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January 31st, 2009 posted by Kelly Burkholder-Allen, RN, MSEd January 31, 2009 @ 8:29 am

DHS deploys cargo-scanning radiation detectors at airports around the country

http://gsn.nti.org/gsn/nw_20090130_1559.php

U.S. Begins Deploying Portal Radiation Sensors to Airports

WASHINGTON — The U.S. Homeland Security Department has deployed more than 1,000 cargo-scanning radiation detectors around the country, but until late last year none could be found at the nation’s airports (see GSN, Sept. 11, 2008).

That changed in September with installation of a radiation portal monitor at Dulles International Airport near Washington, D.C. Another three machines are due to be deployed at unspecified airports this spring and ultimately 30 sites that handle 99 percent of all U.S. airborne cargo could receive the technology.

The intent is to prevent a nuclear or radiological weapon from being smuggled into the country through an airport. It is part of a larger DHS effort that has placed about 1,120 portal units at U.S. seaports and border crossings since 2001.

“The reason we left the airports for last is because we were fully cognizant of the fact that the airports were going to be the most challenging environment to work in,” said Patrick Simmons, head of the Nonintrusive Inspection Division of DHS Customs and Border Protection. “The airport environment is very, very fluid. … We wanted to have our lessons learned and we really wanted to bring our best practices to bear.”

Each monitor costs $450,000 to buy and install. They are capable of detecting any form of radiation but not of identifying the source as a harmless material or potential weapons ingredient.

The technology has been criticized for an excess of “nuisance alarms” — going off after detecting low-level radiation produced by items such as kitty litter or bananas. Some experts have also questioned the portals’ ability to detect weapon-grade material stored inside a shielded container (see GSN, Aug. 17, 2004).

Customs and Border Protection said it could not publicly address which points of entry are considered most likely to be used by smugglers of radioactive material.

The agency began its rollout at Dulles due to the airport’s proximity to an obvious terrorist target and to the lawmakers who maintain what Simmons called “extreme congressional oversight” over federal radiation screening activities (sees GSN, Jan. 9, 2008). “It was an easy place to bring visitors,” he said.

Dulles also needs only one monitor, as there is a single road leading from the tarmac to warehouses where cargo is temporarily stored before being shipped by truck to a final destination.

All cargo with Dulles as its final airport destination must pass through the portal, which consists largely of two yellow posts that each support two white sensor panels. Ultimately, nearly all containers that leave the Virginia facility by air would be screened at another airport that also possesses the detection technology, Simmons said.

“Eventually at some airport it’s got to exit. So we’ll catch it wherever it exits,” he said.

Air cargo is generally stored in pallet-sized containers rather than the larger metal boxes pulled by trucks or stacked on rail cars. Small tractor-like vehicles take the containers off the tarmac and through a gate, passing through the sensor at the airport speed limit of no more than 5 mph.

If the monitor detects radiation, a flashing light goes off ahead of the driver, indicating that the vehicle must stop at a booth a quarter-mile down the road.

Officers who staff the booth at all times would also receive the alert at a sophisticated work station. Their job is then to interview the driver and to use more-precise hand-held detectors capable of identifying the specific isotope that is producing the radiation.

The alarm rate at Dulles is similar to that seen at other U.S. entry points, Simmons said. More than 95,000 “conveyances” — a vehicle pulling one or more cargo containers — passed through the portal between Sept. 8, 2008, and Jan. 4, producing 297 alarms. As has been the case nationwide, none of the alarms led to the discovery of threatening material.

“Sometimes the alarm doesn’t go off” at all during a four-hour shift at the booth, said CBP Officer Stanley Peterson. “Sometimes it goes off once or twice.”

Items found to set off sensors are much the same at Dulles as elsewhere.

“Although the commodities might be less, it’s the same type of commodity,” Simmons said. “We get a lot of earthen ware, a lot of porcelain, a lot of tile. … People are shipping granite via air, which I certainly never would have suspected prior to rolling out this program.”

The top alarm trippers are industrial devices and people who have undergone medical procedures involving radiation, according to CBP officers. Any person or item that passes through the monitor multiple times per day would have to undergo the same scrutiny each time they set off an alarm, they said.

“Being out here, you have to be alert to any type of situation that comes up,” Peterson said.

Next-Generation Technology



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January 31st, 2009 posted by Kelly Burkholder-Allen, RN, MSEd @ 8:24 am

Volcanoes: Are YOU Ready?

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http://www.fema.gov/areyouready/volcanoes.shtm

Are You Ready?

Volcanoes

A volcano is a vent through which molten rock escapes to the earth’s surface. When pressure from gases within the molten rock becomes too great, an eruption occurs. Eruptions can be quiet or explosive. There may be lava flows, flattened landscapes, poisonous gases, and flying rock and ash.

Because of their intense heat, lava flows are great fire hazards. Lava flows destroy everything in their path, but most move slowly enough that people can move out of the way.

Fresh volcanic ash, made of pulverized rock, can be abrasive, acidic, gritty, gassy, and odorous. While not immediately dangerous to most adults, the acidic gas and ash can cause lung damage to small infants, to older adults, and to those suffering from severe respiratory illnesses. Volcanic ash also can damage machinery, including engines and electrical equipment. Ash accumulations mixed with water become heavy and can collapse roofs.

Volcanic eruptions can be accompanied by other natural hazards, including earthquakes, mudflows and flash floods, rock falls and landslides, acid rain, fire, and (under special conditions) tsunamis. Active volcanoes in the U.S. are found mainly in Hawaii, Alaska, and the Pacific Northwest.

Map of volcano locations in the united states

Take Protective Measures

Before a Volcanic Eruption

During a Volcanic Eruption

The following are guidelines for what to do if a volcano erupts in your area:

Protection from Falling Ash

After a Volcanic Eruption

Follow the instructions for recovering from a disaster in Part 5.

Knowledge Check

Read the scenario and answer the question. Check your responses with the answer key.

Scenario
About an hour after the eruption of Mount St. Helens, ash began to fall in Yakima, a city in eastern Washington. The ash fall was so extensive and it became so dark that lights were turned on all day. It took 10 weeks to haul away the ash from Yakima’s streets, sidewalks, and roofs.

Assume you were a resident of Yakima during this time. What would you need to protect yourself when going outside?

For More Information

If you require more information about any of these topics, the following are resources that may be helpful.

Publications
National Weather Service
Heat Wave: A Major Summer Killer. An online brochure describing the heat index, heat disorders, and heat wave safety tips. Available online at: www.nws.noaa.gov/om//brochures/heat_wave.htm

U.S. Geological Survey
Volcano Hazards Program. Website with volcano activity updates, feature stories, information about volcano hazards, and resources. Available online at: volcanoes.usgs.gov



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January 31st, 2009 posted by Kelly Burkholder-Allen, RN, MSEd @ 8:20 am

Maintaining Prehospital Pediatric Airways

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http://www.emsresponder.com/publication/article.jsp?pubId=1&id=8905

Prehospital Pediatric Airway Management

It’s time to reconsider how we maintain pediatric airways

     We are fortunate to live in a time of ongoing research, open discussion and technological advances in prehospital care. EMS providers are dealing with spinal immobilization, “load-and-go” vs. “stay-and-play” situations, medications for rapid sequence airways (RSA) or intubation (RSI), and ways to manage that very first element of patient assessment—the airway.

