Guest guest Posted September 11, 2003 Report Share Posted September 11, 2003 Hi Hank & Matt, I wrote: > IMO it is gross malpractice to reuse AP needles [or any blood- > touching instrument] on another human patient! Never attempt to > clean and resterilise a used needle! Matt Bauer replied: > If you feel this way you [must avoid] dentists. Their practices > are a re-sterilizing nightmare. Unlike the simple, solid shaft AP > needle, dental equipment has a host of factors making proper > sterilization most difficult. Their equipment is expensive which > makes them want to sterilize to a minimum to reduce wear, this > equipment often has porous surfaces in which contaminants can get > trapped greatly complicating sterilization procedures, and many > dental offices are under great pressure to see a high volume of > patients. Matt, I have not been to a dentist for years! I SHUDDER at the thought of the high risks of cross-infection in routine dentistry - probes, elevators, forceps, etc are so easily contaminated by blood/bloody saliva. I cringe at the thought after reading the article by Paul Brown et al, March 2002 (see below). Last year, I had a rocking molar [following several recurrences of an abscess at its root] I extracted it myself in a variant of the old method of tying line around it and whipping it out in one powerful pull. I used a triple- strand of 10kg nylon fishing line as the " lassoo " . It worked fine, and first-time! Hank Barru wrote: > To Phil and group: Some months back on the list there was mention > of prion infection and the possibility of transmitting prions via > reusable acupuncture needles. Can anyone recommend a good source > of information about this hazard, and about prion infections > generally? We are updating the medical asepsis guidelines at my > school, and this is one area we have not yet looked at. Thanks, > Hank Barru Following public concern over the risks of transmission of CJD by hospital equipment [clamps, saws, knives, retractors, etc], I understand that the UK Government appointed a Committee to advise on best practices to be adopted. I understand that the report was not released publicly, but that it recommended destruction after single use of all instruments that contacted brain or nerve tissue of any patient with ANY central encephalopathy/neuropathy. I also understand that the government did NOT act on that report because it would cost many millions of pounds annually to implement the policy. Many countries ban blood donations from donors with neurological symptoms because there is research evidence that prion diseases may be transmitted via blood in animals. Here are copies of earlier mails on the difficulties of sterilising instruments possibly infected with prions. Please forward this to relevant colleagues. Paper 1, below (by Paul Brown et al, March 2002), showed that prion infectivity could withstand ashing at 600 DegC. That suggested the horrific possibility of an INORGANIC template for prion diseases, and the impossibility of disinfecting infected material by practical methods of heating. A new paper by Paul Brown et al (Paper 2, below) suggests a practical way to reduce prion infectivity in meat products. This paper has enormous implications for the meat/food industry. Note that the heaviest treatment (short pressure pulses of 1,200 MPa at running temperatures of 121-137°C) reduced infectivity drastically but it did not remove it completely. Research is still needed to find a way to reduce infectivity of prion-contaminated meat products to zero. Paper 1: New studies on the heat resistance of hamster-adapted scrapie agent: threshold survival after ashing at 600°C suggests an inorganic template of replication. Brown P, Rau EH, Johnson BK, Bacote AE, Gibbs CJ Jr, Gajdusek DC. Proc Natl Acad Sci U S A 2000 Mar 28;97(7):3418-21. Laboratory of Central Nervous System Studies, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA. brownp One-gram samples from a pool of crude brain tissue from hamsters infected with the 263K strain of hamster- adapted scrapie agent were placed in covered quartz-glass crucibles and exposed for either 5 or 15 min to dry heat at temperatures ranging from 150 to 1000°C. Residual infectivity in the treated samples was assayed by the intracerebral inoculation of dilution series into healthy weanling hamsters, which were observed for 10 months; disease transmissions were verified by Western blot testing for proteinase-resistant protein in brains from clinically positive hamsters. Unheated control tissue contained 9.9 log(10)LD(50)/g tissue; after exposure to 150°C, titers equaled or exceeded 6 log(10)LD(50)/g, and after exposure to 300°C, titers equaled or exceeded 4 log(10)LD(50)/g. Exposure to 600°C completely ashed the brain samples, which, when reconstituted with saline to their original weights, transmitted disease to 5 of 35 inoculated hamsters. No transmissions occurred after exposure to 1000°C. These results suggest that an INORGANIC molecular template