Kainan Sun
Research Subjects
Kainan Sun has a total of 6 co-authors. Here are the top co-authors by number of shared publications:
- Brandon J. Patterson
U.S. Health Outcomes & Epidemiology, GSK, Philadelphia, PA
2 shared publications - Catherine Balderston McGuiness
Health Economics and Outcomes Research, Real-World Evidence, IQVIA, Wayne, PA, USA
2 shared publications - Chi-Chang Chen
IQVIA
2 shared publications - Lisa Glasser
Vaccines and Immune Therapies, AstraZeneca , Wilmington, Delaware
2 shared publications - Philip O. Buck
Moderna Inc., Cambridge, MA 02139, USA
2 shared publications - Siyu Ma
GSK, US Health Economics and Outcomes Research, Philadelphia, PA, USA
1 shared publication
Latest Publications
- Open Access
- 1 March 2022
- Published by Elsevier in Journal of the American Pharmacists Association
- Vol. 62 (2) , 526-536.e10
Factors influencing series completion rates of recombinant herpes zoster vaccine in the United States: A retrospective pharmacy and medical claims analysis
- 1 March 2022
- Published by Elsevier in Journal of the American Pharmacists Association
- Vol. 62 (2) , 526-536.e10
Open AccessFactors influencing series completion rates of recombinant herpes zoster vaccine in the United States: A retrospective pharmacy and medical claims analysis
- Open Access
- 13 April 2021
- Published by Taylor & Francis in Human Vaccines & Immunotherapeutics
- Vol. 17 (8) , 2482-2487
Early examination of real-world uptake and second-dose completion of recombinant zoster vaccine in the United States from October 2017 to September 2019
Shingrix (Recombinant zoster vaccine, RZV) was approved in October 2017 in the United States (US) for the prevention of herpes zoster in adults aged 50 years and older. The vaccine is administered in two doses, with the second dose administration recommended between two and six months after the first dose. Examination of uptake and series completion is important to ensure appropriate use, especially at the time of vaccine introduction. This report provides demographic characteristics of patients receiving RZV between October 2017 and September 2019, first- and second-dose uptake, and a cumulative estimation of second-dose completion by month for US adults aged 50 years and older. Monthly uptake increased rapidly since October 2017; overall, 7,097,441 first doses of RZV were administered along with 4,277,636 second doses during the observed timeframe. Among people with an observed first-dose administration, 70% and 80% completed the two-dose series within six and 12 months post initial dose, respectively. This evidence suggests that RZV has rapidly been adopted by a large population in the US and most are following manufacturer or policy recommendations regarding series completion. Further analyses are needed to explore potential patient, provider, and policy-relevant characteristics associated with second-dose completion that could serve as targets for further improvement.
- 13 April 2021
- Published by Taylor & Francis in Human Vaccines & Immunotherapeutics
- Vol. 17 (8) , 2482-2487
Open AccessEarly examination of real-world uptake and second-dose completion of recombinant zoster vaccine in the United States from October 2017 to September 2019
Shingrix (Recombinant zoster vaccine, RZV) was approved in October 2017 in the United States (US) for the prevention of herpes zoster in adults aged 50 years and older. The vaccine is administered in two doses, with the second dose administration recommended between two and six months after the first dose. Examination of uptake and series completion is important to ensure appropriate use, especially at the time of vaccine introduction. This report provides demographic characteristics of patients receiving RZV between October 2017 and September 2019, first- and second-dose uptake, and a cumulative estimation of second-dose completion by month for US adults aged 50 years and older. Monthly uptake increased rapidly since October 2017; overall, 7,097,441 first doses of RZV were administered along with 4,277,636 second doses during the observed timeframe. Among people with an observed first-dose administration, 70% and 80% completed the two-dose series within six and 12 months post initial dose, respectively. This evidence suggests that RZV has rapidly been adopted by a large population in the US and most are following manufacturer or policy recommendations regarding series completion. Further analyses are needed to explore potential patient, provider, and policy-relevant characteristics associated with second-dose completion that could serve as targets for further improvement.