     As Shakespeare’s Hamlet pondered his future with the famous words “To be or not to be,” he had choices; but only one path seemed correct. In that great tragedy, Hamlet chose a path that led to deception and eventually death. All too often, in the world of prehospital pediatric emergencies, we also face an uncomfortable choice: “to tube or not to tube.” Do we attempt a relatively unpracticed procedure that is fraught with danger and potential complications, or do we embrace the future and move forward, toward improved safety for our smallest patients? In this article, we will look at prehospital pediatric airway management, past, present and future. We believe the future of prehospital pediatric airway management for both ALS and BLS providers goes back to basics, back to the past and back to the nonvisualized airways of the future.

     “Airway equipment, including one supraglottic alternative for patients of all ages, should be available on every ambulance.”1

     Research shows that, on average, only 13% of prehospital patients are children.2 We start IV lines on adults every day, and running a full arrest is not an uncommon event. But we don’t often experience a need for invasive procedures on kids. A 2001 study of an urban EMS system found that ALS providers only attempted pediatric IV placement 3.7 times a year, and pediatric intubation was only attempted once every 3 years.3 With such limited actual experience, it is easy to see how real-life proficiency in these procedures is difficult, if not nearly impossible, to maintain.

     “Tracheal intubation (ETI) is considered the method of choice for securing the airway and for providing effective ventilation during cardiac arrest. However, ETI requires skills that are difficult to maintain, especially if practiced infrequently.”4

     Intubation with an endotracheal tube properly placed in the trachea, effectively secured, and with placement confirmed and monitored with capnography is the gold standard for airway management. It allows for continuous assisted ventilation, minimizes the risk of aspiration, and, though not a preferred route, provides a means for delivery of certain emergency medications.5,6 However, intubation is not without risks and potential complications that are generally considered more significant in the uncontrolled and unpredictable prehospital environment. Several studies describe unsuccessful adult intubation rates ranging from 8%–30% and time to intubation ranging from 5–17 minutes.7–11 For our pediatric patients, data from separate studies reveal successful endotracheal intubations in only 50% of the attempts for children under 1 year of age, 54% in children younger than 18 months, and only 57% in those under 12 years.12–14

     “…the addition of out-of-hospital ETI to a paramedic scope of practice that already includes BVM (bag-valve mask) did not improve survival or neurological outcome of pediatric patients treated in an urban EMS system.”14

     A study that opened the eyes of many prehospital providers was conducted in the Los Angeles area.14 The study was developed to evaluate outcome differences between using a bag-valve-mask procedure and intubating children. The methodology used was simple and straightforward. The study population was made up of seriously ill or injured children who were determined to need airway and/or respiratory support. EMS personnel were instructed to intubate children on Mondays, Wednesdays and Fridays, and to use only the bag and mask on other days of the week. Researchers found that pediatric patients who were only bag-mask ventilated did just as well (survival 30%; good neurologic outcome 23%) as those who were intubated (survival 26%; good neurologic outcome 20%).

     Do drugs help? Rapid sequence intubation/rapid sequence airway technique has been used in anesthesia and emergency medicine for many years and is an option in some prehospital care systems as well. RSI/RSA involves pre-treating a patient with a combination of sedative and neuromuscular blocking agents or “paralytic” drugs intended to facilitate airway placement. The purpose of medications in RSI/RSA is to completely eliminate the patient’s ability to resist intubation, voluntarily or involuntarily. Of course, this also means eliminating the patient’s ability to breathe voluntarily or involuntarily. If all goes smoothly, this procedure is very useful. But these techniques are not without their own subset of risks and potential complications, which are increased in the unpredictable EMS setting or in patients with whom we are less comfortable or less familiar (e.g., pediatrics). While research on the use of RSI/RSA techniques in the prehospital setting is ongoing, the subject remains controversial.15–17

     So, if our attempts at pediatric intubation don’t appear to improve patient outcomes, even in a busy urban EMS system, what’s the future direction for prehospital pediatric airway management?

     “Endotracheal intubation is a motor skill that demands practice. EMS providers with limited intubation experience should consider using airway adjuncts other than ETI for respiratory compromise.”18

PEDIATRIC AIRWAY MANAGEMENT     For all prehospital providers, initial airway management in children includes three key elements: positioning (the patient), placement (of the equipment) and providing (supplemental oxygen). In addition to providing appropriate cervical spine precautions, proper positioning of pediatric patients involves remembering a very important principle: Small children have what we call “big head, little body syndrome.” Simply stated, because of their relatively large occiput, infants and small children do not naturally assume a neutral position when supine. Placing a properly sized oral airway is the second key element. Nasal airways are generally too small and are easily clogged with secretions and mucus.6,19 The third element, providing effective bag-mask ventilation, may be the most difficult of the three. Some anesthesia and emergency medicine practitioners suggest that putting the tube in is often the easy part.7 Bagging a patient is a true art.

     These techniques are essential for not only BLS providers, but emergency professionals at all levels. If pediatric airway management is needed, attention to these concepts will serve you and your patients well. Think about it: If a child is not breathing, what do you do before you tube? Ventilate. What do you do after you tube? Ventilate. What do you really have to do if you can’t put the tube in? Ventilate. That’s why bag-mask ventilation is so important. But the skill is not as easy to master as many imagine.

     “A full stomach is probably the most common problem in pediatric anesthesia. Children can never be trusted to fast.”20

     Does bag-mask ventilation work? Yes and especially when a two-rescuer technique is paired with proper positioning and placement of an appropriately sized airway adjunct and mask.7 However, there are complications with bag-mask ventilation, the most notable being aspiration of stomach contents. Think of it as “Bellies + Bag-Mask = Barfing.” We all know that from the mouth everything goes to either the lungs or the belly. If air, which belongs in the lungs, is introduced to the belly, or if stomach contents that belong in the belly are introduced to the lungs, trouble will surely follow. Ideally, the belly is empty and stays that way, and only air goes into the lungs through a perfectly placed ET tube. But we don’t practice in an ideal world. Our patients, especially pediatric patients, are rarely without oral intake for 6 to 12 hours before we see them. So while proper positioning and placement of the oral airway help provide air to the proper area, more often than not, bag-mask ventilation will result in air being forced into the belly, which, unfortunately, is a recipe for aspiration.21,22

     “We believe the time has come to carefully study the validity of the ‘gold standard’ assumption (prehospital intubation) and to evaluate the efficacy of alternative airway management.”23

     If we want to avoid the problems of bagging without an ET tube, and we know that prehospital pediatric intubation is not necessarily the answer (due to inconsistent results), is there a better way for BLS and ALS providers to maintain a pediatric airway? Absolutely, through the use of nonvisualized airways. In the prehospital environment, nonvisualized, or blindly inserted, airways had been limited to esophageal obturator airways (EOAs) or, more recently, the Combitube (see Figure 1). Combitube insertion has become widely accepted for BLS providers, and for ALS providers who, for whatever reason, determine that an endotracheal tube cannot be placed. The Combitube is blindly inserted into the mouth and usually ends up in the esophagus; however, in a small percentage of cases, blind tracheal placement can occur (see Figure 2).5

