Joshua Augustine, MD
- Associate Professor of Medicine
- Cleveland Clinic Lerner College of Medicine Cleveland Clinic Cleveland, Ohio
The of the musculature of the outer third of the continued on next page vagina interfere with sexual intercourse depression symptoms duration buy aripiprazola with paypal. Our marriage is suffering and it feels like a deep chasm is growing between us as sex has become impossible economic depression definition recession purchase 10 mg aripiprazola amex. The sexual dysfunctions are based on the lock-step depression test daily mail purchase 20mg aripiprazola with amex, sequential progression in Masters and Johnsons model of the sexual response cycle depression symptoms nz aripiprazola 15mg discount. However bipolar depression in children and teens aripiprazola 10mg with visa, this may not be the best model for understanding sexual dysfunctions in women depression kills libido cheap aripiprazola 10mg with amex. In this alternative model for females, emotional and physical satisfaction may include orgasm, although not all women need to have an orgasm to feel satised. The cycle starts with sexual neutrality: not feeling very sexual, Sexual neutrality but with an openness to seek or be receptive to sexual Emotional and stimuli. In turn, such sexual stimuli may, depending on physical neurological (and other biological), psychological, and satisfaction seeks or is receptive to social factors operating at that moment, lead to sexual arousal, which in turn leads to a sense of desire and further arousal. The desire creates positive feedback loops that lead to heightened arousal, which Sexual stimuli then leads to emotional and physical satisfaction. This Sexual desire satisfaction in turn produces a sense of emotional and arousal intimacy with her partner, making her more likely to be neurological (and receptive to or seek out sexual stimuli in the future. She other biological), may also feel spontaneous sexual desire, which leads to psychological, positive feedback loops among the rst three phases. Sexual activity that does not end in orgasm is implicitly considered not satisfying (Kleinplatz, 2001). Nevertheless, as noted above, some women feel satised even without having an orgasm. Critics note that the norm promoted by American culture is that of an adolescent male, ever ready for Gender and Sexual Disorders 505 sexual encounters, and able to have erections on demand (Kleinplatz, 2001). The criteria do not include any specic duration; people with symptoms that are transient, perhaps as a result of the aftereffects of surgery or a difficult time in a relationship, are grouped together with people whose symptoms are chronic (Balo, Segraves, & Clayton, 2007). Hypoactive sexual desire disorder in particular has been criticized on several grounds (Basson, 2001). First, it is left to the clinician to determine whether desire is sufficiently lacking (accounting for the individuals age and the context of the problem), and clinicians from diverse cultural and religious or spiritual backgrounds differ in their assessments. In fact, diminished sexual desire may be an appropriate response to a relationship that isnt functioning well (Basson et al. Finally, different types of problems with desire (such as lifelong versus acquired or situational versus generalized) may require different treatments. Many researchers in the eld believe that dyspareunia should not be considered a sexual disorder, but rather a type of pain disorder (Binik, 2005; Binik et al. Understanding Sexual Dysfunctions In a sense, we can view Lauras lack of sexual desire as being related, at least in part, to Mikes sexual difficulties: As Mike pulled back from Laura, Lauras desire for sexual intimacy with Mike waned. Sexuality and any problems related to it develop through feedback loops among neurological (and other biological), psychological, and social factors. Neurological and Other Biological Factors In this section, we rst consider how disease, illness, surgery, and medication can, directly and indirectly, disrupt normal sexuality. We then turn to the effects of normal aging, which can produce sexual difficulties. Sexual Side Effects: Disease, Illness, Surgery, and Medication Disease or illness can produce sexual dysfunction directly, as occurs with prostate cancer or cervical cancer. In addition, surgery can lead to sexual problems: Half of women who survive major surgeries for gynecological-related cancer develop sexual difficulties that do not become better over time (Andersen, Andersen, & DeProsse, Prolonged bike riding can sometimes crush the 1989). Disease or illness can also cause side effects of sexual dysfunction indirectly, as occurs with diabetes or circulation problems that limit blood ow to genital areas. Some physical problems can lead to sexual problems even more indirectly: People N who have had a heart attack may be afraid to engage in sexual activity for fear that P S it will bring on another attack. Aging Researchers have found that normal aging can affect sexual functioning among older people (George & Weiler, 1981). For instance, as weve seen, older women often have a vaginal lubrication problem that arise with menopause; when the lubrication problem is not addressed (for instance, with an over-the-counter lubricant such as Astroglide or K-Y Jelly), the dryness can cause intercourse to be painful and lead to dyspareunia. In addition, as men age, their testosterone levels decrease signi cantly, often making prolonged tactile stimulation necessary to attain erections. Older men are likely to experience reduced penile hardness, decreased urgency to reach climax, and a longer refractory period (Butler & Lewis, 2002; Masters & Johnson, 1966). In addition to the normal biological changes that arise with age, older people of both sexes may develop illnesses or diseases that make sexual activity physically more challenging. They also may take medicaMen and women often experience changes in tions that have side effects that interfere with their sexual response. However, most aspects of sexual performance as they get older, older people say that they continue to enjoy sex. However, most will still experience pleasure from sexual Psychological