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For those charged with resolving the larger conflict, the situation is significantly complicated by the fact that the many different actors have different agendas, that alliances remain fluid and unpredictable, that each country and faction has its own specific interests, and yet that the actions of one inevitably influence others. All these remarkable developments have profoundly complicated the attainment of stability and peace in central Africa. This is well known to include several of the countries centrally involved in the war. Diamonds and gold are also an irresistible lure for mafia-like gangs to make sure the turmoil in the Congo continues in perpetuity. Behind these rogue gangs are often found foreign patrons, some of them legitimate corporations, others more shadowy enterprises, and quietly behind them can be found foreign governments watching out for the interests of their citizens. One academic has urged that more attention be paid to "which multinationals are also placing bets on one faction or another. Congo has few means to repay its $15 billion in external debt, while its remarkable potential development of mineral and non-mineral natural resources, hydroelectric power, and uncultivated arable land goes completely unfulfilled. There should be no misunderstanding of the central historic responsibility of the international community in perpetuating this state of affairs. King Leopold actively pillaged the Congo for its rubber, leading to the deaths of half of its 20 million inhabitants. Theseemingly intractable problem of arms proliferation has continued to grow in recent years, as the International Commission of Inquiry on Rwanda found in 1998. In the report presented to our Panel when he met with us, Commission Chair Mahmoud Kassem stated that, "The uncontrolled illicit flow of arms into Africa fuels conflicts, fortifies extremism and destabilizes the entire conflict. It is clear that many of the arms consignments bound for the Great Lakes Region are intended for. This multitude of rebel groups are inter-linked with an open channel of arms among themselves organized either by outside elements or their own military leaders. Thisconnection has weakened the effectiveness of the two embargoes imposed by the Security Council. There are clear indications that easy access to weapons is also encouraging militant political groups to consider armed rather thandemocratic opposition. As the title suggests, the authors are highly critical of the American role in Africa. When Kabila took power, the Clinton Administration quickly offered military support bydeveloping a plan for new training operations with the armed forces. Within six days of the outbreak of war between Uganda and Rwanda and the Kabila government in August 1998, other African leaders initiated efforts to broker a peace. For the next 10 months Summits took place virtually monthly at both the Ministerialand Presidential levels. And the many violations of the cease-fire ever since is testament to the even greater difficulty of implementing it, as everyone involved well knows. Nevertheless, it is unthinkable for the future of Africa that the accord not eventually be enforced. The agreement contained four main components reflecting the national, regional, and international dimensions of the conflict: 1. The role of these peacemakers is to disarm the militias and supervise the withdrawal of foreign troops. War criminals are to be handed over to the International Criminal Tribunal for Rwanda in Arusha. None of these groups were part of the peace accord or have signed it; all are associated with one or another of the signing governments. Assuming optimistically that the signatory governments abide by a cease-fire, disarming these rebel groups is obviously the key to the future. It will be no easy task, not least because of the vast proliferation of weapons in the region that we have already discussed. This does not give us reason to be optimistic about the will of the international community to take the central African conflict seriously. Beyond that, in order to attain and enforce peace from the Sudanese to the Zambian borders and from the Congo-Brazzaville to the Tanzania borders, studies estimate that 100,000 fully armed soldiers would be required. And if the job is not done now, it is frightening to contemplate the possible consequences. Each of these failures led predictably to the next disaster, just as we can confidently predict that another failure to act decisively in the near future will bring greater turmoil and suffering. This surely creates some kind of inescapable obligation on the part of those countries who have helped create the present situation.

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Historically, moderate-to-severe hearing loss in young children was not detected until well beyond the newborn period, and it was not unusual for diagnosis of milder hearing loss and unilateral hearing loss to be delayed until school age. Surgeon General, on learning of new technology, encouraged that detection of hearing loss be included in the Healthy People 2000 goals for the nation (U. The Healthy People 2010 goals included an objective to "increase the proportion of newborns who are screened for hearing loss by one month, have audiologic evaluation by 3 months, and are enrolled in appropriate intervention services by 6 months" (U. By 2005, every state had implemented a newborn hearing-screening program, and approximately 95% of newborn infants in the United States were screened for hearing loss before hospital discharge. There is a growing body of literature indicating that when identification and intervention occur no later than 6 months of age for newborn infants who are deaf or hard of hearing, the infants perform as much as 20 to 40 percentile points higher on school-related measures (vocabulary, articulation, intelligibility, social adjustment, and behavior; Yoshinaga-Itano, 1995, 2004; Yoshinaga-Itano, Coulter, & Thomson, 2000; Yoshinaga-Itano, Sedey, Coulter, & Mehl, 1998). Despite the fact that approximately 95% of newborn infants have their hearing screened in the United States, almost half of newborn infants who do not pass the initial screening fail to have appropriate follow-up to confirm the presence of a hearing loss and/or initiate appropriate early intervention services. Available data indicate that a significant number of children who need further assessment do not receive appropriate followup