     The Combitube comes with two syringes of different sizes, which are used to inflate the two balloons that secure the Combitube in place and block off the upper airway. Ventilations can be provided through two separate tubes, depending on whether the placement was esophageal or tracheal. The process is quite simple. Once the Combitube is inserted to the correct depth using the marker lines as a guide, inflate the blue pilot balloon (pharyngeal), followed by the white balloon (esophageal). Place a resuscitation bag on the end of the longer blue tube (labeled #1) to see if the tube has been placed in the esophagus as expected. If breath sounds are heard, continue using the blue tube. If breath sounds are not heard, or if there are other indications of gastric insufflation, use the shorter, clear tube (#2). It is important to always confirm the presence of breath sounds and absence of gastric sounds. In the event that both chest and belly sounds are absent, it is possible the tube has been advanced too far into the pharynx. If this occurs, deflate both balloons, pull the tube out approximately 2–3cm, reinflate the balloons and start the assessment process again. Combitube insertion can generally be completed in 30 seconds or less.24–26

     Although Combitubes have been used in prehospital, emergency, critical care and anesthesia for several years as backup airway devices for difficult intubations, it is important to remember that they are designed for use with patients who are at least 4 feet tall, which excludes most pediatric patients.5 Combitubes minimize the risk of pulmonary aspiration, as the device is designed to occlude the esophagus. In addition, if an oral ET tube is to be placed, the Combitube can be moved to the side of the mouth while the ET tube is being placed. However, barring a new, smaller version of the Combitube, this device remains in the prehospital armamentarium for use on only teenage and adult patients.5,7,24,26,27

     “All prehospital services that perform endotracheal intubation should have alternate airways available.”7

     “The laryngeal mask airway (LMA) has become a standard alternative for airway management during general anesthesia.”19

THE FUTURE FOR EMS: LARYNGEAL AIRWAYS—NOT ENDOTRACHEAL     “…Oxygenation, not tracheal intubation, is the main goal when treating emergencies.”1

     For many years, anesthesia professionals knew that not every patient needed to be, or could be, intubated. That knowledge led to the development of laryngeal airway devices. First introduced in the U.K. in 1981 and the U.S. in 1991, laryngeal mask airways (LMAs) are now used in hospital emergency and critical care departments, and in ALS and BLS EMS systems7,28–30 (see Figure 3). In parts of the U.K. and Japan, LMAs have become a primary prehospital airway device.31,32 Several studies suggest that placement of an LMA (generally in 30 seconds or less) is an easier skill at which to become proficient than bag-mask ventilation and certainly endotracheal intubation.19,28,33,34 Like the Combitube, laryngeal airways are designed for “blind” insertion.

     The traditional technique for LMA insertion is to start with the cuff of the device facing the patient’s tongue. Advance the LMA along the roof of the mouth to the posterior pharyngeal wall and into the hypopharynx until resistance is felt. At that point, inflate the cuff with the amount of air listed on the pilot balloon until a seal is formed. The rotational or reverse technique has the cuff initially facing the hard palate and then rotated 180° as the LMA is advanced into position.19,35 When the cuff is inflated, the LMA forms a loose seal around the top of the esophagus and will “pop out” a centimeter or so as the seal is formed. If that outward movement is not observed when the cuff is inflated, it is very likely the LMA is not in the proper position.19 Once proper placement is confirmed (preferably through continuous capnography), it should be adequately secured, as movement of as little as a centimeter can cause displacement of the airway device.19,29

     LMAs do a nice job of quickly getting the air to go where we want it to go, i.e., into the lungs. In addition, an LMA delivers increased effective tidal volumes compared with conventional bag-mask ventilation. Of particular importance is that LMAs are made in baby to adult sizes.36 (The smallest LMA works with a 2.2-lb. baby.) So unless you are doing critical care transport with a neonatal ICU team, there is an LMA for just about every patient we will encounter (see Table I).37 Also available for both adults and children are intubating LMAs through which an endotracheal tube can be placed; however, we strongly recommend waiting until the patient is in a safe and controlled environment (like the ED) before attempting to replace a functional laryngeal airway.

     Since the LMA does not pass through the vocal cords, if the patient vomits, the potential for aspiration is certainly a concern (see Figure 4).6,19,36,38 The good news is that research has shown that patients vomit less when ventilated with an LMA in place (2%) than when using a bag and mask (12%).5,6,21,22,34,39

     Although LMAs allow for effective ventilation for most patients, at inspiratory pressures above 18–20 cm H20, an LMA can pop off, resulting in an airway leak. This is important to remember in a patient with significant lung disease and/or increased airway pressures, as might be the case with ARDS, near-drowning, severe asthma, etc. In those instances, adequate ventilation may not be possible with just an LMA.19,40,41

     “We feel the LT (laryngeal tube) is a simple and timely device that should be given consideration for use as a bridge device or primary airway adjunct in the prehospital arena.”18

KING AIRWAY

     “It looks like an endotracheal tube, works like an esophageal tube, reminds you of a Combitube, and allows you to provide positive pressure ventilation.”42

     Like the LMA, learning to use the King airway is easy (see Figure 5). Both BLS and ALS providers have been found to have an 85%–100% first-time placement success rate, including inexperienced users. Placement generally takes less than 15–30 seconds.18,40,43–47 These airways have two cuffs, which are inflated simultaneously with one syringe. One cuff occludes the esophagus and the other occludes the oropharynx. The proximal cuff blocks the oropharynx and nasopharynx (back of the mouth), allowing air to pass through specially designed ventilatory openings into the trachea and lungs (see Figure 6).42

     The King laryngeal airway is designed to be inserted without direct visualization. It is initially placed laterally into the mouth and rotated back to midline after passing under the tongue (this is important). Once it passes the corner in the posterior pharynx under the base of the tongue, the tube is advanced until resistance is felt or the base of the connector is aligned with the teeth or gums, at which point the tube is in the upper esophagus.48 While King airways are ideally inserted in the “sniffing” position, the angle, shortness and size of the tube allow it to be placed with the patient in a neutral position (i.e., in a cervical collar) with minimal mouth opening or with severe facial trauma.40,47,49 Once it’s placed to maximum depth with the balloons inflated, slowly withdraw the tube until ventilation is easy with equal bilateral breath sounds. During ventilation, air passes into the pharynx, over the epiglottis and into the trachea, because the mouth, nose and esophagus are blocked by the balloons.46 When properly inserted and secured, the King airway almost always goes to the esophagus.18 Though tracheal placement is possible, in studies involving direct laryngoscopic visualization, tracheal placement of the King airway was attempted but not achieved.45,50 Only one published study details tracheal placement in 10% of insertions, but it is important to note that the insertion techniques were different than those recommended by the manufacturer, and the airways used were different from those available in the United States.51,52

     King airways allow for ventilation in most patients, but, like the LMA, they can pop off when airway pressures are significantly elevated. The “pop-off” point for King airways has been listed at pressures above 25–35 cm strong0, significantly higher than with LMA.34,40,46 As previously described, the potential for the airway to lose its seal and leak is an important consideration if the patient has significant lung disease or any other condition that would result in increased airway pressures. Like the LMA, correct placement of the King airway is best confirmed and monitored with continuous capnography, keeping in mind the limitations of CO2 monitoring in cardiac arrest. You should also be able to see appropriate chest rise and auscultate equal breath sounds.

     Though possible, gastric insufflation with potential pulmonary aspiration of stomach contents is minimized, as this device occludes the esophagus.40,48 In addition, newer models like the King LTS-D have an extra port that can be utilized to decompress the stomach. If intubation with an oral endotracheal tube is desired after a King airway has been secured, an intubation catheter or bougie can be passed through the airway’s ventilatory inlet and used as a stylet during removal of the King airway and subsequent replacement with an ET tube using an over-the-catheter technique.42 As mentioned earlier, this substitution should be done in a controlled environment.