Factors: Predisposing, Precipitating, and activities (Leiblum & Seagraves, 2000). Maintaining Sexual Dysfunctions Certain beliefs and experiences can predispose individuals to develop sexual dysfunctions (see Table 11. For example, a woman may believe that women in general lose their sexual desire as they age and a man may believe that real men have intercourse twice a day and that only rock-hard erections will satisfy women (Nobre & Pinto-Gouveia, 2006). Such a belief can lead to a self-fullling prophecy, if the belief produces the perception of a dysfunction and that perception in turn leads to a real dysfunction. Early negative In men, premature ejaculation can develop after hurrying to have conditioning an orgasm quickly for fear of being caught. Sexual trauma Sexual trauma can produce negative conditioning and can lead to a fear of sex, as well as arousal and desire problems. Sources: Bartoi & Kinder, 1998; Becker & Kaplan, 1991; Kaplan, 1981; Laumann, Paik, & Rosen, 1999; LoPiccolo & Friedman, 1988; Masters & Johnson, 1970; Silverstein, 1989. Gender and Sexual Disorders 507 satised by very hard erections may develop a problem as he ages: He may notice that his erections are not as hard as they were when he was younger and then become self-conscious and preoccupied during sex, which does in fact lead him to fail to satisfy his partner. In addition, having been sexually abused as a child also predisposes a person N later to develop sexual dysfunctions. Consider the fact that male victims of childP S hood sexual abuse are three times more likely to have erection problems and twice as likely to have desire problems and premature ejaculation than their peers who did not experience childhood sexual abuse (Laumann, Paik, & Rosen, 1999). Once someone has a problem with desire, arousal, or orgasm, he or she may become anxious that it will happen again, which sets up a self-fullling prophecy and becomes a maintaining factor. Social Factors Although sexuality involves how we see ourselves, it usually also involves other people. The sexual relations of a couple are inuenced by how the partners relate to each other, specically: (1) how conict is expressed and resolved, (2) how they communicate their needs and desires, their likes and dislikes, (3) how they handle stress, and (4) how strongly atBeing chronically preoccupied and anxious about tracted they each are to each other (Tiefer, 2001). That is, from her vantage point, he appeared to have a sexual desire probactivity can interfere with the normal sexual response cycle, and lead to a sexual dysfunction. Such feedback loops best explain why some people, and not others, develop sexual dysfunctions. Current problems in a relationship (social factors) similarly affect sexual functioning, as can having been sexually abused (Bartoi & Kinder, 1998; Becker, 1989; DiLillo, 2001; Laumann, Paik, & Rosen, 1999). Familial and cultural views of sexuality (social factors) can also inuence sexual functioning (psychological and neurological factors): We are all taught various lessons about sexuality both directly (what our parents, teachers, religious leaders, and Figure 11. Some people are taught that sexual relations outside of marriage are wrong, whereas other people are taught that sexual experimentation before marriage is a good thing. Such direct and indirect lessons help shape each persons notion of appropriate or normal sexuality. Depending on what an individual learned about sex, he or she may be primed to have sexual difficulties in some situations. The interplay of factors is seen in the contrasting examples of two men, each of whom has an experience of erectile dysfunction. One man has a history of poor self-esteem and worry (psychological factors), as well as anxiety about his sexual performance (neurological and psychological factors). Although he is very attracted to his partner and generally has a positive view of sex (psychological and social factors), he worries that his partner may get annoyed at his performance failure and perhaps leave him. This leads him to be even more anxious the next time they have a sexual encounter (neurological and social factors), and he again has difficulty attaining or maintaining an erection, and thus develops persistent erectile dysfunction. However, this man does not have the general performance worries of the rst man, nor is he anxious about how his partner may respond. He expects (psychological factor) later to have his usual erections and to be able to satisfy his partner, which is in fact what happens. Thus, neurological, psychological, and social factors inuence each other in complex ways that predispose an individual to develop a sexual dysfunction, and that precipitate and maintain it once it develops. Before sex therapists begin to treat people for sexual dysfunctions, they usually make sure that the patients have a thorough assessment to identify specic factors that contribute to the dysfunction. The results of the assessment guide which factor(s) are targeted for treatment and which specic treatments the therapist suggests. Sexual dysfunctions can be assessed by examining neurological and other biological factors, as well as psychological and social factors. Assessing Neurological and Other Biological Factors Mental health professionals who assess and treat sexual problems want to know about an individuals health status and sexual response cycle. Such information may be obtained through lab tests that measure endocrine and hormone levels, ultrasound imaging to assess internal organs, and tests to assess the functioning of sensory nerves. Testing for men may include a plethysmograph to assess penile response, and testing for women may include vaginal probes to measure lubrication and the vaginas ability to relax and dilate. This information helps the sex therapist determine what specic psychological factors contribute to the patients sexual dysfunction. Assessing Social Factors A sex therapist investigates how relationship issues affect a patients sexuality and whether the sexual difficulties occur only with the patients partner or more generally. For instance, the therapist might ask what function sex serves in the relationship and how unresolved conict