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Research

Role of Pharmacists in the Post-ChatGPT Era

Prepared and Presented by: Dr. Muhammad Shahzad Aslam
Ph.D., M.Phil., Pharm-D, R.Ph
Assistant Professor
School of Traditional Chinese Medicine
Xiamen University Malaysia

The role of pharmacists in the post-ChatGPT era is undergoing a significant transformation. Artificial intelligence (AI) technologies like ChatGPT reshape the landscape of healthcare and pharmacy practice. Traditionally, pharmacists have been essential in dispensing medications, providing patient counseling, and ensuring safe drug interactions. Now, with AI's integration, their responsibilities are expanding beyond these conventional roles.

ChatGPT and other AI-driven systems can streamline many of the time-consuming tasks pharmacists face. These tasks include automating prescription management, processing insurance claims, and providing accurate, real-time drug information to patients. This frees up pharmacists to focus on more patient-centered care, such as personalized medication therapy management and deeper consultations. AI tools can also assist in data analysis. They predict potential health risks. They improve treatment outcomes through more precise medication plans.

Furthermore, as healthcare moves towards a more digital-first approach, pharmacists can leverage AI to enhance telepharmacy services, offering remote consultations and support. In this evolving landscape, pharmacists will not be replaced by AI. They will instead work alongside it. Pharmacists will use these tools to enhance their professional expertise. They will provide higher-quality, more efficient care to patients. The post-ChatGPT era is an exciting frontier. Pharmacists will play a crucial role in navigating the intersection of technology and healthcare.

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Research Uncategorized

Artificial Intelligence Applications Using ChatGPT in Education: Case Studies and Practices

Prepared and Presented by: Dr. Muhammad Shahzad Aslam

email address: aslam.shahzad@xmu.edu.my

Xiamen University Malaysia. 27 August 2024.

Artificial intelligence applications, particularly those leveraging ChatGPT, are transforming the education sector by enhancing personalized learning experiences and improving accessibility. Case studies reveal that educators are using ChatGPT to develop interactive tutoring systems. These systems adapt to individual student needs. They offer real-time feedback and explanations. In classrooms, teachers employ AI-driven tools to facilitate discussions. They generate engaging content and streamline administrative tasks. This allows for a more focused and efficient teaching environment. These practices not only foster deeper understanding and engagement among students but also equip educators with innovative resources to enhance their pedagogical approaches.

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Blog Research

🌍 Call for Chapter Proposals: Global Perspectives on Antiviral Drug Development 🌍

I'm excited to announce a unique opportunity for researchers and professionals in the fields of public health, virology, pharmaceutical sciences, and policy-making! We are currently seeking chapter proposals for our upcoming book titled "Global Perspectives on Antiviral Drug Development." This book will explore how various countries have developed and managed antiviral drugs amidst rapidly evolving viral threats like COVID-19, MERS, Zika, and Monkeypox.

πŸ” Objectives:

  • Enhance evidence-based knowledge about global antiviral strategies.
  • Facilitate innovation by showcasing cutting-edge technologies in drug development.
  • Support informed policy development through data-driven insights.
  • Improve public health outcomes by addressing access and ethical challenges.

πŸ“… Important Dates:

  • Proposal Submission Deadline: September 29, 2024
  • Full Chapters Due: December 1, 2024

We invite you to contribute and share your insights by submitting a chapter proposal (1,000-2,000 words). The proposed chapters should align with the mission and objectives of this book.

πŸ”— Submit Proposal Here: https://www.igi-global.com/publish/call-for-papers/submit/7962

πŸ”— More Information: https://www.igi-global.com/publish/call-for-papers/call-details/7962

Editors:

  • Muhammad Shahzad Aslam
  • Bancha Yingngam
  • Tariq Javed
  • Sana Riaz

Let’s collaborate to drive the future of antiviral drug development and contribute to global public health!

