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But I must explain to you how all this mistaken idea of denouncing pleasure and praising pain was born and will give you a complete account of the system and expound the actual teachings of the great explore

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    Margaret Mary Showel, M.D.

    • Assistant Professor of Oncology

    https://www.hopkinsmedicine.org/profiles/results/directory/profile/0021061/margaret-showel

    Poor bone marrow reserve (platelet count < 100 arthritis diet the body order diclofenac uk, 000/microL arthritis medication without aspirin proven diclofenac 75mg, absolute neutrophil count < 1 arthritis in dogs blog buy cheap diclofenac on-line, 500/microL rheumatoid arthritis simple definition best order diclofenac, bone marrow cellularity < 15%) B arthritis pain cold weather generic diclofenac 75mg amex. In an individual with prior autologous stem cell rescue arthritis pain gloves order generic diclofenac on line, referral to a tertiary care center is highly recommended E. Therefore, a surrogate imaging radionuclide that emits gamma radiation (111In) is required. Immunotherapy either with single agent rituximab or rituximab plus chemotherapy 3. After the first2 rituximab dose on day 1, 111In ibritumomab tiuxetan was administered to assess biodistribution and to aide in dosimetry. No patients received the therapeutic dose of Zevalin if > 20 Gy or 3 Gy was calculated to any non-tumor organ or the red marrow, respectively. Zevalin was administered after the second rituximab dose approximately 1 week days 7 to 9) after the first dose of rituximab and 111In ibritumomab tiuxetan. Individuals with advanced stage disease are usually not cured with conventional treatment. Treatment focuses on the alleviation of symptoms, reversal of cytopenias, and improvement of quality of life. Off-label use of radioimmunoconjugates as single-agent therapy for the management of previously untreated disease Nonrandomized trials support use of radioimmunoconjugates as single-agent therapy for the management of previously untreated disease. While initial reports suggest good response rates and tolerability, long-term follow up of such an approach is limited. Severe (grade 3/4) thrombocytopenia, leukopenia, neutropenia, and lymphopenia were seen in approximately 48%, 34%, 32%, and 20%. A randomized trial comparing 12 and 16 Gy found that the higher dose was associated with a lower relapse rate (12% vs. This would permit targeting of the radiation dose to the tumor cells and marrow with potential reduction in dose to other organs, such as the liver, lungs and kidneys. The most common cytopenias are leucopenia and thrombocytopenia, which are easily managed in the majority of individuals. Survival improvement in patients with medullary thyroid carcinoma who undergo pretargeted anti-carcinoembryonic-antigen radioimmunotherapy: a collaborative study with the French Endocrine Tumor Group. Pivotal study of iodine-131-labeled chimeric tumor necrosis treatment radioimmunotherapy in patients with advanced lung cancer. Allogeneic marrow transplantation in patients with chronic myeloid leukemia in the chronic phase: a randomized trial of two irradiation regimens. Phase I trial results of iodine-131-labeled antitenascin monoclonal antibody 81C6 treatment of patients with newly diagnosed malignant gliomas. Treatment-related myelodysplastic syndrome and acute myelogenous leukemia in patients treated with ibritumomab tiuxetan radioimmunotherapy. Radioiodinated (I-125) monoclonal antibody 425 in the treatment of high grade glioma patients: ten-year synopsis of a novel treatment. A pilot study of the treatment of patients with recurrent malignant gliomas with intratumoral yttrium-90 radioimmunoconjugates. Targeting, toxicity, and efficacy of 2-step, pretargeted radioimmunotherapy using a chimeric bispecific antibody and 131I-labeled bivalent hapten in a phase I optimization clinical trial. Radioimmunotherapy of relapsed indolent non-Hodgkin lymphoma with 131I-rituximab in routine clinical practice: 10-year single-institution experience of 142 consecutive patients. Antibody mass escalation study in patients with castration resistant prostate cancer using 111In-J591: lesion detectability and dosimetric projection for 90Y radioimmunotherapy. Treatment of recurrent and cystic malignant gliomas by a single intracavity injection of 131I monoclonal antibody: feasibility pharmacokinetics and dosimetry. A pilot study: 131I-antitenascin monoclonal antibody 81C6 to deliver a 44-Gy resection cavity boost. Local application of radiolabeled monoclonal antibodies in the treatment of high grade malignant gliomas: a six-year clinical experience. Radioimmunotherapy and Unsealed Radionuclide Therapy and Unsealed Radionuclide Therapy; Conjugated Therapy p. Immunogenicity of iodine 131 chimeric tumor necrosis therapy monoclonal antibody in advanced lung cancer patients. Recommendations for the use of yttrium-90 ibritumomab tiuxetan in malignant lymphoma. Long-term responses in patients with recurring or refractory B-cell non Hodgkin lymphoma treated with yttrium 90 ibritumomab tiuxetan. Unresectable liver only or liver dominant metastases from neuroendocrine tumors. The tumor burden should be liver dominant, not necessarily exclusive to the liver C. Repeat radioembolization is considered medically necessary for new or progressive primary or metastatic liver cancers when: A. Estimated lung dose and combined lung dose from previous embolizations are within acceptable dose volume constraints. The treatment involves catheter-based injection of radioactive Yttrium-90 (90Y) microspheres, in either glass or resin form, through the arterial branch feeding the affected portion of the liver. Radioembolization with Yttrium-90 microspheres has proven safe and effective in palliation of symptoms as well as possible increase in survival in selected cancer patients. Given this proven effect, consideration is now being given to repeating the procedure in an individual who has responded well previously, has good performance status, and has liver dominant disease without other treatment options. In their series of 148 patients diagnosed with neuroendocrine tumor metastases to the liver treated with Yttrium-90 microspheres, Vyleta et al. They also commented on other published studies in which a few patients even received a third treatment. The remaining 6 patients experienced minor side effects with cumulative doses of 2. At this time, requests for a second radioembolization treatment will be considered on a case-by-case basis. Excessive tumor burden in the liver with greater than 70% of the parenchyma replaced by tumor B. Nonobstructive bilirubin elevations generally indicate that liver metastases have caused liver impairment to a degree at which risks outweigh benefits for this therapy. Prior radiation therapy to the liver or upper abdomen that included a significant volume of the liver (clinical judgment by the authorized used required). Treating multiple tumors within the entire liver in a single treatment session is termed whole liver delivery. Treatment to additional lobes may be done if a positive response of the first is achieved as evidenced by any of the following: 1. Page 255 of 263 References: 1. Radioembolization in the treatment of unresectable liver tumors: experience across a range of primary cancers. Radioembolization for unresectable neuroendocrine hepatic metastases using resin 90Y-microspheres: early results in 148 patients. Recommendations for radioembolization of hepatic malignancies using Yttrium-90 microsphere brachytherapy: a consensus panel report from the radioembolization brachytherapy oncology consortium. Patient selection and activity planning guide for selective internal radiotherapy with Yttrium-90 resin microspheres. Summary of Safety and Probably Benefit, Yttrium-90 Glass Microsphere, TheraSphere Issued December 10, 1999. For non-muscle invasive bladder carcinoma verbiage was removed that stated that in patients who have recurrent disease and are medically inoperable, the use of radiation therapy will be considered on a case-by-case basis. For muscle-invasive bladder carcinoma in the preoperative setting, the use of radiation therapy is now considered medically necessary 5. Radium-223 (Xofigo): Updated verbiage from October 2018 press release from Bayer that Xofigo is not recommended for use in combination with abiraterone acetate plus prednisone/prednisolone outside of clinical trials due to increased risk of fractures 6. All requests will go to Medical Review Page 260 of 263 ii. Removed that participation in a clinical trial is encouraged Page 261 of 263 13. Removed verbiage that requests for the treatment of liver metastases from other primaries will be considered on a case-by-case basis. Removed verbiage that requests for repeat radioembolization will be considered on a case-by-case basis. Each medical specialist should claim only those hours of credit that he/she actually spent in the educational activity. In June 2017 Budapest will not only be the center of Europe but also the Capital of hand surgery and hand therapy. An outstanding scienti c program, with more than 900 submitted