and power issues affect the sexual aspect of the relationship (Stock & Moser, 2001). Other questions might address how the couple decides on the timing, duration, or specic activities of sexual relations. Depending on the answers, the sex therapist may target specic social factors as part of the treatment. Treating Sexual Dysfunctions Once the specic nature of the sexual problem has been determined, treatment can target the relevant factors. Targeting Neurological and Other Biological Factors: Medications There has been an increasing trend toward the medicalization of sex therapy, that is, a tendency to target neurological and other biological factors (see Table 11. In the 1990s, medical treatments for erectile dysfunction began in earnest with the advent of the drug Viagra and the marketing campaign for it, which brought the topic of erectile dysfunction from a rarely discussed but relatively common problem among older men to a topic of everyday conversation. Viagra doesnt cause an erection directly; instead, the drug operates by increasing the ow of blood to the penis only when a man is sexually excited. Viagra (and its competitors, such as Cialis) is not a cure but a treatment for impotence, and it is effective only if the man takes a pill before sexual activity. For example, consider a middle-aged man with erectile dysfunction who is given Viagra and resumes sexual intercourse with his postmenopausal wife. However, his wife cannot maintain adequate lubrication or interest during intercourse given her husbands (now) extended erections. Many researchers and clinicians P S maintain that in such cases the woman does not have a disorder, although she may have a relationship problem (Basson et al. One of the main goals of treatments that directly target psychological factors related to sexual dysfunctions is to educate patients about sexuality and the human sexual response. Another goal is to help patients develop strategies to counter negative thoughts, beliefs, or attitudes that may interfere with sexual desire, arousal, or orgasm (Carey & Gordon, 1995). For instance, during sexual activity, some people are preoccupied with nonsexual thoughts that prevent them from reaching full arousal or orgasm. These nonsexual thoughts might be work-related worries, thoughts about household tasks that need to be done, or worries that someone will interrupt the sexual encounter. Cognitive treatment may involve teaching a patient how to lter out such thoughts and (re)focus on the sexual interaction. The therapist might encourage the patient to apply standard cognitive methods (see Chapter 4) to sexual encounters, such as problem solving (You could turn the phone off) or cognitive restructuring (Are you likely to think of a solution to your work problem while making love If not, you can let your mind focus on the physical sensations you are experiencing).
A course of corticosteroid treatment water into the interstitial space; secondary sodium without a renal biopsy is indicated for children without retention develops to compensate for intravascular volume atypical features mood disorder 6 game buy aripiprazola 10 mg mastercard, since responsiveness to steroids is a contraction mood disorder with depressive features 10mg aripiprazola otc. The underfill theory is intuitively attractive better indicator than kidney histology of long-term and data showing that nephrotic patients have contracted prognosis for renal function depression inventory test order generic aripiprazola canada. Renal biopsy is generally intravascular volume mood disorder borderline personality order aripiprazola from india, reduced glomerular filtration rate mood disorder drugs list buy genuine aripiprazola on line, limited to steroid-unresponsive and steroid-dependent and raised renin and aldosterone concentrations support patients mood disorder pathophysiology cheap aripiprazola master card, although it has yet to be shown that this the concept. Therapeutic approaches are nephrotic oedema is a primary defect in sodium excretion. Traditionally, not universally accepted and may not be sufficient to patients receive divided doses but once-daily treatment explain oedema formation in childhood nephrotic also seems to be effective. The underfill and overfill mechanisms are not been a shift in the past decade to longer courses of necessarily mutually exclusive, dependent on the stage corticosteroid treatment for first episodes of nephrotic of nephrotic syndrome, the rate of development of syndromes in an effort to decrease the relapse rate. In hypoproteinaemia, and absolute plasma oncotic support of this approach was the study by the pressure. By contrast, patients with chronic forms of prednisone on alternate days for 6 weeks than among persistent nephrotic syndrome may have continuing patients who received the then standard 8-week sodium retention and thus be more prone to oedema from treatment. In a meta-analysis of the five randomised controlled trials involving children with a first episode of steroidHyperlipidaemia responsive nephrotic syndrome, longer duration of Hyperlipidaemia, with raised serum cholesterol and treatment significantly decreased the risk of relapse at 12 triglyceride concentrations, is a hallmark of nephrotic and 24 months without an increase in adverse events. Steroid-induced side-effects Although steroid treatment is normally continued beyond develop in a high proportion of these patients. Currently 8 weeks even in steroid-resistant patients, and it remains a there are no data on the preferred second-line drug. Use component of most subsequent treatment, we have no of cyclophosphamide, chlorambucil, ciclosporin, and adequate evidence from randomised controlled clinical levamisole to reduce the risk of relapses is supported by a trials to provide clear guidance for subsequent dosing. In a summary of nine paediatric any 12-month period) reportedly achieve a longer series published in 1984, 30% of steroid-unresponsive remission with alkylating agents than do children with patients responded to cyclophosphamide. Given the risks of seizures also induce remission, whether this route of associated with chlorambucil, cyclophosphamide is more administration is safer or more