with a decomposition point near 600°C can nucleate the biological replication of the scrapie agent. PMID: 10716712 [PubMed - indexed for MEDLINE] Paper 2: Ultra-high-pressure inactivation of prion infectivity in processed meat: A practical method to prevent human infection (food processing | scrapie | bovine spongiform encephalopathy | new variant Creutzfeldt-Jakob disease | prion disease). Paul Brown*, Richard Meyer , Franco Cardone & Maurizio Pocchiari* (2003) Preprint, May 5, Proc. Natl. Acad. Sci. USA, http://www.pnas.org/cgi/content/abstract/1031826100v1 National Institutes of Health, Bethesda, MD 20892; Washington Farms, Tacoma, WA 98443; and Istituto Superiore di Sanità, 00161 Rome, Italy. Bovine spongiform encephalopathy contamination of the human food chain most likely resulted from nervous system tissue in mechanically recovered meat used in the manufacture of processed meats. We spiked hot dogs with 263K hamster- adapted scrapie brain (10% wt/wt) to produce an infectivity level of 9 log10 mean lethal doses (LD50)/g paste homogenate. Aliquots were subjected to short pressure pulses of 690, 1000, and 1200 MPa at running temperatures of 121-137°C. Western blots of PrPres were found to be useful indicators of infectivity levels, which at all tested pressures were significantly reduced as compared with untreated controls: from 103 LD50/g at 690 MPa to 106 LD50/g at 1200 MPa. The application of commercially practical conditions of temperature and pressure could ensure the safety of processed meats from bovine spongiform encephalopathy contamination, and could also be used to study phase transitions of the prion misfolded state. See also the Medline Preprint of the same abstract at: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=retrieve & db=pub med & list_ui ds=12732724 & dopt=Abstract On 29 Jan 2003 Mangala wrote: > ... The NCCAOM book of 'Clean Needle Technique', says : " While > disposable needles are not essential for Clean Needle Technique, > they are recommended The protocol of sterilization is clearly > defined. Autoclave is the method of choice. 'It is critical that a > pressurized steam bath, as provided by an autoclave, be maintained > at 250 degrees Farenheit, 15 pounds of pressure for 30 minutes. The > pressure must be released quickly at the end of the sterilization > cycle.' Dry heat sterilizers : 2 hrs of exposure to 338 degrees > Farenheit. In case of rebbers and plastics instruments that can > melt under this temperature :, it is acceptable to use high level > disinfectants, in a correct concentration and for a specified > immertion time. Amongst the 'Unacceptable' procedures are : Glass > Bead Devices, Boiling Water, Alcohol and Pressure Cookers. Thanks. > Mangala In reply to this, I wrote: This is a plea to ALL medical professionals with political clout. Please try to have a National Ban in your country on the sterilisation and re-use of all needles for human use (including spinal and biopsy needles). Autoclaving and dry heat, and the usually accepted ways of sterilising instruments simply CANNOT guarantee freedom from prion-infectivity. The evidence is that PRIONS have an INORGANIC template. Prion infectivity REMAINS after ASHING of infective material at 600 DegC This is recent evidence and the implications for doctors, nurses, dentists, acupuncturists, etc are horrific. Human prion diseases range far wider than CJD and Kuru! There are MANY others known in humans. Some papers even suggest a prion-link in Alzheimer's Disease. Needles cost very little. Why run the risk of transmitting an INCURABLE disease for the sake of a few cents? Need I say more? Because of risks of transmitting AIDS, hepatitis, CJD, etc, one should ALWAYS use disposable single-use needles and NOT attempt to resterilise them. The same applies to 7-star (hammer- type) needles, lancets, etc. An exception is if patients are given their OWN needles for their OWN use only. Best regards, WORK : Teagasc Staff Development Unit, Sandymount Ave., Dublin 4, Ireland WWW : Email: < Tel : 353-; [in the Republic: 0] HOME : 1 Esker Lawns, Lucan, Dublin, Ireland WWW : http://homepage.eircom.net/~progers/searchap.htm Email: < Tel : 353-; [in the Republic: 0] Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 11, 2003 Report Share Posted September 11, 2003 Ouchhhhhhhhhhhhhhhhhhhhhhhhhhhh ) Thanks for the article it is impressive. Vanessa >>Last year, I had a rocking molar [following several recurrences of an abscess at its root] I extracted it myself in a variant of the old method of tying line around it and whipping it out in one powerful pull. I used a triple- strand of 10kg nylon fishing line as the " lassoo " . It worked fine, and first-time! >> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 11, 2003 Report Share Posted September 11, 2003 Wow Phil! You really are concerned about sterility. Not to freak you out any more but, the most difficult piece of equipment to keep clean in a dental practice are the suction tubes that draw out