I’m excited to announce that I will be co-chairing the 2015 SHEA meeting with Susan Huang. The new format will combine the highly regarded SHEA Basic Training Course in Healthcare Epidemiology with plenary, abstracts and symposia focused on infection prevention topics including long-term care, implementation science, science communication, MDROs, device infections and antibiotic stewardship. A strong emphasis will be placed on networking and mentoring sessions. The meeting will take place in Orlando, Florida (May 14-17th). The abstract site will be open from August 1, 2014 to January 16, 2015 and awards will be given to the top abstracts and posters at all career levels. So, get busy making science and look forward to seeing you in Orlando!
Pondering vexing issues in infection prevention and control
Showing posts with label hospital acquired infections. Show all posts
Showing posts with label hospital acquired infections. Show all posts
Monday, June 2, 2014
SHEA 2015 - New Format - Abstracts - May 14-17
I’m excited to announce that I will be co-chairing the 2015 SHEA meeting with Susan Huang. The new format will combine the highly regarded SHEA Basic Training Course in Healthcare Epidemiology with plenary, abstracts and symposia focused on infection prevention topics including long-term care, implementation science, science communication, MDROs, device infections and antibiotic stewardship. A strong emphasis will be placed on networking and mentoring sessions. The meeting will take place in Orlando, Florida (May 14-17th). The abstract site will be open from August 1, 2014 to January 16, 2015 and awards will be given to the top abstracts and posters at all career levels. So, get busy making science and look forward to seeing you in Orlando!
Thursday, April 25, 2013
The Environment and HAI – Where does Biological Plausibility Come In?
This May's Infection Control and Hospital Epidemiology (ICHE) contained a randomized trial of copper-coated surfaces in ICU settings which reported a 50-70% reduction in several aggregate outcomes that included hospital-acquired infections and colonization with MRSA and VRE. In this guest blog post, physician-scientists Dr. Matthias Maiwald from the KK Women’s and Children’s Hospital in Singapore and Dr. Stephan Harbarth from University of Geneva Hospitals in Geneva, Switzerland question the plausibility of these findings and put them in the larger context of what actually causes HAIs.In 1965, Sir Austin Bradford Hill published a landmark paper, entitled “The Environment and Disease: Association or Causation?” in which he outlined what would become known as the “Bradford Hill Criteria.” The “Hill Criteria” help distinguish association from causation in epidemiological research. One of nine criteria was biological plausibility. Quoting: “It will be helpful if the causation we suspect is biologically plausible. But this is a feature I am convinced we cannot demand. What is biologically plausible depends upon the biological knowledge of the day.” As commented elsewhere, the spirit of this criterion is to check whether the proposed causation violates any of the known laws and facts of science of biology, and as Hill outlines, this depends on currently available knowledge. It is said that Hill did not intend the criteria to be applied rigidly in the sense of a checklist approach; instead, he regarded them as “viewpoints” that would merely help in the assessment.
Fast-forward to the May 2013 Special Topic Issue of ICHE concerning the role of the environment in infection prevention. In the issue’s introduction, Weber and Rutala quote figures from a 1991 article by Weinstein concerning the biologically plausible sources of healthcare-acquired infections (HAIs): “patients’ endogenous flora, 40-60%; cross infection via the hands of personnel, 20-40%; antibiotic-driven changes in flora, 20-25%; and other (including contamination of the environment), 20%.”
In the same issue, an article by Salgado and colleagues caught our attention. This clinical trial compares 614 patients randomly placed into standard ICU rooms or into rooms where 6 frequently-touched items (e.g. bed rails, overbed tables, intravenous poles, etc.) had been replaced with copper alloy surfaces. The measured primary outcomes, according to the paper’s methods, were:
(a) any HAIs and
(b) colonization with methicillin-resistant Staphylococcus aureus (MRSA) or vancomycin-resistant enterococci (VRE). Besides HAI and colonization, outcomes presented in the results section included the numbers of patients who had
(c) both HAI and colonization,
(d) HAI and/or colonization,
(e) HAI only but no colonization (i.e. number of patients who had HAI minus the ones who had both HAI and colonization), and
(f) colonization only but no HAI.
Are you confused? Separate data for outcomes in each trial arm were only reported for (d-f) but not (a-c).
