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Daniel Bainbridge, MD, FRCPC

  • Associate Professor
  • Anesthesia and Perioperative Medicine
  • Schulich School of Medicine
  • University of Western Ontario
  • London, Ontario, Canada

Adverse effects Renal impairment is a caution or contraindication for all bisphosphonates muscle relaxant essential oils purchase skelaxin 400mg online. This is minimized by taking alendronic acid or risedronate when sitting upright or standing spasms 1st trimester buy discount skelaxin 400mg, on an empty stomach before breakfast spasms with spinal cord injury generic 400 mg skelaxin overnight delivery, and remaining standing for half an hour before eating muscle relaxant prescriptions buy skelaxin 400 mg otc. Inhibit bone resorption by osteoclasts; etidronate also inhibits mineralization with chronic use 303 muscle relaxant reviews buy generic skelaxin 400 mg online. Oral absorption is poor; short t1/2 in plasma and long t1/2 in bone; renal clearance spasms near kidney skelaxin 400 mg. Food and/or calcium-containing antacids further reduce gastrointestinal absorption of bisphosphonates. The most common side effects are gastro-intestinal disturbances (Note: with regard to oesophagitis and ulceration with alendronic acid, this drug must be taken with water and the patient must be able to stand for 30 minutes post-ingestion). Calcitonin lowers calcium levels more rapidly than bisphosphonates, and may be used concomitantly in severe cases. They disappear rapidly from the blood, distributing to bone, where their effects are long lived. Within 24 hours, approximately 50% of the absorbed dose is excreted unchanged in the urine, but the remainder is excreted over many weeks. It is given daily by subcutaneous injection for periods up to 18 months, monitoring serum calcium, phosphate, alkaline phosphatase, creatinine and electrolytes. Case history A 52-year-old woman has had epilepsy since childhood, treated with phenytoin 300 mg/day and her fits have been well controlled. Since the loss of her job and the death of her husband she has become an alcoholic. Neurological examination of her legs is normal apart from signs of thigh and hip muscle weakness and slight wasting. Clinical investigations reveal that haemoglobin, white blood and platelets are normal, but her erythrocyte sedimentation rate is 30 mm per hour, her blood glucose level is 5. Question What is the likely cause of her metabolic disturbance and leg weakness, and how would you treat it? Answer this patient has hypocalcaemia with hypophosphataemia and a raised alkaline phosphatase, but no evidence of renal dysfunction. The mechanism of these effects is complex and relates to several actions of the drug. Phenytoin is a potent inducer of hepatic drug metabolizing enzyme systems, including the enzymes involved in vitamin D metabolism, specifically metabolism of calciferol to 25 -hydroxycholecalciferol by the liver, and its further metabolism to inactive products. Treatment of this form of drug-induced osteomalacia consists of giving the patient oral Ca2 supplements together with low-dose 1-hydroxy vitamin D (0. Uses Synthetic or recombinant salmon calcitonin (salcatonin) is used to lower the plasma calcium concentration in hypercalcaemia, especially from malignancy, and in the treatment of pain and some of the neurological complications. Calcitonin is given by subcutaneous or intramuscular injection, or as a nasal spray. Plasma calcium, phosphate, alkaline phosphatase and if possible urine hydroxyproline excretion are monitored. Mechanism of action the main action of calcitonin is on bone; it inhibits bone resorption by binding to a specific receptor on osteoclasts inhibiting their action. In the kidney, it decreases the reabsorption of both Ca2 and phosphate in the proximal tubules. These adverse effects may have reflected a calcium-deficient diet and incorrect dosing. Recent evidence indicates that strontium ranelate reduces bone reabsorption and increases bone formation, and reduces vertebral and hip fractures in women with post-menopausal osteoporosis. It is given by mouth at night to older women with osteoporosis and a history of bone fracture when bisphosphonates are contraindicated or not tolerated. Comparative safety of bone remodeling agents with a focus on osteoporosis therapies. The effects of strontium ranelate on the risk of vertebral fracture in women with postmenopausal osteoporosis. Recombinant human parathyroid hormone: osteoporosis is proving amenable to treatment. Thus glucocorticosteroids produce a delayed but profound anti-inflammatory effect. Adverse effects Adverse effects of glucocorticosteroids are common to all members of the group, and will be discussed before considering the uses of individual drugs. Features include: · · · · · · · Cushingoid physical appearance; impaired resistance to infection; salt and water retention; hypokalaemia; hypertension; hyperglycaemia; osteoporosis; glucocorticosteroid therapy is weakly linked with peptic ulceration, and can mask the symptoms and signs of gastrointestinal perforation; mental changes: anxiety, elation, insomnia, depression and psychosis; posterior cataracts; proximal myopathy; growth retardation in children; aseptic necrosis of bone. Glucocorticosteroids influence carbohydrate and protein metabolism, and play a vital role in the response to stress. Glucocorticosteroids stimulate the mobilization of amino acids from skeletal muscle, bone and skin, promoting their transport to the liver where they are converted into glucose (gluconeogenesis) and stored as glycogen. The major therapeutic uses of the glucocorticosteroids exploit their powerful anti-inflammatory and immunosuppressive properties. They reduce circulating eosinophils, basophils and T-lymphocytes, while increasing neutrophils. Applied topically to skin or mucous membranes, potent steroids can cause local vasoconstriction and massive doses administered systemically can cause hypertension due to generalized vasoconstriction. However, even in patients who have been successfully weaned from chronic treatment with glucocorticosteroids, for one to two years afterwards a stressful situation (such as trauma, surgery or infection) may precipitate an acute adrenal crisis and necessitate the administration of large amounts of sodium chloride, glucocorticosteroids, glucose and water. Suppression of the adrenal cortex is unusual if the daily glucocorticosteroid dose is lower than the amount usually secreted physiologically. The rate at which patients can be weaned off glucocorticosteroids depends on their underlying condition and also on the dose and duration of therapy. After long-term glucocorticosteroid therapy has been discontinued the patient should continue to carry a steroid card for at least one year. At physiological concentrations, it plays little if any part in controlling blood glucose, but it does cause hyperglycaemia (and can precipitate frank diabetes mellitus) when administered in pharmacological doses. This is caused by enhanced gluconeogenesis combined with reduced sensitivity to insulin. Hydrocortisone is given (usually with fludrocortisone to replace mineralocorticoid) as replacement therapy in patients with adrenocortical insufficiency. High-dose intravenous hydrocortisone is used short term to treat acute severe asthma (usually followed by oral prednisolone) or autoimmune inflammatory diseases. Hydrocortisone cream is relatively low in potency and is of particular use on the face where more potent steroids are contraindicated. Key points Glucocorticosteroids ­ major side effects Adrenal suppression, reduced by once daily morning or alternate-day administration. The plasma t1/2 is approximately 90 minutes, but the biological t1/2 is longer (six to eight hours). Key points Glucocorticosteroids ­ pharmacodynamics and pharmacokinetics · They have a potent anti-inflammatory action which takes six to eight hours to manifest after dosing. They act as positive transcription factors for proteins involved in inhibition of the production of inflammatory mediators. Mineralocorticoid effects decrease as the antiinflammatory potency of synthetic glucocorticoids increases. Glucocorticosteroids have relatively short half-lives and are metabolized to inactive metabolites. Used in a wide range of inflammatory disorders of lung, gut, liver, blood, nervous system, skin and musculoskeletal systems, and for immunosuppression in transplant patients. The anti-inflammatory effect of prednisolone can improve inflammatory symptoms of connective tissue and vasculitic diseases (see Chapter 26), but whether this benefits the underlying course of the disease is often unclear. Treatment must therefore be re-evaluated regularly and if long-term use is deemed essential, the dose reduced to the lowest effective maintenance dose. Alternate-day dosing produces less suppression of the pituitary­adrenal axis, but not all diseases are adequately treated in this way. Prednisolone is considered in progressive rheumatoid arthritis when other forms of treatment have failed, or as an interim measure while a disease-modifying drug, such as methotrexate, has time to act. Low doses of prednisolone may be symptomatically useful in the short-term management of patients with severe articular symptoms from systemic lupus erythematosus and larger doses may be appropriate for limited periods in such patients with steroid-responsive forms of glomerulonephritis or with progressive central nervous system involvement. Other diseases where prednisolone may be indicated include severe asthma and some interstitial lung diseases. The immunosuppressant effect of prednisolone is further utilized in transplantation, usually in combination with ciclosporin or azathioprine, in order to prevent rejection (Chapter 50). Clinical features include nocturia, hypokalaemia, hypomagnesaemia, weakness, tetany, hypertension and sodium retention. Spironolactone and eplerenone are mineralocorticoid antagonists (see Chapters 31 and 36) that compete with aldosterone and other mineralocorticoids for the cytoplasmic mineralocorticosteroid receptor. They are used as potassium-sparing diuretics and to treat primary or secondary