     Like LMAs, King airways must be well secured at all times, as displacement in a transport environment can occur with even minimal movement.21 Of note for prehospital pediatric patients, the smallest King airway is currently recommended for children over 12 kg (25lbs) or 35″ in length. Finally, laryngeal tubes are much simpler than Combitubes, as they have only one syringe with which to inflate the cuff(s) and only one tube to ventilate the patient.25 Guesswork and the concomitant potential for error are eliminated.

KEEPING THE AIRWAY IN PLACE     Following are some simple suggestions to help avoid potential airway management complications. First, we highly recommend that prehospital and hospital providers remove the bag from the airway device when the patient is being moved. The ventilation bag is a significant weight if not completely supported or removed. Imagine trying to keep your neck straight with a brick hanging from it. Not easy to do, especially if you don’t weigh much more than the brick.

     Second, an airway device that is not carefully secured to the patient can easily become displaced or dislodged, especially in an infant or child. Movement of 1cm in an adult ET tube may be insignificant, but that same 1 cm movement in an infant’s 3.0 ET tube may pull it completely out of the trachea.

     Third, if you are transporting a pediatric patient with an airway in place, make sure the patient is also secured. Many airway disasters occur after a successful intubation. Critical care transport teams routinely place intubated patients (with or without a history of trauma) in hard cervical collars to minimize head and neck movement and the subsequent effect on the airway.

     Fourth, it is critical to monitor the airway, ideally through continuous capnography. The difference between an unexpected airway event and a disaster is often simply the amount of time between recognition and remedy.

     You may not be able to control all eventualities, so be prepared. If something happens to the airway device, you will need a mask for your patient. We suggest taping the mask onto something that will always be with the patient, such as the head blocks, monitor or even the patient’s forehead, so you always know where it is. It’s also a good idea to have a back-up airway device on hand in case something happens.

     In the world of prehospital pediatric emergencies, managing your patient’s airway will present certain challenges and opportunities. Non-visualized laryngeal airways and other new modalities make it possible to treat children more effectively while minimizing adverse events. With increased knowledge, proper planning, preparation and practice, we can enhance our comfort level and competence and continue to improve patient care and outcomes.

     The authors wish to thank Michael Abernethy, MD, from the University of Wisconsin and Madelyn Kahana, MD, from the University of Chicago for their expert and helpful reviews of this article.

References

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17. Davis D. Should invasive airway management be done in the field? Can Med Assoc J 178(9):1171–1173, 2008.

18. Russi C, Wilcox C, House H. The laryngeal tube device: A simple and timely adjunct to airway management. Am J Airway Management 25:263–267, 2007.

19. Wheeler M, Cote C, Todres I. Pediatric airway. In, A Practice of Anesthesia for Infants and Children, 3rd Ed., pp. 79–120. Cote C, et al (eds). Philadelphia, PA: Saunders, 2001.

20. Cote C, Todres D, Ryan J, Goudsouzian N. Preoperative evaluation of pediatric patients. In, A Practice of Anesthesia for Infants and Children, 3rd Ed., pp. 37–54. Cote C, et al. (eds). Philadelphia, PA: Saunders, 2001.

21. Kette F, Reffo I, Giordani G, et al. The use of laryngeal tube by nurses in out-of-hospital emergencies: Preliminary experience. Resuscitation 66:21–25, 2005.

22. Stone B, Chantler P, Baskett P. The incidence of regurgitation during cardiopulmonary resuscitation: A comparison between the bag valve mask and the laryngeal mask airway. Resuscitation 38:3–6, 1998.

23. Giesecke A, Montgomery W. The role of anesthesiologists in paramedic training. American Society of Anesthesiologists Newsletter 69(11):1–3, 2005.

24. Frass M. Combitube: What is new? Difficult Airway 2(2):26–31.

25. Trabold B, Schmidt C, Schneider B, et al. Application of three airway devices during emergency medical training by health care providers: A manikin study. Am J Emerg Med 26(7):783–788, 2008.

26. Lefrancois D, Dufour D. Use of the esophageal tracheal Combitube by basic emergency medical technicians. Resuscitation 52(1):77–83, 2002.

27. Ochs M, Vilke G, Chan T, et al. Successful prehospital airway management by EMT-Ds using the Combitube. Prehosp Emerg Care 4(4):333–337, 2000.

28. Chen L, Hsiao A. Randomized trial of endotracheal tube versus laryngeal mask airway in simulated prehospital pediatric arrest. Pediatrics 122:E294–E297, 2008.

29. Silvestri S, Ralls G, Ho A. Prehospital laryngeal mask airway use by emergency medical technician-basics. Paper presented at the annual meeting of the National Association of EMS Physicians. www.allacademic.com/meta/p66726_index.html.

30. Deakin C, Peters R, Tomlinson P, Cassidy M. Securing the prehospital airway: A comparison of laryngeal mask insertion and endotracheal intubation by UK paramedics. Emerg Med J 22:64–67, 2005.

31. O’Malley R, O’Malley G, Ochi G. Emergency medicine in Japan. Ann Emerg Med 38(4):441–446, 2001.

32. Ridgway S, Hodzovic I, Woolard M, Latto I. Prehospital airway management in ambulance services in the United Kingdom. Anaesthesia 59(11):1091–1094, 2004.

33. Smith I, White P. Use of laryngeal mask airway as an alternative to a face mask during outpatient arthroscopy. Anesthesiology 77:850–855, 1992.

34. Ocker H, Wenzel V, Schmucker P, et al. A comparison of the laryngeal tube with the laryngeal mask airway during routine surgical procedures. Anesthesia & Analgesia 95:1094–1097, 2002.

35. Kuvaki B, Kucukguclu S, Lyilikci L, et al. The Soft Seal disposable laryngeal mask airway in adults: Comparison of two insertion techniques without intra-oral manipulation. Anaesthesia. E-publication ahead of print, 2008.

36. Gandini D, Brimacombe J. Manikin training for neonatal resuscitation with the laryngeal mask airway. Paediatric Anaesthesia 14(6):493–494, 2004.

37. King C, Henretig F, King B, et al. Management of the Difficult Airway. In, King C, et al. (eds). Textbook of Pediatric Emergency Procedures, p. 199. LWW: Philadelphia, 2007.

38. Dorges V, Ocker H, Wenzel V, Schmucker P. The laryngeal tube: A new simple airway device. Anesthesia & Analgesia 90:1220–1222, 2000.

39. Brimacombe J, Berry A. The incidence of aspiration associated with the laryngeal mask airway: A meta-analysis of published literature. J Clin Anesthesia 4:297–305, 1995.

40. Hagberg C, Bogomolny Y, Gilmore C, et al. An evaluation of the insertion and function of a new supraglottic airway device, the King LT, during spontaneous ventilation. Anesthesia & Analgesia 102:621–625, 2006.

41. Asai T, Morris S. The laryngeal mask airway: Its pediatric airways, effects, and role. Can J Anaesthesia 41:930–960, 1994.

42. Fowler R. King LT-D to the rescue. J Emerg Med Serv 30(7): 90–92, July 2005.

43. Brimacombe J, Keller C, Brimacombe L. A comparison of the laryngeal mask airway ProSeal and the laryngeal tube airway in paralyzed anesthetized adult patients undergoing positive pressure-controlled ventilation. Anesthesia & Analgesia 96:1535, 2003.