abstracts, more than 70 scienti c sessions, more than 300 free paper presentations, 17 instructional course sessions including all topics of hand surgery focusing on the available evidence based data will be an excellent opportunity to refresh your knowledge. The already registered more than 1500 participants, hand surgeons of all generations are ready to present their cases, their results and share their experience. Joint sessions with hand therapists can build an even closer relation between surgeons and therapists. Needless to say, that beside a high level scienti c program the well known Hungarian hospitality, gastronomy and cultural life are also waiting for you in the Capital of Hungary. Many members have been actively involved in the societies work and Antal Renner was one of founding motors of that European idea in Hand Surgery. In a special meeting a great number of experienced members, have tried to establish an organizational framework for best conducting this meeting. We will have to analyze the e ects of our inputs and adapt the organizational structure annually according to the needs of European Hand Surgeons. This is why I wish to invite all of you, to take part to our Delegates Assembly on Thursday in the afternoon. Everybody is welcome, voting rights are reserved to the national delegate of each society. The Hungarian Society and Asszisztencia were waiting very much to organize this meeting. I wish them and you an interesting congress with a fruitful exchange of scienti c, technological, surgical, cultural and social experiences in Budapest. You will have the opportunity to choose your preferred topics from the concurrent programs, and with the chance of mixing both lectures and workshops, this will provide an interesting and versatile entity for therapists from di erent backgrounds and work settings. In addition to the compact scienti c program, the social program will allow you to meet and spend time with colleagues and see beautiful Budapest. Budapest o ers you a great location to combine the scienti c event to culture, history, sights and urban life. I o er you a warm welcome to the Eurohand 2017 Congress and look forward to seeing you in Budapest! A laptop will be provided at each presentation hall that should be used for presentation. If your presentation contains videos, make sure to embed them in the presentation le or upload them also during slide check. Slides must be clear and easy to read from a distance charts with detailed data are to be avoided. Please report to this room to upload your presentation not later than 2 hours before your talk. The le is copied on the main server, on the backup server and immediately in the right room. Speakers who want to change their presentation material will be able to do so in this area. As a safety measure, bring with you a second pen drive with a back-up copy of your presentation. For viewing the e-posters big touchscreens will be provided at the slide checking area of the congress venue. The overall aim of the session is to: Provide clinicians with an understanding of how Woodcast products can be used to manage traumatic injuries a ecting the hand and wrist. The key areas of focus will be management of: peripheral nerve injury, 5th metacarpal fractures base of thumb fractures. Bernd Maydell1, David Le1, 2, Kristian Welle2, Khabir K2, Christof Burger2, Martin Richter1 | 1Hand Centre, Order of Malta-Hospital, Bonn, Germany; 2Dept. Igor Shvedovchenko1, 2, Andrej Koltsov1, Boris Kasparov1 | 1Federal State Institution St. Petersburg Scienti c and Practical Centre of Medical and Social Expertise, Prosthetics and Rehabilitation named after G. Albrechtof the 46 Ministry of Labour and Social Protection of the Russian Federation, St. Functional outcome and complications following surgery for Dupuytrens disease: a multi-centre cross sectional study by J.

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    Health care providers should become familiar with action plans that are relevant to their local health care system arthritis diet foods to avoid mayo buy diclofenac 50 mg line, treatment options arthritis special diet purchase diclofenac uk, and cultural and literacy context arthritis paleolithic diet quality diclofenac 100mg. Details of the specific treatment adjustments that can be recommended for written asthma action plans are described in the next chapter (Box 4-2 arthritis pain vitamins generic diclofenac 50 mg, p arthritis in horses front feet generic 75mg diclofenac. Treating to control symptoms and minimize future risk 61 Regular review by a health care provider the third component of effective asthma self-management education is regular review by a health care provider arthritis in hips for dogs buy diclofenac. Comorbidities may contribute to respiratory symptoms and impaired quality of life, and some contribute to poor asthma control. Active management of comorbidities is recommended because they may contribute to symptom burden, impair quality of life, and lead to medication interactions. In addition, lack of fitness and reduction in lung volume due to abdominal fat may contribute to dyspnea. Because of other potential contributors to dyspnea and wheeze in obese patients, it is important to confirm the diagnosis of asthma with objective measurement of variable airflow limitation (Box 1-2, p. Asthma is more common in obese than non-obese patients, 47 but both over and under diagnosis of asthma occur in obesity. Increased exercise alone appears to be insufficient (Evidence B);290 however a weight loss program plus Deleted. Asymptomatic gastroesophageal reflux is not a likely cause of poorly controlled asthma. For patients with asthma and symptoms suggestive of reflux, an empirical trial of anti-reflux medication, such as a proton pump inhibitor or motility agent, may be considered, as in the general population. If the symptoms do not resolve, specific investigations such as 24-hour pH monitoring or endoscopy may be considered. In summary, symptomatic reflux should be treated, but patients with poorly controlled asthma should not be treated with anti-reflux therapy unless they also have symptomatic reflux (Evidence A). Diagnosis Although several tools are available for screening for anxious and depressive symptomatology in primary care, the majority have not been validated in asthma populations. Difficulties in distinguishing anxiety or depression from asthma symptoms may therefore lead to misdiagnosis. It is important to be alert to possible depression and/or anxiety in people with asthma, particularly when there is a previous history of these conditions. Where appropriate, patients should be referred to psychiatrists or evaluated with a disease-specific psychiatric diagnostic tool to identify potential cases of depression and/or anxiety. Management There have been few good quality pharmacological and non-pharmacological treatment trials for anxiety or depression in patients with asthma, and results are inconsistent. A Cochrane review of 15 randomized controlled trials of psychological interventions for adults with asthma included cognitive behavior therapy, psychoeducation, relaxation, and biofeedback. Drug treatments and cognitive behavior therapy305 have been described as having some potential in 64 3. Treating to control symptoms and minimize future risk patients with asthma; however, current evidence is limited, with a small number of studies and methodological shortcomings. Food allergy and anaphylaxis Clinical features Rarely, food allergy is a trigger for asthma symptoms (<2% of people with asthma). In patients with confirmed food induced allergic reactions (anaphylaxis), co-existing asthma is a strong risk factor for more severe and even fatal reactions. Children with food allergy have a four-fold increased likelihood of having asthma compared with children without food allergy. This may include appropriate allergy testing such as skin prick testing and/or blood testing for specific IgE. Management Patients who have a confirmed food allergy that puts them at risk for anaphylaxis must be trained and have an epinephrine auto-injector available at all times. They, and their family, must be educated in appropriate food avoidance strategies, and in the medical notes, they should be flagged as being at high risk. It is especially important to ensure that their asthma is well controlled, they have a written action plan, understand the difference between asthma and anaphylaxis, and are reviewed on a regular basis. Rhinitis, sinusitis and nasal polyps Clinical features Evidence clearly supports a link between diseases of the upper and lower airways. Rhinosinusitis is defined as inflammation of the nose and paranasal sinuses characterized by more than two symptoms including nasal blockage/obstruction and/or nasal discharge (anterior/posterior nasal drip). Rhinosinusitis is defined as acute when symptoms last <12 weeks with complete resolution, and chronic when symptoms occur on most days for at least 12 weeks without complete resolution. Chronic rhinosinusitis is an inflammatory condition of the paranasal sinuses that encompasses two clinically distinct entities: chronic rhinosinusitis without nasal polyposis and chronic rhinosinusitis with nasal