Fentiman’s Toxic Legacy

After two years of misinformation, deceit and outright lies, fake “Cambridge graduate microbiologist” Rick Fentiman has to admit that his Deprox process leaves hospital rooms and equipment contaminated with highly toxic silver nitrate dust. A recent investigation at the University College London NHS Trust revealed the following figures:

  • Silver Nitrate content of Deproxin solution: 10 – 25mg/l
  • Silver Nitrate deposited on room surfaces after a single cycle: 1.5 – 2.5mg/m2

An independent test of the same parameters by Butterworth gave similar results:

  • (Deproxin) Silver expressed as Ag (by Plasma Emission Spectroscopy) 51.0mg/l
  • (Deproxin) Nitrate expressed as NO(by ion chromatography)  35.1mg/l

Surface deposits after single cycle:

  • (Surface) Silver expressed as Ag (by Plasma Emission Spectroscopy) 2.5mg/m2
  • (Surface) Nitrate expressed as NO(by ion chromatography) 1.8mg/m2

Silver nitrate is persistent in the environment, and will build up cumulatively each time a room is processed. The permitted level of silver nitrate dust in the air is vanishingly small. The legal maximum is 0.01mg/m³ –  250 times this amount of the chemical is deposited on each square metre of surface per process! 

This presents a particular danger to hospital staff making up the bed after a Deprox process – laying down the mattress and placing sheets will disturb clouds of the fine dust at very hazardous levels. Staff should certainly be provided with appropriate respiratory equipment for this task, and silver nitrate dust levels should be monitored before readmitting patients. 

Rooms that have become heavily contaminated by multiple processes may need decontaminating by Hazchem professionals.

Silver Nitrate deposits at the Royal Liverpool Hospital

capture

Isolation rooms at the Royal Liverpool University Hospital have become so heavily contaminated with silver nitrate that patients have complained, mistaking the black deposits on the windows for dirt. Director of nursing Lisa Grant admitted that the Hydrogen Peroxide Vapour (HPV) bio-decontamination system leaves a “sterile residue” but was apparently unaware that it is silver nitrate. The photo above was submitted to The Liverpool Echo by a patient who attempted to remove the chemical with a tissue. There is enough silver nitrate on the tissue to cause unpleasant chemical burns to the skin. Even more seriously, the AgNO3 dust levels in the room must have been far in excess of the legal maximum, which is an invisibly small 0.01mg/m³ – that’s 1/100,000th of a gram per cubic metre of air.

Rick Fentiman

Rick Fentiman claims to be a "Cambridge graduate microbiologist"

Fentiman’s UCLH Hoax

 

A letter published this week by Prof. Wilson of UCLH finally proves how Hygiene Solutions’ (Deprox) director Rick Fentiman cheated both the UCLH and rival HPV system manufacturer Bioquell Plc, in a widely publicized comparative test in 2015. The results of this test apparently demonstrated that the Deprox, vapourising a 5% Hydrogen peroxide solution had identical germicidal efficacy as the Bioquell system vapourising 35% hydrogen peroxide solution.

I published an article in 2016 in which I analyzed the test results as published by Professor Wilson and colleagues in the Journal of Hospital Infection, and concluded that Fentiman had in fact filled the internal tank of the Deprox machine with a 35% solution prior to the test. New data published in the letter proves this claim beyond reasonable doubt.

In Wilson’s original test, neither the aerial concentration of H2O2 vapour , or the concentration of the liquid solutions was  measured.

In response to widespread concern and comment as to the rather surprising results obtained, Wilson recently again obtained the use of a Bioquell and a Deprox system and measured the concentrations of both the liquid and aerial vapour phases throughout their test cycles, as detailed in this week’s letter.

The Deprox was using 5% H2O2 solution, and produced peak vapour concentrations of 29 to 46ppm. The Bioquell machine was using a 35% solution, and produced 450 to 640ppm of vapour.