44. Asai T, Murao K, Shingu K. Efficacy of the laryngeal tube during intermittent positive-pressure ventilation. Anaesthesia 55:1099–1102, 2000.

45. Genzwuerker H, Hilker T, Hohner E, Kuhnert-Frey B. The laryngeal tube: A new adjunct for airway management. Prehosp Emerg Care 4:168–172, 2000.

46. Gaitini L, Vaida S, Somri M, et al. An evaluation of the laryngeal tube during general anesthesia using mechanical ventilation. Anesthesia & Analgesia 96:1750–1755, 2003.

47. Guyette F, Wang H, Cole J. King airway use by air medical providers. Prehosp Emerg Care 11(4):473–476, 2007.

48. Asai T, Hidaka I, Kawachi S. Efficacy of the laryngeal tube by inexperienced personnel. Resuscitation 55:171–175, 2002.

49. Asai T. Use of the laryngeal tube in a patient with an unstable neck. Can J Anesthesia 49(6):642–643, 2002.

50. Genzwuerker H, Hilker T, Hohner E, Kuhnert-Frey, B. Der larynxtubus: Eine alternative fur die vorubergehende oxygenierung bei schwieriger intubation? Anaesteshiol Intens 40:158, 1999.

51. McGrail T. Personal communication with Tom McGrail, R&D Director, King Systems, Sep 20, 2008.

52. Kikuchi T, Kamiya Y, Ohtsuka T, et al. Randomized prospective study comparing the Laryngeal Tube Suction II with the ProSeal Laryngeal Mask Airway in anesthetized and paralyzed patients. Anesthesiology 109(1):54–60, 2008.

Bibliography     Aijian P, Tsa A, Knopp R, Kallsen G. Endotracheal intubation of pediatric patients by paramedics. Ann Emerg Med 18:489–494, 1989.

     Baskett P. The use of the laryngeal mask airway by nurses during cardiopulmonary resuscitation: Results of a multicentre trial. Anaesthesia 49:3–7, 1994.



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January 31st, 2009 posted by Kelly Burkholder-Allen, RN, MSEd @ 8:06 am

Ice-caked Kentuckians cry for help!

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http://www.google.com/hostednews/ap/article/ALeqM5jv320qXrVAVFqDYU3nglqZySw6YgD9621HN03

Ice-battered Kentucky pleads for help from storm

By BRUCE SCHREINER – 3 hours ago

MARION, Ky. (AP) — A crippling winter storm has plunged about a million customers into the dark from the Midwest to the East Coast, and thousands of people in ice-caked Kentucky have sought refuge in motels and shelters.

Dozens of deaths have been reported and many people are pleading for a faster response to the power outages. Some in rural Kentucky ran short of food and bottled water, and resorted to dipping buckets in a creek.

Thousands fled frigid, powerless homes for hotels and even a heated auditorium at Murray State University that was converted into a shelter following Monday’s storm that left some areas in up to 1 inch ice.

Utility workers hoped to speed up efforts Saturday to turn the lights back on. Still, rural communities feared it could be days or even weeks before workers got to areas littered with downed power lines.

Temperatures were expected to rise just above freezing Saturday for the first time in days.

At least 42 people have died in the icy arc of destruction that began in the Midwest. At least nine deaths were reported in Arkansas, six each in Texas and Missouri, three in Virginia, two each in Oklahoma, Indiana and West Virginia and one in Ohio. Most were blamed on hypothermia, traffic accidents and carbon monoxide poisoning from generators.

In Kentucky, where 11 people had died, a man and two women were the latest victims after they were found dead in a southwestern Louisville home. One woman was found in a bed; the other two were found in the garage with a generator, police spokesman Phil Russell said.

Meanwhile, the uncertainty of when power might be restored had many appealing for help. Officials urged those in dark homes to leave.

“We’re asking people to pack a suitcase and head south and find a motel if they have the means, because we can’t service everybody in our shelter,” said Crittenden County Judge-Executive Fred Brown, who oversees about 9,000 people, many of whom spent a fifth night sleeping in the town’s elementary school.

Local officials grew angrier at what they said was a lack of help from the state and the Federal Emergency Management Agency.

In Kentucky’s Grayson County, about 80 miles southwest of Louisville, Emergency Management Director Randell Smith said the 25 National Guardsmen who have responded have no chain saws to clear fallen trees. He said roads are littered with fallen trees and people shivering in bone-chilling cold are in need.

“We’ve got people out in some areas we haven’t even visited yet,” Smith said. “We don’t even know that they’re alive.”

Smith said FEMA was still a no-show days after the storm.

“I’m not saying we can’t handle it,” Smith said. “We’re handling it. But it sure would have made life a lot easier.”

FEMA spokeswoman Mary Hudak said some agency workers had begun working Friday in Kentucky and more help was on the way. Hudak said FEMA also has shipped 50 to 100 generators to the state to supply electricity to such facilities as hospitals, nursing homes and water treatment plants.



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January 31st, 2009 posted by Kelly Burkholder-Allen, RN, MSEd @ 8:00 am

Seven Chinese nationals die and many more are injured in bus crash near Hoover Dam!

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http://www.nytimes.com/2009/01/31/us/31hoover.html

January 31, 2009

7 Die in Bus Crash Near Hoover Dam

DOLAN SPRINGS, Ariz. (AP) — A tour bus overturned on a highway near the Hoover Dam on Friday, killing seven Chinese nationals and injuring at least 10 other people, the authorities said.

Six fatalities were confirmed at the scene, about 190 miles northwest of Phoenix; a seventh person died at a hospital, said Cmdr. Dean Nyhart of the Arizona Department of Public Safety.

Commander Nyhart said investigators were not certain how many people were on the 24-passenger bus or how many had been transported to hospitals in Kingman, Ariz., and Las Vegas.

The bus was traveling north on U.S. 93 when it veered left and then right across the median, Commander Nyhart said. It rolled at least once. He said many of the victims killed at the scene had been ejected from the bus.



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January 31st, 2009 posted by Paul Rega, MD, FACEP @ 2:16 am

For the Good of Us All

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January 31st, 2009 posted by Paul Rega, MD, FACEP @ 2:12 am

Minnesota talks to her citizens: Rationing Medicine in a Pandemic

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Intro:  Hats off to  the Minnesota Department of Health for putting this all together and then having the public comment on it.  It certainly is more than what many, if not most, other states are doing. 

1

Minnesota Department of Health

News Release

January 30, 2008

Contact information


Public invited to comment on recommendations for allocating medical resources in an influenza pandemic
Health officials say possibility of pandemic still a major concern

Minnesotans are invited to review and comment on a proposed new ethical framework for allocating scarce medical resources during a major influenza pandemic. The framework includes recommended strategies for rationing key types of medical supplies that would be needed during a severe flu pandemic, like the one that occurred worldwide in 1918.
The recommendations were developed by a specially-convened panel of Minnesotans, with the support of experts in a variety of fields. The public can view and comment on the framework document online at http://www.ahc.umn.edu/mnpanflu/ through March 16. The recommendations are posted in two parts – a report outlining the panel’s recommendations, and a separate document outlining recommendations for implementation.
The project was organized by the Minnesota Center for Health Care Ethics (MCHCE) and the University of Minnesota Center for Bioethics, under a contract with the Minnesota Department of Health (MDH). MCHCE is a community-based ethics center sponsored by Fairview Health Services, HealthEast Care System and the Sisters of St. Joseph of Carondelet. The Center for Bioethics is a multidisciplinary program whose goals include “fostering public discussion and debate through community outreach activities, and assisting in the formulation of public policy.”
The kinds of medical resources considered in the recommendations include vaccines that are matched to the virus strain causing the pandemic; antiviral drugs; protective masks (technically known as respirators); and mechanical ventilators for patients with severe breathing problems.
All of these items could be in extremely short supply if there is ever another pandemic like the one in 1918. Health officials have estimated that a 1918-style pandemic could sicken up to 30 percent of our state’s population, resulting in over 30,000 deaths in Minnesota alone. It is estimated that as many as 170,000 Minnesotans could require hospitalization.