polyposis. Chronic rhinosinusitis is associated with more severe asthma, especially in patients with nasal polyps. Examination of the upper airway should be arranged for patients with severe asthma. A Comment [A32]: Lohia 2013 meta-analysis added recent placebo-controlled trial of nasal mometasone in adults and children with chronic rhinosinusitis and poorly controlled asthma showed no benefit for asthma outcomes, suggesting that, while chronic rhinosinusitis can contribute to respiratory symptoms. Also refer to the Diagnosis of respiratory symptoms in special populations section of Chapter 1 (p. It is possible to build capacity of primary health care teams, including nurses and other health professionals, for the development of an integrated approach to the most common diseases and symptoms, including asthma. Asthma control may improve or worsen, although remission of asthma is seen more commonly in males than females. This may involve the transition from a pediatric to an adult health care facility. During consultations, the adolescent should be seen separately from the parent/carer so that sensitive issues such as smoking, adherence and mental health can be discussed privately, and confidentiality agreed. An empathic approach should be used to identify beliefs and behaviors that may be barriers to optimal treatment; for example, adolescents may be concerned about the impact of treatment on their physical or sexual capabilities. Treating to control symptoms and minimize future risk reviews arranged regularly so that the medication regimen can be adjusted for changing needs. Information about local youth-friendly resources and support services should be provided, where available. However, shortness of breath or wheezing during exercise may also relate to obesity or a lack of fitness, or to comorbid or alternative conditions such as vocal cord dysfunction. Athletes Clinical features Athletes, particularly those competing at a high level, have an increased prevalence of various respiratory conditions compared to non-athletes. Airway hyperresponsiveness is common in elite athletes, often without reported symptoms. Asthma in elite athletes is commonly characterized by less correlation between symptoms and pulmonary function; higher lung volumes and expiratory flows; less eosinophilic airway inflammation; more difficulty in controlling symptoms; and some improvement in airway dysfunction after cessation of training. Management Preventative measures to avoid high exposure to air pollutants, allergens (if sensitized) and chlorine levels in pools, particularly during training periods, should be discussed with the athlete. They should avoid training in extreme cold or pollution (Evidence C), and the effects of any therapeutic trials of asthma medications should be documented. Treating to control symptoms and minimize future risk 67 Pregnancy Clinical features Asthma control often changes during pregnancy; in approximately one-third of women asthma symptoms worsen, in one-third they improve, and in the remaining one-third they remain unchanged. Pregnant women appear to be particularly susceptible to the effects of viral respiratory infections, 326 including influenza. Exacerbations and poor symptom control are associated with worse outcomes for both the baby (pre-term delivery, low birth weight, increased perinatal mortality) and the mother (pre-eclampsia). For this reason, using medications to achieve good symptom control and prevent exacerbations is justified even when their safety in pregnancy has not been unequivocally proven. Deleted: treatment Despite lack of evidence for adverse effects of asthma treatment in pregnancy, many women and doctors remain concerned. During labor and delivery, usual controller medications should be taken, with reliever if needed. Neonatal hypoglycemia may be seen, especially in preterm babies, when high doses of beta-agonists have been given within the last 48 hours prior to delivery. These women tend to be older, have more severe asthma, a higher body mass index, a longer duration of asthma, and a greater likelihood of aspirin exacerbated respiratory disease. They more often have dysmenorrhea, premenstrual syndrome, shorter menstrual cycles, and longer menstrual bleeding. Occupational asthma Clinical features In the occupational setting, rhinitis often precedes the development of asthma (see p9 regarding diagnosis of occupational asthma). Once a patient has become sensitized to an occupational allergen, the level of exposure necessary to induce symptoms may be extremely low; resulting exacerbations become increasingly severe, and with continued exposure, persistent symptoms and irreversible airflow limitation may result. The early identification and elimination of occupational sensitizers and the removal of sensitized patients from any further exposure are important aspects of the management of occupational asthma (Evidence A). Attempts to reduce occupational exposure have been successful, especially in industrial settings. Older patients may not report asthma symptoms, and may attribute breathlessness to normal aging or comorbidities such as cardiovascular disease and obesity. Asthma costs may be higher amongst older patients, because of higher hospitalization rates and medication costs. Side-effects of beta2-agonists such as cardiotoxicity, and corticosteroid side effects such as skin bruising, osteoporosis, and cataracts, are more common in the elderly than in younger adults. Factors such as arthritis, muscle weakness, impaired vision and inspiratory flow should be considered when choosing inhaler devices for older 3. Treating to control symptoms and minimize future risk 69 patients, 337, 339 and inhaler technique should be checked at each visit. Older patients may have difficulties with complex medication regimens, and prescribing of multiple inhaler devices should be avoided if possible. Large print versions may be needed for written information such as asthma action plans. Patients with cognitive impairment may require a carer to help them use their asthma medications. Surgery and asthma Clinical features There is no evidence of increased peri-operative risk for the general asthma population. The incidence 1 of severe peri-operative bronchospasm in people with asthma is low, but it may be life threatening. For patients requiring emergency surgery, the risks of proceeding without first achieving good asthma control should be weighed against the need for immediate surgery. More immediate intra-operative issues relating to asthma management are reviewed in detail elsewhere. It is usually accompanied by rhinorrhea, nasal obstruction, conjunctival irritation, and scarlet flush of the head and neck, and may sometimes progress to severe bronchospasm, shock, loss of consciousness, and respiratory arrest. Aspirin challenge (oral, bronchial or nasal) is the gold standard for diagnosis349, 350 as there are no reliable in vitro tests, but oral aspirin challenge tests must only be conducted in a specialized center with cardiopulmonary resuscitation capabilities because of the high risk of severe reactions. An additional option is desensitization, which may be conducted under specialist care in a clinic or hospital. Severe asthma includes patients with refractory asthma, and those in whom response to treatment of comorbidities is incomplete. Clinical features Many people with severe or difficult-to-treat asthma experience frequent or persistent asthma symptoms, frequent exacerbations, persistent loss of lung function, substantial impairment of quality of life, and troublesome comorbidities such as anxiety and depression. In patients with adult-onset asthma, smoking history is an independent risk factor for progression to severe asthma. Additional investigations that should be considered for patients suspected of having severe asthma, and additional therapies or strategies that may assist in their management, are shown in Box 3-14. When potential reasons for a lack of treatment response have been considered and addressed, a compromise level of asthma control may need to be accepted and discussed with the patient to avoid futile over-treatment (with its attendant cost and potential side-effects) (Evidence D). The objective is then to minimize exacerbations and the need for emergency medical interventions while achieving as high a level of symptom control as is feasible. In difficult-to-treat asthma, adherence and health outcomes may be improved with a comprehensive adherence-promoting intervention. Carefully controlled trials are important as a large placebo effect has been seen in studies to date. The place of these therapies and strategies in severe asthma has not been established. Response of symptoms, oxygen saturation and lung function should be reviewed after 1 hour. For management of asthma exacerbations in children 5 years and younger, see Chapter 6, p. Identifying patients at risk of asthma-related death In addition to factors known to increase the risk of asthma exacerbations (Box 2-2, p. The presence of one or more of these risk factors should be quickly identifiable in the clinical notes, and these patients should be encouraged to seek urgent medical care early in the course of an exacerbation.