hyperaldosteronism in the contexts of hypertension and/or heart failure (Chapters 28 and 36). It binds to the mineralocorticoid steroid receptor and mimics the action of aldosterone. It undergoes significant presystemic metabolism, but unlike aldosterone is active by mouth. Uses Dexamethasone is powerfully anti-inflammatory, but is virtually devoid of mineralocorticoid activity. It has no glucocorticoid activity, but is about 1000 times more active than hydrocortisone as a mineralocorticoid. Aldosterone acts on the distal nephron, promoting Na /K exchange, causing sodium retention and urinary loss of potassium Adrenaline (epinephrine) is the main hormone produced by the adrenal medulla. It is used in emergency situations, such as cardiac arrest (Chapter 32), anaphylactic shock (Chapter 50) and other life-threatening disorders that require combined potent - and -agonist activity. It is used to prolong the action of local anaesthetics (via its vasoconstrictor action). Dipivefrine is a prodrug eye-drop formulation of adrenaline used to treat chronic open angle glaucoma (Chapter 52). Tumours of the adrenal medulla that secrete adrenaline and other pharmacologically active catecholamines (phaeochromocytoma) are treated surgically; in these patients preoperative blockade with phenoxybenzamine, a long-acting -blocker, followed by -blockade is essential. Glucocorticosteroids, primarily in the form of hydrocortisone (cortisol), are secreted in a diurnal pattern from the zona fasciculata. Case history A 32-year-old man presents after collapsing in the street complaining of severe lower abdominal pain. His relevant past medical history is that for 10 years he has had chronic asthma, which is normally controlled with 2-agonists and inhaled beclometasone 2000 g/day. Initial assessment shows that he has peritonitis, and emergency laparotomy reveals a perforated appendix and associated peritonitis. His immediate post-operative state is stable, but approximately 12 hours post-operatively he becomes hypotensive and oliguric. The hypotension does not respond well to intravenous dobutamine and dopamine and extending the spectrum of his antibiotics. By 16 hours post-operatively, he remains hypotensive on pressor agents (blood pressure 85/50 mmHg) and he becomes hypoglycaemic (blood glucose 2. Answer In a chronic asthmatic patient who is receiving high-dose inhaled steroids (and may have received oral glucocorticosteroids periodically), any severe stress. In this case, the development of refractory hypotension in a patient who is on antibiotics and pressors, and the subsequent hypoglycaemia, should alert one to the probability of adrenal insufficiency. This possibility is further supported by the low sodium, slightly increased potassium and elevated urea levels. The treatment consists of immediate administration of intravenous hydrocortisone and intravenous glucose. Hydrocortisone should then be given eight hourly for 24­48 hours, together with intravenous 0. With improvement, the patient could then be given twice his normal dose of prednisolone or its parenteral equivalent for five to seven days. This unfortunate clinical scenario could have been avoided if parenteral hydrocortisone was given preoperatively and every eight hours for the first 24 hours postoperatively. Glucocorticosteroids should be continued at approximately twice their normal dose for the next two to three days post-operatively, before reverting to his usual dose (clinical state permitting). The main hormones secreted by the ovary are oestradiol17, oestrone, progesterone and androgens. Oestrogens influence the development of secondary sexual characteristics, including breast development and the female distribution of fat, as well as ovulation during the reproductive years. From the start of menses until the menopause, the primary oestrogen is oestradiol-17, whereas in post-menopausal women oestrone predominates. Uses Oestrogens are used in: · oral contraception; · the treatment of symptoms of menopause; · the prevention of osteoporosis. Fractures of the spine, wrist and hips are reduced by 50­70% and there is about a 5% increase in spinal bone density in those women treated with oestrogen within three years of the onset of menopause and for five to ten years thereafter. Ethinylestradiol, a synthetic oestrogen, is an alternative for many of the above indications. Oestrogens are no longer used to suppress lactation because of the risk of thromboembolism. Salt and water retention with oedema, hypertension and exacerbation of heart failure can occur with pharmacological doses. Oestrogens are carcinogenic in some animals and there is an increased incidence of endometrial carcinoma in women who have uninterrupted treatment with exogenous oestrogen unopposed by progestogens. Pharmacokinetics Oestrogens are absorbed by mouth and via the skin and mucous membranes. The most potent natural oestrogen is oestradiol-17 which is largely oxidized to oestrone and then hydrated to produce oestriol. All three oestrogens are metabolized in the liver and excreted as glucuronide and sulphate conjugates in the bile and urine.