For HAI and/or colonization (d), the article reported what amounted to a 49% reduction in the copper rooms vs. non-copper rooms (21 vs. 41 patients; p=.02), for HAI only (e) a 62% reduction in the copper rooms (10 vs. 26; p=.013), and for colonization only (f), a 67% reduction (4 vs. 12; p=.063, NS). What was was not reported were the numbers of patients with (a) HAI and (b) colonization, listed separately for each trial arm, but the article concluded – in the discussion – that copper surfaces in rooms reduced the risk of HAIs by more than half. Conventional wisdom, however, would suggest that (a) any HAIs and (b) any colonization events, would be the most biologically relevant outcomes, and that it may not be so informative to combine these two events (under d) in the same statistical calculation, because they are biologically very different from each other. So, we extracted the missing numbers from the other numbers presented and arrived at (a) HAIs 17 vs. 29, and (b) colonization, 11 vs. 15 events. Putting these into our statistics calculator, they were – non-significant.
Now, let us revisit possible transmission routes in hospitals. We have: (i) endogenous transmission, from within the patient’s own flora, (ii) exogenous transmission via direct transfer, (e.g. as in handborne without surfaces), and (iii) exogenous transmission via surfaces and secondary transmission from surfaces onto the patients. If we look at (a) HAIs and (b) colonization with MRSA or VRE, then all three pathways can lead to HAIs, while only the two exogenous pathways can lead to colonization. If there is a >50% reduction of HAIs through copper surfaces (pathway iii), this would mean that the overall proportion of transmission from pathways (i) and (ii) plus the proportion of transmission from the remaining non-copper surfaces in the copper-treated rooms among pathway (iii) among all HAIs together would contribute less than 50% to overall HAIs.
The obvious question comes to mind: is that consistent with the known proportions of the different pathways leading to HAIs? The preliminary answer, given the Weinstein data (see above), would be, “given the biological knowledge of the day, apparently not.” It is also noted that the overall numbers of HAI and colonization events in the present article are relatively small.
Finally, anyone of us engaging in research can accidentally have outcomes that are surprising or do not quite add up with existing knowledge in the field. That is, in our opinion, where the intended purpose and scope of a discussion section of an article comes in, and where the Hill Criteria provide important food for thought. As one of us has put forward (Teleclass Feb. 7, 2013) on a different occasion and concerning a different topic, we would welcome the broad application of a check for biological plausibility when findings from clinical trials – and even systematic reviews – are reported. But we are not confident that our voices will be heard.
Image of Sir Austin Bradford Hill, source: toxipedia
Sunday, April 21, 2013
Nosocomial listeriosis
The Sydney Morning Herald is reporting that 3 patients in 2 Sydney hospitals have developed listeriosis after consuming profiteroles served to patients at the hospitals. The infecting strain in all patients was identical. One of the patients has died from an apparently unrelated cause.
Nosocomial foodborne illnesses, particularly those of bacterial origin, are seemingly uncommon. I suspect this is likely due to a lack of appetite in many hospitalized patients, and the highly processed nature of hospital foods (sometimes I'm not sure it's actually food).
A few weeks ago, while making morning rounds on the inpatient infectious diseases consult service, I went to see an immunosuppressed patient with pneumonia. As I was about to leave his room, I noted a clear plastic container of macaroni salad on his overbed table that had been served the evening before. My paranoia of foodborne infections must have been palpable. He thought it was quite funny that I alarmingly said, "Don't eat that!" While laughing at me, he said, "that's old Doc, I'm not gonna eat that." Just to be sure, I threw it in the garbage, which made him laugh all the more.
Photo: Culinary Catastrophy
Nosocomial foodborne illnesses, particularly those of bacterial origin, are seemingly uncommon. I suspect this is likely due to a lack of appetite in many hospitalized patients, and the highly processed nature of hospital foods (sometimes I'm not sure it's actually food).
A few weeks ago, while making morning rounds on the inpatient infectious diseases consult service, I went to see an immunosuppressed patient with pneumonia. As I was about to leave his room, I noted a clear plastic container of macaroni salad on his overbed table that had been served the evening before. My paranoia of foodborne infections must have been palpable. He thought it was quite funny that I alarmingly said, "Don't eat that!" While laughing at me, he said, "that's old Doc, I'm not gonna eat that." Just to be sure, I threw it in the garbage, which made him laugh all the more.
Photo: Culinary Catastrophy
Tuesday, November 13, 2012
Q: What are Iowans doing to prevent hospital-acquired infections?
A: Quite a bit, actually. Thanks for asking!Just last week, University of Iowa researchers Tara Smith, Marin Schweizer, and Phil Polgreen all sat down with Iowa Public Radio's Ben Kieffer (picture to the left) to discuss the latest science in HAI prevention including the epidemiology of MRSA in animal populations, the importance of environmental control in hospital settings and the latest hand-hygiene surveillance technologies.
Click on over to have a listen!
