Cherdsak Duangchan

Dr. Cherdsak Duangchan

Princess Agrarajakumari Faculty of Nursing, Chulabhorn Royal Academy, Bangkok, Krung Thep Maha Nakhon, Thailand
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Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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TJThanakrit Jeamjitvibool
Thanakrit Jeamjitvibool
Cherdsak DuangchanCherdsak Duangchan
Cherdsak Duangchan
AMAndria Mousa
Andria Mousa
Wiriya MahikulWiriya Mahikul
Wiriya Mahikul
This study examined the association between resilience and psychological distress in healthcare workers, the general population, and patients during the COVID-19 pandemic. We searched the PubMed, Web of Science, PsycInfo, Science Direct, and Nursing and Allied Health databases. Included articles examined healthcare workers (e.g., physicians and nurses), the general population, and patients during the COVID-19 pandemic. Studies of exposure to other infectious diseases related to epidemics or pandemics (e.g., SARS and MERS) were excluded. This study was performed following the Cooper matrix review method and PRISMA guidelines, followed by a meta-analysis of study results using R version 4.1.2. A random effect model was used for the pooled analysis. This study was registered with PROSPERO (registration No. CRD42021261429). Based on the meta-analysis, we found a moderate negative relationship between overall resilience and psychological distress (r = −0.42, 95% confidence interval [CI]: −0.45 to −0.38, p < 0.001). For the subgroup analysis, a moderately significant negative relationship between overall resilience and psychological distress was found among healthcare workers (r = −0.39, 95% CI: −0.44 to −0.33, p < 0.001), which was weaker than in the general population (r = −0.45, 95% CI: −0.50 to −0.39, p < 0.001) and in patients (r = −0.43; 95% CI: −0.52 to −0.33; p < 0.001). This association was robust, although the heterogeneity among individual effect sizes was substantial (I2 = 94%, 99%, and 74%, respectively). This study revealed a moderate negative relationship between resilience and psychological distress in healthcare workers, the general population, and patients. For all these populations, interventions and resources are needed to improve individuals’ resilience and ability to cope with psychological distress during the COVID-19 pandemic and in future disease outbreaks.

Suchanart InwannaSuchanart Inwanna
Suchanart Inwanna
Cherdsak DuangchanCherdsak Duangchan
Cherdsak Duangchan
AMAlicia K. Matthews
Alicia K. Matthews
Medication non-adherence is a leading cause of poor treatment outcomes among Thai patients with psychiatric disorders and creates challenges for psychiatric nurses. This systematic review synthesized research on intervention effectiveness for antipsychotic medication adherence in Thai schizophrenic populations. Following PRISMA guidelines, searches were completed in seven databases, including PubMed, PsycINFO, CINAHL, Web of Science, Scopus, ThaiJO, and Google Scholar. No restriction dates were used. Screening and extraction of data were performed systematically. Eligible studies consisted of nine quasi-experimental and two randomized control trial studies. The Joanna Briggs Institute Meta-Analysis of Statistics Assessment and Review Instrument (JBI-MAStARI) was used to assess the studies’ methodological quality. This review revealed that individual counseling combined with cognitive-behavioral therapy (CBT) and motivational interviewing (MI) techniques improved and maintained medication adherence behavior over time. Post-testing after intervention completion and at 3- and 6-month follow-ups showed that treatment group participants were more adherent than control group participants (p < 0.01). These findings suggest that incorporating CBT and MI into clinical practice can enhance medication adherence behavior. Booster session efficacy for reinforcing and sustaining adherence should be investigated. Greater rigor is warranted in future intervention studies based on a quality appraisal of previous studies.

11 March 2021 in Research in Nursing & Health
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Cherdsak DuangchanCherdsak Duangchan
Cherdsak Duangchan
AMAlicia K. Matthews
Alicia K. Matthews

1 December 2023 in Ethnicity & Disease
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Journal Article
Open access
AMAlicia K. Matthews
Alicia K. Matthews
ASAlana D. Steffen
Alana D. Steffen
LBLarisa A. Burke
Larisa A. Burke
GDGeri Donenberg
Geri Donenberg
Cherdsak DuangchanCherdsak Duangchan
Cherdsak Duangchan
DDDarcy Dodd
Darcy Dodd
Purpose: To describe the training, preliminary results, and lessons learned from using patient navigators to increase the enrollment of low-income patients in a health system–supported and electronic health record–linked patient portal. Methods: Patient navigators (n=4) were trained to assist patients in a federally qualified health center to enroll in and use patient portals. Patient navigators were stationed at 3 clinic locations. Data from the electronic health record system (Epic) were used to compare MyChart patient portal activation rates and use among patients for the 8 months before and after patient navigation services were offered. Results: Navigators offered 83% of eligible patients with activation assistance. Sixty-four percent of the patients (n=1062) offered MyChart enrollment assistance accepted help. Seventy-four percent of assisted patients with no prior MyChart enrollment activated their accounts during that clinic visit. The primary reason for declining MyChart assistance was a lack of access to or comfort with technology. Patient portal activation increased during the 8 months when navigators were at the clinics (51%) compared to the previous 8 months (44%). Most new users viewed lab results and read a message [χ2(1)=49.3, p<.001], with significant increases evident for African Americans [44% before, 49% during; χ2(1)=40.4, p<.001] and Latinx patients [52% before, 60% during; χ2(1)=6.15, p=.013]. Conclusion: Study results suggest that using patient navigators is feasible and beneficial for increasing patient enrollment in the Federally Qualified Health Centers context. However, patient-, clinic-, and system-level factors were identified as barriers and should be addressed in future research studies.

1 December 2021 in European Journal of Oncology Nursing
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Closed access
Cherdsak DuangchanCherdsak Duangchan
Cherdsak Duangchan
ASAlana Steffen
Alana Steffen
AMAlicia K. Matthews
Alicia K. Matthews

1 February 2023 in Health Equity
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Journal Article
Open access
LBLarisa Ann Burke
Larisa Ann Burke
ASAlana D. Steffen
Alana D. Steffen
SKSandeep Kataria
Sandeep Kataria
KWKarriem S. Watson
Karriem S. Watson
RWRobert A. Winn
Robert A. Winn
AMAlicia K. Matthews
Alicia K. Matthews
Purpose: To examine the association of cigarette use and smoking-related health conditions by race/ethnicity among diverse and low-income patients at a federally qualified health center (FQHC). Methods: Demographics, smoking status, health conditions, death, and health service use were extracted from electronic medical data for patients seen between September 1, 2018, and August 31, 2020 (n=51,670). Smoking categories included everyday/heavy smoker, someday/light smoker, former smoker, or never smoker. Results: Current and former smoking rates were 20.1% and 15.2%, respectively. Males, Black, White, non-partnered, older, and Medicaid/Medicare patients were more likely to smoke. Compared with never smokers, former and heavy smokers had higher odds for all health conditions except respiratory failure, and light smokers had higher odds of asthma, chronic obstructive pulmonary disease, emphysema, and peripheral vascular disease. All smoking categories had more emergency department visits and hospitalizations than never smokers. The associations between smoking status and health conditions differed by race/ethnicity. White patients who smoked had a greater increase in odds of stroke and other cardiovascular diseases compared with Hispanic and Black patients. Black patients who smoked had a greater increase in odds of emphysema and respiratory failure compared with Hispanic patients. Black and Hispanic patients who smoked had a greater increase in emergency care use compared with White patients. Conclusion: Smoking was associated with disease burden and emergency care and differed by race/ethnicity. Health Equity Implications: Resources to document smoking status and offer cessation services should be increased in FQHCs to promote health equity for lower income populations.