1.Bibliography of Clinical Research in Malaysia: Methods and Brief Results
Cheong Lieng Teng ; Zuhanariah Mohd Nordin ; Chun Sien NG ; Cheng Chun Goh
The Medical Journal of Malaysia 2014;69(Supplement A):4-7
This article describes the methodology of this bibliography. A
search was conducted on the following: (1) bibliographic
databases (PubMed, Scopus, and other databases) using
search terms that maximize the retrieval of Malaysian
publications; (2) Individual journal search of Malaysian healthrelated
journals; (3) A targeted search of Google and Google
Scholar; (4) Searching of Malaysian institutional repositories;
(5) Searching of Ministry of Health and Clinical Research
Centre website. The publication years were limited to 2000-
2013. The citations were imported or manually entered into
bibliographic software Refworks. After removing duplicates,
and correcting data entry errors, PubMed’s Medical Subject
Headings (MeSH terms) were added. Clinical research is
coded using the definition “patient-oriented-research or
research conducted with human subjects (or on material of
human origin) for which the investigator directly interacts with
the human subjects at some point during the study.” A
bibliography of citations [n=2056] that fit the criteria of clinical
research in Malaysia in selected topics within five domains
was generated: Cancers [589], Cardiovascular diseases [432],
Infections [795], Injuries [142], and Mental Health [582]. This
is done by retrieving citations with the appropriate MESH
terms, as follow: For cancers (Breast Neoplasms; Colorectal
Neoplasms; Uterine Cervical Neoplasms), for cardiovascular
diseases (Coronary Disease; Hypertension; Stroke), for
infections (Dengue; Enterovirus Infections, HIV Infections;
Malaria; Nipah Virus; Tuberculosis), for injuries (Accidents,
Occupational; Accidents, Traffic; Child Abuse; Occupational
Injuries), for mental health (Depression; Depressive Disorder;
Depressive Disorder, Major; Drug Users; Psychotic Disorders;
Suicide; Suicide, Attempted; Suicidal Ideation; SubstanceRelated
Disorders).
2.Pharmacological and Safety Profile of Dexlansoprazole: A New Proton Pump Inhibitor - Implications for Treatment of Gastroesophageal Reflux Disease in the Asia Pacific Region.
Khean Lee GOH ; Myung Gyu CHOI ; Ping I HSU ; Hoon Jai CHUN ; Varocha MAHACHAI ; Udom KACHINTORN ; Somchai LEELAKUSOLVONG ; Nayoung KIM ; Abdul Aziz RANI ; Benjamin C Y WONG ; Justin WU ; Cheng Tang CHIU ; Vikram SHETTY ; Joseph C BOCOBO ; Melchor M CHAN ; Jaw Town LIN
Journal of Neurogastroenterology and Motility 2016;22(3):355-366
Although gastroesophageal reflux disease is not as common in Asia as in western countries, the prevalence has increased substantially during the past decade. Gastroesophageal reflux disease is associated with considerable reductions in subjective well-being and work productivity, as well as increased healthcare use. Proton pump inhibitors (PPIs) are currently the most effective treatment for gastroesophageal reflux disease. However, there are limitations associated with these drugs in terms of partial and non-response. Dexlansoprazole is the first PPI with a dual delayed release formulation designed to provide 2 separate releases of medication to extend the duration of effective plasma drug concentration. Dexlansoprazole has been shown to be effective for healing of erosive esophagitis, and to improve subjective well-being by controlling 24-hour symptoms. Dexlansoprazole has also been shown to achieve good plasma concentration regardless of administration with food, providing flexible dosing. Studies in healthy volunteers showed no clinically important effects on exposure to the active metabolite of clopidogrel or clopidogrel-induced platelet inhibition, with no dose adjustment of clopidogrel necessary when coprescribed. This review discusses the role of the new generation PPI, dexlansoprazole, in the treatment of gastroesophageal reflux disease in Asia.
Asia*
;
Blood Platelets
;
Delayed-Action Preparations
;
Delivery of Health Care
;
Dexlansoprazole*
;
Efficiency
;
Esophagitis
;
Gastroesophageal Reflux*
;
Healthy Volunteers
;
Plasma
;
Prevalence
;
Proton Pump Inhibitors
;
Proton Pumps*
;
Protons*