Congenital toxoplasmosis in Austria: Prenatal screening for prevention is cost-saving

被引:62
作者
Prusa, Andrea-Romana [1 ]
Kasper, David C. [2 ]
Sawers, Larry [3 ]
Walter, Evelyn [4 ]
Hayde, Michael [1 ]
Stillwaggon, Eileen [5 ]
机构
[1] Med Univ Vienna, Dept Pediat & Adolescent Med, Toxoplasmosis Reference Lab, Vienna, Austria
[2] Med Univ Vienna, Dept Lab Med, Vienna, Austria
[3] Amer Univ, Dept Econ, Washington, DC 20016 USA
[4] Inst Pharmaecon Res, Vienna, Austria
[5] Gettysburg Coll, Dept Econ, Gettysburg, PA 17325 USA
关键词
POLYMERASE-CHAIN-REACTION; FREE-RANGE CHICKENS; GONDII INFECTION; HIGH PREVALENCE; RISK-FACTORS; PREGNANCY; TRANSMISSION; GENOTYPES; CHILDREN; MANIFESTATIONS;
D O I
10.1371/journal.pntd.0005648
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background Primary infection of Toxoplasma gondii during pregnancy can be transmitted to the unborn child and may have serious consequences, including retinochoroiditis, hydrocephaly, cerebral calcifications, encephalitis, splenomegaly, hearing loss, blindness, and death. Austria, a country with moderate seroprevalence, instituted mandatory prenatal screening for toxoplasma infection to minimize the effects of congenital transmission. This work compares the societal costs of congenital toxoplasmosis under the Austrian national prenatal screening program with the societal costs that would have occurred in a No-Screening scenario. Methodology/Principal findings We retrospectively investigated data from the Austrian Toxoplasmosis Register for birth cohorts from 1992 to 2008, including pediatric long-term follow-up until May 2013. We constructed a decision-analytic model to compare lifetime societal costs of prenatal screening with lifetime societal costs estimated in a No-Screening scenario. We included costs of treatment, lifetime care, accommodation of injuries, loss of life, and lost earnings that would have occurred in a No-Screening scenario and compared them with the actual costs of screening, treatment, lifetime care, accommodation, loss of life, and lost earnings. We replicated that analysis excluding loss of life and lost earnings to estimate the budgetary impact alone. Our model calculated total lifetime costs of (sic)103 per birth under prenatal screening as carried out in Austria, saving (sic)323 per birth compared with No-Screening. Without screening and treatment, lifetime societal costs for all affected children would have been (sic)35 million per year; the implementation costs of the Austrian program are less than (sic)2 million per year. Calculating only the budgetary impact, the national program was still cost-saving by more than (sic)15 million per year and saved (sic)258 million in 17 years. Conclusions/Significance Cost savings under a national program of prenatal screening for toxoplasma infection and treatment are outstanding. Our results are of relevance for health care providers by supplying economic data based on a unique national dataset including long-term follow-up of affected infants.
引用
收藏
页数:24
相关论文
共 69 条
[41]   Prevention of congenital toxoplasmosis in Slovenia by serological screening of pregnant women [J].
Logar, J ;
Petrovec, M ;
Novak-Antolic, Z ;
Premru-Srsen, T ;
Cizman, M ;
Arnez, M ;
Kraut, A .
SCANDINAVIAN JOURNAL OF INFECTIOUS DISEASES, 2002, 34 (03) :201-204
[42]   Serologic diagnosis of congenital toxoplasmosis [J].
Lourdes Roc, Maria ;
Pilar Palacian, Maria ;
Lomba, Elena ;
Luisa Monforte, Maria ;
Rebaje, Victor ;
Revillo Pinilla, Maria Jose .
ENFERMEDADES INFECCIOSAS Y MICROBIOLOGIA CLINICA, 2010, 28 (08) :517-519
[43]   EARLY AND LONGITUDINAL EVALUATIONS OF TREATED INFANTS AND CHILDREN AND UNTREATED HISTORICAL PATIENTS WITH CONGENITAL TOXOPLASMOSIS - THE CHICAGO COLLABORATIVE TREATMENT TRIAL [J].
MCAULEY, J ;
BOYER, KM ;
PATEL, D ;
METS, M ;
SWISHER, C ;
ROIZEN, N ;
WOLTERS, C ;
STEIN, L ;
STEIN, M ;
SCHEY, W ;
REMINGTON, J ;
MEIER, P ;
JOHNSON, D ;
HEYDEMAN, P ;
HOLFELS, E ;
WITHERS, S ;
MACK, D ;
BROWN, C ;
PATTON, D ;
MCLEOD, R .
CLINICAL INFECTIOUS DISEASES, 1994, 18 (01) :38-72
[44]   Outcome of treatment for congenital toxoplasmosis, 1981-2004: The national collaborative Chicago-based, congenital toxoplasmosis study [J].
McLeod, R ;
Boyer, K ;
Karrison, T ;
Kasza, K ;
Swisher, C ;
Roizen, N ;
Jalbrzikowski, J ;
Remington, J ;
Heydemann, P ;
Noble, AG ;
Mets, M ;
Holfels, E ;
Withers, S ;
Latkany, P ;
Meier, P .
CLINICAL INFECTIOUS DISEASES, 2006, 42 (10) :1383-1394
[45]   Prematurity and Severity Are Associated With Toxoplasma gondii Alleles (NCCCTS, 1981-2009) [J].
McLeod, Rima ;
Boyer, Kenneth M. ;
Lee, Daniel ;
Mui, Ernest ;
Wroblewski, Kristen ;
Karrison, Theodore ;
Noble, A. Gwendolyn ;
Withers, Shawn ;
Swisher, Charles N. ;
Heydemann, Peter T. ;
Sautter, Mari ;
Babiarz, Jane ;
Rabiah, Peter ;
Meier, Paul ;
Grigg, Michael E. .
CLINICAL INFECTIOUS DISEASES, 2012, 54 (11) :1595-1605
[46]  
Moncada PA, 2012, EXPERT REV ANTI-INFE, V10, P815, DOI [10.1586/ERI.12.58, 10.1586/eri.12.58]
[47]  
OECD, 2015, AV ANN WAG
[48]  
OECD, 2012, MORT RISK VAL ENV HL
[49]   Severe Congenital Toxoplasmosis in the United States Clinical and Serologic Findings in Untreated Infants [J].
Olariu, Tudor Rares ;
Remington, Jack S. ;
McLeod, Rima ;
Alam, Ambereen ;
Montoya, Jose G. .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2011, 30 (12) :1056-1061
[50]  
Peyron F, 2000, COCHRANE DB SYST REV, DOI DOI 10.1002/14651858.CD001684