    Surgery should be considered in patients who have an aortic arch a b Recommendations Class Level aneurysm with a maximal diameter 55 mm or who present symp Surgery is indicated in patients who have toms or signs of local compression arthritis relief gnc buy diclofenac 75 mg online. In cases of Marfan disease arthritis back brace generic 75mg diclofenac with visa, surgery should be preferred over gSee text in section 8 arthritis of the knee buy generic diclofenac. Therearenodatatoprovide guresandasensiblecase-by-caseapproachistheonly order to get initial stabilization as a bridge to de nitive surgical option arthritis in neck and shoulder pain discount diclofenac online amex. Its disadvantages include non-visualization between the aneurysmal and disease-free zones is not well deli of calci cations and the usual contraindications arthritis in collie dogs buy cheapest diclofenac. Several countries have may be present but should not be awaited in order to reach a diagno not implemented such a programme arthritis foundation grants cheap diclofenac 75 mg online, despite national guidelines in sis. Indeed, some doubts have been cast ination may detect a pulsatile abdominal mass, but its sensitivity is over the good results of the trials performed during the 1990s, since poor. The most appealing situation for cardiol aneurysmal sac, and may misjudge the aortic diameter. The measures addressed below will focus only on risk was more than twice as high in non-users of aspirin vs. Aftera rstimagingoftheabdominal logical stress from blood loss and uid shifts may be strong triggers aorta, those with an aorta diameter, 25 mm can be considered to be for acute ischaemic events. The pooled estimate of operative mortality rate Unites States, there was the Open Vs. Signs suggesting this condition include a large aneurysm sac, increase of aneurysm size, a thrombus and high Recommendations Classa Levelb Ref. Also, unreport populations (children and young adults, or adults) and designs (aten ed speci c alterations were revealed, some shared between the olol vs. The disease frequently involves the thoracic and abdominal Patients display altered facial features (elongated face, blepharophi aorta, the renal, mesenteric, iliac, and femoral arteries, as well as the 426 mosis and down-slanting palpebral ssures, a beaked nose, a highly vertebral and carotid arteries (extra and intra-cranial). Arteries archedpalate, and micrognathia) and various signs of a moregeneral can dissect without previous dilation and are thus unpredictable. A more recent study in families of the fragility of tissue, haemorrhagic tendency, and poor wound mostly European origin reported on adult patients, with less healing confer an added surgical risk. Prolonged post-operative moni 434 428 frequent aneurysms and a less-severe vascular phenotype. Males are more often affected than females, with follow-up, according to family history of vascular events. True bicuspid valves and unicommisural valves first-degree relatives (siblings and parents) are very rare. Therearesomeindicationsonracialdifferences molecular) is established or ruled out. Chronic chest, neck, untreated aortic dilation at the time of aortic valve replacement, the and back pain can be atypical signs of a dilated aorta. Dyspnoea, in 15-year rate of aortic surgery or complications was reported to be as spiratory stridor, and recurrent airway infection may indicate com highas86%whentheinitialaorticdiameterwas, 40 mm, 81%withdia pression of major airways. Coarctation of the aorta istypically locatedat the areaof ductus arter Recommendations for the management of aortic root iosus insertion, and occurs ectopically (ascending, descending, or ab dilation in patients with bicuspid aortic valve dominalaorta)inrarecases. Notably, despite intervention, antihypertensive extent of disease when the ascending aorta is surgically manipulated. Atherosclerotic lesions of the Intraoperative (epiaortic ultrasonography) or pre-operative diag nosis and surgical techniques such as intra-aortic lters, off-pump aorta coronary artery bypass, single aortic clamp or no clamping, and 9. Thromboemboli are usually large, and commonly occlude medium-to-large arteries, causing stroke, transient ischaemic 9. Cholesterol Aortic atheroma can be subdivided in small, moderate, and severe crystal emboli tend to occlude small arteries and arterioles, and aortic atherosclerosis, or even semi-quantitatively into four grades (Web Table 3). This condition may be No randomized trials are available to support the use of statins for either asymptomatic or present with sudden onset of intermittent patients with stroke caused by atheroembolism. Treatment may retrospective study of 519 patients with severe aortic plaque, only be bypass grafting or aorto-iliac endarterectomy. Surgery for atherothrombotic severe atherosclerosis of the aorta causes an eggshell-like appearance diseaseintheaorticarchisofahigh-risknatureandcannotberecom visualizedonchestX-ray(porcelainaorta). Off-pump coronary bypass and the im plantation of transcatheter aortic heart valves may render a solution Recommendations Classa Levelb in patients requiring, respectively, coronary bypass grafting and In the presence of aortic atherosclerosis, I C aortic valve replacement with porcelain aorta [15. The aetiology and pathogenesis are still uncertain al though it has been proposed that calci cation of a brin-platelet thrombus may result in this lesion. Aortitis thrombi of the aortic arch, only four cases presented thrombophilic states. The clinical ous antibiotics with broad antimicrobial coverage of the most likely presentation of Takayasu arteritis varies across a spectrum of symp pathological organisms (particularly Staphylococcal and gram toms and clinical signs, ranging from back or abdominal pain with negative species). In ammation-associated of the aorta thrombusformationintheaorticlumenwithperipheralembolization Primarymalignanttumoursoftheaortaareanextremelyrareclassof 528, 532 has also been reported. Leiosarcomas and brosar 541 modalities play an important role in the diagnosis and follow-up of comas originate from the media or adventitia of the aortic wall. The most characteristic and frequently reported clinical ening of the aortic wall with a uniform smooth internal surface. Competitive sports and isometric the prognosis for aortic sarcomas is poor, with metastatic disease heavy weight lifting should be discouraged, to reduce aortic wall leading to death in a short time in most patients. Long-term follow-up of aortic Beta-blockers have been seen to be associated with reduced aneur diseases ysmal degeneration of the dissected aorta and reduced incidence of late dissection-related aortic procedures in non-randomized Patients with aortic disease usually require life-long surveillance, re studies. A recent meta-analysis showed that the sensitiv exclude the presence of early complications. In an observational study alizemetallicstentstrutsandshouldthusbesupplementedbychest using Medicare data, repair of incisional hernia was required in 5. Web addenda dins; Lebanon: Lebanese Society of Cardiology, Elie Chammas; Lithuania: Lithuanian Society of Cardiology, Regina Jonkaitiene; All Web Figures and Web Tables are available in the online addenda Malta: Maltese Cardiac Society, Andrew Cassar; Norway: Norwe at. References Society of Interventional Radiology, Society of Thoracic Surgeons, and Society for Vascular Medicine. Ann Thorac Population-based outcomes of open descending thoracic aortic aneurysm repair. Fattori R, Cao P, De Rango P, Czerny M, Evangelista A, Nienaber C, Rousseau H, 16. Interdisciplinary expert consensus document on management of Noppeney T, Umscheid T, Wenk H. Impact of hospital volume and type on outcomes of canCollegeofRadiology, AmericanStrokeAssociation, SocietyofCardiovascular open and endovascular repair of descending thoracic aneurysms in the United Anesthesiologists, Society for Cardiovascular Angiography and Interventions, States Medicare population. Measurementof Quantitative determination of age-related geometric changes in the normal ab intracardiacdimensionsandstructuresinnormalyoungadultsubjectsbytranseso dominal aorta. Relationship of aortic cross the infrarenal aortic diameter in relation to age: only part of the population in sectionalareatoheightratioandtheriskofaorticdissectioninpatientswithbicus older age groups shows an increase. Ab acicaortadiameterdiagnosedby multislicecardiaccomputedtomographyinmen dominal aortic aneurysms, increasing infrarenal aortic diameter, and risk of total versuswomenandinpersonsaged23to50years, 51to65years, 66to80years, and mortality and incident cardiovascular disease events: 10-year follow-up data 81 to 88 years. A multidetector computed tomography: age and sex-speci c reference values in new ultrasonographic index using the wrist