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  • Professor, Department of Clinical Pharmacy, West Virginia University School of Pharmacy
  • Infectious Diseases Clinical Specialist, West Virginia University Medicine, Morgantown, West Virginia

https://directory.hsc.wvu.edu/Individual/Index/31914

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Observe Fig 26 where the etched lines are relative to the skin prior to extending the Stylet once it is docked. Warning: If the Stylet trajectory is not monitored by fuoroscopy, there is a potential for pedicle or anterior wall breach, potentially resulting in neurological damage or damage to the great vessels. This can be used to track the position of the Stylet while it is being advanced into the pedicle. Use the depth markings on the X-Tab to monitor the travel of the implant relative to the skin. Holding the Red Stylet Control Handle will retract the Stylet as the screw is advancing into the pedicle. As a result, the tip of the Stylet will not advance further into vertebral body as the screw is inserted. If the Red Stylet Control Handle is not held, the Stylet will remain extended and advance in front of the screw, Fig 30 potentially leading to a anterior wall breach, neurological damage or damage to the great vessels. Reference the etched lines on the X-Tab to check that they move relative to the skin to ensure the screw is advancing. The tip of the Stylet is now approximately 3 mm beyond the tip of the screw and can be confrmed by the red line position on the Stylet Depth Gauge at the proximal end of the Inserter. At this point, release the Red Stylet Control Handle and insert the screw the remaining distance using the proximal handle until the screw is fully seated. If the length of the subsequent screw is the same, the Stylet and Depth Adjustor do not need to be changed. If the length of the subsequent screw is different, remove the Depth Adjustor using the Set Screw Driver. Open the retaining sleeve and move the Stylet fange to the appropriate slot for the new screw length. Attachment of Additional Alignment Devices Repeat until Alignment Devices are attached to all levels intended for cement augmentation. Use of the alignment guide will prevent undue stress from being applied to the cannula. Placement can be verifed by ensuring that the circumferential lines on the shafts of the Rod Gauge align with the top of each X-Tab. The X-Tabs must be parallel to each other and the Rod Gauge should be laid on the body so that the legs are perpendicular to the tabs to ensure accurate measurement. Etch lines should be aligned with the outside edge of the X-Tabs for straight rod measurements. If the measurement is between two lengths, it is recommended to select the longer rod. Ensure that Fig 39 the Push Rod is fully seated before inserting the Threaded Shaft. It is necessary for the distal end of the rod to be below the fascia before proceeding. Fig 43 the rod is fully seated when the laser-etch line on the stem of the Rod Holder is aligned with the top of the X-Tabs. If the tab is able to rotate, the rod is not contained within the tab and rod placement should be re-attempted. Fluoroscopy should be used to verify adequate rod overhang at each end of the construct. This will prevent other set screws from inadvertently becoming dislodged during set screw loading. This will allow the Set Screw Driver to fully reduce the rod into the head of the polyaxial screw and reduce the chance of tab splay and subsequent set screw cross threading. If further correction is needed, remove the set screw Driver and proceed to next step.