Diseases

  • Hyperhomocysteinemia
  • Delirium tremens
  • Tracheoesophageal fistula symphalangism
  • Renal tubular acidosis, distal, type 3
  • Tay syndrome ichthyosis
  • Tourette syndrome
  • Albers Schonberg disease
  • Cholemia, familial

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Cultural and Linguistic Aspects of Sexual Assault Care 103 Evaluation and Management of the Sexually Assaulted or Sexually Abused Patient ii muscle relaxant in pregnancy trusted skelaxin 400 mg. No flip flops infantile spasms 8 months discount skelaxin 400mg fast delivery, white coat thrown over unprofessional clothing muscle relaxant dosage purchase 400 mg skelaxin overnight delivery, tobacco smoke smell or gum chewing spasms in lower abdomen buy 400 mg skelaxin free shipping. Some will want to move quickly through the exam while others muscle relaxant india cheap skelaxin 400 mg with mastercard, perhaps elderly patients spasms after stroke buy discount skelaxin 400mg on-line, will need a pause for each step. Any laughter, loud noises, loud talking or knocking on the door can be disruptive or even traumatizing to the patient. If possible, the zone in which the exam is taking place should be maintained as a quiet area. Male examiners have had the same patient satisfaction rates as female examiners in many programs and in some cases to be cared for by a competent, compassionate and caring male provider may minimize post sexual assault "male phobias. However, much like interpreters, most have not had any cultural and linguistic competency education. The terminology we use to communicate with sexual assault patients is critical and it begins when you enter the room. Make sure you professionally address your patient when you enter the examination room. Post Examination Considerations a) Discharge Instructions Specifically because many sexual assault patients are lost to follow up, it is essential that their discharge instructions be clearly understood. Working with an interpreter is essential at this stage, as important and time sensitive follow up medical, law enforcement, advocacy, and privacy issues must clearly be understood. If you are not providing actual medications, you should make sure your patient has the funds to purchase them. You (along with the advocate) should also inquire about their access to transportation to a pharmacy, to follow up advocacy, or back to the hospital. Although males are a minority of sexual assault cases, you should also inquire about specific male advocacy services. Most advocacy centers are intimidating for male survivors to even approach, because all their literature, pictures, etc. General principles of cultural and linguistic care As noted initially, it is impossible to be knowledgeable of all the cultural and linguistic issues that may impact the care of any individual patient. The difference is somewhat subtle, but a generalization is similar to the beginning of the conversation where all possible conclusions are remain open for consideration. Fifth, "evidence based care" is only as good as the diversity/inclusion within the research and must always be balanced with individual patient and family centered principals of care. Comparing heart failure patient literacy levels with available educational materials. Commentary: Linking cultural competence training to improved health outcomes: Perspectives from the field. Improving comprehension for cancer patients with low literacy skills: Strategies for clinicians. Legislation as intervention: A survey of cultural competence policy in health care. Executive summary of adult literacy in America: a first look at the results of the national adult literacy survey. Improving Patient Safety through Informed Consent for Patients with Limited Health Literacy. A Comprehensive Framework and Preferred Practices for Measuring and Reporting Cultural Competency: A Consensus Report. Unifying efforts to achieve quality care for all American: Five year summary, American Medical Associaton, 2009. Advancing Effective Communication, Cultural Competence, and Patient- and Family-Centered Care: A Roadmap for Hospitals. Emergency departments discharge instructions and patient literacy: A problem of disparity. Unifying efforts to achieve quality care for all Americans: Five year summary, American Medical Association, 2009. Elderly female victims of sexual assault are more likely to sustain injury as a result of decreased estrogen levels. Bruising often incorrectly attributed to aging process, medications, or to injuries sustained during routine care. Memory impairment may hinder reporting, cooperation with investigation, and getting appropriate follow up. Hearing impairment and physical limitations may make the medical forensic examination somewhat challenging. Children with mental or intellectual impairments appear to be among the most vulnerable, with 4. Adults with mental health conditions are at nearly four times the risk of experiencing violence. Developmental disability increases risk of sexual assault 4­10 times above rest of population; perpetrators most often caretakers. For hearing impaired patients, use interpreters with experience regarding sexual violence. In cases of physical disability, ask what assistance a patient may require during the examination, and provide assistance only with permission. Includes an executive summary of the report health Literacy and video clips or patients discussing their literacy experiences. However, depending upon the type of contact, perpetrators may be more likely than victims to have probative evidence on their bodies and clothing. This is especially true in cases involving oral copulation of the suspect and digital penetration of the mouth, vagina, or rectum. This should be done as a collaborative effort between law enforcement, forensic medical personnel, and prosecutors. Rates of sexual victimization did not vary based on commonly cited characteristics of facilities, including size or age of facility, crowding, inmate-to-staff ratios, or gender composition of staff. The forensic examiner should not ask the custodial officer to step out of the room during the exam. No restraining devices should be removed or modified without consulting with accompanying law enforcement. Consent should be obtained for each portion of the forensic medical exam as it would be for any other patient. Although local practices may vary, if a corrections officer is the accused perpetrator, a different law enforcement agency may need to conduct the investigation. A suspect exam should be considered an additional expense associated with the investigation and as such it is reasonable that costs may be recovered from victim compensation programs, the suspect upon conviction, or from the investigating law enforcement or prosecuting agency. Because there is no medical indication for the evaluation, health care insurance cannot be billed for the exam. Special Considerations intoxicated or Unconscious Patients Special Considerations · · · · · Patients are unable to give consent for forensic examination if intoxicated or unconscious. Due to the limited time window in which evidence