circumference as a body build refer adults without evident cardiovascular disease. Aorticsizeassessmentbynoncontrastcardiaccomputed dards for endovascular aortic aneurysm repair. Useofspiralcomputedtomog dimensional workstation is useful for measuring the correct size of abdominal raphy for the assessment of blunt trauma patients with potential aortic injury. Abdominal Aortic Aneurysm Detection and Management Veterans patients undergoing myocardial perfusion imaging. Repetitive 18F uorodeoxyglucose positron emission tomography interobserver variability in the measurements of abdominal aortic and common in giant cell arteritis: a prospective study of 35 patients. Recommendationsfor tomical variations in the branches of the human aortic arch in 633 angiographies: transoesophageal echocardiography: update 2010. Evangelista A, Aguilar R, Cuellar H, Thomas M, Laynez A, Rodriguez-Palomares J, 93. Usefulness of real-time three dictionofcardiovasculareventsall-causemortalitywithcentralhaemodynamics:a dimensional transoesophageal echocardiography in the assessment of chronic systematic review, meta-analysis. Mancia G, Fagard R, Narkiewicz K, Redon J, Zanchetti A, Bohm M, Christiaens T, 72. Abdominalaortic geal echocardiography, helical computed tomography, and magnetic resonance aneurysm expansion: risk factors and time intervals for surveillance. A Randomized Comparison of the Dose-Dependent study of incidence and mortality rates. Retrograde ascending aortic dissection during or after thoracic aortic stent graft 128. Opensurgicalrepairof2286thoracoabdominal placement: insight fromthe European registryon endovascularaortic repaircom aortic aneurysms. Cao P, De Rango P, Czerny M, Evangelista A, Fattori R, Nienaber C, Rousseau H, thoracoabdominal aneurysm repair. KhaladjN, ShresthaM, MeckS, PeterssS, KamiyaH, KallenbachK, WinterhalterM, aortic arch dissections and other arch diseases. Diagnosis of an cated by mesenteric malperfusion: observations from the International Registry eurysm of the thoracic aorta. Kaji S, Akasaka T, Horibata Y, Nishigami K, Shono H, Katayama M, Yamamuro A, aortic diseases. A decision analysis to determine a testing threshold for com patients with type a aortic intramural hematoma. Rule out of acute aortic dissection aortic dissection: image reconstruction with use of 180 degrees and 360 degrees with plasma matrix metalloproteinase 8 in the emergency department. Optimal guidance for intimal ap fenestration in aortic dissection by and Blood Flow in Aortic Aneurysm Using Tagging Cine Magnetic Resonance transvenous two-dimensional and Doppler ultrasonography. Endovascular fenestration in aortic dissection with acute malperfusion syndrome: 194. Contemporary results of surgery in acute type A aortic dissection: the Treatment of acute type a dissection by percutaneous endovascular stent-graft International Registry of Acute Aortic Dissection experience. The location of the primary entry tear in acute type B aortic dissection WeigangE. Valve-sparing aortic root repair in 30-day results of the Valiant Captivia registry. Extended total arch replacement for acute type a aortic dissection: ex raphyinthediagnosisandmanagementofacutetypeAaorticsyndrome. De nitive diagnosis of intramural hematoma of the thoracic aorta acic aorta: early and mid-term results. Evangelista A, Dominguez R, Sebastia C, Salas A, Permanyer-Miralda G, atheroscleroticulcerofthedescendingthoracicaortaandarch. Acute type A intramural hematoma: analysis of current management strat KienbaumP, PetersJ, JakobH, ErbelR, BaumgartD. Are penetrating aortic ulcers best treated using an endovas hematoma: an analysisfromthe International Registryof Acute Aortic Dissection. Re-operations on the proximal thoracic aorta: results and predictors of short and long-term mortality in a series of 174 patients. KitaiT, Kaji S, YamamuroA, Tani T, Kinoshita M, EharaN, Kobori A, Kim K, Kita T, 273. Traumatic aortic injury score ography in patients with acute aortic intramural hematoma. Penetratingathero aortic injury: a lesion associated with advancing diagnostic techniques. Endovascular repair of traumatic thoracic aortic injury: sectionsextendingintoinvolvingtheaorticroot.

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    The appearance of a blue procedural Control Line provides several forms of internal control: (1) capillary flow occurred; and (2) functional integrity of the test strip was maintained arthritis after back fusion discount diclofenac 50mg overnight delivery. If the blue procedural Control Line does not develop at 5 minutes x rays of arthritis in fingers discount diclofenac 50 mg, the test result is considered invalid arthritis diet not to eat cheap diclofenac online american express. A built-in negative control is provided by the clearing of red background color arthritis pain relief finger joints order genuine diclofenac line, verifying that the test has been performed correctly arthritis zealand purchase diclofenac amex. The result area should be white-to-light pink within 5 minutes and not interfere with interpretation of the test result rheumatoid arthritis home remedies diclofenac 75mg on-line. If background color appears which interferes with interpretation of the test result, the result is considered invalid. Should this occur, review the procedure and repeat the test with a new Test Cassette. External Quality Control External controls also may be used to demonstrate that the reagents and assay procedure perform properly. Add two drops of the Positive or Negative Control Solution to the Sample Well using a new Test Cassette; continue with the assay as described in the Test Procedure using these controls in place of a patient sample. If the Positive and Negative Controls do not perform as expected, repeat the test or contact Quidel Technical Support. Caution: Follow universal precautions when handling potentially infectious materials. The Test Cassette should not be moved until the assay is complete and ready for interpretation. Positive Result: Any shade of a pink-to-red Test Line near the letter "T" and a blue procedural Control Line near the letter "C" within 5 minutes indicates the presence of H. Negative Result: Only a blue procedural Control Line near the letter "C" at 5 minutes indicates the absence of H. Invalid Result: the test result is considered invalid if the blue procedural Control Line is not visible at 5 minutes after sample application, even if the Test Line is visible. If the result is invalid, retest using a new Test Cassette or contact Quidel Technical Support. The test should be used only to evaluate adult patients with clinical signs and symptoms suggestive of gastrointestinal disease. Performance characteristics for persons under the age of 18 have not been established with this test. A positive QuickVue result only indicates the presence of specific IgG antibodies to H. Additional follow-up testing is recommended if the QuickVue result is negative and H. The factors that lead from colonization with the organism to infection are unknown. The prevalence rate of colonization appears to be age related with 50% of adults shown to be colonized with the organism by age sixty. Eighty to 100% of individuals with signs and symptoms of other gastrointestinal conditions such as duodenal ulcers, are 10 reported to be positive for H. Serum specimens were obtained from 342 patients undergoing endoscopic examination. Three (3) specimens were equivocal and 21 were positive, indicating the presence of H. Because sampling errors may occur during biopsy due to the sporadic distribution of the bacteria in the gastric mucosa, the actual bacteria may not be sampled during biopsy, making it difficult to detect the bacterium by histology. Antibody detection tests, therefore, are more likely to determine if an infection is present, provided that the patient is not immunosuppressed and is actually producing antibodies to H. Altering the hematocrit ranging from 20 to 60% did not affect the accuracy of the test. The proficiency panel contained negative, moderate positive and high positive specimens. Each specimen level was tested a minimum of six replicates at each site over a period of three days. If outside the United States, contact your local distributor or technicalsupport@quidel. Prospective doubleblind trial of duodenal ulcer relapse after eradication of Campylobacter pylori. Effect of treatment of Helicobacter pylori infection on the long term recurrence of gastric or duodenal ulcer. Evaluation of techniques for isolation, subcultivation and preservation of Helicobacter pylori. Evaluation of a new immunodiagnostic assay for Helicobacter pylori antibody detection. Date Patient Negative Positive Test Results Lot Technician Name Procedural Procedural At 5 minutes Number Control Control and Exp. Date/Date External External Lot Number Technician