The maximum aerial concentration of H2O2 that can be generated is limited by the concentration of the original solution. Henry’s law can be used to prove that about 50ppm is the maximum sustained aerial concentration that can be generated from a 5% solution. The figure of 46ppm for Deprox from Wilson’s retest of the machine is thus exactly what would be expected.

In the original comparative test, both the Deprox and the Bioquell systems demonstrated practically identical efficacies of log 5.1 for spores and log 6.3 for vegetative bacteria. A very large number of biological indicators of several species were used over multiple tests, and no significant difference in performance between the two systems was found.

Therefore, inescapably, both systems must have generated the same aerial concentration of H2O2 vapour, and that must have been in the region of 400 to 700ppm. (There are numerous published papers demonstrating a log 6 efficacy for HPV systems using 30-35% H2O2 solutions)

It is physically impossible to generate anything close to these levels of vapour by evaporating or aerosolizing a 5% solution. Quite apart from Henry’s law, the volume of water that would have to be evaporated along with the H2O2 would quickly push the relative humidity to saturation, and prevent further evaporation from taking place.

Therefore, in the original comparative tests as published in the Journal of Hospital Infection, the Deprox was NOT running on a 5% H2O2 solution as claimed, but on a 35% solution, the same as the Bioquell system.

How then was this deception accomplished?

There are some aspects of the way in which the original UCLH tests were conducted that  are very suggestive:

At the time of the tests, Hygiene Solutions had a contract with UCLH, and had 4 Deprox machines permanently on site, which were operated daily by Hygiene Solutions employees. UCLH had a definite rule that the equipment was not to be operated by their staff – hence no UCLH staff were trained in the use of the equipment.

The paper states:  “The HPS1 unit was operated by a trained engineer (Bioquell), while the HPS2 module was operated by hospital staff following training by a dedicated member of the issuing manufacturer (i.e. Hygiene Solutions).”

I have two independent witnesses that the two Deprox machines were used in the trial were not the machines already on site, but were specially prepared at the Kings Lynn depot, with all new piezo discs and calatytic deactivation media. The machines were driven up to UCLH personally by Rick Fentiman, who stayed for the duration of the tests then drove the machines back to Lynn. Apparently no other Hygiene Solutions staff were involved. The “dedicated member” therefore was Rick Fentiman, and he instructed and supervised some unidentified member of the “hospital staff” in the operation of the equipment “on the spot”.

The paper says: “However, during this study, both parties provided storage of equipment and hydrogen peroxide stock solutions off-site.” In the case of the Deprox units, this was  the large van in which they were transported. Clearly then there would have been opportunity for Mr Fentiman to have filled the internal storage tank of the test machines with a 35% solution and disposed of or diluted any residual fluid after the test, without either his own employees or the UCLH staff being aware of the substitution.

It is pertinent that (unknown to the UCLH) the Deprox has a substantial internal storage tank, of about 8 litres capacity.

capo2

Illustration from the Deprox patent.

The evaporation unit draws from the bottom of this tank, and the 2 litre Deproxin refill bottles trickle feed in to the top of the tank. I assume that for the sake of authenticity, a genuine Deproxin refill was inserted in to the top of the machine for the tests, hence even if Prof Wilson had tested the concentration of the fluid, he would have found it to be as stated. As concentrated H2O2 solution is substantially denser than water, a trickle of dilute solution in to the top of the tank would have no significant effect over the course of a few cycles of the machine.

Deprox salesman Tom Lister stalls when faced with a direct question about the UCLH tests. The machines had been filled with a 35% hydrogen peroxide solution, where UCLH were told it was a 5% solution. Tom knows this, and his guilty conscience shows very clearly in his body language and facial expressions. Rather than answer he says “Where did you say you were from?” although I had just told him, and was wearing a badge with the answer in large type!

 

Wilson exposes Deprox fraud!