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The 3 additional admits will only need a progress note because the H&P will have been done by night float or resident the day before. On post post-call day, a resident can transfer his/her old patient(s) to the intern. The resident may pick up additional patients admitted by the night float team or resident during the day as long as their total census is <14 and total new patients <16 within 48 hours. Once a cap has been reached, any more admissions will be given to the hospitalist on call unless the patient is a clinic patient. Post Post-call team is limited to 1 admission (only for Clinic and Care clinic patients only). Please call the chief(s) prior to activating the Jeopardy, and if it appears that Jeopardy activation is imminent. No resident (on a one intern team) can be responsible for the ongoing care of more than 14 patients. Bounce-back: to assure the continuity of patient care, a patient who needs to be re-admitted after discharge is a bounce-back to the resident team that discharged the patient. For example, if Team A resident has 2 patients on his/her own that he/she is unable to transfer to the intern, then the co-resident (pre-call team) will have to write these 2 notes and assume their care in the interim. Resident should sign-out verbally or by email to the co-resident covering for them on all patients, so that they can perform pre-rounding adequately with interns. This requires the resident to keep the intern updated on all patients on the service. It is highly recommended that residents transfer patients to interns prior to their day off; cross-covering residents should not write notes for interns when the intern census is <10. During a pre-call or on-call day, a resident cannot take patients from the intern to reduce the number of potential admits for the resident. Residents are responsible for hand-writing an addendum H&P with their own physical exam. However, the intern must give a written discharge summary for the resident to dictate from within 48 16 hours. Off-service note: when Interns change rotations, off-services notes need to be done for patients who have been on the service for more than 48hrs. Off service notes must be written or typed using the yellow progress notes in the same format as a discharge summary, to assist your colleagues when they have to do the transfer and/or discharge summaries. Residents & interns are allowed to leave clinic only after approval by the Clinic Attending. Each resident may be assigned a day during their 4 week block to present an interesting case during afternoon report. This will familiarize housestaff with the patients when they start the new rotation. Interns should arrive earlier than 6am if they require more time to see their patients. Intern should sign-out to the on-call team if they have clinic that afternoon and their resident is post-call from an overnight shift. After clinic, the intern should return to get an update on their patients and answer any questions the on-call team has before leaving for the day. Resident should sign-out verbally or by email to the weekend resident covering for them. The weekend resident may have the responsibility of writing progress notes and needs to be familiar with the patients. Off-service note: when Interns change rotations, off-services notes must be written for patients who have been on the service for more than 48hrs. Off service notes must be written or typed using the yellow progress notes in the same format as a discharge summary (this will assist your colleagues when they have to write transfer summaries).

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However, the dentist of record shall be changed when the dentist of record leaves the practice where the treatment was being rendered and the patient elects to continue treatment in the office where treatment began. The records shall include, but not be limited to, patient history, examination results, test results, and, if taken, X rays. This subsection does not relieve the dentist of record in a multidentist practice of the responsibility to maintain patient records. Further, the dentist of record may be relieved of the responsibility to maintain the original or duplicate patient records if she or he leaves the practice where the treatment was rendered, transfers custody of the records to the owner of the practice, and retains, in lieu of the records, a written statement, signed by the dentist of record, the owner of the practice, and two witnesses, that lists the date and the records that were transferred. The board shall adopt rules to carry out the intent of this section, the purpose of which shall be to regulate the manner of such advertising in keeping with the provisions hereof. A registered dental laboratory shall disclose in writing at the time of delivery of the final restoration to the prescribing dentist the materials and all certificates of authenticity that constitute each product manufactured and the point of origin of manufacture of each restoration, including the address and contact information of the dental laboratory. The file of prescriptions to be kept by the dentist and the dental laboratory shall be open to inspection at any reasonable time by the department or its constituted agent. Failure of the dentist to keep records of each prescription shall subject the dentist to suspension or revocation of her or his license to practice dentistry in this state. This section does not preclude a registered dental laboratory from working for another registered dental laboratory if that work is performed pursuant to written authorization, in a form to be prescribed by rule of the board, which evidences that the originating laboratory has obtained a valid prescription and which sets forth the work to be performed and the resulting material certifications to be provided. A dental laboratory accepting prescriptions from dentists is liable for damages caused by inaccuracies in the material disclosure, certificates of authenticity, or point of origin provided by the dental laboratory to the prescribing dentist. This section does not preclude a registered laboratory from providing its services to dentists licensed and practicing in another state if that work is requested or otherwise authorized in written form that clearly identifies the name and address of the requesting dentist and sets forth the work to be performed and otherwise complies with all applicable laws and treaties. In performing such service, any member of a peer review Revised 11/2019 23 organization or committee shall, pursuant to s. Any such peer review committee member shall be afforded the privileges and immunities of any other complainant or witness which are provided by s. Furthermore, a professional organization or association of dentists which sponsors, sanctions, or otherwise operates or participates in peer review activities is hereby afforded the same privileges and immunities afforded to any member of a duly constituted medical review committee by s. Further, no person who voluntarily serves on a peer review committee or who investigates a complaint for the committee shall be permitted or required to testify in any such disciplinary proceeding as to any evidence or other matters produced or presented during the proceedings of such organization or committee or as to any findings, recommendations, evaluations, opinions, or other actions of such organization or committee or any members thereof. However, nothing in this section shall be construed to mean that information, documents, or records otherwise available and obtained from original sources are immune from discovery or use in any such disciplinary proceeding merely because they were presented during proceedings of a peer review organization or committee. Members of peer review organizations shall assist the department in identification of such original sources when possible. For the purpose of this section, official records of peer review organizations or committees include correspondence between the dentist who is the subject of the complaint and the organization; correspondence between the complainant and the organization; diagnostic data, treatment plans, and radiographs used by investigators or otherwise relied upon by the organization or committee; results of patient examinations; interviews; evaluation worksheets; recommendation worksheets; and peer review report forms. In addition, dental hygienists may expose dental X-ray films, apply topical preventive or prophylactic agents, and perform all tasks delegable by the dentist in accordance with s. The board by rule shall determine whether such functions shall be performed under the direct, indirect, or general supervision of the dentist. Revised 11/2019 24 However, the dentist issuing such prescription shall remain responsible for the care of such patient. The purpose of the limitation shall be to protect the health and safety of patients and to ensure that procedures which require more than general supervision be adequately supervised.