#antiviral #drugdevelopment #globalhealth #publichealth #pharmaceuticals #research #innovation #policydevelopment #opportunity #callforchapters #academia #globalhealthsecurity #igiGlobal

Categories
Research

[Call for Book Chapter]Artificial Intelligence (AI) for Precision Medicine in Treating Rare Disorders:

A Roadmap for Healthcare Practitioners in treating rare disorders is a groundbreaking exploration of the convergence of artificial intelligence (AI) and precision medicine, revolutionizing the future of healthcare. This comprehensive book offers a unique perspective on how cutting-edge AI technologies are reshaping the field of medicine, enabling personalized and targeted treatment approaches with unprecedented accuracy and efficiency.

Drawing upon the latest advancements in AI and its applications in healthcare, this book delves into the realm of deep precision medicine. It explores the synergy between AI algorithms, big data analytics, and genomic profiling, unraveling the potential for precise diagnosis, prognosis, and treatment selection across various diseases.

Through real-world case studies and expert insights, readers will gain a deep understanding of the role of AI in deciphering complex molecular data, identifying novel therapeutic targets, and predicting patient responses to various treatments. The book explores how AI-driven models can optimize drug discovery, streamline clinical trials and improve patient outcomes by enabling tailored interventions based on individual genetic profiles, biomarkers, and clinical data in treating rare diseases.

Covering a broad spectrum of topics, including machine learning, deep learning, NLP, and medical imaging analysis, this book provides a comprehensive roadmap for healthcare professionals, researchers, and students to navigate the integration of AI and precision medicine. It also delves into the ethical and regulatory considerations surrounding AI in healthcare, ensuring responsible and equitable implementation of these transformative technologies.

Submission Procedure:

The researcher can submit the book chapter directly through an e-mail address (aslam.shahzad@xmu.edu.my). The book will be published in CRC affiliated publishing house. There is no publication charges.

Categories
Research

Epistemology and Diabetic Care

Dear researchers, academics, and professionals,

We are pleased to announce the Call for Papers for the upcoming topic title as "Epistemology and Diabetes Care".
This topic aims to bring together scholars and experts from various disciplines to explore the intersection of epistemology and diabetes care.
We invite you to submit your original research papers and contribute to this intellectually.
Scope and Themes:
The Epistemology and Diabetes Care issue seeks to delve into the philosophical and theoretical aspects of knowledge generation, acquisition, and dissemination in the field of diabetes care.
We encourage submissions that explore the following themes:
Epistemological foundations of diabetes research: Examining the underlying assumptions, methodologies, and paradigms in diabetes care research and their impact on knowledge production.
The role of evidence-based practice: Exploring the use of empirical evidence and its integration with clinical expertise and patient values in diabetes care decision-making.
Patient perspectives and knowledge: Investigating the epistemic role of patients in the management of their own diabetes, including the challenges they face and their contributions to knowledge creation.
Ethics and epistemology in diabetes care: Addressing ethical considerations related to knowledge acquisition, communication, and implementation in the field of diabetes care.
Epistemic injustices in diabetes care: Examining the presence of epistemic biases, inequalities, and injustices in the diagnosis, treatment, and management of diabetes.

Submit your manuscript here.

https://www.frontiersin.org/research-topics/57130/epistemology-and-diabetes-care

Categories
Research Research Survey

A Retrospective, Non-Interventional, Multi-Centre Cohort Study on Olfactory and Gustatory outcomes among Long COVID-19 patients

Patient information sheet

You are invited to participate in a research study being and looking at the incidence of sensory symptoms in participants who have COVID-19 symptoms developed during or after an infection and continuing for more than 12 weeks; and/or ongoing symptomatic COVID symptoms between 4 and 12 weeks after the start of acute symptoms. We will also study the incidence of psychological symptoms in post-covid participants. In addition, recent literature suggests that some patients who survive COVID-19 are likely to have some psychological and neurological symptoms.  

1.What is the purpose of the study?

