Elamin Elbasha

Dr. Elamin Elbasha

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Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

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

Representative Publications

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1 January 2007 in Emerging Infectious Diseases
Verified
Journal Article
Open access
EEElamin Elbasha
Elamin Elbasha
EDErik J. Dasbach
Erik J. Dasbach
RIRalph P. Insinga
Ralph P. Insinga
We present a transmission dynamic model that can assess the epidemiologic consequences and cost-effectiveness of alternative strategies of administering a prophylactic quadrivalent (types 6/11/16/18) human papillomavirus (HPV) vaccine in a setting of organized cervical cancer screening in the United States. Compared with current practice, vaccinating girls before the age of 12 years would reduce the incidence of genital warts (83%) and cervical cancer (78%) due to HPV 6/11/16/18. The incremental cost-effectiveness ratio (ICER) of augmenting this strategy with a temporary catch-up program for 12- to 24-year olds was US $4,666 per quality-adjusted life year (QALY) gained. Relative to other commonly accepted healthcare programs, vaccinating girls and women appears cost-effective. Including men and boys in the program was the most effective strategy, reducing the incidence of genital warts, cervical intraepithelial neoplasia, and cervical cancer by 97%, 91%, and 91%, respectively. The ICER of this strategy was $45,056 per QALY.

29 July 2009 in BMC Infectious Diseases
Verified
Journal Article
Open access
PDF file
RIRalph P Insinga
Ralph P Insinga
EDErik J Dasbach
Erik J Dasbach
EEElamin Elbasha
Elamin Elbasha
Natural history models of human papillomavirus (HPV) infection and disease have been used in a number of policy evaluations of technologies to prevent and screen for HPV disease (e.g., cervical cancer, anogenital warts), sometimes with wide variation in values for epidemiologic and clinical inputs. The objectives of this study are to: (1) Provide an updated critical and systematic review of the evidence base to support epidemiologic and clinical modeling of key HPV disease-related parameters in the context of an HPV multi-type disease transmission model which we have applied within a U.S. population context; (2) Identify areas where additional studies are particularly needed.

7 April 2006 in Bulletin of Mathematical Biology
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Journal Article
Closed access
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EEElamin Elbasha
Elamin Elbasha
AGAbba B. Gumel
Abba B. Gumel

1 September 2005 in Mathematical Biosciences
Verified
Journal Article
Closed access
EEElamin Elbasha
Elamin Elbasha
AGAlison P. Galvani
Alison P. Galvani

8 October 2008 in Bulletin of Mathematical Biology
Verified
Journal Article
Closed access
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EEElamin Elbasha
Elamin Elbasha
EDErik J. Dasbach
Erik J. Dasbach
RIRalph P. Insinga
Ralph P. Insinga

12 July 2007 in Infectious Agents and Cancer
Verified
Journal Article
Open access
PDF file
RIRalph P Insinga
Ralph P Insinga
EDErik J Dasbach
Erik J Dasbach
EEElamin Elbasha
Elamin Elbasha
KLKai-Li Liaw
Kai-Li Liaw
EBEliav Barr
Eliav Barr
We describe type-specific progression, regression and persistence of incident human papillomavirus (HPV)-6-11-16 and -18 infections, along with type distribution in cervical intra-epithelial neoplasia (CIN) lesions.