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For higher organisms such as humans, Nickel consumed with food is relatively Silver is much less toxic. However, about 17% of the also been used in dental alloys since female population are already sensitised artificial dental restorations were first to Nickel; they are at risk if supplied developed. Zinc deficiency, which ous to humans, but it is not released is relatively common, causes immune from precious metal dental alloys. However, the toxic doses ported to parts of the body where it is identified in animal experimentation are needed. Allergies against Cerium are not of Zinc per day, which can be easily known to date. Allergic reactions to Zinc are not known at this time, and they are not expected given the high essential dose. Some daily intake values are taken from the literature; others were estimated based on the composition of typical foods. Information on systemic toxicity comes from different sources in toxicological literature. Cytotoxicity information particularly takes into account examinations on murine fibroblasts. High cytotoxicity also results in a high antibacterial effect, which can certainly be considered a positive characteristic if the element has other positive biological properties. It is proven and only possible with steadily increasing market share, to be one of the leading alloy manufactures. Code solder 800 non-preciousalloys Herador solder V 800 1583 0000 Stahlgold solder 750 1380 0000 Stahlgold solder 910 1360 0000 Caution! Stahlgold solder 910 contains nickel and must not be used for individuals with known nickel sensitivity. The casting features and 1g training lot 1 mechanical properties of training metals 6460 2012 1g training lot 2 are so similar to those of Type 3 (acc.