Deprox Hygiene Solutions

In a letter published today in the Journal of Hospital Infection, Professor Peter Wilson and colleagues report on their retesting of the Deprox (Hygiene Solutions Ltd) HPV decontamination system. The retesting was in response to concerns widely raised that the earlier tests of the system, which purported to give a log 6 efficacy, were the result of the manufacturer misrepresenting the concentration and/or constituents of the Deproxin solution.

In brief, the retest reveals the following:

  • The efficacy of the system, when using the correct 5% H2O2 solution, is around log 4 – similar to other, much less expensive fogging systems on the market. Hygiene Solutions Ltd will now be taxed to explain why on the initial test by Prof. Wilson, a log 6 efficacy was found. This 100 fold drop in efficacy comes between the first test series, in which the solution concentration was not checked, and the second series in which the concentration was independently measured. It seems highly likely that in the initial test series, the Deprox was running on a 30% H2O2 solution, rather than a 5% H2O2 solution as claimed.
  • The aerial H2O2 concentration on re-entering the room at the end of the cycle was 3.3ppm which is in excess of both short term and long term H2O2 exposure health limits. This is in spite of a hasty retrofit of catalysts to the whole Deprox fleet, and the manufacturer’s claim that their system monitored the H2O2 levels, and would only allow re-entry when the level was below the 1ppm safety standard.
  • Deproxin is confirmed to contain 10-20ppm silver nitrate, and this is indeed deposited on surfaces in the room, and may well be a contributor to the efficacy achieved. Hygiene Solutions informed the HSE over a year ago that Deproxin does not contain silver nitrate. This has now been exposed as untrue – and raises the question as to whether it is currently legal to sell or use the Deprox system.
  • Poor efficacy results for two more sheltered locations is attributed to inhomogeneous vapour distribution, due to inadequate circulation of the vapour. This raises serious doubts as to Hygiene Solutions’ claims that the Deprox will decontaminate “inside small crevices and complex equipment”

It is very much to the credit of Professor Wilson and colleagues that they have thoroughly retested the system in response to widespread concerns. It is sad that commercial interests would abuse the trust and confidence of highly qualified academics in this way by misrepresenting the basic test parameters.

For those without access to the Journal of Hospital Infection, I have reproduced the letter below, and a PDF is downloadable here.


Sir,

In response to the letter from Dr Singh commenting on our paper.[1], [2]

The objective of our study was to evaluate the reductions in environmental contamination during in-use operation of two commercially-available hydrogen peroxide whole-room disinfection systems.2 Both manufacturers agreed test parameters prior to the trial to ensure methodology followed manufacturer instructions. Our findings suggested similar efficacy of the two systems against both surface contamination and biological indicators of common pathogens. Inocula used on the indicators far exceeded the likely levels seen in the environment.

Additional studies were performed as part of the original work using the same methodology with four strains each of MRSA, Klebsiella pneumoniae, Clostridium difficile spores and Acinetobacter baumannii. Three HPV decontamination cycles were evaluated for each system. Of 305/320 samples, >4-log10 reduction was achieved.

Aerial concentrations of hydrogen peroxide and relative humidity were monitored continuously during a further 6 cycles of both systems using a sensor (C-16 Portasens II Gas Detector; Analytical Technology Inc., Collegeville, PA, USA). In addition, horizontal surfaces in the near-patient vicinity were swabbed and analysed to detect fallout of silver and nitrate at the end of HPV decontamination cycles (n=3). Surfaces were swabbed and analysed for silver by titration (Silver Test Kit, DTK Water, Wellingborough, UK) and nitrate using Quantofix semi-quantitative test strips (Macherey-Nagel, Düren, Germany).

For the Deprox (Hygiene Solutions, King’s Lynn, UK) system, peak aerial values of 29-46 ppm hydrogen peroxide were achieved with similar bacteriological efficacy as other cycles. The mean level at the end of the cycles was 3.3ppm for 41.8% (30.8-58.1%) mean relative humidity at start of cycles. Silver and nitrate were detected on surfaces at 1.5-2.5mg/m2 following cycles with the Deprox system.