effective has not been commonly prescribed. Standardised guidelines for the dose and important data on safety and efficacy have been added. To achieve Overall, when used to treat steroid-responsive nephrotic remission, the initial target plasma trough concentrations syndrome, remission can be achieved in 85% of patients. Concerns higher plasma concentrations may be necessary to achieve about nephrotoxic effects mandate careful monitoring of adequate tissue ciclosporin concentrations. Despite the very promising as effective as cyclophosphamide in frequently relapsing initial outcome reported with this therapeutic protocol, nephrotic syndrome. Ethnic composition of the study population is an cases of agranulocytosis, vasculitis, and encephalopathy. Prophylactic treatment with varicella zoster immune globulin is recommended for non-immune patients taking immunosuppressive treatments. No one laboratory test can reliably predict the However, with the high rate of end-stage renal disease real thrombotic risk. Fibrinogen concentration has been among patients unresponsive to traditional doses of proposed as a surrogate marker. Other factors that glucocorticoids and ciclosporin, this approach is often increase thrombotic risk in nephrotic patients include considered. They can be divided into two major subgroups: acute complications related to the nephrotic state, especially infections and thromboembolic disease, and long-term sequelae of nephrotic syndrome and its treatment, especially effects on bones, growth, and the cardiovascular system. A third important area is the psychological impact and social demands on children who have nephrotic syndrome, and their families. Pulmonary Susceptibility to bacterial infection is related to multiple thromboemboli in the nephrotic syndrome. Impaired complementwith copyright permission from Springer-Verlag, Heidelberg, Germany. Multicentre clinical trials are needed to improve hyperlipidaemia and limit its complications. Changing trends of Other potential medical complications include drug toxic histopathology in childhood nephrotic syndrome. Although diuretics and albumin infusions can successfully 5 Bonilla-Felix M, Parra C, Dajani T, et al. Changing patterns in the treat symptomatic oedema, injudicious use can lead to histopathology of idiopathic nephrotic syndrome in children. Changing trends of histopathology in childhood nephrotic dependent on the cause of oedema. Racial differences in the incidence and renal Natural history and prognosis outcome of idiopathic focal segmental glomerulosclerosis in children. Not all in the family: mutations of podocin in sporadic sustained remission with one of the second-line or thirdsteroidresistant nephrotic syndrome. Germline mutations in the Wilms tumor suppressor gene are associated with abnormal urogenital inevitable. Insight into podocyte differentiation from the study For patients who have familial forms of nephrotic of human genetic disease: nail-patella syndrome and transcriptional regulation in podocytes. Focal 22 Frishberg Y, Rinat C, Megged O, Shapira E, Feinstein S, segmental glomerular sclerosis among patients infected with hepatitis Raas-Rothschild A. Circulating mediators of proteinuria in idiopathic minimal pathophysiological concept. Effects of plasma volume expansion on renal salt factors in the nephrotic syndrome: a compendium and prospectus. Atrial recurrence of nephrotic syndrome following renal transplantation in natriuretic peptide and the renal response to hypervolemia in children. Pathogenesis of edema formation in the with increased glomerular permeability to albumin in recurrent focal nephrotic syndrome. Effect of protein A mechanisms in the impaired salt excretion of experimental nephrotic immunoadsorption in nephrotic syndrome of various etiologies. Transmission of glomerular Considerations on the sodium retention in nephrotic syndrome. A critique of the overfill hypothesis of 32 Carraro M, Caridi G, Bruschi M, et al. Should hyperlipidemia in children with the nephrotic patients with focal segmental glomerulosclerosis. Up-regulation of acyl-coenzyme A:cholesterol 34 Koyama A, Fujisaki M, Kobayashi M, Igarashi M, Narita M. Dominant T cells in recommendations for kidney biopsy in nephrotic syndrome need idiopathic nephrotic syndrome of childhood. Severe hypercholesterolemia inhibits cyclosporin initial treatment of idiopathic nephrotic syndrome in children: A efficacy in a dose-dependent manner in children with nephrotic Arbeitsgemeinschaft fur Padiatrische Nephrologie. Tacrolimus treatment established at the National Kidney Foundation conference on for steroidand cyclosporin-resistant minimal-change nephrotic proteinuria, albuminuria, risk, assessment, detection, and elimination syndrome. Management of minimal lesion glomerulonephritis: with steroid-resistant idiopathic nephrotic syndrome treated with evidence-based recommendations. Unfavorable response to cyclophosphamide of steroid-resistant focal segmental glomerulosclerosis in native in steroid-dependent nephrotic syndrome. A meta-analysis of affinity immunoadsorption strongly decreases proteinuria in patients cytotoxic treatment for frequently relapsing nephrotic syndrome in with relapsing nephrotic syndrome. Extracorporeal plasma treatment in primary therapy in frequently relapsing nephrotic syndrome. Peritonitis in childhood renal induced tubulointerstitial lesions in children with minimal change disease. Infectious Diseases, technical report: prevention of pneumococcal 87 Yoshioka K, Ohashi Y, Sakai T, et al. A multicenter trial of infections, including the use of pneumococcal conjugate and mizoribine compared with placebo in children with frequently polysaccharide vaccines and antibiotic prophylaxis. Prevention of serious bacterial infection in treatment for primary glomerular diseases. Contemporary issues in nephrology: pediatric and peritonitis in nephrotic children. Hypercoagulability, intraglomerular cyclosporine in steroid-resistant idiopathic nephrotic syndrome. Treatment of childhood steroid-resistant idiopathic 121 Citak A, Emre S, Sairin A, Bilge I, Nayir A. Calcium and vitamin D metabolism in risk of coronary heart disease associated with nephrotic syndrome. Premature acute