bloody saliva. These tubes are now fitted with back-flow valves to help prevent back-flow of contaminated waste, but are prone to failures and must be carefully and regularly flushed. Some on the list may be interested to learn there was a study done in the late 1970's-early 1980's in Hong Kong in which the rates of hepatitis for those who had acupuncture, tattoos, and electrolysis were followed. The authors concluded those who had tattoos and electrolysis had slightly higher rates of hepatitis while acupuncture patients showed no higher rates than the general population. Matt Bauer - Acupuncture research in the UK and beyond. Cc: traditional_Chinese_Medicine Thursday, September 11, 2003 11:23 AM Re: Prion infection & SINGLE-USE needles, lancets, etc. Hi Hank & Matt, I wrote: > IMO it is gross malpractice to reuse AP needles [or any blood- > touching instrument] on another human patient! Never attempt to > clean and resterilise a used needle! Matt Bauer replied: > If you feel this way you [must avoid] dentists. Their practices > are a re-sterilizing nightmare. Unlike the simple, solid shaft AP > needle, dental equipment has a host of factors making proper > sterilization most difficult. Their equipment is expensive which > makes them want to sterilize to a minimum to reduce wear, this > equipment often has porous surfaces in which contaminants can get > trapped greatly complicating sterilization procedures, and many > dental offices are under great pressure to see a high volume of > patients. Matt, I have not been to a dentist for years! I SHUDDER at the thought of the high risks of cross-infection in routine dentistry - probes, elevators, forceps, etc are so easily contaminated by blood/bloody saliva. I cringe at the thought after reading the article by Paul Brown et al, March 2002 (see below). Last year, I had a rocking molar [following several recurrences of an abscess at its root] I extracted it myself in a variant of the old method of tying line around it and whipping it out in one powerful pull. I used a triple- strand of 10kg nylon fishing line as the " lassoo " . It worked fine, and first-time! Hank Barru wrote: > To Phil and group: Some months back on the list there was mention > of prion infection and the possibility of transmitting prions via > reusable acupuncture needles. Can anyone recommend a good source > of information about this hazard, and about prion infections > generally? We are updating the medical asepsis guidelines at my > school, and this is one area we have not yet looked at. Thanks, > Hank Barru Following public concern over the risks of transmission of CJD by hospital equipment [clamps, saws, knives, retractors, etc], I understand that the UK Government appointed a Committee to advise on best practices to be adopted. I understand that the report was not released publicly, but that it recommended destruction after single use of all instruments that contacted brain or nerve tissue of any patient with ANY central encephalopathy/neuropathy. I also understand that the government did NOT act on that report because it would cost many millions of pounds annually to implement the policy. Many countries ban blood donations from donors with neurological symptoms because there is research evidence that prion diseases may be transmitted via blood in animals. Here are copies of earlier mails on the difficulties of sterilising instruments possibly infected with prions. Please forward this to relevant colleagues. Paper 1, below (by Paul Brown et al, March 2002), showed that prion infectivity could withstand ashing at 600 DegC. That suggested the horrific possibility of an INORGANIC template for prion diseases, and the impossibility of disinfecting infected material by practical methods of heating. A new paper by Paul Brown et al (Paper 2, below) suggests a practical way to reduce prion infectivity in meat products. This paper has enormous implications for the meat/food industry. Note that the heaviest treatment (short pressure pulses of 1,200 MPa at running temperatures of 121-137°C) reduced infectivity drastically but it did not remove it completely. Research is still needed to find a way to reduce infectivity of prion-contaminated meat products to zero. Paper 1: New studies on the heat resistance of hamster-adapted scrapie agent: threshold survival after ashing at 600°C suggests an inorganic template of replication. Brown P, Rau EH, Johnson BK, Bacote AE, Gibbs CJ Jr, Gajdusek DC. Proc Natl Acad Sci U S A 2000 Mar 28;97(7):3418-21. Laboratory of Central Nervous System Studies, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA. brownp One-gram samples from a pool of crude brain tissue from hamsters infected with the 263K strain of hamster- adapted scrapie agent were placed in covered quartz-glass crucibles and exposed for either 5 or 15 min to dry heat at temperatures ranging from 150 to 1000°C. Residual infectivity in the treated samples was assayed by the intracerebral inoculation of dilution series into healthy