Received Positive Control Negative and Exp. Patients with advanced stages of atrophic gastritis should be followed up with a Patients with chronic atrophic gastritis or intestinal meta high quality endoscopy every 3 years. Biopsies should of atrophic gastritis, and reduces the risk of gastric cancer be taken from at least two topographic sites (antrum and in patients with these conditions, and it is recommended. Moderate quality evidence, strong recommendation Working groups were set up to cover the following topics: (94% agree [94% strongly or moderately agree]). Diverse efforts have been made then sent to every participant and statements were voted to stage or classify individuals according to the severity and/or upon online. Advanced stages of atrophic gastritis statements with less than 75% agreement were excluded. For adequate stagingand grading of time diagnostic uppergastrointestinal endoscopy should include gastric precancerous conditions, at least four non-targeted biopsies of gastric biopsies bothfor Helicobacter pylori infection diagnosis and twotopographic sites (at thelesser and greater curvature, from both for identificationof advancedstages of atrophic gastritis (moderate theantrum and the corpus) should betaken and clearly labelled in qualityevidence, strongrecommendation) separate vials; additionaltarget biopsies of lesions should betaken 9 Biopsies of at least two topographic sites (fromboththe antrum andthe corpus, at the lesser andgreater curvature of each) should betakenandclearlylabelledintwo separatevials. Additional biopsies of visible neoplastic suspicious lesions shouldbe taken (moderate qualityevidence, strong recommendation) 8 Systems for histopathological staging. If these systems are used to stratify patients, additional biopsyof the incisura should be consid ered(moderate qualityevidence, weakrecommendation) 9 Serumpepsinogen levels can predict extensiveatrophic gastritis 10 In patients with low pepsinogen test levels, H. Gastric dysplasia represents the penultimate stage of the gastric carcinogenesis sequence. High quality evidence, strong recommendation (94% High grade intraepithelial neoplasia/dysplasia comprises neo agree [94% strongly or moderately agree]). Moreover, some biopsies may be negative for dys fines carcinomas that invade the lamina propria and are dis plasia in the face of a true neoplastic lesion [27]. The diagnosis of intramucosal carcinoma scopic resection specimens, concluded that the overall discre means that there is an increased risk of lymphatic invasion pancy rate was 32% [27]. However, the authors concluded that few studies High quality evidence (94% agree [94% strongly or mod addressed interobserver reliability and that there was no valida erately agree. External validation of this clas the diagnosis of gastric precancerous conditions, by guid sification in a prospective multicenter study involving five inter ing biopsy for staging atrophic and metaplastic changes national Western centers (some using near-focus and second and by helping to target neoplastic lesions. A regular and circular/oval mucosal pattern with regular thin/peripheral (body) or thick/central (antrum) vessels is highly predictive of a normal mucosa. In general, these areas of mucosa alternate with areas of normal but atrophic mucosa. Irregular vessels and glands (upper panel, high grade dysplasia lesion), or absent glands with complete architectural loss of the mucosal and vascular pattern (lower panel, intramucosal adenocarcinoma) predict neoplastic changes of the mucosa. More biopsies will allow better stag such as i-Scan digital contrast and flexible spectral imaging col ing. This is used to support an additional microscopy, endocytoscopy, Raman spectroscopy, and polari biopsy of the incisura. The updated Sydney system is the most metry, may have a future role but at this stage cannot be re widely accepted protocol for the classification and grading of commended for routine clinical use [59]. It recommends at least five biopsies: two from the an trum (from the greater and lesser curvature, 3cm from the py 4. However, the need to sample tions, a first-time diagnostic upper gastrointestinal the incisura was based mostly on the notion that atrophic/me endoscopy should include gastric biopsies both for taplastic changes appear first in the incisura even though there H. Additional biopsies of visible neoplastic three studies (two European studies including nonselected po suspicious lesions should be taken. All found that the incisura biopsy increased the propor (94% agree [82% strongly or moderately agree]). Another European used to stratify patients, additional biopsy of the incisura study evaluated classification systems in a high risk population should be considered. In fact, these are therefore recommend a minimum of two biopsies from the an widely accepted cutoff values for gastric cancer screening in trum and two biopsies from the corpus, noting that adding an Japan [76]. However, they note that there was great this additional biopsy will allow more precise evaluation of heterogeneity between studies. In fact, different methods may be corpus mucosa can be easily distinguished in the absence of se used for pepsinogen quantification and results may differ be vere atrophic changes, use of a single vial cannot be recom tween tests [77]. Future studies should evaluate specific ular assay should be used, and cannot be generalized to all as scenarios when antrum, incisura, and corpus samples can be says. In a Moderate quality evidence, strong recommendation 2014 cohort of 4655 patients followed up for 16 years, there (88% agree [76% strongly or moderately agree]). In this meta-analysis, the summary sensitivity these tests is not sufficient and further studies are required be and summary specificity for gastric cancer diagnosis were 0. In conclusion, pepsinogen serum levels are currently the Corresponding values for atrophic gastritis diagnosis were 0. A systematic review and meta there are no studies addressing the clinical usefulness of geno analysis reported that approximately 10% of the patients with typing H. The rate of missed lesions of the gastric mucosa, leading to mucosal atrophy and pro tended to be higher in primary care and screening settings than gression to cancer. A recent Swedish study, that to the best of our knowl edge is the largest follow-up study to date among patients with gastric precancerous conditions, suggested a lower risk of gastric cancer for patients with dysplasia. However, they excluded the first 2 years of follow-up and concluded that this might be the reason for the lower risk of gastric cancer since many lesions might have been there already [110]. Another study found that reassessment of indefinite for dys plasia biopsies by three expert gastrointestinal pathologists Pimentel-Nunes Pedro et al. If a lesion is seen and the endoscopic assessment sug gests dysplasia, we recommend resection without need of fur ther biopsies. With the above considerations in mind, patients with a diag nosis of indefinite for dysplasia/neoplasia or of dysplasia/intra mucosal carcinoma in random biopsies. An Italian prospective study found a significantly increased risk Pimentel-Nunes Pedro et al. For these reasons, when reported, atrophy were significantly more frequent in gastric cancer pa this information can have prognostic value and can aid in the tients [118]. Another study using endoscopic grading of atro selection of patients for surveillance. A Korean study reported that some kind of familial aggregation occurs in 10% of cases [128]. It is believed that this familial clustering of endoscopic atrophy were also identified as independent risk gastric cancer is due to an inherited genetic susceptibility, factors in a prospective Korean study with follow-up >3 years shared environmental or lifestyle factors, shared susceptibility [121]. Interestingly, it showed that a second tion and precancerous conditions/lesions, as well as an in endoscopic surveillance with biopsies can have significant creased risk for gastric cancer. However, additional studies are required before subtyping can be routinely recommended. If expert revision does not confirm the diagnosis of dysplasia then the patient may be released from intensive follow-up. In sum, there is a significantly higher risk of progression to targeted biopsies and restaging, if this was not previously done. We thus recommend (based on expert opinion) 3 years in patients at higher risk for gastric cancer. However, the cost-effectiveness of a 2-year many patients included in these studies may have had low vita interval for every patient may not be ideal and the evidence is min B12 serum levels because of conditions other than auto not strong enough to change the recommended 3-year surveil immune gastritis. Nevertheless, there is no recommen gree