myocardial hyperparathyroid bone disease in patients with nephrotic syndrome. Pathophysiology of acute renal failure in idiopatic patients with persistent nephrotic syndrome. Influence of age at onset on the outcome of steroidtherapy improves brachial artery endothelial function in nephrotic sensitive nephrotic syndrome. Lipid abnormalities in the nephrotic syndrome: year relapses in children with nephrotic syndrome. Hyperlipidaemia, diet and simvastatin dependency in children with idiopathic nephrotic syndrome. Management of hyperlipidemia significance of the early course of minimal change nephrotic in children with refractory nephrotic syndrome: the effect of statin syndrome: report of the International Study of Kidney Disease in therapy. Clinical picture Retinal detachment Jennifer Ng, James Cleland, Peter Bergin A 75-year-old woman presented with a 6-week history fundoscopy through the undilated pupil showed only a of seeing raindrops and triangles throughout her field benign pigmented lesion over the right optic disc. The of vision, which progressed to near-total painless visual visual acuity of her left eye was normal, as was the loss in the right eye 4 days before presentation. Magnetic resonance examination we found mild bilateral chemosis and imaging of the brain and orbits, done to exclude a retrosubtle proptosis of the right eye. She was able to count orbital mass lesion, showed retinal detachment in the fingers in the temporal field of her right eye, while in the right eye (figure, arrow). References have been expanded and updated for those interested in more in-depth reading on this subject. Our goal is to make this a reference for the health-care provider on the front lines, whether on the battlefield or in a clinic, who needs basic summary and treatment information quickly. We want your feedback so that we might make future editions more useful and readable. The exclusion of anyone on this page is purely accidental and in no way lessens the gratitude we feel for contributions received. As you review this handbook, you will find specific therapies and prophylactic regimens for the diseases mentioned. The majority of these are based upon standard treatment guidelines; however, some of the regimens noted may vary from information found in standard reference materials. The reason for this is that the clinical presentation of certain diseases caused by a weaponized biological agent may vary from the endemic form of the disease. For ethical reasons, human challenge studies can only be performed with a limited number of these agents. Therefore, treatment and prophylaxis regimens may be derived from in vitro data, animal models, and limited human data. These products are not available commercially, and can only be given under a specific protocol with informed consent. In certain other cases, licensed pharmaceuticals are discussed for use in a manner or for a condition other than that for which they were originally licensed. This executive order does not intend to alter the traditional physicianpatient relationship or individual physician prescribing practices.
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Recirculating systems are common in indoor research settings where high-density housing systems are often needed mood disorders kitchener cheap aripiprazola 10mg amex. Most recirculating systems are designed to exchange a specifc volume of water per unit time and periodically introduce fresh water into the system depression symptoms diabetes buy generic aripiprazola 10 mg online. These systems are the most mechanically advanced depression definition pubmed buy aripiprazola mastercard, containing biologic flters (bioflters) that promote conversion of ammonia to nitrite and nitrate via nitrifying bacteria anxiety 800 numbers buy aripiprazola no prescription, protein skimmers (foam fractionators) and particulate flters to remove undissolved and dissolved proteins and particulate matter depression test game trusted 10mg aripiprazola, carbon flters to remove dissolved chemicals mood disorder research articles discount aripiprazola express, and ultraviolet or ozone units to disinfect the water. The systems generally contain components to aerate and degas the water (to prevent gas oversaturation) and to heat or cool it, as well as automated dosing systems to maintain appropriate pH and conductivity. Not all elements are present in all systems and some components may accomplish multiple functions. The development and maintenance of the bioflter is critical for limiting ammonia and nitrite accumulation in recirculating systems. The microorganisms supported by the bioflter require certain water quality parameters. Continuous or timed fow-through systems can be used where suitable water is available to support the species to be housed. Static systems vary in size from small tanks to large inground ponds, and may use mechanical devices to move and aerate water. Temperature, humidity, and Ventilation the general concepts discussed in the Terrestrial Animals section also apply to the aquatic setting. Most aquatic or semiaquatic species (fsh, amphibians, and reptiles) used in research are poikilotherms, which depend, for the most part, on the temperature of their environment to sustain physiologic processes, such as metabolism, reproduction, and feeding behavior (Browne and Edwards 2003; Fraile et al. Temperature requirements are based on the natural history of the species and can vary depending on life stage (Green 2002; Pough 1991; Schultz and Dawson 2003). Water temperature may be controlled at its source, within the life support system, or by controlling the macroenvironment. The volume of water contained in a room can affect room temperature, temperature stability, and relative humidity. Likewise the thermal load produced by chiller/heater systems can affect the stability of the macroenvironmental temperature. Macroenvironmental relative humidity levels are generally defned by safety issues and staff comfort, since room humidity is not critical for aquatic species; however, excessive moisture may result in condensation on walls, ceilings, and tank lids, which may support microbial growth and serve as a source of contamination or create a