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Severe and permanent conditions 77,700 to 96,800 Complex and multiple fractures to the tibia and fbula which required extensive surgery and extended healing but may result in an incomplete union and the possibility of having or has achieved arthritic changes and degeneration of the knee or ankle joint and affects the ability to walk unaided. Ankle Soft Tissue (excluding Achilles Tendon) Any of the ankle/foot ligaments may be partially ruptured (sprained) or involve complete rupture. Ankle ligament and tendon sprains are commonly classifed as minor, moderate and severe. Minor up to 23,100 Minor sprains are mild injuries where there is no tearing of the ligament, and often no function is lost, although there may be tenderness and slight swelling which has substantially recovered. Moderate 23,000 to 56,600 Moderate sprains are caused by a partial tear in the ligament. These sprains are characterised by obvious swelling, extensive bruising, pain, diffculty walking and reduced function of the ankle but with a full recovery expected. Severe and permanent conditions 38,900 to 62,300 Severe sprains are caused by complete tearing of the ligament or a rupture, where there is severe pain, loss of grip, widespread swelling and bruising and the inability to bear weight. Achilles Tendon Injuries the Achilles tendon is a major tendon that makes up the ankle joint and is responsible for the majority of movement to the ankle joint. Damage to the Achilles tendon will typically require surgery in order for it to resolve. Minor up to 12,600 Minor sprains are mild injuries where there is no tearing of the ligament and often no function is lost, although there may be tenderness and slight swelling which has substantially recovered. Moderate 14,600 to 25,700 Moderate Achilles tendon sprains are caused by a partial tear in the ligament. These sprains are characterised by obvious swelling, extensive bruising, pain, diffculty walking and reduced function of the ankle with a full recovery expected. These sprains are characterised by obvious swelling, extensive bruising, pain, diffculty walking, and reduced function of the ankle. With surgery the tendon would have been repaired but may have resulted in a permanent loss of movement to the ankle. Severe and permanent conditions 41,200 to 51,600 Severe Achilles tendon ruptures are caused by complete tearing of the ligament or a rupture, where there is severe pain, widespread swelling and bruising and the inability to bear weight. Surgery will have been required and despite this the tendon would still result in a permanent loss of function of the ankle. Dislocations Ankle dislocations normally heal without ligament instability and generally have a good outcome with little, if any, residual disability. Where the dislocation involves open wounds infection is a constant concern and a permanent disability may arise. Minor 22,100 to 49,300 these injuries will have made substantially recovered and may have required the joint to be replaced back into the original position. Moderate 41,100 to 77,100 these injuries will have required manipulation of the joint back into normal position and will have taken longer to recover with extensive treatment but with a full recovery expected. Severe and permanent conditions 56,800 to 82,800 these injuries will have required manipulation of the joint back into normal position and may have included more invasive treatment or even surgery to keep the joint in the position. Fractures that involve the joint are usually considered more complicated than others due to the increased impact on limb movement. The more severe injuries involve displacement and ligament damage (which may be treated with either open or closed reduction). Minor up to 54,700 these injuries will include simple non-displaced fracture in the ankle which has substantially recovered. Moderate 39,100 to 87,600 these injuries will include displaced fractures to a single bone in the ankle, or non displaced fractures to multiple bones with a full recovery expected with treatment. Moderately Severe 79,900 to 89,300 Multiple fractures that have resolved but with ongoing pain and stiffness which impacts on movement of the ankle. Severe and permanent conditions 80,500 to 93,300 these injuries include all three bones of the ankle structure which required extensive surgery and extended healing but may result in an incomplete union and the possibility of having or has achieved arthritic changes and degeneration of the ankle joint and may affect the ability to walk unaided. Foot sprains are treated with the application of ice, possibly the use of walking aids during the acute phase, physiotherapy, protective taping, anti-infammatory medication and possibly analgesics for pain depending on the severity of the injury.

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Alternate method three: Bilateral Media for recording centric relation position manipulation of the mandible A number of media can be used to record centric rela Some dentists prefer to use bilateral manipulation of the tion. These include waxes, modeling plastics, acrylic resins, mandible when recording centric relation. The bilateral elastomeric impression materials, impression pastes, dental manipulation technique is significantly different from those plasters, and dental stones. The material selected for recording centric relation de pends on the number and location of the remaining teeth. When using bilateral manipulation, four fingers of each If there are a sufficient number of widely spaced occlusal hand should be positioned on the lower border of the contacts (at least three widely separated areas of contact), mandible, and the thumbs should be placed near the record bases are not needed and any recording medium prominence of the chin (Fig 6-35). If the edentulous areas are extensive or the is rotating freely, the dentist should exert firm, upward teeth are not favorably distributed, record bases and oc pressure with the fingers. The thumbs should be used clusion rims should be used to accurately relate the dental to apply pressure in a downward and backward direc casts (Fig 6-37). These actions result in a posterior, rotational used, the selection of a suitable recording medium be movement of the mandible. When the dentist is confident that the mandible has terial should be used to minimize the danger of record been properly positioned, a centric relation record base displacement. More recent additions such as polyvinyl siloxane and polyether registration pastes also may be Alternate method four: Use of an used. These materials are accurate, dimensionally stable, occlusal splint durable, and easy to trim (Fig 6-38). Patients with severe splinting or hypertonicity of the mus cles or with acute symptoms of temporomandibular joint Occlusal vertical dimension dysfunction will usually provide inconsistent and inaccurate results. The construction of an occlusal device to be worn In most instances, patients will have two or more teeth for a time in an attempt to relieve symptoms and to pre that contact at the original occlusal vertical dimension. Jaw re using wax lation records should then be made at the determined oc clusal vertical dimension. A more in-depth discussion of Wax is often used as a recording medium when there are occlusal vertical dimension is included in chapter 14. Despite to occlusal vertical dimension occur when there is occlusal its widespread use, wax also is the most unreliable and un contact with an apparent overclosure of the mandible (see predictable material used for making centric relation Fig 5-7). Therefore, the heating, tended period to ensure that the proposed change in oc handling, and storage of wax records is critical. If the patient Two distinctly different types of waxes are used for in can tolerate the proposed change in occlusal vertical terocclusal records. Hard baseplate wax often is used dimension, definitive treatment may be undertaken. Using the erty minimizes errors that may occur when dental casts maxillary diagnostic cast as a guideline, the wax should be are placed into baseplate wax records. The mandible metallic filler in the form of finely ground powder (eg, Alu should be guided into centric relation and gently closed Wax, Alu-wax Dental Products; Coprwax, Heraeus Kulzer). This maxillomandibular rela the filler permits uniform heating and cooling of the wax. To speed In addition, the metallic powder provides increased heat this process, the practitioner may use a gentle stream of retention and an extended working time. Unfortunately, the record should be removed from the mouth and metal-impregnated waxes are relatively soft and may be inspected for thickness (Fig 6-44). Complete penetration of Considerable care must be exercised when either type the wax usually indicates contact of opposing teeth. Suggested techniques are provided in the contact must be avoided since it may cause the mandible following sections. Hence, the record should be remade if these criteria are Use of hard baseplate wax not satisfied. The following equipment and supplies are needed to At this stage, the wax record should be placed into a make an interocclusal record with hard baseplate wax: bowl of cool water (Fig 6-45).

