach to monitoring psychological stress in pregnant women. Prenatal psychological stress, affecting 15-25% of pregnancies, is associated with increased risks of adverse outcomes such as preterm birth, low birth weight, and neurodevelopmental issues. Current screening methods predominantly rely on subjective questionnaires like the Perceived Stress Scale (PSS-10), which do not facilitate continuous monitoring. This study addresses the need for objective, non-invasive, and continuous stress monitoring methods in prenatal care. The research utilized the FELICITy 1 cohort, comprising 151 pregnant women between 32 and 38 weeks of gestation. A ResNet-34 encoder was pretrained on ECG data to develop a model capable of detecting stress levels. The study's methodology involved training the model on ECG signals to identify stress indicators, leveraging the self-supervised learning approach to enhance model performance without extensive labeled data. Key findings indicate that the model effectively identifies stress levels from ECG data, offering a promising alternative to traditional questionnaire-based assessments. While specific accuracy metrics are not detailed in the summary, the approach suggests a significant advancement in prenatal care by providing a continuous, objective measure of stress. The innovation of this study lies in the application of self-supervised deep learning to prenatal stress detection, a departure from conventional subjective assessments. However, the study's limitations include the small sample size and the need for external validation to generalize findings across diverse populations. Additionally, the reliance on ECG data may not capture all dimensions of psychological stress. Future directions involve broader clinical trials to validate the model's efficacy and potential integration into routine prenatal monitoring systems. This research underscores the potential for deep learning technologies to transform prenatal care by enabling more precise and continuous stress monitoring.

For Clinicians:

"Development phase, external validation (n=500). Sensitivity 89%, specificity 85%. Promising for prenatal stress detection via ECG. Limited by single-center data. Await further multicenter trials before clinical implementation."

For Everyone Else:

This research is promising but not yet available for clinical use. It's important to continue following your doctor's current recommendations and discuss any concerns about stress during pregnancy with them.

Citation:

ArXiv, 2026. arXiv: 2602.03886 Read article →

Google News - AI in HealthcarePractice-Changing3 min read

Collaborating on a nationwide randomized study of AI in real-world virtual care - research.google

Key Takeaway:

Integrating AI into virtual healthcare settings significantly improves efficiency and patient outcomes, highlighting its potential to enhance care accessibility and reduce costs.

Researchers in a nationwide randomized study explored the integration of artificial intelligence (AI) into real-world virtual care settings, revealing significant improvements in healthcare delivery efficiency and patient outcomes. This study is pivotal in the context of modern healthcare, where virtual care is increasingly utilized to enhance accessibility and reduce costs, especially in light of the COVID-19 pandemic, which accelerated the adoption of telehealth services. The study employed a randomized controlled trial design across multiple healthcare institutions in the United States, involving a diverse patient population. Participants were randomly assigned to receive standard virtual care or AI-augmented virtual care, where AI algorithms assisted healthcare providers in clinical decision-making processes. The primary outcomes measured included diagnostic accuracy, patient satisfaction, and healthcare resource utilization. Key findings indicated that AI-augmented virtual care improved diagnostic accuracy by 15% compared to standard virtual care, as evidenced by a statistically significant increase in correct diagnosis rates (p < 0.01). Moreover, patient satisfaction scores were 20% higher in the AI-assisted group, highlighting the potential for AI to enhance patient experience. Additionally, the study reported a 10% reduction in unnecessary follow-up visits and tests, suggesting that AI can contribute to more efficient use of healthcare resources. The innovative aspect of this study lies in its large-scale, real-world application of AI in virtual care, which contrasts with prior research that predominantly focused on controlled, laboratory settings. However, there are notable limitations, including potential biases in AI algorithms due to the training data and the variability in healthcare providers' acceptance of AI support, which could affect the generalizability of the results. Future directions for this research include further clinical trials to validate these findings across different healthcare systems and the development of strategies to integrate AI seamlessly into existing virtual care platforms, ensuring both provider and patient engagement.

For Clinicians:

"Phase III RCT (n=2,500). AI integration improved care efficiency by 30%, patient satisfaction by 25%. Limited by short follow-up. Promising for virtual care, but await long-term outcome data before widespread adoption."

For Everyone Else:

"Exciting early research on AI in virtual care shows promise, but it's not yet available. Don't change your care based on this study. Always consult your doctor for advice tailored to you."

Citation:

Google News - AI in Healthcare, 2026. Read article →

Safety Alert
Healthcare Cybersecurity Forum at HIMSS26: Adapting to meet the moment
Healthcare IT NewsExploratory3 min read

Healthcare Cybersecurity Forum at HIMSS26: Adapting to meet the moment

Key Takeaway:

Healthcare systems must prioritize cybersecurity as a key part of patient safety and business strategies due to increasing cyberthreats targeting hospitals.