conducive environment for metal corrosion. Some amphibians and reptiles may need elevated microenvironmental humidity (in excess of 50-70% relative humidity), which may require maintaining elevated macroenvironmental humidity levels (Pough 1991; St. For fsh and some aquatic amphibians, the microenvironmental air quality may affect water quality. As the aerosolization of water can lead to the spread of aquatic animal pathogens. Illumination Aquatic and semiaquatic species are often sensitive to changes in photoperiod, light intensity, and wavelength (Brenner and Brenner 1969). Lighting characteristics will vary by species, their natural history, and the research being conducted. Gradual changes in room light intensity are recommended, as rapid changes in light intensity can elicit a startle response in fsh and may result in trauma. Some aquatic and semiaquatic species may need full-spectrum lighting and/or heat lamps to provide supplemental heating to facilitate adequate physiological function. Noise and Vibration General concepts discussed in the Terrestrial Animals section apply to aquatic animals. These animals may be sensitive to noise and vibration, which are readily transmitted through water. Vibration through foors can be reduced by using isolation pads under aquaria racks. Aquatic Housing Microen ironment (Primary Enclosure) the primary enclosure (a tank, raceway, pond, or pen holding water and the animal) defnes the limits of an animals immediate environment. In some poikilothermic reptiles and amphibians, microenvironmental temperature gradients may be needed for certain physiologic functions such as feeding and digestion. En ironmental Enrichment and Social housing Environmental enrichment strategies for many aquatic species are not well established. When used, enrichment should elicit speciesappropriate behaviors and be evaluated for safety and utility. Generally, schooling fsh species are housed with conspecifcs, and many amphibians, especially anuran species, may be group housed. Improved breeding success in enriched environments has been reported but further research in this area is needed (Carfagnini et al. Most semiaquatic reptiles spend some time on land (basking, feeding, digesting, and ovipositing) and terrestrial areas should be provided as appropriate. Sheltered, Outdoor, and Naturalistic housing Animals used in aquaculture are often housed in situations that mimic agricultural rearing and may be in outdoor and/or sheltered raceways, ponds, or pens with high population densities. In these settings, where natural predation and mortalities occur, it may be appropriate to measure animal numbers by using standard aquaculture techniques such as fnal production biomass (Borski and Hodson 2003). Space Space recommendations and housing density vary extensively with the species, age/size of the animals, life support system, and type of research (Browne et al. In the United States, for example, adult zebrafsh (danio rerio) in typical biomedical research settings are generally housed 5 adult fsh per liter of water (Matthews et al. This guidance is not necessarily relevant for other species of fsh, and may change as research advances (Lawrence 2007). To avoid damage to the protective mucus layers of the skin and negative effects on immune function (De Veer et al. Appropriate handling techniques vary widely depending on the species, age/size, holding system, and specifc research need (Fisher 2000; Matthews et al. The use of appropriate nets by well-trained personnel can reduce skin damage and thus stress. Nets should be cleaned and disinfected appropriately when used in different systems and should be dedicated to animals of similar health status whenever possible. Exercise and activity levels for aquatic species are minimally described but informed decisions may be extrapolated from studies of behavior of the same or similar species in the wild (Spence et al. Some aquatic species do not rest and constantly swim; others may rest all or a signifcant portion of the day. Food should be stored in a type-appropriate manner to preserve nutritional content, minimize contamination, and prevent entry of pests. Food delivery methods should ensure that all animals are able to access food for a suffcient period of time while minimizing feeding aggression and nutrient loss. Feeding methods and frequency vary widely depending on the species, age/size of species, and type of life support system. Many aquatic or semiaquatic species are not provided with food ad libitum in the tank, and in some cases may not be fed daily. In aquatic systems, particularly in fsh rearing or when maintaining some amphibian and reptile species, the use of live foods. Water (see also section on Water Quality) Aquatic animals need access to appropriately conditioned water. Fully aquatic animals obtain water in their habitat or absorb it across their gills or skin. Some semiaquatic amphibians and reptiles may need bowls of water for soaking and drinking, and water quality should be appropriate (see Terrestrial Animals section). Chlorine or chloramines may be present in tap water at levels that could be toxic to some species. Substrate Substrates can provide enrichment for aquatic animals by promoting species-appropriate behavior such as burrowing, foraging, or enhanced spawning (Fisher 2000; Matthews et al. They may be an integral and essential component of the life support system by providing increased surface area for denitrifying bacteria. System design and species needs should be evaluated to determine the amount, type, and presentation of substrate. Sanitation Sanitation of the aquatic environment in recirculating systems is provided through an appropriately designed and maintained life support system, regular removal of solid waste materials from the enclosure bottom, and periodic water changes. However, sanitation measures in aquatic systems differ from those for terrestrial systems because much of the nitrogenous waste (feces and urine) and respiratory output (carbon dioxide) is dissolved in the water. A properly functioning life support system, designed to process the bioload, will maintain nitrogenous wastes within an acceptable range. Solids may be removed in a