For the Bioquell Q10 system with the R10 aeration unit (Bioquell, Andover, UK), the peak aerial levels of hydrogen peroxide were 450-640ppm. The mean level at the end of the cycles was 0.0ppm with starting mean relative humidity 42.5% (34.5-49.7%). No silver or nitrate was detected on surfaces following cycles with the Bioquell Q10 system.

The aqueous concentration of hydrogen peroxide in a Hygiene Solutions cartridge (Deprox) tested on one occasion at the point of insertion into the machine was 5%. Nitrate was detected in the aqueous solution at 10-25mg/L. The aqueous hydrogen peroxide concentration in the Bioquell Q10 cartridge (Bioquell HPV-AQ) was 35% and no silver or nitrate was detected.

Dr Singh suggests C. difficile spores (but not the other organisms) persisted underneath the bed and on the window frame after decontamination using the Deprox system. The persistence of spores may have been minimised during the Bioquell Q10 cycles by the inclusion of an oscillating fan to facilitate aerial distribution and aid breakdown of hydrogen peroxide vapour.

As Dr Singh suggests, settling of active silver onto biological indicator coupons during a cycle of aerial HPV decontamination may have contributed to the bactericidal/sporicidal activity of the Deprox system. However further studies would be required to elucidate its role.

“They deserve answers” – Theresa May.

rick fentiman

“We have evidence that warnings were ignored and that these products continued to be used despite the warnings and that following the infections…[there was] a cover-up,”  – Andy Evans, chairman of campaign group Tainted Blood

Speaking to the BBC, Mrs May said: “They deserve answers, and the inquiry that I have announced today will give them those answers, so they will know why this happened, how it happened”

These quotations from today’s news refer not to the Deprox, but to the tragic suffering and loss of life from infected blood administered by the NHS in the 70s and 80s. At last, there is to be an inquiry, and the victims’ relatives will know how and why 2,400 NHS patients died.

Meanwhile a disturbingly similar tragedy is unfolding right here and now – and again the NHS turns a blind eye for fear of negligence lawsuits, and the corrupt medical suppliers hastily reap the profits before the mounting evidence of fraud and corruption forces them back to the dark places that spawned them.

The victims – the frail elderly, the cancer patients, the cystic fibrosis sufferers, have no idea that the C. difficile or MRSA infections they have suffered from were preventable. They are assured that the hospital rooms and equipment have been sterilised by the best technology available – the Deprox – which according to the Hygiene Solutions Ltd. website, “…achieves a log 6 reduction of even the most virulent of organisms.”

The truth is in stark contrast to this glib fabrication; – leaked emails and the testimony of former Hygiene Solutions employees prove that the Deprox units are turned up to their maximum output of  RH30 when tested, but in everyday use are turned down to output levels of RH 5 to RH 15 – with directly proportional reductions in H2O2 concentration and germicidal efficacy.

To compound this error, a recent letter published in the Journal of Hospital Infection revealed that most of the tested efficacy of the Deprox process could be attributed to the exceptionally high silver nitrate content of the Deproxin solution – an illegal additive which Hygiene Solutions now claims to have removed.

What residual efficacy remains absent this powerful cytotoxin remains untested and unproven.

The shocking and highly persuasive statistics from the UCLH hospitals, showing a substantial upwards step change in C. difficile rates corresponding exactly with the years of Deprox use, cannot be denied. These are public data sets, and the 75 or so extra infections over this period demand explanation.

We need an inquiry in to the Deprox scandal NOW, while lives can still be saved – not in 30 years time.