evaluations. Principles All children with hearing loss should have access to resources necessary to reach their maximum potential. All infants should have access to hearing screening using a physiologic measure no later than 1 month of age. All infants who do not pass the initial hearing screening and the subsequent rescreening should have appropriate audiologic and medical evaluations to confirm the presence of hearing loss no later than 3 months of age. All infants with confirmed permanent hearing loss should receive early intervention services as soon as possible after diagnosis but no later than 6 months of age. A simplified, single point of entry into an intervention system appropriate for children with hearing loss is optimal. Families should have access to information about all intervention and treatment options and counseling regarding hearing loss. The child and family should have immediate access to high-quality technology, including hearing aids, cochlear implants, and other assistive devices when appropriate. Continued assessment of communication development should be provided by appropriate professionals to all children with or without risk indicators for hearing loss. Appropriate interdisciplinary intervention programs for infants with hearing loss and their families should be provided by professionals knowledgeable about childhood hearing loss. Intervention programs should recognize and build on strengths, informed choices, traditions, and cultural beliefs of the families. Studies have demonstrated that current screening technologies are effective in identifying hearing loss of moderate 5 Year 2007 Position Statement: Principles and Guidelines for Early Hearing Detection and Intervention Programs Position statement and greater degree (Norton et al. In addition, studies of children with permanent hearing loss indicate that moderate or greater degrees of hearing loss can have significant effects on language, speech, academic, and social-emotional development (Carney & Moeller, 1998). Recent evidence suggests, however, that current hearing screening technologies fail to identify some infants with mild forms of hearing loss (Cone-Wesson et al. All infants, regardless of newborn hearing screening outcome, should receive ongoing monitoring for development of age-appropriate auditory behaviors and communication skills. Any infant who demonstrates delayed auditory and/or communication skills development, even if he or she passed newborn hearing screening, should receive audiologic evaluation to rule out hearing loss. The roles and responsibilities of each team member should be well defined and clearly understood. Essential team members are the birth hospital, families, pediatricians or primary health care professionals. Additional services including genetics, ophthalmology, developmental pediatrics, service coordination, supportive family education, and counseling should be available (Calderon, Bargones, & Sidman, 1998). From this foundation, families usually develop an urgent desire to understand and meet the special needs of their infant. Families gain knowledge, insight, and experience by accessing resources and through participation in scheduled early intervention appointments including audiologic, medical, habilitative, and educational sessions. Informed family choices and desired outcomes guide all decisions for these children. The transfer of responsibilities from families to their child develops gradually and increases as their child matures, growing in independence and selfadvocacy. A medical home is defined as an approach to providing health care services where care is accessible, family centered, continuous, comprehensive, coordinated, compassionate, and culturally competent. The primary health care professional acts in partnership with parents in a medical home to identify and access appropriate audiology, intervention, and consultative services needed to develop a global plan of appropriate and necessary health and habilitative care for infants identified with hearing loss and infants with risk factors for hearing loss. An audiologist is a person who, by virtue of academic degree, clinical training, and license to practice, is qualified to provide services related to the prevention of hearing loss and the audiologic diagnosis, identification, assessment, and nonmedical and nonsurgical treatment of persons with impairment of auditory and vestibular function, and to the prevention of impairments associated with them.

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These photoisomers can be excreted into the bile without conjugation to glucuronic acid. Determination of bilirubin concentration: Bilirubin is commonly measured by the van den Bergh reaction, in which diazotized sulfanilic acid reacts with bilirubin to form red azodipyrroles that are measured colorimetrically. Catecholamines Dopamine, norepinephrine, and epinephrine are biologically active (biogenic) amines that are collectively termed catecholamines. Dopamine and norepinephrine are synthesized in the brain and function as neurotransmitters. Norepinephrine and epinephrine are released from storage vesicles in the adrenal medulla in response to fright, exercise, cold, and low levels of blood glucose. They increase the degradation of glycogen and triacylglycerol as well as increase blood pressure and the output of the heart. These effects are part of a coordinated response to prepare the individual for stress, and are often called the "fight-or-flight" reactions. Synthesis: the catecholamines are synthesized from tyrosine, as shown in Figure 21. Parkinson disease, a neurodegenerative movement disorder, is due to insufficient dopamine production as a result of the idiopathic loss of dopamineproducing cells in the brain. In the neuron, this enzyme oxidatively deaminates and inactivates any excess neurotransmitter molecules (norepinephrine, dopamine, or serotonin) that may leak out of synaptic vesicles when the neuron is at rest. This causes activation of norepinephrine and serotonin receptors and may be responsible for the antidepressant action of these drugs. Histamine Histamine is a chemical messenger that mediates a wide range of cellular responses, including allergic and inflammatory reactions and gastric acid secretion. Histamine has no clinical applications, but agents that interfere with the action of histamine have important therapeutic applications. Serotonin has multiple physiologic roles including pain perception, regulation of sleep, appetite, temperature, blood