“People may have a false sense of security because we haven’t had a pandemic yet, after all of the publicity about ‘bird flu’ a couple of years ago,” said Dr. Sanne Magnan, Minnesota Commissioner of Health. “However, that same avian strain of influenza is still making people sick and causing deaths in Asia and Africa, and it could still cause a pandemic.”

“Even if that strain never acquires the ability to cause a pandemic, history tells us that we will have another global pandemic, sooner or later. We need to be prepared, and the new ethical framework is part of that preparation.”

A panel convened by MCHCE and the University, was responsible for drafting the framework. In addition to health ethicists, the panel also included representatives of faith communities, hospitals, health care providers, ethnic and racial communities, populations with special needs, business and government.

The panel developed a separate set of priorities for allocating each of the major types of health care resources they considered – antivirals, vaccines, masks and ventilators.

Rather than relying solely on clinical decision-making criteria, or resorting immediately to a possible lottery when medical resources are in short supply, they recommended that a number of other factors also be considered in determining who gets which resources.

The panel also looked at the impact of resource allocation decisions on the overall health of the population, public safety and civil order, as well as the essential fairness of allocation decisions.
Fairness goals considered by the panel included:

Seeking public input and comment is an essential step in developing the guidelines, Dr. Magnan noted.

“If this framework is to be useful, it is vitally important that they reflect our shared values, and that they are accepted by the broader community,” she said. “From the beginning, we recognized that community outreach would be a critical part of this project.”

In addition to seeking public comment through the website, organizers of the project will also be using two additional vehicles to seek input on the panel’s recommendations. The public will be able to provide comment at two town hall meetings, to be held later in Owatonna and Duluth. Then, following the town hall meetings, small groups of individual citizens will be invited to take part in a series of focus groups, to be held at six different locations around the state. These facilitated small group discussions will provide an opportunity for a more intensive and structured discussion of the issues raised by the two reports.

A separate report will be developed once all of the community engagement activities have been completed, summarizing comments and reaction from the public. That report, which is expected by the end of the year, will be made public and formally presented to the panel that drafted the ethics recommendations.

The panel will then consider revisions to its original ethics and implementation recommendations in response to the public input report, and present those recommendations to MDH for implementation.



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January 31st, 2009 posted by Paul Rega, MD, FACEP @ 2:06 am

Peanut Corp. of America undergoing a criminal investigation

Intro:  Have you heard anyone from PCA talk about what’s been happening? I haven’t.  That noise you hear is not the cracking of peanut shells.  It’s the shredding on incriminating documents.

                                           1

Click on Going to Jail?  for the full story.

CIDRAP News, 1/30/09

“The US Food and Drug Administration said today it is starting a criminal investigation of Peanut Corp. of America (PCA), the company whose peanut processing plant in Georgia has been linked with a Salmonella outbreak involving more than 500 cases nationwide…
…”I can confirm that the FDA Office of Criminal Investigation is involved with the Justice Department in an investigation of Peanut Corp. of America,” Stephen Sundlof, DVM, head of the FDA’s Center for Food Safety and Applied Nutrition (CFSAN), said at a press teleconference this afternoon.

“It’s an open investigation at this time and we can’t talk at all about the investigation,” he said.

The announcement comes 3 days after the FDA first reported that PCA had sold peanut products that had initially tested positive for Salmonella. In an inspection report published on Jan 28, the FDA said that in 12 cases over the past 18 months, initial tests had detected Salmonella in various PCA peanut products. In each case the company had the product retested and then sold it after the second test was negative, according to the FDA…”



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January 31st, 2009 posted by Paul Rega, MD, FACEP @ 1:40 am

MRSA & Football

MMWR, 1/30/09  

Methicillin-Resistant Staphylococcus aureus Among Players on a High
School Football Team

New York City, 2007

 

On September 12, 2007, the New York City Department of Health and Mental Hygiene (DOHMH) was notified of three players on a Brooklyn high school football team with culture-confirmed methicillin-resistant Staphylococcus aureus (MRSA) skin and soft tissue infections (SSTIs). During August 19–24, the team had attended a preseason football training camp, where all 59 players on the team lived together in the school gymnasium. An investigation by DOHMH revealed four culture-confirmed and two suspected cases of MRSA among 51 players interviewed (11.8% attack rate). Of the six cases, three involved abscesses that required incision and drainage. The risk for MRSA infection was higher among those who shared towels during the training camp than among those who did not (relative risk [RR] = 8.2). In addition, the six players with MRSA infections had a mean body mass index (BMI) that was significantly higher than the mean for those who were not infected. Multivariable logistic modeling determined that sharing towels during camp (adjusted odds ratio [AOR] = 15.7) and higher BMI (AOR = 1.4) were associated independently with MRSA infection. Similar outbreaks have been reported among football teams in which inadequate hygiene, combined with skin injuries and living in close quarters, contributed to the spread of MRSA infection. Such outbreaks might be prevented by better educating players and coaches regarding SSTIs and by better promoting proper player hygiene, particularly during training camps.

1

Initial investigation by DOHMH began on September 12. Investigators learned that all 59 players had attended a preseason training camp during August 19–24. The players had lived together in the school gymnasium, slept on cots in close proximity to each other, and showered in the school locker room, usually only once at the end of the day. The school had supplied antibacterial soap in pump dispensers in the showers; however, several players brought their own soap. Players supplied their own towels. Players reported that they usually left their towels on their cots or on the floor when not in use. The school offered a daily laundry service for uniforms and towels during the camp; however, most players did not have their towels washed and wore their uniforms two or three times between launderings. Players often remained in sweat-soaked clothes between the morning and afternoon practices. The school did not have whirlpools or hot tubs.

Investigators hypothesized that sharing facilities and equipment, previous skin injuries, player position, inadequate player hygiene, and having a higher BMI might be risk factors linked to MRSA infections (1–3). To find additional cases, identify risk factors for infection, and implement infection control measures, DOHMH conducted face-to-face interviews on September 14 with 51 of the 59 players, using a close-ended questionnaire; the eight remaining players could not be contacted. In addition, a DOHMH physician further examined the five players reported by the school nurse as potentially infected.

A confirmed MRSA case was defined as a clinically compatible SSTI with a positive MRSA culture in a team member during August 5–September 14, a period ranging from 2 weeks before to 3 weeks after the end of the training camp. A suspected MRSA case was defined as a clinically compatible SSTI or systemic infection with no culture confirmation. Date of symptom onset was defined as the date an infected player reported first noticing an infected wound.

Among the 51 players interviewed, four confirmed and two suspected MRSA cases were identified (11.8% attack rate). Molecular typing with pulsed-field gel electrophoresis revealed that three of the confirmed cases were USA300, a strain usually considered to be a community-associated MRSA. An isolate from the fourth player with confirmed MRSA was not available for typing. Symptom onsets ranged from August 24, the last day of training camp, to September 6, a total of 13 days after the camp (Figure 1).