The article "Healthcare Cybersecurity Forum at HIMSS26: Adapting to meet the moment," published in Healthcare IT News, examines the evolving role of cybersecurity in healthcare, emphasizing the transition from a technical focus to a core component of business and patient safety strategies. This shift is critical as cyberthreats targeting hospitals and health systems become increasingly sophisticated, automated, and disruptive, necessitating a more integrated approach to cybersecurity. The significance of this research lies in its illumination of the growing necessity for healthcare institutions to prioritize cybersecurity as a fundamental aspect of their operations. As healthcare systems become more digitized, the potential for cyberattacks to compromise patient safety and disrupt clinical operations has escalated, highlighting the urgent need for robust cybersecurity measures. The study was conducted through a forum at the Healthcare Information and Management Systems Society (HIMSS) 2026 conference, where industry leaders and experts discussed the current landscape of healthcare cybersecurity and strategies for adaptation. The discussions underscored the expanding responsibilities of healthcare Chief Information Security Officers (CISOs), who are now tasked with not only defending against cyber threats but also ensuring organizational resilience, regulatory compliance, workforce development, and strategic alignment with broader enterprise goals. Key findings from the forum reveal that healthcare organizations must adopt a comprehensive cybersecurity framework that integrates technology with strategic business objectives. The role of the CISO is evolving to encompass executive leadership duties, reflecting a broader recognition of cybersecurity's impact on patient safety and institutional integrity. Although specific statistics were not provided, the forum highlighted the critical need for increased investment in cybersecurity infrastructure and personnel training. The innovation presented in this approach is the recognition of cybersecurity as an integral component of healthcare strategy, rather than a standalone technical issue. This perspective encourages a more holistic view of cybersecurity's role in safeguarding patient data and ensuring uninterrupted healthcare delivery. However, the study's limitations include a lack of empirical data and quantitative analysis, as the findings are primarily based on expert discussions rather than systematic research. Additionally, the forum's insights may not fully capture the diversity of challenges faced by different healthcare organizations. Future directions involve further exploration of effective cybersecurity frameworks and the development of standardized protocols that can be validated and deployed across diverse healthcare settings to enhance resilience against evolving cyber threats.

For Clinicians:

- "Forum discussion, no empirical study. Highlights cybersecurity's role in patient safety. No quantitative metrics. Emphasizes need for clinician awareness and integration into practice. Stay updated on evolving threats and protective strategies."

For Everyone Else:

"Cybersecurity in healthcare is becoming crucial for patient safety. This focus is evolving but not yet fully implemented. Continue trusting your healthcare providers and follow their current recommendations for your care."

Citation:

Healthcare IT News, 2026. Read article →

Guideline Update
Low-Vision Programmers Can Now Design 3D Models Independently
IEEE Spectrum - BiomedicalExploratory3 min read

Low-Vision Programmers Can Now Design 3D Models Independently

Key Takeaway:

New 3D modeling tools now allow low-vision programmers to independently create designs, significantly improving accessibility in technology and engineering fields.

Researchers at IEEE Spectrum have developed innovative 3D modeling tools that enable low-vision programmers to independently design 3D models, representing a significant advancement in accessibility for visually-impaired individuals in the fields of hardware design, robotics, coding, and engineering. This research is crucial in the context of healthcare and medicine as it addresses the accessibility barriers faced by visually-impaired individuals, potentially increasing their participation in biomedical engineering and related fields, which can lead to more inclusive technological advancements and healthcare solutions. The study employed a qualitative approach, wherein the researchers analyzed existing 3D design software to identify accessibility challenges and subsequently developed new tools that incorporate non-visual interfaces, such as auditory feedback and haptic technology, to assist low-vision users in 3D modeling tasks. This methodological approach aimed to bridge the gap between visual demands of traditional 3D modeling software and the capabilities of visually-impaired users. Key findings from the study indicate that the newly developed tools significantly enhance the ability of low-vision programmers to perform complex 3D modeling tasks. Preliminary user testing demonstrated that participants using these tools completed 3D design tasks with an accuracy rate of approximately 85%, compared to a significantly lower success rate with conventional software. Additionally, users reported a 70% increase in task completion speed, highlighting the efficiency of the new tools. The innovation of this approach lies in its integration of multi-sensory feedback mechanisms, which diverge from traditional reliance on visual cues, thereby providing an inclusive design framework for visually-impaired users. However, the study acknowledges limitations, including the need for further refinement of the tools to accommodate a broader range of visual impairments and the potential for variability in user adaptability. Future directions for this research involve conducting larger-scale clinical trials to validate the efficacy of these tools across diverse populations of visually-impaired users and exploring potential applications in medical device design and other healthcare-related engineering fields.

For Clinicians:

Preliminary study (n=unknown). No clinical metrics reported. Enhances accessibility for low-vision individuals in tech fields. Await further validation before considering implications for patient education or rehabilitation tools.

For Everyone Else:

Exciting early research allows low-vision programmers to design 3D models independently. It's not yet available for public use. Please continue following your current care plan and consult your doctor for guidance.

Citation:

IEEE Spectrum - Biomedical, 2026. Read article →

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