pressure, cognitive functions, and mood (causes a feeling of well-being). Creatine Creatine phosphate (also called phosphocreatine), the phosphorylated derivative of creatine found in muscle, is a high-energy compound that provides a small but rapidly mobilized reserve of high-energy phosphates that can be reversibly transferred to adenosine diphosphate (Figure 21. Degradation: Creatine and creatine phosphate spontaneously cyclize at a slow but constant rate to form creatinine, which is excreted in the urine. The amount excreted is proportional to the total creatine phosphate content of the body and, therefore, can be used to estimate muscle mass. When muscle mass decreases for any reason (for example, from paralysis or muscular dystrophy), the creatinine content of the urine falls. In addition, any rise in blood creatinine is a sensitive indicator of kidney malfunction, because creatinine normally is rapidly removed from the blood and excreted. Melanin Melanin is a pigment that occurs in several tissues, particularly the eye, hair, and skin. It is synthesized from tyrosine in melanocytes (pigment-forming cells) of the epidermis. The major sites of heme biosynthesis are the liver, which synthesizes a number of heme proteins (particularly cytochrome P450 enzymes), and the erythrocyte-producing cells of the bone marrow, which are active in hemoglobin synthesis. In the liver, the rate of heme synthesis is highly variable, responding to alterations in the cellular heme pool caused by fluctuating demands for hemeproteins. In contrast, heme synthesis in erythroid cells is relatively constant and is matched to the rate of globin synthesis. Porphyrias are caused by inherited (primarily autosomal-dominant) or acquired defects in heme synthesis, resulting in the accumulation and increased excretion of porphyrins or porphyrin precursors. Enzymic defects early in the pathway cause abdominal pain and neuropsychiatric symptoms, whereas later defects cause photosensitivity. Degradation of hemeproteins occurs in the reticuloendothelial system, particularly in the liver and spleen. The first step in the degradation of heme is the production by heme oxygenase of the green pigment biliverdin, which is subsequently reduced to bilirubin. Bilirubin is transported to the liver, where its solubility is increased by the addition of two molecules of glucuronic acid.

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As discussed further below, severe hypoglycemia is a potent marker of high absolute risk of cardiovascular events and mortality (38). Providers should be vigilant in preventing hypoglycemia and should not aggressively attempt to achieve near-normal A1C levels in patients in whom such targets cannot be safely and reasonably achieved. Setting and Modifying A1C Goals Numerous factors must be considered when setting glycemic targets. Glycemic targets must be individualized in the context of shared decision making to address the needs and preferences of each patient and the individual characteristics that influence risks and benefits of therapy for each patient. Less stringent control (A1C up to 8% [64 mmol/mol]) may be recommended if the life expectancy of the patient is such that the benefits of an intensive goal may not be realized, or if the risks and burdens outweigh the potential benefits. Severe or frequent hypoglycemia is an absolute indication for the modification of treatment regimens, including setting higher glycemic goals. Thus, a goal that might be appropriate for an individual early in the course of the disease may change over time. Newly diagnosed patients and/or those without comorbidities that limit life expectancy may benefit from intensive control proven to prevent microvascular complications. Thus, a finite period of intensive control to near-normal A1C may yield enduring benefits even if control is subsequently deintensified as patient characteristics change. Over time, comorbidities may emerge, decreasing life expectancy and the potential to reap benefits from intensive control. Also, with longer duration of disease, diabetes may become more difficult to control, with increasing risks and burdens of therapy. Thus, A1C targets should be reevaluated over time to balance the risks and benefits as patient factors change. The recommendations include blood glucose levels that appear to correlate with achievement of an A1C of,7% (53 mmol/mol). Elevated postchallenge (2-h oral glucose tolerance test) glucose values have been associated with increased cardiovascular risk independent of fasting plasma glucose in some epidemiologic studies, but intervention trials have not shown postprandial glucose to be a cardiovascular risk factor independent of A1C. In subjects with diabetes, surrogate measures of vascular pathology, such as endothelial dysfunction, are negatively affected by postprandial hyperglycemia. It is clear that postprandial hyperglycemia, like preprandial hyperglycemia, contributes to elevated A1C levels, with its relative contribution being greater at A1C levels that are closer to 7% (53 mmol/mol). Therefore, it is reasonable for postprandial testing to be recommended for individuals who have premeal glucose values within target but have A1C values above target. These findings support that premeal glucose targets may be relaxed without undermining overall glycemic control as measured by A1C. Postprandial glucose may be targeted if A1C goals are not met despite reaching preprandial glucose goals. Caregivers, school personnel, or family members of these individuals should know where it is and when and how to administer it. B Hypoglycemia is the major limiting factor in the glycemic management of type 1 and type 2 diabetes. Recommendations regarding the classification of hypoglycemia are outlined in Table 6. Level 1 hypoglycemia is defined as a measurable glucose concentration,70 mg/dL (3. Because many people with diabetes demonstrate impaired counterregulatory responses to hypoglycemia and/or experience hypoglycemia unawareness, a measured glucose level,70 mg/dL (3. Lastly, level 3 hypoglycemia is defined as a severe event characterized by altered mental and/or physical functioning that requires assistance from another person for recovery. Studies of rates of level 3 hypoglycemia that rely on claims data for hospitalization, emergency department visits, and ambulance use substantially underestimate rates of level 3 hypoglycemia (45), yet find high burden of hypoglycemia in adults over 60 years of age in the community (46).