In the four confirmed cases, infections initially appeared as a blister on the ankle, calf, hip, or instep. One suspected case involved impetigo on the upper arm; the other suspected case involved impetigo on the arms and eyebrow. Three players reported their wounds to the school nurse or a physician only after blisters had developed into infections requiring medical attention. The six players with confirmed or suspected MRSA infections were referred to their personal physicians for treatment. Three of the players had abscesses that required incision and drainage. Three of the players with confirmed cases were treated with Bactrim and doxycycline, clindamycin and mupirocin, and Bactrim and mupirocin, respectively. One of the players with suspected MRSA infection was treated with ciprofloxacin. Antibiotics used to treat the remaining two players were unknown.

Interviews with the players revealed that 33 (65%) had sustained at least one cut, abrasion, or turf burn during the preseason camp or regular season. The players reported that, unless the skin injuries were severe, they had cleaned, dressed, or bandaged them by themselves. No players reported sharing towels or soap during the regular season, because players went home after practice to shower. However, 10 (20%) had shared towels and six (12%) had shared soap during training camp, when the players showered on site.

In a retrospective cohort analysis, after combining confirmed and suspected MRSA cases, bivariate RRs and their 95% confidence intervals (CIs) were calculated to identify risk factors associated with infection. Multivariable logistic regression was used to evaluate the independent association of multiple risk factors, including BMI, which was modeled as a continuous variable because the small number of cases did not allow for tests based on BMI categories (i.e., normal, overweight, and obese).

Sharing towels during training camp significantly increased the risk for MRSA infection (RR = 8.2) (Table). Sharing protective pads, sharing soap, showering less than once a day, having more than one skin injury, and washing uniforms less than once a day were not significant risk factors for infection. Playing at lineman or linebacker and wide receiver or cornerback positions (previously shown to be potential risk factors in football MRSA outbreaks [2,4]) also were not significant risk factors (Table).

The six players with MRSA infection had a mean BMI of 29.1 (CI = 24.7–33.3), which was significantly higher by t-test (t = 2.56; p=0.014) than the mean BMI of 23.8 (CI = 22.8–25.0) for the 45 players without infection. Using CDC’s child and teen BMI-for-age weight status categories,* five of the six (83%) players with MRSA infection could be classified as overweight or obese, compared with 20 of the 45 (44%) players without infection (Figure 2). A bivariate analysis using logistic regression revealed that higher BMI was associated with higher risk for infection (OR = 1.3 per unit increase in BMI; CI = 1.1–1.7). A multivariable logistic model confirmed that both sharing towels during training camp (AOR = 15.7; CI = 1.5–167.4) and BMI (AOR = 1.4; CI = 1.1–1.9) were associated independently with MRSA infection.

Reported by: P Kellner, MPH, A Yeung, MPH, HA Cook, MPH, J Kornblum, PhD, M Wong, MPH, F Eniola, MPH, D Weiss, MD, New York City Dept of Health and Mental Hygiene. HP Nair, PhD, EIS Officer, CDC.

Editorial Note:

 

Since 2000, outbreaks of MRSA SSTIs have been reported among players on high school, college, and professional football teams with attack rates similar to those described in this report (1–4). Despite education efforts by CDC and state and local health departments, MRSA infections continue to be a problem among football players. A 2007 CDC survey of high school athletic trainers revealed that 53% had treated MRSA infections in football players (1). The results of this investigation suggest that sharing of towels among players at a preseason training camp was associated with MRSA infection, a risk factor previously linked to football-related MRSA outbreaks (1–3). These results are also consistent with three previous reports that identified MRSA infections in football teams temporally linked to training camps (2–4), which might be a setting that increases risk behaviors for infection (4). Living in close quarters for an extended period, a potential risk factor identified in other settings (5), might have further contributed to the outbreak.

The results also indicated that higher BMI among team players was associated with higher risk for MRSA infection, independent of sharing towels. These results are consistent with those of two other football-related outbreaks (5) and published reports linking higher BMI with a range of infections, including skin infections (6). The possibility that higher BMI is confounded by player positions (e.g., lineman) involving heavier players and more frequent contact is not supported by the data, which found no differences by player position. Evaluating player position in general is statistically problematic because sample sizes vary substantially by position on most football rosters.

The findings in this report are subject to at least two limitations. First, the small number of cases reduced the precision of the point estimates, as reflected in the wide CIs. Second, because players were not interviewed until 3 weeks after the first reported symptom onsets, they might not have been able to accurately recall events, leading to misclassification of players by risk factor.

High school football programs might be able to reduce the risk for MRSA outbreaks by improving their procedures and facilities to promote optimal player hygiene, particularly during training camps. Improvements might include providing a towel service and collecting used towels from players on a daily basis. Skin injuries should be monitored closely by coaches and trainers, rather than by players alone. Living arrangements might be modified so that players are not living in close quarters for extended periods. Education on SSTI identification, prevention, and intervention might be included as a standard component of football training camps.

Acknowledgments

This report is based, in part, on contributions by M Marx, PhD, J Nguyen, MPH, M Layton, MD, Bur of Communicable Disease; L Thorpe, PhD, K Konty, PhD, Div of Epidemiology; T Matte, MD, Div of Environmental Surveillance and Policy, New York City Dept of Health and Mental Hygiene. J Magri, MD, Office of Workforce and Career Development, CDC.

References

 

  1. Brinsley-Rainisch K, Goding A, Sinkowitz-Cochran R, Pearson M, Hageman J, the National Athletic Trainers’ Association. MRSA infections in athletics: perceptions and practices of certified athletic trainers [Poster]. Presented at the Society for Healthcare Epidemiology of America 17th Annual Meeting, Baltimore MD; April 15, 2007.
  2. Begier EM, Frenette K, Barrett NL, et al. A high-morbidity outbreak of methicillin-resistant Staphylococcus aureus among players on a college football team, facilitated by cosmetic body shaving and turf burns. Clin Infect Dis 2004;39:1446–53.
  3. Romano R, Lu D, Holtom P, et al. Outbreak of community-acquired methicillin-resistant Staphylococcus aureus skin infections among a collegiate football team. J Athl Train 2006;41:141–5.
  4. Kazakova SV, Hageman JC, Matava M, et al. A clone of methicillin-resistant Staphylococcus aureus among professional football players. N Engl J Med 2005;352:468–75.
  5. Campbell KM, Vaughn AF, Russell KL, et al. Risk factors for community-associated methicillin-resistant Staphylococcus aureus infections in an outbreak of disease among military trainees in San Diego, California, in 2002. J Clin Microbiol 2004;42:4050–3.
  6. Falagas M, Kompoti M. Obesity and infection. Lancet Infect Dis 2006;6:438–46.


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January 31st, 2009 posted by Paul Rega, MD, FACEP @ 1:34 am

The PB Recall Express

1                     “First, it’s Blagojevich.  Now, they’re after us.  Sigh!”

Voluntary Recall Alert: Chef Pierre Chocolate Peanut Butter Silk Pie (January 30)
Fri, 30 Jan 2009 12:55:00 -0600

 

Sara Lee North American Foodservice is conducting a voluntary recall of Chef Pierre Chocolate Peanut Butter Silk Pie, a foodservice product. This voluntary recall is being conducted as a precautionary measure due to this product containing peanut pieces subject to the expanded recall of products produced by Peanut Corporation of America’s (PCA) Blakely, Georgia facility. This PCA facility is the subject of an investigation by the U.S. Food and Drug Administration (FDA) concerning a recent salmonella outbreak. No other Sara Lee Corporation products are involved in this recall.