may be collected, if there are no family members present and the patient is unable to provide consent, a medical forensic examination may be completed and the kit stored until the patient is able to consent to release to law enforcement. If the patient is not expected to regain normal mental status, law enforcement may request a court order to obtain the kit and associated documentation. Prevalence and risk of violence against adults with disabilities: a systematic review and meta-analysis of observational studies. Discussion with law enforcement and prosecution should occur in order to determine a reasonable length of time to maintain these records. Evidence Kits Evidentiary kits are often supplied by law enforcement or the crime lab that analyzes the kit. If a program desires they may also compile a kit specific to suspect examinations. Commercial suspect specific kits are available from several forensic supply companies. Different rooms should be used and the examiner needs to change gowns and gloves and wash hands well between exams, and document they have done so. Alternative sites to conduct the examination includes the police station or the jail. Consent Forensic examination of suspects presents unique issues regarding consent. In some cases, examinations may be obtained from suspects who have consented to the examination and collection of evidence. More commonly, a court order or warrant may have been issued for the collection of specific pieces of evidence. This part of the process should be clearly worked out by all agencies prior to doing any suspect exams. The suspect will need to be informed of any and all evidence that will be obtained. The suspect has the right to decline portions of the examination and to abort evidence collection at any time. If evidence is being collected with a court order, the suspect may not refuse the examination. Because the forensic examiner is acting as an agent of the investigating officer, a Miranda warning must be provided prior to the examination. Both the law enforcement officer and the forensic examiner should document any spontaneous statements made by the suspect during the exam. Occasionally a suspect is uncooperative during the exam and becomes aggressive or hostile requiring the use of restraints. It is the duty of law enforcement, not medical personnel, to restrain the individual. If the suspect does not invoke his right to remain silent the forensic examiner should obtain a medical history, including information on anal or genital injuries, surgeries, or procedures that may affect the interpretation of examination findings. Obtain consent from suspect, or if applicable, review search warrant/court order and what has been authorized to be collected. If bite mark is present: photograph, collect swabs using the double swab technique, and consider forensic odontologist consult J. As during a victim exam, the examiner should document vital signs and a brief medical history. Areas of pain or tenderness and visible injuries, birthmarks, tattoos, etc, should be described using written documentation, photography, and/or body diagrams. The examiner should collect trace evidence, such as grass and soil, as it may link the suspect to a crime scene. Penile identifiers such as scars, tattoos, warts, and color variations should also be documented. In cases in which no previous intimate relationship existed between the two individuals, this information may add credence to the allegation that a sexual encounter occurred. The body of published studies evaluating suspect exam evidence collection, including areas most likely to yield results and the time course of evidence degradation, is still in its infancy. This is in part due to the paucity of programs participating is suspect evidence collection. Swabs from each of these areas should be collected separately as opposed to a single swab of the entire area. Fingernails should be swabbed especially in cases that include digital penetration of the mouth, vagina and /or rectum of the victim. All evidence collection should follow standardized forensic sample collection protocols. All swabs should be allowed to dry, be labeled, and packaged according to local protocols. In summary, forensic examination of a suspect in a sexual assault case can yield valuable information placing the suspect at the scene and supporting the allegation of sexual contact. While the evidence may not prove a lack of consent, it may be probative or informative in value and is likely to assist with the prosecution of a difficult to prove crime. Sexual Assault Suspect Evidential Examination, California Medical Protocol for Examination of sexual assault and child sexual abuse victims, 2001. High-quality performance in court depends on the appearance of the sexual assault examiner as an unflappable, well-prepared expert who is able to explain and teach his/her findings to the judge and jury. For the sexual assault examiner, as for any witness, emanating that confident demeanor in court includes maintaining eye contact with the questioning attorney, judge and jury members to make sure that they hear and understand you well, speaking at a moderate pace, dressing appropriately for court and conveying evidence by working in concert with the examining attorney. The section which follows will describe some basic ways of achieving this kind of performance. Order of Events A basic understanding the order of events usually involved in trying a sexual assault case is helpful in allowing the sexual assault examiner to be well prepared for testimony. Although this sequence can vary significantly between jurisdictions, what follows is a general outline. The victim and/or information/findings obtained by the witnesses are interviewed by police and an assailant is accused, or the police work in concert with crime scene investigators and/or sexual assault examiner to determine the identity of the assailant. The nature of the charges is based on type of crime committed and the weapons involved in perpetration of the crime (if any). This means that the charges against the assailant are reviewed, found credible and confirmed. The accurate and intelligible documentation of injuries by the sexual assault examiner is integral to this process. Most important in many sexual assault cases is for the prosecution to prove that the victim did not consent to the sexual encounter. The accused assailant is arrested (this often occurs before formal indictment, however the accused can only be held for a finite amount of time and must be freed unless indictment occurs promptly). This means that the accused perpetrator comes to court to be formally advised of the charges against him/her. At this hearing, a judge hears brief testimony, most often from the victim, and makes sure that legal requirements to go forward with the case are met3. Receiving a subpoena means that you are required by law to appear in court for the purpose of giving testimony. The subpoena will be headed by the name of the state versus the name of the defendant, and will tell the location of the court and the date(s) upon which you will be required to appear.

