National Institute of Allergy and Infectious Disease (NIAID) Funding for Studies of Hospital-Associated Bacterial Pathogens: Are Funds Proportionate to Burden of Disease?
© Perencevich et al; licensee BioMed Central Ltd. 2011
Received: 27 December 2011
Accepted: 26 January 2012
Published: 26 January 2012
Hospital-associated infections (HAIs) are associated with a considerable burden of disease and direct costs greater than $17 billion. The pathogens that cause the majority of serious HAIs are Enterococcus faecium, Staphylococcus aureus, Clostridium difficile, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter species, referred as ESCKAPE. We aimed to determine the amount of funding the National Institute of Health (NIH) National Institute of Allergy and Infectious Diseases (NIAID) allocates to research on antimicrobial resistant pathogens, particularly ESCKAPE pathogens.
The NIH Research Portfolio Online Reporting Tools (RePORT) database was used to identify NIAID antimicrobial resistance research grants funded in 2007-2009 using the terms "antibiotic resistance," "antimicrobial resistance," and "hospital-associated infection."
Funding for antimicrobial resistance grants has increased from 2007-2009. Antimicrobial resistance funding for bacterial pathogens has seen a smaller increase than non-bacterial pathogens. The total funding for all ESKCAPE pathogens was $ 22,005,943 in 2007, $ 30,810,153 in 2008 and $ 49,801,227 in 2009. S. aureus grants received $ 29,193,264 in FY2009, the highest funding amount of all the ESCKAPE pathogens. Based on 2009 funding data, approximately $1,565 of research money was spent per S. aureus related death and $750 of was spent per C. difficile related death.
Although the funding for ESCKAPE pathogens has increased from 2007 to 2009, funding levels for antimicrobial resistant bacteria-related grants is still lower than funding for antimicrobial resistant non-bacterial pathogens. Efforts may be needed to improve research funding for resistant-bacterial pathogens, particularly as their clinical burden increases.
The National Institutes of Health (NIH) has been successful over the past 60 years in funding research that has greatly advanced modern medicine. However, given limited resources, many have begun to question how these research funds are allocated to various diseases.[1–3] The NIH has listed five major criteria for the allocation of research funds: public health needs, the scientific quality of research, the probability of success, the maintenance of a diverse portfolio, and the maintenance of an adequate scientific infrastructure. While the Institute of Medicine panel has embraced these criteria as an appropriate framework for funding, they also concluded that the NIH does not adequately describe how public health need is assessed, and recommended the use of burdens and costs of diseases in strengthening their assessment and use of health data.
The relationship between burden of disease and research funding is an important metric to consider when determining funding priorities that impact public health. Hospital-acquired infections (HAIs) are associated with a considerable burden of disease. The Centers for Disease Control and Prevention (CDC) estimates that each year in the United States there are about 1.7 million HAIs and 99,000 associated deaths. The mean direct costs of HAIs (in 2005 dollars) range from $1,257 per case for catheter-associated urinary tract infections to $22,875 per case for ventilator-associated pneumonia.
The pathogens that cause the majority of serious HAIs are Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter species- commonly referred to as ESKAPE bacteria. Recently though, Clostridium difficile has emerged as an important nosocomial pathogen. In 2007, C. difficile was ranked as one of the 20 leading causes of death for people aged 65 and older. Thus, this study has included C. difficile in the ESKAPE bacteria definition, henceforth known as ESCKAPE bacteria.
The aim of this study was to determine the amount of funding the NIH's National Institute of Allergy and Infectious Diseases (NIAID) allocates to research on antimicrobial nosocomial pathogens, particularly ESCKAPE pathogens and to compare this funding to the burden of disease caused by two ESCKAPE pathogens.
Identifying Grants Using NIH RePORT Database
The NIH Research Portfolio Online Reporting Tools (RePORT) database was used to identify NIH-funded research grants. Searches were done during the month of November 2011 among all available fiscal years for retrospective grant funding data using the search terms "antibiotic resistance," "antimicrobial resistance," and "hospital-associated infection" that included the National Institute of Allergy and Infectious Diseases (NIAID) as the administration or funding agency. Over 11,000 grants were screened to exclude duplicates from the search terms.