Arico Natural Foods Company Announces US and Canadian Recall of Arico Peanut Butter Cookies and Cookie Bars Because of Possible Health Risk (January 29)
Fri, 30 Jan 2009 12:32:00 -0600

 

Beaverton, Oregon based Arico Natural Foods Company announced today a voluntary recall of Arico Peanut Butter Cookies and Cookie Bars as a precautionary measure due to yesterday’s expanded recall of peanut ingredients from Peanut Corporation of America’s Blakely, Georgia facility, which is the subject of an FDA investigation concerning the recent Salmonella outbreak.

Orchard Valley Harvest Announces Urgent Nationwide Voluntary Recall for Peanuts Because of Possible Health Risk (January 29)
Fri, 30 Jan 2009 12:12:00 -0600

 

Orchard Valley Harvest initiated a nationwide voluntary recall of certain conventional and organic peanuts roasted and packed for Safeway because the product may be contaminated with Salmonella. Product was sourced from Peanut Corporation of America.

Select Simbree Energy Foods Products Recalled Because of Possible Health Risk (January 30)
Fri, 30 Jan 2009 12:45:00 -0600

 

No known illnesses have been reported to date in connection with these products. The recall was initiated after it was determined that the peanut product received was manufactured by Peanut Corporation of America. Simbree Energy Foods has informed FDA of its actions and is fully cooperating with the Agency.

Rain Creek Baking Corporation Announces An Expanded Voluntary Withdrawal of Peanut Butter Turtles, Peanut Butter Baskets and Peanut Butter Princesses Due to Possible Health Risk (January 30)
Fri, 30 Jan 2009 12:15:00 -0600

 

Due to the expanded recall of Peanut Butter Corporation’s peanut butter products on January 28th, Rain Creek Baking Corporation announces an expanded precautionary voluntary withdrawal of Sinbad, Michael’s and Rain Creek Baking Company branded dessert products produced with peanut butter because the products have a potential of being contaminated with Salmonella.

Galliker Dairy Announces Voluntary Recall of Rocky Road Ice Cream and Sundae Nut Cones Because of Possible Health Risk (January 30)
Fri, 30 Jan 2009 12:24:00 -0600

 

The Galliker Dairy Co. is voluntarily recalling all three-gallon containers of Galliker-brand Rocky Road ice cream and Galliker-brand Sundae Nut Cones sold to foodservice and retail outlets in Pennsylvania and West Virginia.

Country Maid Expands Upon Previous Voluntary Nationwide Recall of Classic Breaks Peanut Butter Cookie Dough Due to Possible Health Risk (January 29)
Fri, 30 Jan 2009 10:17:00 -0600

 

Due to the second expanded recall from the Peanut Corporation of America, additional lot numbers of peanut butter are now included that were used to manufacture the peanut butter cookie dough. The peanut butter used to make the cookie dough was supplied by Peanut Corporation of America and may be contaminated with Salmonella.

Hy-Vee Inc. recalls two bakery products with peanuts distributed in seven states due to possible health risk (January 29)
Fri, 30 Jan 2009 09:41:00 -0600

 

Hy-Vee Inc. is voluntarily recalling its freshly made party mix and peanut brittle because the products contain whole peanuts that have the potential to be contaminated with salmonella. All sell-by dates are included in this recall. The products are sold in various types of packaging and have a Hy-Vee price label attached. The items should be destroyed or returned to Hy-Vee for a full refund.

Meijer Announces Voluntary Recall for Some Meijer Brand Peanuts and Ice Cream Novelties Citing Possible Health Risk (January 30)
Fri, 30 Jan 2009 09:27:00 -0600

 

Meijer initiated a voluntary recall of two types of its Meijer Brand dry-roasted peanuts and four types of Meijer Brand ice cream novelties sold in all of its stores in Michigan, Ohio, Indiana, Illinois and Kentucky. Meijer removed all identified products from its stores and gas stations. All sell-by dates are impacted by this recall.

Fieldbrook Foods Corp. Announces Nationwide Voluntary Recall of Select Ice Cream Novelty Products Due to Possible Health Risk (January 29)
Fri, 30 Jan 2009 07:09:00 -0600

 

Fieldbrook Foods Corp. announced a voluntary nationwide recall of select ice cream novelty products containing granulated peanuts as the products have the potential to be contaminated with Salmonella.

Lesserevil Brand Snack Co. Issues a Nationwide Voluntary Recall of Lesserevil Brand Peanut Butter and Choco Kettle Corn (January 30)
Fri, 30 Jan 2009 17:40:00 -0600

 

LesserEvil announces a voluntary recall of PEANUT BUTTER AND CHOCO KETTLE CORN because the peanut butter in this product was purchased from Peanut Corporation of America (PCA). Peanut butter products produced by PCA have been the subject of an investigation by the US Food and Drug Administration (FDA) and are linked in a national outbreak of Salmonella.

Wells’ Dairy Expands Voluntary Recall of Select Blue Bunny Products (January 30)
Fri, 30 Jan 2009 17:20:00 -0600

 

Wells’ Dairy, Inc., today expands its voluntary recall of its Blue Bunny Personals Bunny Tracks 8 fl oz. sold at retail and foodservice levels to include Lot Number 80030 “Best Used By” date 11/17/2009. The lot number can be found printed on the side of the carton. The affected product was shipped to the following states: Virginia, Iowa, Ohio, Nebraska, Washington, Tennessee, Michigan, Wisconsin, Indiana, North Carolina, Pennsylvania, and Oregon. This product contains peanuts from the Peanut Corporation of America (PCA), which is the focus of an ongoing Salmonella investigation.

NutriSystem Expands Voluntary United States Recall of Peanut Butter Granola Breakfast Bar to Include Canada Due to Possible Peanut Corporation Of America (PCA) Contamination and Potential Health Risk (January 30)
Fri, 30 Jan 2009 16:48:00 -0600

 

NutriSystem Inc., a leading provider of weight management products and services, today announced an expanded voluntary recall of its NutriSystem-branded Peanut Butter Granola Bar due to the expanded recall from Peanut Corporation of America (PCA) to include all peanut products manufactured from January 1, 2007 to the present.

House of Flavors Issues Voluntary Recall in Eastern United States Due to Possible Health Risk (January 30)
Fri, 30 Jan 2009 16:56:00 -0600

 

House of Flavors Ice Cream Company is voluntarily recalling all Hannaford Denali Nutty Moose Tracks ice cream sold in Hannaford Stores in Maine, New Hampshire, Vermont, Massachusetts, New York and Sweetbay Stores in Florida. The product is packed in 56 (UPC 41268 15394) and 16 (UPC 41268 15447) fluid ounce paper containers stamped date code prior to 09028.

Turkey Hill Dairy Announces Voluntary Recall of Select Ice Cream Flavors Following Expanded FDA Investigation of Peanut Corporation of America (January 30)
Fri, 30 Jan 2009 16:33:00 -0600

 

Turkey Hill Dairy of Lancaster County, PA, is voluntarily recalling six select ice cream and frozen yogurt items because the products contain ingredients that have been voluntarily recalled by our suppliers.



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