variety of ways, depending on the design of the system; generally they are removed by siphoning (hydrocleaning) and/or fltration. Depending on the type, flters need routine cleaning or replacement or, if self-cleaning, proper maintenance; in saltwater systems dissolved proteins may be removed by protein skimmers. Reducing organic solids limits the quantities of nitrogen and phosphorus that need to be removed from the system, both of which can accumulate to levels that are toxic to fsh and amphibians. The biologic flter (denitrifying bacteria) typically removes ammonia and nitrite, potential toxins, from aquatic systems. Nitrate, the end product of this process, is less toxic to aquatic animals but at high levels can be problematic; it is generally removed through water changes, although large systems may have a specialized denitrifcation unit to reduce levels. Chlorine and most chemical disinfectants are inappropriate for aquatic systems containing animals as they are toxic at low concentrations; when used to disinfect an entire system or system components, extreme care must be taken to ensure that residual chlorine, chemical, and reactive byproducts are neutralized or removed. The type of monitoring and frequency varies depending on the disinfection method, the system, and the animals. Algal growth is common in aquatic systems and increases with the presence of nitrogen and phosphorus, particularly in the presence of light. Algal species seen with recirculating systems are generally nontoxic, although species capable of producing toxins exist. Limiting algal growth is important to allow viewing of the animals in the enclosure. Cyanobacteria (commonly called blue-green algae) growth is also possible and may be common in freshwater aquaculture. As with algae, while most species are harmless, some species can produce clinically relevant toxic compounds (Smith et al. Tank (cage) changing and disinfection are conducted at frequencies using methods that often differ from terrestrial systems. Because waste is dissolved in the water and/or removed as solids by siphoning or fltration, regular changing of tanks is not integral to maintaining adequate hygiene in typical aquatic systems. The frequency of cleaning and disinfection should be determined by water quality, which should permit adequate viewing of the animals, and animal health monitoring. System components such as lids on fsh tanks, which may accumulate feed, may require sanitation as often as weekly depending on the frequency and type of feed and the systems design. Cleaning and disinfection of the Macroen ironment As with terrestrial systems, all components of the animal facility, including animal rooms and support spaces. Cleaning agents should be chosen and used with care to ensure there is no secondary contamination of the aquatic systems. Cleaning implements should be made of materials that resist corrosion and withstand regular sanitation. They should be assigned to specifc areas and should not be transported between areas with different risks of contamination without prior disinfection. Pest Control Terrestrial animal pest control principles apply to aquatic systems but, due to transcutaneous absorption, aquatic and semiaquatic species may be more sensitive to commonly used pest control agents than terrestrial animals. Before use, an appropriate review of chemicals and methods of application is necessary. Emergency, Weekend, and holiday Care As with terrestrial species, aquatic animals should receive daily care from qualifed personnel who have a suffcient understanding of the housing system to identify malfunctions and, if they are unable to address a system failure of such magnitude that it requires resolution before the next workday, access to staff who can respond to the problem. Automated monitoring systems are available and may be appropriate depending on system size and complexity. Appropriate emergency response plans should be developed to address major system failures. Population Management Identifcation Identifcation principles are similar to those for terrestrial animals. Identifcation methods available for use in aquatic species include fn clipping, genetic testing (Matthews et al. Because it can be diffcult to individually identify some small aquatic animals throughout their life, group identifcation may be more appropriate in some situations (Koerber and Kalishman 2009; Matthews et al. Aquatic Animal Recordkeeping Adequate recordkeeping is necessary in aquatic system management. In general, the same standards used for terrestrial animals apply to aquatic and semiaquatic species, although modifcations may be necessary to account for species or system variations (Koerber and Kalishman 2009). Records of water quality testing for system and source water and maintenance activities of the life support system components are important for tracking and ensuring water quality. The exact water quality parameters tested and testing frequency should be clearly established and will vary with such factors as the type of life support system, animals, and research, as discussed under Water Quality. Detailed tracking of animal numbers in aquatic systems is often possible with accurate records of transfers, breeding, and mortalities (Matthews et al. In large-scale aquaculture research it may be more appropriate to measure biomass of the system versus actual numbers of animals (Borski and Hodson 2003).