JHI letter damns Wilson’s Deprox test

A letter published on May 31st in the Journal of Hospital Infection shows Prof Peter Wilson’s controversial Deprox test results can be attributed to the very high level of (now illegal) silver nitrate in the Deproxin disinfectant solution. Wilson’s paper had already been strongly criticised by Dr Jon Otter of Imperial College, who suggested that Deprox manufacturer Hygiene Solutions Ltd. had added “A dash of peracetic acid” to the mix in order to achieve the improbable results.

However, as Dr Singh points out in the letter, the explanation is that Deproxin contains a whopping 2000ppm of silver nitrate, forty times as much as the ASP Glosair system that Dr Otter was comparing it to. The spray of silver nitrate solution settles on the BIs (conveniently unpouched and placed face up) and is concentrated by evaporation to highly germicidal levels. Meanwhile the volatile hydrogen peroxide component is dispersed and diluted through the volume of the room, and may play relatively little part in the process.

This substantial silver nitrate content is confirmed by a Daily Mail report from the Royal Liverpool Hospital, where a patient complained of “black grime” on the inside of the windows. The Hospital explained that it was a “sterile residue” from the hydrogen peroxide decontamination process. The hospital was using the Deprox process at the time.

Deprox mail

By an interesting coincidence, the JHI “articles in press” also has another paper on the antimicrobial efficacy of silver nitrate. This paper shows the MIC (Minimum Inhibitory Concentration) of silver nitrate for a range of vegetative bacteria, as below:

“The silver nitrate MIC was tested on a total of 443 isolates, ranging from 16 to 32 mg/L for the majority of the tested strains with or without sil genes. For Enterobacter and Klebsiella spp., elevated MIC (≥64 mg/L) for silver nitrate was recorded in E. cloacae (15/99, 15%), E. aerogenes (2/29, 7%), K. oxytoca (2/59, 3%), and K. pneumoniae (2/95, 2%).”

Note that 1mg/L = 1ppm. These bacterial strains were inhibited by just 16 to 32ppm AgNO3, compared to 2000ppm in Deproxin. No wonder the BIs were sterilised!

Hygiene Solutions Ltd is now between the devil and the deep blue sea. Do they remove the silver nitrate from the Deproxin, in which case their already shaky “validated to achieve a log 6 reduction” claim collapses, or do they continue the ludicrous pretense that the silver nitrate is actually just “silver” – in spite of the obvious point that metallic silver is a powerful catalyst for the decomposition of hydrogen peroxide?

This is a dilemma for hospital staff also, as according to the HSE it is illegal to use a PT2 (i.e. fogging or airborne) product containing silver nitrate. There can be no question that silver nitrate is an “active ingredient” in Deproxin. The Deprox unit contains a palladium catalyst to remove the hydrogen peroxide at the end of the process – however, this catalyst will not remove the silver nitrate, leaving an extremely fine dust or droplets of silver nitrate solution in the air when the room is re-entered. This chemical is highly toxic by inhalation, with a legal limit of just 0.01mg/m³. Certainly it would be risky to re-enter treated rooms without some kind of measurement process to assess the air quality.

Deprox nitrate

For those without access to the JHI, I have reproduced Dr Singh’s letter below.

Sir,

I note with interest the May 2016 article by S. Ali et al. “Efficacy of two hydrogen peroxide vapour aerial decontamination systems for enhanced disinfection of meticillin-resistant Staphylococcus aureus, Klebsiella pneumoniae and Clostridium difficile in single isolation rooms.”[1]

The two systems compared in this study use very different concentrations of hydrogen peroxide, and yet showed almost indistinguishable efficacy in these tests.

This would lead to the conclusion that the bactericidal and sporicidal efficacy of H2O2 is independent of concentration, which seems improbable – indeed, previous comparative evaluations of a high-concentration (30%) hydrogen peroxide system (Bioquell) with a low-concentration (5%) hydrogen peroxide system (ASP Glosair) by Fu et al.[2] Holmdahl et al.[3] and Beswick et al.[4] have demonstrated that the low-concentration fogging only achieved log reduction factors (LRF) of between 2 and 4, which was much smaller that the LRF of 6 generally achieved with the higher hydrogen peroxide concentration.