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A regimen of cisplatin plus ifosfamide muscle relaxant 4212 order skelaxin 400 mg otc, with or without an anthracycline spasms after hemorrhoidectomy purchase skelaxin 400mg overnight delivery, is recommended for patients with advanced carcinosarcoma (Gadducci et al muscle relaxant exercises order skelaxin 400 mg with visa. Hormonal treatment should be planned on the basis of hormone receptor status (Gadducci et al muscle relaxant headache order skelaxin 400mg without prescription. Radiation therapy is most useful when used in palliative treatment to distant sites muscle relaxant use in elderly generic skelaxin 400mg free shipping, such as bone or brain metastasis (Gadducci et al spasms posterior knee purchase 400mg skelaxin visa. Recurrent Disease the treatment of recurrent gynecologic sarcoma often requires the use of multiple therapeutic modalities. Except for rare cases of resectable, isolated pulmonary metastases, such patients are not considered curable (Hensley et al. Enrollment into clinical trials is strongly encouraged to facilitate the identification of new active agents for these malignancies. In women with poorer performance status or multiple comorbidities, palliative measures and supportive care should be the mainstay of treatment. Summary Uterine sarcomas are a group of rare gynecologic tumors that usually have an aggressive clinical course and poor prognosis. The rarity of these sarcomas and their aggressive behavior has resulted in a paucity of literature. Total abdominal hysterectomy and bilateral salpingo-oophorectomy remains the surgical standard of care. Lymph node dissection is indicated for carcinosarcomas because of their high incidence of nodal involvement. Adjuvant pelvic radiotherapy may improve local control but has no significant affect on survival. Evidence in the literature is scant to support the routine use of adjuvant chemotherapy, except in carcinosarcomas. Further evaluation of adjuvant treatment in prospective trials clearly is warranted. Oncology nurses collaborating with medical and surgical oncologists is pivotal to ensuring quality care. Patient and family education regarding the details of the sarcoma treatment plan provides support to women from time of initial diagnosis and at the time of recurrence. Low grade endometrial stromal sarcoma of uterine cor- Radiation the role of adjuvant radiotherapy in nonmetastatic disease is controversial. Although this therapy reduces the rate of local recurrences, it has no significant impact on overall survival, as most patients with recurrent disease have distant failures (Gadducci et al. Estrogen and progesterone receptor expression in patients with uterine smooth muscle tumors. Prognostic parameters in endometrial stromal sarcoma: A clinicopathologic study in 31 patients. Surveillance, epidemiology, and end results analysis of 2,677 cases of uterine sarcoma 1989­1999. Uterine carcinosarcoma: Immunohistochemical studies on tissue microarrays with focus on potential therapeutic targets. A clinicopathologic analysis of ten cases of a distinctive type of Mьllerian mixed tumor. Long-term sequelae of conservative treatment by surgery, brachytherapy, and chemotherapy for vulval and vaginal rhabdomyosarcoma in children. Long-term tamoxifen treatment: A possible aetiological factor in the development of uterine carcinosarcoma: Two case-reports and review of the literature. Retrospective review of 208 patients with leiomyosarcoma of the uterus: Prognostic indicators, surgical management, and adjuvant therapy. Uterine sarcomas and carcinosarcomas: Advances for advanced disease and updates for adjuvant therapy. Recurrent endometrial stromal tumors with smooth-muscle differentiation and a protracted clinical course. Adenosarcoma of the uterus: A Gynecologic Oncology Group clinicopathologic study of 31 cases. Estrogen and progesterone receptor expression in uterine and extrauterine leiomyosarcomas: An immunohistochemical study. Surgical resection of pulmonary and extrapulmonary recurrences of uterine leiomyosarcoma. Tissue microarray immunohistochemical expression of estrogen, progesterone, and androgen receptors in uterine leiomyomata and leiomyosarcoma. Uterine carcinosarcomas (malignant mixed Mьllerian tumors) are metaplastic carcinomas. Endometrial stromal tumor: An update on a group of tumors with a protean phenotype. Epithelioid endometrial and endometrioid stromal tumors: A report of four cases emphasizing their distinction from epithelioid smooth muscle tumors and other oxyphilic uterine and extrauterine tumors. Expression of estrogen and progesterone receptors in low-grade endometrial stromal sarcomas. Is pre-operative radiotherapy superior to postoperative radiotherapy in the treatment of soft tissue sarcoma? Exogenous sex hormone use, correlates of endogenous hormone levels, and the incidence of histologic types of sarcoma of the uterus. Clinical outcome after neoadjuvant thermoradiotherapy in high grade soft tissue sarcomas. Primary ovarian sarcoma: Analysis of prognostic