family history of gastric cancer, may benefit from a tighter ded follow-up interval to date. These Since the largest excess risk of gastric cancer incidence recommendations do not apply to hereditary/familial diffuse among patients with pernicious anemia has been found during gastric cancer, for which there are specific guidelines [134]. One study [147] performed follow-up gastroscopies Low quality evidence, weak recommendation (82% agree 3 years after primary screening examination of 56 patients and [76% strongly or moderately agree]). Another study [142] followed up a group of 27 patients for 6 to 7 years after Autoimmune gastritis is a chronic progressive inflammatory initial investigation. None of the patients had developed gastric condition that results in the replacement of the parietal cell cancer since the initial endoscopy and the distribution of dys mass by atrophic and metaplastic mucosa, leading to a corpus plasia was virtually unchanged. Both gastric carcinoma and neuroendocrine tumors or 48-month follow-up interval [148]. No gastric cancer was are the most dreaded long-standing complications of perni found in either group, but a patient from the 48-month group cious anemia. Individuals with pernicious anemia year intervals in patients with autoimmune gastritis. However, the diagnosis of auto immune gastritis in this study was rather flawed as it was solely 6. A Swedish study followed 21 265 patients with per duces the risk of gastric cancer in patients with nicious anemia for an average of 7. These patients nonatrophic and atrophic gastritis, and, therefore, it is had a significant excess risk for gastric cancer distal to the car recommended in patients with these conditions. High quality evidence, strong recommendation (87% the excess risks increased with increasing follow-up duration.

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    Those involved should be clear about their own roles and should ensure that the woman is carefully guided along a planned care pathway by fully briefed and supportive staff (section 6) arthritis in the knee bone on bone discount 75mg diclofenac amex. All staff involved in the care of a woman or couple facing a possible termination of pregnancy must adopt a non-directive rheumatoid arthritis physical therapy order diclofenac 50 mg without a prescription, non-judgemental and supportive approach (section 6) arthritis medication with coumadin order diclofenac 75mg without prescription. It should not be assumed that arthritis in dogs and incontinence buy diclofenac 100mg visa, even in the presence of an obviously fatal fetal condition such as anencephaly arthritis in feet after pregnancy purchase line diclofenac, a woman will choose to have a termination rheumatoid arthritis in fingers and toes purchase generic diclofenac canada. A decision to decline the offer of termination must be fully supported (section 6). Live birth following termination of pregnancy before 21+6 weeks of gestation is very uncommon. Nevertheless, women and their partners should be counselled about this unlikely possibility and staff should be trained to deal with this eventuality (section 8). Live birth becomes increasingly common after 22 weeks of gestation and, when a decision has been reached to terminate the pregnancy for a fetal abnormality after 21+6 weeks, feticide should be routinely offered. Where the fetal abnormality is not compatible with survival, termination of pregnancy without prior feticide may be preferred by some women. In such cases, the delivery management should be discussed and planned with the parents and all health professionals involved and a written care plan agreed before the termination takes place (section 8). Where the fetal abnormality is not lethal and termination of pregnancy is being under taken after 21+6 weeks of gestation, failure to perform feticide could result in live birth and survival, an outcome that contradicts the intention of the abortion. A fetus born alive with abnormalities incompatible with life should be managed to maintain comfort and dignity during terminal care (section 8). After a termination for fetal abnormality, well-organised follow-up care is essential (section 6). The Working Party recognises the need for the National Health Service Fetal Anomaly Screening Programmes to be linked to databases that enable detection rates of specific congenital abnormalities to be monitored and the impact of the programmes to be evaluated. An appropriately funded and centrally coordinated system of congenital anomaly x ascertainment that covers all parts of the country is essential (section 4). Outcome data on children born with specific abnormalities are required to provide better information on natural history and prognosis. The Working Party recommends that the envisaged 2-year data collection for preterm infants should be expanded to collect outcome data for infants with abnormalities (section 4). Abortion statistics for England and Wales for 2008 report that 124 terminations for fetal anomalies (Ground E) were performed of pregnancies over 24 weeks of gestation. As numbers in most categories of abnormality were fewer than ten, the nature of the abnor malities is not disclosed and trends or patterns in termination cannot be determined. We recommend that such information is published in the Department of Health Abortion Statistics on a 3 and 6-year cycle (section 4). Introduction the Working Party was set up by the Royal College of Obstetricians and Gynaecologists in 2008 to produce updated guidance on the termination of pregnancy for fetal abnormality, taking into account changes that have occurred since the College report of 1996. The report is also designed to help staff to provide appropriate care both for those women who elect to have an abortion as well as those who decide not to have the pregnancy terminated. Over the 13 years since the last guidance was issued, there has been a range of developments in the detection and treatment of congenital abnormalities that has resulted in earlier diagnosis and clearer indications for the offer of termination of pregnancy. Data from improved imaging with follow-up of specific abnormalities has allowed a better understanding of the natural history of many fetal abnormalities and has resulted in a more accurate assessment of prognosis and better informed counselling. In addition, screening is now an integral part of routine antenatal care and most women accept the offer of screening. This has resulted in the development of clear auditable standards for fetal anomaly screening and better access for women. Of the total number of terminations, around 1% (1988) were performed under Section 1(1)(d), known as Ground E, of the Abortion Act (see section 2 of this report), namely that there was a substantial risk that, if the child were born, it would suffer physical or mental abnormalities that would result in serious handicap. However, despite improved antenatal screening programmes to detect fetal anomalies, there has been little change in the number of abortions carried out under Ground E over the past 5 years. In 2008, for residents of England and Wales, 1308 of the 1988 (66%) terminations of pregnancy for fetal abnormality were performed before 20 weeks of gestation; 309 (16%) were carried out in the first 12 weeks. About one-third (37%) of pregnancies terminated under Ground E were reported to be for chromosomal abnormalities. Trisomy 21 (Down syndrome) was the most common reported chromosomal abnormality and accounted for 22% of all Ground E cases. Structural abnor malities accounted for 48% of terminations in this group; most were for nervous system (24%) and musculoskeletal system abnormalities (7%). Structural abnormalities constitute a major cause of mortality, accounting for about 23% of neonatal deaths and 16% of stillbirths in 2006. Of these, 28 were for trisomy 21, 86 for other chromosomal anomalies and 38 for neural tube defects and other abnormalities. Legal status of termination of pregnancy the law governing termination of pregnancy by doctors is found in four different Acts of Parliament: G the Offences Against the Person Act 1861 G the Infant Life (Preservation) Act 1929 G the Abortion Act 1967 G the Human Fertilisation and Embryology Act 1990. The Offences Against the Person Act 1861, Section 58, prohibits the unlawful medical or surgical induction of a miscarriage. Compliance with the provisions of the Abortion Act 1967 in effect creates a series of defences to the Offences Against the Person Act and the Infant Life (Preservation) Act. This includes the legal requirement that a pregnancy can only be terminated by a registered medical practi tioner where two registered medical practitioners are of the opinion, formed in good faith, (except in an emergency) that one of the stipulated grounds is met. It