To screen post-COVID-19 patients OR long COVID-hauler for olfactory, gustatory and psychological symptoms . The current study is design to collect the data two times (12 month each) during 24 months of the study. The knowledge will assist in deepening understanding of the long-term or Post-exposure impact of COVID-19 population thus facilitate strategies, prevention and treatment of olfactory, gustatory and psychological symptoms.

2.Who is conducting this study?

The current study involve multi-center research team at private Traditional and Chinese Medicine (T&CM) clinic in collaborated with Xiamen university Malaysia MoU’s (T&CM) private sector to observational study with Long COVID-19 patients.

3.Why have I been invited to participate in this study?

According to the NICE guidelines on long-COVID-19; Post-COVID-19 syndrome (symptoms developed during or after an infection and continuing for more than 12 weeks; and ongoing symptomatic COVID (symptoms between 4 and 12 weeks after the start of acute symptoms) is the definitions of the current study.

4.What if I don't want to take part in this study or if I want to withdraw later?

Participation in this study is voluntary and your decision will not affect the medical management.  If you wish to withdraw from the study you can do so at any time without justifying your decision.  If you do withdraw from the study, all of the data already collected about you as part of the study will be destroyed and no data or information collected will be used in anyway by the researchers or sent outside this institution. No additional information will be collected for the purposes of this study and you will not be contacted again.

5.What does this study involve?

Participation in this study involves allowing the study investigators to interview. The study involve questionnaire.  The recruitment was made initially according to eligible criteria. One of the research investigators will meet you at private Traditional and Chinese Medicine (T&CM) clinic. A follow up survey will be done at 12 months after first survey. The follow-up survey will be in the form of telephonic interview answering a series of questions in-case if participant unable to visit the clinic. This will assist us to determine if there have been any changes during that course of time. The research will be using a set of screening tools (questionnaire) called Post Traumatic Stress Scale (PTSS-14); Impact of Events Scale-Revised (IES-R); Depression Anxiety Stress Scales (DASS 21). The following tools measure some of the symptoms you may be experiencing as a result of being through post-COVID-19.  

6.Will my taking part in this study be kept confidential?

You have the right to privacy and all information that is collected during this study is confidential to the extent permitted by the applicable laws and regulations.  Your study data will be made anonymous by the assignment of a unique number to you alone.  All data collected from you will then be identified by this number. No data which could be used to identify you will be transferred from your medical notes. The medical information collected during this study will then be transferred into study database(s) and processed to allow the results of this study to be analysed and reported or published for scientific purposes. Paper records including contact information will be stored in locked room accessible only to authorized study personnel.  Electronic information will be kept on password-protected computers accessible only to authorized study personnel. Your identity will be kept confidential at all times. Your personal information will only be disclosed with your permission, except as required by law.

7.Are there risks to me in taking part in this study?

No questions will be asked of you about any specific instances or memories of your time during COVID-19 pandemic. However, it is possible that you may experience some discomfort or distress as you may recollect some unpleasant memories during your COVID-19 time. Participation in the study will ensure that distress can be potentially diagnosed and appropriate referral made. In the unlikely event that you do feel distressed by any of the questions, we would encourage you to discuss any concerns with the study coordinator or your General Practitioner.

8.Will I benefit from the study?

This study aims to look at the olfactory, gustatory and psychological simpact of post-COVID-19 and gain further medical knowledge. This study may help to improve treatment for others with similar conditions, and the results of the study will be published in a major international medical journal. You may not receive any direct benefits from this research.

9.Will taking part in this study cost me anything, and will I be paid?

Participation in this research study will not cost you anything. You will not be paid or receive any financial benefits from taking part in this research study.

10.What happens with the results?

The results obtained will be collated and published in medical journals, conference presentations and other professional forums.  In any publication, information will be provided in such a way that you cannot be identified. Results of the study will be provided to you, if you wish.

11.What should I do if I want to discuss this study further before I decide?

When you have read this information, the study investigator will discuss it with you and clarify any queries you may have. If you would like to know more at any stage, please do not hesitate to contact the study coordinator.