variables and the role of surgical cytoreduction. Primary spindle cell sarcoma of the vagina treated with neoadjuvant radiation and pelvic exenteration. Prognostic factors and the impact of adjuvant chemotherapy for uterine leiomyosarcoma. Pathologic variables and adjuvant therapy as predictors of recurrence and survival for patients with surgically evaluated carcinosarcoma of the uterus. Asymptomatic intracardiac metastasis from a low-grade endometrial stromal sarcoma with successful surgical resection. Immunohistochemical markers in differential diagnosis of endometrial stromal sarcoma and cellular leiomyoma. It encompasses a spectrum of interrelated neoplasms ranging from benign to metastatic. Although the etiology of trophoblastic disease is not definitive, a combination of defects in gametogenesis and fertilization, as well as certain risk factors such as personal or family history of trophoblastic disease, maternal age, use of oral contraceptives, history of infertility, or low parity, contribute to this group of pregnancy-related disorders (Smith, 2003). All variants of trophoblastic disease arise following a gestational event resulting in abnormal growth of placental trophoblastic cells. Although trophoblastic neoplasms are interrelated, they are histologically distinct variants. Epidemiology of Trophoblastic Variants Historically, comparing epidemiologic data across geographic locations and among racial/ethnic groups in a meaningful manner has been complicated. This difficulty existed because of discrepancies in data collection methods and reporting. For example, estimates regarding incidence may differ as a result of using population-based versus hospital-based pregnancy data (Garner, Goldstein, Feltmate, & Berkowitz, 2007; Smith & Kim, 2003; Steigrad, 2003). Furthermore, incidence rates were based on diverse denominators such as woman years (adult female population at risk), live births, or pregnancies. However, over the last two to three decades, registries dedicated to the study of trophoblastic disease have been established throughout the world. Common to these registries is the use of population-based statistics, which enhances the worldwide comparison of epidemiologic data (Smith & Kim, 2003). Invasive mole occurs in 15% of women with complete molar pregnancies (Berkowitz & Goldstein, 2003). Problems in estimating the incidence of choriocarcinoma are compounded by the rarity of the disease and by differences in data collection methods and reporting. In contrast, when using woman years as the denominator, the reported incidence is 0. In addition, advances in diagnostic imaging and biochemical testing has enabled earlier intervention, improved clinical outcomes, and systematic follow-up. This triploid karotype occurs in 90%­93% of partial moles (Berkowitz & Goldstein, 1996). A nonviable fetus may be present with identifiable multiple congenital anomalies and growth retardation (Berkowitz & Goldstein, 1996; Garner et al. Etiology Complete and partial molar pregnancies share several social, demographic, and physiologic risk factors. Risk factors include reproductive history, age, and socioeconomic status (see Figure 10-2). For example, there is a higher incidence of choriocarcinoma with lower survival rates among African Americans compared with Caucasians (Smith et al. Also, an increased incidence of hydatidiform mole in Asian countries is reported (Berman, DiSaia, & Tewari, 2004). Although these relationships are unclear, the variation in incidence may be attributed to nutritional and/or socioeconomic factors (Berkowitz & Goldstein, 2005; Hurteau, 2003) or genetics (Tham, Everard, Tidy, Drew, & Hancock, 2003). Researchers continue to explore role of genetics in the development and progression of trophoblastic variants, including the underlying explanation for racial/ethnic differences. Gestational Trophoblastic Disease Chromosomal Characteristics Moles are genetically determined and the characteristic trophoblastic hyperplasia appears to be associated with more than one set of paternal chromosomes (Paradinas, Sebire, & Rees, 2003). Analysis of chromosomal differences between complete and partial moles enhances diagnostic accuracy. Complete hydatidiform mole results from the fertilization of an ovum that is without a nucleus. The sperm duplicates its own chromosomes creating embryonic tissue that is totally uniparental, in this case, paternally derived. Berkowitz and Goldstein (1996) and Soper (2006) theorized that it occurs when an anuclear ovum is fertilized by two sperm. Partial molar pregnancy results from the fertilization of one ovum with two sperm resulting in three sets of chromosomes instead of the usual two sets (Kurowski & Yakoub, 2003; Smith, 2003). Embryonic tissue is composed of one set of chromo- Clinical Presentation and Diagnostic Evaluation Women with hydatidform mole initially have amenorrhea and may experience either characteristic or exaggerated signs or symptoms of pregnancy. First-trimester vaginal bleeding is the most common presenting symptom regardless of type of molar