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230 The Claimant testified in her own behalf. At the time of the attack, she was 46 years of age, four feet, eleven inches 4' 11" ; tall, and weighed approximately 113 pounds. She had six children and began working outside her home in November 1972. She worked part time for three different employers while raising her six children through April 1980. She began x-ray training at Illinois Central College. After graduating as an x-ray technician, she found full-time employment with Correctional Health Services and was assigned to the Pontiac Correctional Center in July 1983. Ms. Zimmerman participated in the conversation between Assistant Warden Washington and Dale Bent. During that conversation, she expressed concern for her safety, especially in the darkroom and processing room. She also expressed concern about the response time of officers in the event of a problem. A memo from Ms. Zimmerman to Assistant Warden Washington, dated March 18, 1985, was introduced into evidence. The memo suggested that a doorway be installed between the x-ray room and Mr. Bent's lab, and also referred to Bent's memo of March 15, 1985. There was never a response from Assistant Warden Washington, nor any action taken as of October 29, 1986, to improve access to the x-ray suite. No alarm system or monitors were installed in the x-ray area. As stated previously, there were no windows between the lab and the hallway. Ms. Zimmerman was never given instructions with regard to self-defense or security when dealing with prisoners. She was not supplied with self-defense equipment; in fact, such items were expressly prohibited. When prisoners were to be x-rayed, they would come into the x-ray lab with either a requisition from the prison doctor or a pass. The Claimant would let them into. Variations in MH presentation can complicate diagnosis and treatment. This case report demonstrates delayed clinical presentation of MH in patient who had had two previous prolonged anesthetics without difficulty as well as recrudescence, in spite of high-dose dantrolene. The patient was later proven to be MH susceptible by in vitro contracture testing. MH has been reported to occur in patients with a history of a previous uneventful anesthetic 1, 2 ; . In recent review of 503 cases of MH, 24% of the adults and 17.5% of the pediatric patients had a median of two prior general anesthetics without complications. In most of these cases, volatile anesthetics and depolarizing and nondepolarizing muscle relaxants were used 3 ; . In our case, the patient had a thoracotomy, a craniotomy, and two brain biopsies without incident. There have been several case reports of delayed postoperative triggering up to 11 after anesthesia 4, 5 ; . The etiology is uncertain, but postsurgical stress may be a factor. MH has also been reported in susceptible patients who underwent "safe" anesthesia without triggering drugs ; with stress again being postulated as the etiology 7, 10, 11 ; . The described episodes are inconclusive, and may represent residual effects from the anesthetic or other factors. Our patient had an 8-h procedure which included continuous ETco, and temperature monitoring. There was no evidence of a hypermetabolic state during surgery. The patient was transferred for a radiologic procedure at which time HR, BP, and pulse oximetry were monitored and remained stable. However, once the patient arrived in the PACU, he was clearly in a hypermetabolic state as documented by initial ABGs, temperature, and vital signs. Our patient may have triggered during transfer to radiology or during the second anesthetic for the evacuation of the pneumocephalus. Stress should not have been a significant factor, since the patient was sedated continuously throughout the early postoperative period. There have been case reports of large doses of dantrolene required for treatment of MH 6, 7 ; explanation for these large doses is not found readily. Blank and Boggs 8 ; reported 42 mg kg of dantrolene was needed to overcome severe muscle rigidity in a 6-yrold, 25-kg female 4 ; . They postulated that decreases in blood flow to the affected muscles during rigidity might have resulted in a decrease in the amount of drug delivered. It is possible that adequate blood levels of dantrolene are not attained initially with the loading dose 6 ; . The standard recommendation for dantrolene treatment in MH is 2.5 mg kg initially with additional doses up to 10 mg kg if symptoms do not resolve, followed by IV maintenance doses of 1 mg * kg-' * 6 h-' for 24-48 h, for instance, teraazosin dosing. Is illustrated in Figure 2. 1. Unless clinically contraindicated, all patients should first receive a trial with prazosin at an appropriate dose. The most cost-effective approach to treating BPH is prazosin even if some patients cannot tolerate the occasional side effects. 2. For patients who can not tolerate prazosin or who fail to respond to it, then terazodin is a viable cost-effective alternative. 3. Finasteride is the least cost-effective therapy, and should be considered only in those patients in whom alpha-blockers are contraindicated, or in those patients who fail an adequate trial with prazosin or terazosin. 4. Doxazosin, at present, provides no advantage compared to prazosin or terazosin. This situation could change if tablet breaking strategies were shown to be effective. Preferred Drug List and tiazac. IFIS IFIS is newly identified, and is characterised by loss of muscle tone in the iris the part of the eye that controls pupil dilations and contractions and thus the amount of light entering the eye ; . During cataract surgery, IFIS is characterised by three features: a floppy iris that billows in response to normal irrigation currents in the anterior chamber; a marked tendency for the iris to prolapse to the phaco and side-port incisions; and progressive pupil constriction.1 Because the pupil must remain stable and dilated properly for effective cataract removal, IFIS is a potentially serious problem because it might cause surgical complications and might increase the risk of posterior capsular rupture. Chang and Campbell1 discussed data from a retrospective study and a prospective study, which support an association between tamsulosin and IFIS. The retrospective study assessed 706 eyes in 511 patients who underwent cataract surgery, 27 5% ; of whom were receiving systemic -1 adrenoceptor antagonists 16 tamsulosin, and 11 prazosin, terazosin, or doxazosin ; . The researchers noted a so-called floppy iris in 10 of the 16 patients given tamsulosin, and recorded poor or moderately poor preoperative dilation in patients taking prazosin, terazosin, or doxazosin but no actual cases of IFIS were identified ; . In the prospective study, IFIS was diagnosed in 21 of 900 cataract surgeries, and in 16 of 741 patients about 2% ; . 14 of the 16 patients were taking tamsulosin at the time of cataract surgery, and 1 patient had stopped tamsulosin 1 year before surgery. Of the 725 patients who did not have IFIS patients, none were receiving tamsulosin. Frequency of IFIS in both studies, totalling more than 1600 eyes and 1250 patients, was reported as 2% of patients having cataract surgery, and was regarded as associated with tamsulosin. Chang and Campbell1 suggest that tamsulosin has a particular high affinity and specificity for the -1A receptor, which might account for the difference between tamsulosin and other selective -1 adrenoceptor antagonists and risk of IFIS. Tamsulosin not only blocks -1A receptors in the prostate, but also is thought to block selectively -1A receptors that are common in the iris dilator muscle as shown in animals.2, 3 A lack of dilator smooth-muscle tone can cause iris billowing and a tendency for the iris to prolapse. Treatment. In fact, the current information sharing process is too slow to help patients in pressing medical situations. We are in a position to improve that, " says Barry Bershow, M.D., Fairview quality and informatics medical director, and an architect of the shared electronic database. Patients often arrive in emergency rooms without their prescription information and only general descriptions about recent tests and resulting outcomes. At worst, missing information can lead to poor patient care. It can also be costly, because tests must be repeated. The participating systems have already received a $500, 000 planning grant from the Agency for Healthcare Research and Quality AHRQ ; . They hope to hear this fall about a three.
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