I would suggest that the unexpectedly high efficacy of the 4.9% hydrogen peroxide system evaluated by S. Ali et al. may be attributable to the relatively high level of silver nitrate in the proprietary Deproxin solution. The Deproxin MSDS[5] states: “CAS: 7761-88-8 Silver <0.2% EINECS: 231-853-9”. While “Silver” is given as the description, the CAS and EINECS numbers show that this is in the form of silver nitrate. In terms of ppm, 0.2% equates to 2000ppm. By contrast, the ASP Glosair system evaluated in the three papers mentioned above contained “<50ppm silver nitrate”. The solution used by S. Ali et al. thus apparently contained around forty times more “silver” than solutions used in systems previously evaluated.

Even at 2000ppm, the silver nitrate in Deproxin is considerably less concentrated than the hydrogen peroxide, by a factor of 25. (0.2% AgNO3: 4.9%H2O2) However, there is an important difference in the mode of distribution for these two active ingredients that may tend to preferentially concentrate the silver nitrate in the vicinity of the biological indicators. The hydrogen peroxide is volatile and unstable, and as the fog droplets evaporate, it is distributed throughout the whole volume of the room (about 60m3 in the example given), where the concentration then drops substantially with elapsed time as it spontaneously decays to oxygen and water. The silver nitrate however is not at all volatile, and is persistent.

The final distribution of the silver nitrate is hard to predict, but it may be assumed that much of it eventually drops to the floor or other horizontal surfaces in the room, either as solid particles or as droplets of solution that have been concentrated by partial evaporation. In the tests performed by S. Ali et al., biological indicators(BIs) were placed in horizontal, upwards facing orientation. If these BIs became saturated with a film of Deproxin solution from the fogging process, it can be expected that as the water evaporated during the “deactivation” cycle, the concentration of the silver nitrate would rise from the initial figure of around 2000ppm to substantially higher levels. It is of note that according to S.R.K. Pandian et al.[6] the MIC (Minimum Inhibitory Concentration) of silver nitrate for the spore-forming Bacillus licheniformis is only 5mM, which is equivalent to 850ppm.

There is some circumstantial evidence to support this explanation. S Ali et al. referring to the Deprox system state; “When rooms were disinfected using HPS2, C. difficile persisted most frequently underneath the bed and window frame in 6/21 cases (28.6%).” The “window frame” position is described as being “approximately 2m above floor” where the room height is given as 2.7m. The two positions pointed up as showing the lowest LRFs for the fogging system were those positions with the most restricted headspace – 0.7m in one case and presumably the same or less under the bed. These positions would have received the least precipitation from settling fog droplets or dust, so may have received proportionally less of the silver nitrate.

It would be very instructive to repeat the experiment without the hydrogen peroxide, and thus determine the log reduction attributable to a 2000ppm silver nitrate solution alone.

Conflict of interest

None.

References

  1. S. Ali, M. Muzslay, M. Bruce, A. Jeanes ,G. Moore, A.P.R. Wilson et al. Efficacy of two hydrogen peroxide vapour aerial decontamination systems for enhanced disinfection of meticillin-resistant Staphylococcus aureus, Klebsiella pneumoniae and Clostridium difficile in single isolation rooms. J Hosp Infect. 2016; 93: 70–77
  2. Fu, T.Y., Gent, P., and Kumar, V. Efficacy, efficiency and safety aspects of hydrogen peroxide vapour and aerosolized hydrogen peroxide room disinfection systems. J Hosp Infect. 2012; 80: 199–205
  3. Holmdahl, T., Lanbeck, P., Wullt, M., and Walder, M.H. A head-to-head comparison of hydrogen peroxide vapor and aerosol room decontamination systems. Infect Control Hosp Epidemiol. 2011; 32: 831–836 Beswick, A.J., Farrant, J., Makison, C. et al. Comparison of Multiple Systems for Laboratory Whole Room Fumigation. Applied Biosafety. 2011; 16
  4. Sevron Safety Solutions. http://sevron.co.uk/msds/deproxin-msds-download-2/[accessed 11.05.17]
  5. Pandian, S.R.K., Deepak, V., Kalishwaralal, K. et al. Mechanism of bactericidal activity of Silver Nitrate – a concentration dependent bi-functional molecule. Braz J Microbiol. 2010; 41: 805–809