gestation (Berkowitz & Goldstein, 1996; Berman et al. Risk Factors for Gestational Trophoblastic Neoplasia · Lower socioeconomic status (Hurteau, 2003) · Nulliparous, low parity (Smith, 2003) · Age extremes (Altman et al. Bleeding may be intermittent or continuous and ranges from brisk hemorrhage to a dark-brown watery discharge resembling prune juice (Berkowitz & Goldstein, 2004; Berman et al. The prune juice­like discharge is caused by liquefaction of intrauterine clots (Evans, Soper, & Hammond, 2003). Vaginal discharge may contain pieces of molar tissue (vesicles) that resemble grapelike clusters representing indisputable evidence of a molar pregnancy (Kurowski &Yakoub; Soper). In addition to vaginal bleeding, some individuals may present with fatigue and shortness of breath secondary to anemia from blood loss. Classic manifestations of complete moles typically present in the second trimester (Kurowski & Yakoub, 2003). However, clinical practice changes have allowed for the diagnosis of molar pregnancies and subsequent molar evacuations in the first trimester. Consequently, the classic presentation is less common at time of diagnosis (Berkowiz & Goldstein, 1996; Evans et al. Although the current trend is for earlier diagnosis, some women may not be diagnosed with a molar pregnancy until the second trimester. They most likely will present with classic manifestations and subsequent medical complications at this stage (Kurowski & Yaloub, 2003). Women presenting with a uterus greater than 14­16 weeks gestational size also may present with classic manifestations (Soper, 2006). Moreover, the classic presentation of molar pregnancies may be more common in countries without well-developed health care (Evans et al. Increased uterine size results from retained intrauterine clots, enlarged chorionic villi, and trophoblastic proliferation (Berkowitz & Goldstein, 2003; Leiser & Aghajanian, 2006). These fluidfilled cysts may be as large as 20 cm (Berkowitz & Goldstein) and usually are bilateral. Cysts greater than 6 cm may cause severe abdominal pain (Kurowski & Yakoub, 2003). Untreated or poorly controlled hyperthyroidism may precipitate development of thyroid storm, also known as thyrotoxic crisis, at the time of anesthesia induction for molar evacuation (Berkowitz & Goldstein, 2003; Berman et al. In thyroid storm, all hyperthyroid manifestations are heightened and may lead to heart failure or shock. This medical emergency may be prevented by treatment with beta adrenergic blocking agents. These agents aid in preventing or rapidly reversing many of the cardiovascular and metabolic complications of thyroid storm (Berkowitz & Goldstein; Garner et al. Symptoms of hyperthyroidism disappear subsequent to evacuation of the molar pregnancy (Berkowitz & Goldstein; Berman et al. The clinical presentation of a partial mole is considerably less dramatic than with a complete mole (Cunningham et al. Partial moles have less trophoblastic overgrowth than is characteristically found in complete moles and, in fact, trophoblastic excess may not be detected if the tissue is not thoroughly examined (Paradinas et al. Physical examination findings may include a nontender uterus that is generally small for gestational age, palpable fetal parts, and a fetal heart beat (Kurowski & Yakoub, 2003). Pathologic examination of an aborted conceptus is the only way to make a definitive diagnosis.

Indian Kudzu (Kudzu). Skelaxin.

  • What is Kudzu?
  • Symptoms of alcohol hangover (headache, upset stomach, dizziness and vomiting), chest pains, treatment of alcoholism, menopause, muscle pain, measles, dysentery, stomach inflammation (gastritis), fever, diarrhea, thirst, cold, flu, neck stiffness, promoting sweating (diaphoretic), high blood pressure, abnormal heart rate and rhythm, stroke, and other conditions.
  • Are there safety concerns?
  • Are there any interactions with medications?
  • Dosing considerations for Kudzu.
  • How does Kudzu work?

Source: http://www.rxlist.com/script/main/art.asp?articlekey=96732

References

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  • Hovding G, Sjursen H: Bacterial contamination of drops and dropper tips of in-use multidose bottles. Acta Ophthalmol 60:213, 1982.
  • Bishop CV, Renwick WE, Hogan C, et al: Recombinant activated factor VII: Treating postoperative hemorrhage in cardiac surgery, Ann Thorac Surg 81:875-879, 2006.
  • Van den Ouweland JMW, Lemkes HHPJ, Ruitenbeek W, et al. Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. Nat Genet 1992;1:368.
  • Hadziselimovic F, Hoecht B: Testicular histology related to fertility outcome and postpubertal hormone status in cryptorchidism, Klin Padiatr 220(5):302n307, 2008.
  • Triest, J.A., Bukowski, T.P. Multicystic dysplastic kidney as cause of gastric outlet obstruction and respiratory compromise. J Urol 1999;161:1918-1919.
  • Vermeulen SH, Hanum N, Grotenhuis AJ, et al: Recurrent urinary tract infection and risk of bladder cancer in the Nijmegen bladder cancer study, Br J Cancer 112:594n600, 2015.
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