Classifying Grants into Pathogen Categories
Abstracts of the remaining grants were viewed in detail and categorized by the pathogen of interest (e.g. bacteria, virus, fungi, parasites). If the pathogen was classified as bacteria, the grant was further analyzed for drug resistance and type of bacterial species. If unclear, the grant was reviewed by a second reviewer. Bacterial grants were then classified as hospital-associated and non-hospital-associated based on the type of pathogen. Special emphasis was placed on ESCKAPE bacteria.
National mortality data for MRSA and C. difficile were obtained from prior publications by the CDC's Active Surveillance Core and National Vital Statistics.[9, 10] Funding amounts for MRSA and C. difficile were then divided by the most recent national mortality statistics to estimate the dollar amount funded per death for each pathogen.
Number of NIAID Grants and Amounts by Search Term and Year
Fiscal Year (FY)
Total Amount ($)
Total Number of Grants
Amount per Grant ($)
Approximate NIAID budget
In 2005, there were an estimated 18,650 deaths among people infected with MRSA. Based on FY2009 funding data for Staphylococcus aureus, approximately $1,565 of research funding was spent per death. In 2007, 6,372 people infected with Clostridium difficile died. Based on FY2009 funding data, approximately $750 of research funding was spent per C. difficile death. According to the NIH RePORT database, NIAID funding for HIV/AIDS was estimated to be $1.302 billion. This is similar to previous reports of $1.244 billion of NIAID funds allocated to HIV/AIDS in 2009. Roughly 17,000 - 18,000 HIV deaths occur annually in the U.S. Based on these rough numbers approximately $72,000 - $76,000 per HIV/AIDS death was spent for research.
Using NIH RePORTER we also attempted to evaluate grants funded by other agencies for ESCKAPE pathogens during the FY2007 - 2009. We focused on three major agencies; CDC, the Agency for Healthcare Research and Quality (AHRQ), and Veteran's Health Administration (VHA). No information was obtained for AHRQ and no funding amounts were listed for VHA. During the search, there were only four grants listed for VHA in the FY2009. Nine grants related to ESCKAPE pathogens were funded by the CDC in FY2007-08 and decreased to six grants in FY2009. Funding amounts decreased over the same period from approximately $3 million in FY2007 to approximately $1.9 million in FY2009.
Currently, the antibiotic era is threatened by the convergence of three adverse circumstances: high levels of antibacterial resistance among important pathogens, a dwindling supply of novel classes of antibacterials, and a dramatic reduction in the number of pharmaceutical companies engaged in the discovery and development of antibacterial agents. While 10 new classes of antibiotics were discovered from the 1930s to the 1960s, only two new classes have been approved since 1970. In addition, due to the relatively unfavorable return on investment, pharmaceutical companies have been steering away from engaging in antibiotic-drug discovery.[14, 15]
The response to the public-health crisis of antibacterial resistance could be similar to the strategies used to counter HIV. For the past 30 years, NIH-funded research has made great progress in implementing various prevention measures, including reducing the transmission rate of perinatal HIV, HIV drug development and treatment, and a potential vaccine.[16, 17] In 2009, the NIH awarded $1.302 billion in research funding for HIV/AIDS.[NIH Research Portfolio Online Reporting Tools (RePORT) http://projectreporter.nih.gov]. As a marker of NIH's HIV research success, in the U.S. in 2005, there were more deaths attributed to MRSA infections than attributable to HIV/AIDS.
The NIH is not blind to the emerging problem of antibiotic resistance, and in response created the 'antimicrobial resistance' funding category. However, the title 'antimicrobial' includes viruses and parasites as well as antibiotic-resistant bacteria. Even though funding continues to increase in the antibiotic-resistance category, we found that only half of the funding is going to antibacterial research and the large increases in funding have targeted non-bacterial pathogens. The ESCKAPE pathogens are inherently different compared to viruses such as HIV and other pathogens such as Mycobacterium tuberculosis, thus they require specific attention. From a mortality stand point, even though in the United States MRSA and HIV may be on par with each other, the research dollars invested shows a stark difference ($1,565 vs. $72,000 per death) when only considering NIAID research dollars. Considering other agency dollars, not to mention funding from pharmaceutical companies, will only widen this gap further. In order to have the hope in making the tremendous advances seen in HIV research, antibacterial research would need increased backing. Separate RCDC funding categories in "Antibacterial Resistance" and "Hospital-acquired infections" might be needed in order to highlight the need for more research dollars and attention to this ongoing crisis.