intro duced a time limit on most abortions of 24 weeks of gestation but permitted termination at any gestation on grounds of serious fetal anomaly. The ground that there is substantial risk that if the child were born it would suffer from such physical or mental abnormalities as to be seriously handicapped is known as Ground E in practice and is referred to as Ground E in this report. The Act draws a distinction between pregnancies of up to 24 weeks and those of later gestation. Pregnancies of up to 24 weeks of gestation can be terminated under Section 1(1)(a), since many doctors believe in good faith that the continuation of any pregnancy that a woman wishes to terminate involves a greater risk to her physical and mental health than its termination. Thus, up to 24 weeks, doctors dealing with fetal abnormality have the option of choosing either 1(1)(a) or 1(1)(d). A pregnancy may be terminated at any stage for fetal abnormality under Section 1(1)(d) (Ground E), which specifies that there is a substantial risk that if the child was born it would suffer from such physical and mental abnormalities as to be severely handicapped. What constitutes substantial risk and severe handicap is clearly germane to decisions about termination of pregnancy after 24 completed weeks of gestation. As discussed below, there is no legal definition of substantial risk or severe handicap. Two practitioners believe in good faith Each of the grounds for termination of pregnancy has to be believed by two medical practi tioners in good faith and, if challenged, they would have to be able to persuade the court that their belief is honestly held. There has only been one prosecution of a doctor found not to hold a belief in good faith under the Abortion Act (R v. He was convicted on the grounds that he had not in good faith attempted to balance the risks of pregnancy and termination. A medical view put forward in evidence by one or more doctors is no substitute for the verdict of the jury. The legality of the procedure depends upon both doctors holding the belief in good faith. Thus, if it turns out that one of the two did not hold the requisite belief, the whole procedure will have been unlawful. In such cases, the termination would be unlawful and thereby would expose those participating in the termination to criminal prosecution. Selective feticide the law on selective feticide for a woman carrying more than one fetus was obscure until 1990, since the procedure involved the demise of a fetus but the woman remained pregnant. The Abortion Act now provides that the procedure must be treated as an abortion, so that it will be lawful only if one of the four statutory grounds is satisfied. Most specialists in this area believe that the continuation of multiple pregnancies could involve a greater risk to the woman than the termination of one of the fetuses and Ground 1(1)(a) is usually relied upon in pregnancies of under 24 weeks of gestation. A fetus that is born alive after termination of pregnancy is deemed to be a child, irrespective of the gestational age at birth, and should be registered as a live birth. Thus, before deciding on the means of terminating the pregnancy, it is important to define whether the fetus will be born alive; in practice, this means that doctors have to distinguish those capable of being born alive. In law, a child is born alive when it is capable of maintaining an existence independent of its mother. If it is anticipated that the fetus may die during the delivery process or that the child may die as a result of an abnormality that is incompatible with survival, some parents may request delivery without feticide. As a result, a child may be born alive and subsequently die after it has achieved a life of its own. In such situations, termination of pregnancy should only be undertaken after careful discussion between attending obstetric, midwifery and neonatal staff and the woman and her family, with all parties agreeing a written care plan before the termi nation takes place. When a child dies following termination, the question arises as to whether a prosecution could be brought for murder or manslaughter. There is no binding authority on this point and there is nothing in the Abortion Act authorising the destruction of the child. If the child is born alive, there is little doubt that, whatever the intention of those who brought 6 about its premature delivery and whatever the wishes of the woman or the doctor inducing delivery, the fetus becomes entitled to the legal protection available to any other child. This moment of transition alters the moral and legal status of the fetus/child and has been considered carefully in the Nuffield Council on Bioethics Working Group Report entitled Critical Care Decisions in the Fetus and Newborn. This applies equally to situations when a child is born with or without a serious congenital abnormality, such as one of sufficient seriousness to lead to termination. These recommendations have recently been considered and adopted in the development of a professional framework for care. Guidelines are in preparation for the conduct of perinatal palliative care in such situations (British Association of Perinatal Medicine). Where this is likely to happen, there should be careful discussion between attending obstetric, midwifery and neonatal staff and the woman and her family. Before the termination takes place, all parties should agree a written care plan and, in such situations, the Working Party believes that all parties act from their firm belief and in good faith within the terms of the Abortion Act. A more difficult situation arises when the termination results in a liveborn child suffering from a condition for which the outcome is predicted to be very poor but for whom survival is likely in the first instance. Such children should receive the neonatal support, including resuscitation, and intensive care that is in their best interests, as judged by the criteria usually applied to their condition. Events taking place before birth are unlikely to be relevant to the determi nation of their best interests. Once a child is established in neonatal care, the situations in which the neonatal team would consider offering discontinuation of neonatal supportive care are described within the Royal College of Paediatrics and Child Health document, Withholding or Withdrawing Life Sustaining Treatment in Children: A Framework for Practice. Although the child may be able to survive with treatment, the degree of physical or mental impairment will be so great that it is unreasonable to expect them to bear it. The child and/or family feels that, in the face of progressive and irreversible illness, further treatment is more than can be borne. They wish to have a particular treatment withdrawn or to refuse further treatment, irrespective of the medical opinion that it may be of some benefit. The amended Abortion Act sets out the legal framework within which an abortion may be legally carried out and, in effect, creates a series of defences to prosecution under the former two Acts. G What constitutes a serious handicap becomes a particular issue for doctors when termi nation of pregnancy is likely to take place after 24 weeks of gestation, when abortion is no longer lawful under Ground 1(1)(a) of the Abortion Act. G Termination for fetal abnormality will only be lawful when two registered medical practi tioners are of the opinion, formed in good faith, that the grounds for termination of pregnancy are met; in the final analysis a jury would have to determine that these beliefs are appropriate on the totality of the evidence. G A fetus born alive after termination for a fetal abnormality is deemed to be a child and must be treated in his or her best interests and managed within published guidance for neonatal practice. A fetus born alive with abnormalities incompatible with long-term survival should be managed to maintain comfort and dignity during terminal care. Definition of substantial risk and serious handicap When a fetal abnormality has been detected, the pregnancy can be terminated before 24 weeks of gestation under Ground 1(1)(a) of the Abortion Act but after 24 weeks of gestation it can only be carried out if there is a substantial risk that the child if born would be seriously handi capped. Thus, much of the discussion around late termination of pregnancy for fetal anomalies has focussed on what constitutes a substantial risk of serious handicap. Whether a risk is substantial depends upon factors such as the nature and severity of the condition and the timing of diagnosis, as well as the likelihood of the event occurring. It has been argued that, since neither substantial risk nor serious handicap is defined, each can be interpreted on a largely subjective basis.

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