Friday, October 14, 2011
Climate change and hospital pathogens
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| Do hospital pathogens like living in a Greenhouse? |
Back in 2006, Judy and I were sitting on a park bench (it was a nice day) discussing the upcoming ICAAC abstract deadline and pondering what we should submit, when she suggested we look for seasonal variation in Gram-negative pathogens. Judy mentioned some data suggesting Gram-negative infections were more common in tropical countries and we also discussed the high incidence of Acinetobacter infections in troops returning from Iraq. Sure, we also knew that others had noticed summer peaks in certain pathogens, but the prior research didn't control for meteorologic factors and also combined summer data from across the entire US (hint: Maine ≠ Texas). Thus, we felt there was room for further exploration.
In our initial analysis, published in ICHE (2008), we reported that summer season (vs. winter) was associated with 28% more P. aeruginosa, 46% more E. cloacae, 12% more E. coli and 21% more A. baumannii clinical cultures over 8 years. Importantly, we found that for each 10°F increase in temp, there was a 17% increase in the monthly rates of infection caused by P. aeruginosa and also A. baumanii. Of course, this was a single center study, so we needed more proof.
Mike Eber and our group have just published a follow-up study in PLoS One looking at BSI data from 132 hospitals over 8 years. Using 211,697 inpatient blood isolates, we again found that Gram-negative organisms were more frequent in summer months ranging from 12.2% higher rates for E. coli to 51.8% higher for Acinetobacter spp. And more interestingly, we reported that independent of season, monthly humidity, monthly precipitation, and long-term trends, each 10°F rise in mean monthly temperature was associated with higher Gram-negative bacterial BSI frequencies ranging between 3.5% for E. coli to 10.8% for Acinetobacter spp. Thus, warm temps = more Gram-negative bacteremias; that is, even a warm winter is a bad thing. Lots more work to do to figure out why this might be, but I think it's an interesting first (or second) step. Cheers.
Note: Special thanks to Ramanan Laxminarayan and Extending the Cure for supporting this project.
Wednesday, November 17, 2010
DHHS releases 2010 Adverse Events in Hospitals report
The Department of Health and Human services just released an 81-page report titled: Adverse Events in Hospitals: National Incidence among Medicare Beneficiaries. Using a nationally representative random sample of 780 Medicare beneficiaries discharged in October 2008, physicians determined (1) whether an adverse event occurred, (2) whether the event was an NQF Serious Reportable Event or a Medicare hospital-acquired conditions, (3) what the level of harm was to the patient, and (4) whether the event was preventable. Using this sample, they estimated that 13.5% of all hospitalized Medicare patients experienced an adverse event and in 1.5% the AE contributed to their deaths. These extrapolate to 134,000 adverse events and 15,000 deaths in a single month. Multiply by 11.7498 (or 365.2425/31) if you want yearly estimates for an average year. Yes, I'm being a smart a**, but multiplying by 12 is incorrect.
One thing we're always concerned about on this blog is the percent of HAIs that are actually preventable in the current 'get to zero' world that we live in. In the DHHS report, physicians estimated that 44% of the AEs were preventable, 51% were not preventable and in 5% they were unsure. The costs were $324 million in October 2008 or 3.5% of all hospitalization costs. They suggest that the FY2009 attributable costs of AEs were $4.4 billion, with two-thirds of the costs being associated with extended hospital stays.
So what about HAIs? Table 3 in the report classifies the 128 AEs into categories and 19 or 15% of the AEs were HAIs. Thus, 2.5% of all hospitalized Medicare patients had an HAI. There were 5 UTIs, 4 CLABSI, 4 other BSI, 4 RTIs and 2 SSIs. The physicians classified only 60% of the infections as preventable. I wonder if this will help Mike achieve one of his wishes for the 2010 New Year? I could probably dig deeper but I've got work to do and I don't want to ruin all of your fun.
Link: November 2010 DHHS Adverse Events in Hospitals report.
h/t: Megan McKenna
One thing we're always concerned about on this blog is the percent of HAIs that are actually preventable in the current 'get to zero' world that we live in. In the DHHS report, physicians estimated that 44% of the AEs were preventable, 51% were not preventable and in 5% they were unsure. The costs were $324 million in October 2008 or 3.5% of all hospitalization costs. They suggest that the FY2009 attributable costs of AEs were $4.4 billion, with two-thirds of the costs being associated with extended hospital stays.
So what about HAIs? Table 3 in the report classifies the 128 AEs into categories and 19 or 15% of the AEs were HAIs. Thus, 2.5% of all hospitalized Medicare patients had an HAI. There were 5 UTIs, 4 CLABSI, 4 other BSI, 4 RTIs and 2 SSIs. The physicians classified only 60% of the infections as preventable. I wonder if this will help Mike achieve one of his wishes for the 2010 New Year? I could probably dig deeper but I've got work to do and I don't want to ruin all of your fun.
Link: November 2010 DHHS Adverse Events in Hospitals report.
h/t: Megan McKenna
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