weanling hamsters, which were observed for 10 months; disease transmissions were verified by Western blot testing for proteinase-resistant protein in brains from clinically positive hamsters. Unheated control tissue contained 9.9 log(10)LD(50)/g tissue; after exposure to 150°C, titers equaled or exceeded 6 log(10)LD(50)/g, and after exposure to 300°C, titers equaled or exceeded 4 log(10)LD(50)/g. Exposure to 600°C completely ashed the brain samples, which, when reconstituted with saline to their original weights, transmitted disease to 5 of 35 inoculated hamsters. No transmissions occurred after exposure to 1000°C. These results suggest that an INORGANIC molecular template with a decomposition point near 600°C can nucleate the biological replication of the scrapie agent. PMID: 10716712 [PubMed - indexed for MEDLINE] Paper 2: Ultra-high-pressure inactivation of prion infectivity in processed meat: A practical method to prevent human infection (food processing | scrapie | bovine spongiform encephalopathy | new variant Creutzfeldt-Jakob disease | prion disease). Paul Brown*, Richard Meyer , Franco Cardone & Maurizio Pocchiari* (2003) Preprint, May 5, Proc. Natl. Acad. Sci. USA, http://www.pnas.org/cgi/content/abstract/1031826100v1 National Institutes of Health, Bethesda, MD 20892; Washington Farms, Tacoma, WA 98443; and Istituto Superiore di Sanità, 00161 Rome, Italy. Bovine spongiform encephalopathy contamination of the human food chain most likely resulted from nervous system tissue in mechanically recovered meat used in the manufacture of processed meats. We spiked hot dogs with 263K hamster- adapted scrapie brain (10% wt/wt) to produce an infectivity level of 9 log10 mean lethal doses (LD50)/g paste homogenate. Aliquots were subjected to short pressure pulses of 690, 1000, and 1200 MPa at running temperatures of 121-137°C. Western blots of PrPres were found to be useful indicators of infectivity levels, which at all tested pressures were significantly reduced as compared with untreated controls: from 103 LD50/g at 690 MPa to 106 LD50/g at 1200 MPa. The application of commercially practical conditions of temperature and pressure could ensure the safety of processed meats from bovine spongiform encephalopathy contamination, and could also be used to study phase transitions of the prion misfolded state. See also the Medline Preprint of the same abstract at: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=retrieve & db=pub med & list_ui ds=12732724 & dopt=Abstract On 29 Jan 2003 Mangala wrote: > ... The NCCAOM book of 'Clean Needle Technique', says : " While > disposable needles are not essential for Clean Needle Technique, > they are recommended The protocol of sterilization is clearly > defined. Autoclave is the method of choice. 'It is critical that a > pressurized steam bath, as provided by an autoclave, be maintained > at 250 degrees Farenheit, 15 pounds of pressure for 30 minutes. The > pressure must be released quickly at the end of the sterilization > cycle.' Dry heat sterilizers : 2 hrs of exposure to 338 degrees > Farenheit. In case of rebbers and plastics instruments that can > melt under this temperature :, it is acceptable to use high level > disinfectants, in a correct concentration and for a specified > immertion time. Amongst the 'Unacceptable' procedures are : Glass > Bead Devices, Boiling Water, Alcohol and Pressure Cookers. Thanks. > Mangala In reply to this, I wrote: This is a plea to ALL medical professionals with political clout. Please try to have a National Ban in your country on the sterilisation and re-use of all needles for human use (including spinal and biopsy needles). Autoclaving and dry heat, and the usually accepted ways of sterilising instruments simply CANNOT guarantee freedom from prion-infectivity. The evidence is that PRIONS have an INORGANIC template. Prion infectivity REMAINS after ASHING of infective material at 600 DegC This is recent evidence and the implications for doctors, nurses, dentists, acupuncturists, etc are horrific. Human prion diseases range far wider than CJD and Kuru! There are MANY others known in humans. Some papers even suggest a prion-link in Alzheimer's Disease. Needles cost very little. Why run the risk of transmitting an INCURABLE disease for the sake of a few cents? Need I say more? Because of risks of transmitting AIDS, hepatitis, CJD, etc, one should ALWAYS use disposable single-use needles and NOT attempt to resterilise them. The same applies to 7-star (hammer- type) needles, lancets, etc. An exception is if patients are given their OWN needles for their OWN use only. Best regards, WORK : Teagasc Staff Development Unit, Sandymount Ave., Dublin 4, Ireland WWW : Email: < Tel : 353-; [in the Republic: 0] HOME : 1 Esker Lawns, Lucan, Dublin, Ireland WWW : http://homepage.eircom.net/~progers/searchap.htm Email: < Tel : 353-; [in the Republic: 0] Quote Link to comment Share on other sites More sharing options...
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