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Most training programs provide limited instruction on how to properly document operational and clinical processes, and almost no practice. Most providers learn this skill on the job, and often proficient mentors are sparse. Some more experienced providers use it as they find telling the story from start to finish works best to organize their thoughts. A drawback to this method is that it is easy to forget to include facts because of the lack of structure. It minimizes the likelihood of forgetting information and ensures documentation is consistent between records and providers. Medications Given Showing Positive Action Using Pertinent Negatives 347 For medications that are required by protocol. If a patient had the intended therapeutic response to the medication, but a side effect that caused a clinical deterioration in another body system, then "Improved" should be chosen and the side effects documented as a complication. The patient condition deteriorated or continued to deteriorate because either the medication: i. Had a sub-therapeutic effect that was unable to stop or reverse the decline in patient condition; or iii. Was the wrong medication for the clinical situation and the therapeutic effect caused the condition to worsen. Not Applicable: the nature of the procedure has no direct expected clinical response. An effective procedure that caused an improvement in the patient condition may also have resulted in a procedure complication and the complication should be documented. In the case of worsening condition, documentation of the procedure complications may also be appropriate. Currently there are three versions of the data standard available for documentation and in which data is stored: a. These fields require real data and do not accept Nil (Blank) values, Not Values, or Pertinent Negatives. However, required fields allow Nil (blank) values, Not Values, or Pertinent Negatives to be entered and submitted. Values can be left blank, which can either be an accidental or purposeful omission of data. Value fields can appropriately and purposefully be left blank if there was nothing to enter. There are 11 possible Pertinent Negative values and the available list for each field varies as appropriate to the field. The element numbering structure reflects the dataset and the text group name of the element 5. Some software systems allow the visible text name to be modified or relabeled to meet local standards or nomenclature; this feature can help improve data quality by making documentation easier for the provider. However, the technical structure of the fields has made their practical use limited as all the data is collected as a separate, self contained group, rather than as part of the procedures group. However, solutions are currently far from practical, functional, effective, or uniform in how they are being implemented or used across various systems. Reference: Trade names, class, pharmacologic action and contraindications (relative and absolute) information from the website. Additional references include the 2015 American Heart Association Guidelines for Cardiopulmonary Resuscitation and Emergency Cardiovascular Care, position statements from the American Academy of Clinical Toxicology and the European Association of Poison Control Centers clintox. When reuptake is prevented, a strong antidopaminergic, antiserotonergic response occurs.

References:

  • http://www.marionpublichealth.org/docs/Position-Descriptions.pdf
  • https://ecfsapi.fcc.gov/file/1060927842647/irradiated.pdf
  • https://www.asge.org/docs/default-source/about-asge/newsroom/doc-gerd_infographic_final.pdf
  • https://www.auanet.org/documents/education/NMSC-Adult-UTI.pdf
  • http://www.londoncancer.org/media/84331/london-cancer-head-and-neck-radiotherapy-protocol-march-2013.pdf