Our estimates may be limited since we only assessed NIAID funding, and not other institutes in the NIH or other agencies such as the CDC, the Agency for Healthcare Research and Quality (AHRQ), or Veteran's Health Administration. However, NIAID is the major agency within NIH that focuses on antimicrobial research. NIAID currently spends $800 million per year in antimicrobial research, which includes $200 million annually in research to better understand the causes, consequences, and treatments of drug resistance. CDC has allocated approximately $17 million for antimicrobial resistance, which is mainly for preparedness, detection, and control purposes not for research. Congress appropriated $5 million for MRSA and related hospital-associated infections in 2007-2008, then in 2009 $17 million ($8 million for MRSA and the remaining for other HAI) to AHRQ. The VHA receives approximately $500 million in medical research but most of the funding is divided among other projects such as Gulf War illnesses, genomics, prosthetics, diabetes, and heart disease. Very little is given to antimicrobial research. The combined total from these various agencies is a fraction of what the NIAID funds, thus our research is representative of the funding situation of antimicrobial research. Our data may be limited by missing information in the NIH RePORT website. However, this is the best public access source of NIAID research funding and should be up to date for FY2007-2009. Finally, our estimates of the amount of research funding spent per S. aureus or C. difficile death may be an overestimate or underestimate since we do not have mortality data from FY2009. However, the number of deaths associated with MRSA or C. difficile should not have significantly declined because no new antibiotics have become available since 2005.
In summary, although it is impressive that the funding for ESCKAPE pathogens has increased over a relatively short period of time, funding levels for antimicrobial-resistant bacteria related grants is still lower than funding for antimicrobial-resistant, non-bacteria related grants. Annual NIAID funding for MRSA and C. difficile infections remains below $2,000 per death. Steps should be made in order to match the funding for ESCKAPE pathogens to their disease burden. If we are to have any hope in holding back the tide of antibacterial resistant pathogens as a cause of community and hospital-acquired infections, it is likely that funding will have to increase to the levels successfully employed in HIV-related research during the past three decades. NIAID should be encouraged to make a clear public commitment to increasing funding for the development of new antibacterials and expand the knowledge base around infection prevention.
Funding: ENP is supported by the US Department of Veterans Affairs Health Services Research and Development [grant IIR-09-099]. MLS is supported by the National Institute of Health/National Center for Research Resources [CTSA grant KL2 RR024980-04S1].
- Istook E: Research funding on major diseases is not proportionate to taxpayers' needs. J NIH Res. 1997, 9 (8): 26-8.Google Scholar
- Anderson C: NIH budget: A new kind of earmarking. Science. 1993, 260 (5107): 483View ArticlePubMedGoogle Scholar
- Marshall E: Lobbyists seek to reslice NIH's pie. Science. 1997, 276 (5311): 344-6. 10.1126/science.276.5311.344.View ArticlePubMedGoogle Scholar
- National Institutes of Health Working Group on Priority Setting: Setting research priorities at the National Institutes of Health. 1997, Bethesda, MD: National Institutes of HealthGoogle Scholar
- Committee on NIH Research Priority-Setting Process: Scientific opportunities and public needs: Improving priority setting and public input at the national institutes of health. 1998Google Scholar