Freedom of Information request reveals exact C. difficile/Deprox correlation.

C. difficile 1

A Freedom of Information request¹ to UCLH disclosed the starting and finishing dates of their disastrous Deprox decontamination contract with Hygiene Solutions Ltd. The Deprox operations started in June 2013 and ran continuously, 7 days per week through to October 2016. The contract called for at least 4 Deprox units to be at the hospital, and 6 or more processes to be completed daily.

However, due to frequent breakdowns, Hygiene Solutions struggled to meet their obligations, and on occasion asked engineers to put a non-functional Deprox unit in a room, tape up the door and “run” a process – thus not only defrauding the NHS but leaving a dangerously contaminated room that the staff believed to have been sterilized.

Plotting the contract dates against the quarterly UCLH C. difficile data² (extended through 2016 with mandatory government reporting data)³  reveals an exact correlation between the period of Deprox deployment and a substantial step change in the number of C.difficile infections  – approximately 70 extra cases over the 29 month period.

According to the March 2016 government report on C. difficile mortality, the 30 day mortality rates for the London area were about 17%. –  suggesting that approximately 12 deaths in this period could be attributed to Deprox operations. Any patients who acquired C. difficile or any other Heathcare Associated Infection, (HAI) in the UCLH hospitals between June 2013 and October 2015 should consider contacting a medical negligence solicitor and seeking compensation.

Deprox pushed UCLH in to high risk category for C. diff – CQC reports.

The CQC (Care Quality Commission) makes regular evaluations of NHS trusts using a list of critical indicators. These are the Intelligent Monitoring reports. The extracts from a series of these reports below show how the “Incidence of C. difficile” indicator moved from “No evidence of risk” to “Elevated Risk” when the Deprox program was implemented. The complete reports can be found at: http://www.cqc.org.uk/provider/RRV/reports

Deprox UCLH

[1] https://www.uclh.nhs.uk/aboutus/wwd/Annual%20reviews%20plans%20and%20reports%20archive/Infection%20Control%20Annual%20Report%202015-16.pdf  (See graph, p.17)

[2] https://www.gov.uk/government/statistics/clostridium-difficile-infection-monthly-data-by-nhs-acute-trust

[3] https://www.uclh.nhs.uk/aboutus/FOI/FOI%20disclosure%20list/FOI2017271Response.pdf

https://www.dropbox.com/s/71u3j3fcdqwqfnj/ResponseFOI2017271.xlsx%20%28~13%20KB%29.URL?dl=0

Deprox fails log 6 test even in tiny test chamber.

 

deprox box

Hygiene Solutions claim a single Deprox unit has the capacity to decontaminate rooms with a volume of 380m3, e.g. a 12 bed ward bay. A typical hospital side ward (single room with ensuite) has a volume of 60m3.

However, the chamber used by Hygiene Solutions Ltd  to test the Deprox is 1.5m x 1.5m x 2.8m. Total volume 6.3m3 , just 10% of the volume of a hospital single bedroom, and 1.7% of the maximum volume that Deprox is guaranteed to disinfect. It is barely larger than a telephone box.

Hygiene Solutions internal testing, published here for the first time reveals that the Deprox, in spite of being boosted with 50% more concentrated hydrogen peroxide solution than the standard “Deproxin” was incapable of a log 6 decontamination of even this tiny test chamber.