- Klevens RM, Edwards JR, Richards CL, Horan TC, Gaynes RP, Pollock DA, Cardo DM: Estimating health care-associated infections and deaths in U.S. hospitals, 2002. Public Health Rep. 2007, 122 (2): 160-6.PubMed CentralPubMedGoogle Scholar
- Perencevich EN, Stone PW, Wright SB, Carmeli Y, Fisman DN, Cosgrove SE, Society for Healthcare Epidemiology of America: Raising standards while watching the bottom line: Making a business case for infection control. Infect Control Hosp Epidemiol. 2007, 28 (10): 1121-33. 10.1086/521852.View ArticlePubMedGoogle Scholar
- Rice LB: Federal funding for the study of antimicrobial resistance in nosocomial pathogens: No ESKAPE. J Infect Dis. 2008, 197 (8): 1079-81. 10.1086/533452.View ArticlePubMedGoogle Scholar
- Xu JQ, Kochanek KD, Murphy SL, Tejada-Vera B: Deaths: Final data for 2007. National vital statistics reports. 2010, Hyattsville, MD: National Center for Health StatisticsGoogle Scholar
- Klevens RM, Morrison MA, Nadle J, Petit S, Gershman K, Ray S, Harrison LH, Lynfield R, Dumyati G, Townes JM, Craig AS, Zell ER, Fosheim GE, McDougal LK, Carey RB, Fridkin SK, Active Bacterial Core surveillance (ABCs) MRSA Investigators: Invasive methicillin-resistant Staphylococcus aureus infections in the United States. JAMA. 2007, 298 (15): 1763-71. 10.1001/jama.298.15.1763.View ArticlePubMedGoogle Scholar
- National Institutes of Health National Institute of Allergy and Infectious Diseases: Congresional justification. 2008, Bethesda, MD: National Institutes of HealthGoogle Scholar
- Centers for Disease Control and Prevention: HIV surveillance report. 2008, [http://www.cdc.gov/hiv/topics/surveillance/resources/reports/]Google Scholar
- Wenzel RP: The antibiotic pipeline--challenges, costs, and values. N Engl J Med. 2004, 351 (6): 523-6. 10.1056/NEJMp048093.View ArticlePubMedGoogle Scholar
- Projan SJ: Why is big pharma getting out of antibacterial drug discovery?. Curr Opin Microbiol. 2003, 6 (5): 427-30. 10.1016/j.mib.2003.08.003.View ArticlePubMedGoogle Scholar
- Carlet J, Collignon P, Goldmann D, Goossens H, Gyssens IC, Harbarth S, Jarlier V, Levy SB, N'Doye B, Pittet D, Richtmann R, Seto WH, van der Meer JW, Voss A: Society's failure to protect a precious resource: Antibiotics. Lancet. 2011, 378 (9788): 369-71. 10.1016/S0140-6736(11)60401-7.View ArticlePubMedGoogle Scholar
- Burr CK, Lampe MA, Corle S, Margolin FS, Abresh C, Clark J, National Organizations' Collaborative to Eliminate Perinatal HIV in the US: An end to perinatal HIV: Success in the US requires ongoing and innovative efforts that should expand globally. J Public Health Policy. 2007, 28 (2): 249-60. 10.1057/palgrave.jphp.3200126.View ArticlePubMedGoogle Scholar
- Long EF, Owens DK: The cost-effectiveness of a modestly effective HIV vaccine in the United States. Vaccine. 2011, 29 (36): 6113-24. 10.1016/j.vaccine.2011.04.013.PubMed CentralView ArticlePubMedGoogle Scholar
- Bancroft EA: Antimicrobial resistance: It's not just for hospitals. JAMA. 2007, 298 (15): 1803-4. 10.1001/jama.298.15.1803.View ArticlePubMedGoogle Scholar
- Peters NK, Dixon DM, Holland SM, Fauci AS: The research agenda of the National Institute of Allergy and Infectious Diseases for antimicrobial resistance. J Infect Dis. 2008, 197 (8): 1087-93. 10.1086/533451.View ArticlePubMedGoogle Scholar
- FY2009 budget submission center for disease control and prevention discretionary all-purpose table [Internet]. Available from: http://www.cdc.gov/fmo/fmofybudget.htm
- Agency for Healthcare Research and Quality: AHRQ's efforts to prevent and reduce healthcare-associated infections: FY2009 projects. Rockville, MD: Agency for Healthcare Research and QualityGoogle Scholar
- Panangala SV: U.S. Congressional Research Service. Veterans medical care: FY2009 appropriations (RL34598; July 29, 2008).Google Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.