The Deprox was thoroughly tested over a period of months by David Sempere Aracil, a well qualified chemist. David placed Log 6 biological indicator discs (Apex Biological Indicator #HMV-091) in 8 different locations around the inside walls of the test chamber. The Deprox unit (“Trusted by leading hospitals around the world”) was sealed in the chamber, and the process was run. The log6 BIs were incubated – they were all alive.

David tried substituting Sanosil SO15 which at 7.5% H2O2 is 50% more concentrated than Deproxin. Now some of the BIs would be sterilised, sometimes. Over several weeks in late 2014, David did a series of 12 tests in the test chamber, all with 7.5% H2O2 rather than the 5% Deproxin. He tried turning the ΔRH up and down, but to no avail. In 5 of these tests, all 8 BIs remained viable. None of the tests sterilised more than 6 out of 8.

 

In summary then:

Deprox, running on a 5% H2O2 solution, is claimed to give a log6 decontamination of an entire 380m3 ward, including inside small crevices and complex equipment. In Hygiene Solutions’ own tests, the Deprox running on a 7.5% solution, and thus generating a 50% higher aerial H2O2 concentration than the standard process, completely failed to give a log6 decontamination of a 6.3m3 box in multiple tests.

Hygiene Solutions continued to promote and sell the Deprox with exactly the same claims, but in 2015, they turned the whole Deprox fleet down from ΔRH20 to ΔRH5. See https://deproxfraud.info/2017/03/13/leaked-emails-prove-test-cheating-bodily-harm-and-massive-fraud/

Fortunately, (or unfortunately for Hygiene Solutions) David’s notes of these tests survived.

deproxy

Explanation of table.

This table is a summary of 15 tests done by David Sempere Aracil, assisted by Tautvydas Karitonas, over a period of months. Both are university graduates with extensive research experience, and David has a PhD in Chemistry. The tests were done with a standard production model Deprox machine, the purpose of the tests was to determine if the extremely low efficacy of the Deprox process could be rectified by increasing the concentration of the hydrogen peroxide solution from the standard 5% to 7.5%.

The results were recorded in 3 A4 hardcover notebooks. Each of the 15 tests was recorded in more detail on preceding pages of the notebook. In addition to the efficacy tests, the notebooks contain extensive details of tests on prototype catalyst systems, and constitute proof that HS was well aware of both the low efficacy and residual gas issues with Deprox.

Heading: “Sanosil 015 forte” refers to Sanosil S015, which is a disinfectant intended for water systems. It is 7.5% Hydrogen peroxide solution. Note that this is more concentrated than the 5% Deproxin solution that is used in production Deprox machines.

Col.1. The test number. These are not sequential, as some tests did not use Biological indicators (BIs) and were not recorded in this resume.

Col. 2 Duration of test measured from when the machine starts vapourising. (It takes several minutes for the machine to fill the piezo tank at the beginning of each test)

Col. 3 Delta HR setting of machine. This is adjusted by using unmarked pressure sensitive switches below the LCD display. – see How to test your Deprox.

Col. 4 HRO This is the original relative humidity in the test chamber before the machine starts.

Col. 5 TO Temperature in the chamber before the machine starts

Col. 6 CMAX Hydrogen peroxide concentration in PPM, maximum level reached during process.

Results columns. The first 12 tests were done in the test chamber (wardrobe). Each number represents a specific marked location on the test chamber wall where an exposed stainless steel Bacillus subtilis log6 biological indicator was placed. The chamber is a crude wood and plasterboard structure in an essentially unheated warehouse. It is approximately 5’ x 5’ x 9’ and the indicators were placed at various heights on the interior walls of the chamber. The last 3 tests were done in the company board room which is approximately 12’ x 25’.

A” +” indicates that the BI still contained viable bacteria, a “–“ indicates that all bacteria on this indicator were killed.

Final column. This is the percentage of BIs that were killed.