Include in education and training programs mood disorder lesson plan purchase aripiprazola 15mg visa, information concerning 17 depression jokes aripiprazola 15 mg amex, 611 bipolar depression 4 years buy genuine aripiprazola, use of vaccines as an adjunctive infection control measure 690 bipolar depression 31 aripiprazola 20mg with mastercard, 874 anxiety uncertainty theory buy generic aripiprazola 20mg. Enhance education and training by applying principles of adult learning anxiety xr order 20 mg aripiprazola visa, using reading level and language appropriate material for the target audience, and using online educational tools available to 658, 694, 695, 697, 698, 700, 966 the institution. Provide instructional materials for patients and visitors on recommended hand hygiene and Respiratory Hygiene/Cough Etiquette practices and the 9, 709, 710, 963 application of Transmission-Based Precautions. Apply the following epidemiologic principles of infection surveillance 673 969 663 664. Develop and implement strategies to reduce risks for transmission and 566, 673, 684, 970 963 971 evaluate effectiveness. When transmission of epidemiologically-important organisms continues despite implementation and documented adherence to infection prevention and control strategies, obtain consultation from persons knowledgeable in infection control and healthcare epidemiology to review 566 247 687 the situation and recommend additional measures for control. Review periodically information on community or regional trends in the incidence and prevalence of epidemiologically-important organisms. Standard Precautions Assume that every person is potentially infected or colonized with an organism that could be transmitted in the healthcare setting and apply the following infection control practices during the delivery of health care. When hands are visibly dirty, contaminated with proteinaceous material, or visibly soiled with blood or body fluids, wash hands with either a nonantimicrobial soap and water or an antimicrobial soap 559 and water. The preferred method of 562, 978 hand decontamination is with an alcohol-based hand rub. Frequent use of alcohol-based hand rub immediately following handwashing with nonantimicrobial soap may increase 559 the frequency of dermatitis. After contact with blood, body fluids or excretions, mucous 664 membranes, nonintact skin, or wound dressings. If hands will be moving from a contaminated-body site to a clean-body site during patient care. After contact with inanimate objects (including medical 72, 73, 88, 800, 981 equipment) in the immediate vicinity of the patient 982. Wash hands with non-antimicrobial soap and water or with antimicrobial soap and water if contact with spores. The physical action of washing and rinsing hands under such circumstances is recommended because alcohols, chlorhexidine, iodophors, and 559, 956, 983 other antiseptic agents have poor activity against spores. Do not wear artificial fingernails or extenders if duties include direct contact with patients at high risk for infection and associated 30, 31, 559, adverse outcomes. Develop an organizational policy on the wearing of non-natural nails by healthcare personnel who have direct contact with 984 patients outside of the groups specified above. Wear gloves when it can be reasonably anticipated that contact with blood or other potentially infectious materials, mucous membranes, nonintact skin, or potentially contaminated intact skin. Wear disposable medical examination gloves or reusable utility gloves for cleaning the environment or medical equipment. Remove gloves after contact with a patient and/or the surrounding environment (including medical equipment) using proper technique to prevent hand contamination (see Figure). Do not wash gloves for the purpose of reuse since this practice has been associated with transmission of 559, 728, 741-743, 988 pathogens. Change gloves during patient care if the hands will move from a contaminated body-site. Wear a gown, that is appropriate to the task, to protect skin and prevent soiling or contamination of clothing during procedures and patient-care activities when contact with blood, body fluids, 739, 780, 896 secretions, or excretions is anticipated. Select masks, goggles, face shields, and combinations of each according to the need anticipated by 113, 739, 780, 896 the task performed. Educate healthcare personnel on the importance of source control measures to contain respiratory secretions to prevent droplet and fomite transmission of respiratory pathogens, especially during seasonal outbreaks of viral respiratory tract infections. Implement the following measures to contain respiratory secretions in patients and accompanying individuals who have signs and symptoms of a respiratory infection, beginning at the point of initial encounter in a healthcare setting. Provide resources and instructions for performing hand hygiene in or near waiting areas in ambulatory and inpatient settings; provide conveniently-located dispensers of alcohol-based hand rubs and, where sinks are available, supplies for handwashing 559, 903. During periods of increased prevalence of respiratory infections in the community. Some facilities may find it logistically easier to institute this recommendation year-round as a standard of practice. Include the potential for transmission of infectious agents in patientplacement decisions. Establish policies and procedures for containing, transporting, and handling patient-care equipment and instruments/devices that may 18, 739, 975 be contaminated with blood or body fluids. Remove organic material from critical and semi-critical instrument/devices, using recommended cleaning agents before high level disinfection and sterilization to enable effective 836 991, 992 disinfection and sterilization processes. Establish policies and procedures for routine and targeted cleaning of environmental surfaces as indicated by the level of patient 11 contact and degree of soiling. Clean and disinfect surfaces that are likely to be contaminated with pathogens, including those that are in close proximity to the patient. Review the efficacy of in-use disinfectants when evidence of continuing transmission of an infectious agent. In facilities that provide health care to pediatric patients or have waiting areas with child play toys. Include multi-use electronic equipment in policies and procedures for preventing contamination and for cleaning and disinfection, especially those items that are used by patients, those used during delivery of patient care, and mobile devices that are moved in and 850 851, 852, 997 out of patient rooms frequently. Handle used textiles and fabrics with minimum agitation to avoid 739, 998, 999 contamination of air, surfaces and persons. If laundry chutes are used, ensure that they are properly designed, maintained, and used in a manner to minimize dispersion of 11, 13, 1000, 1001 aerosols from contaminated laundry. Use aseptic technique to avoid contamination of sterile injection 1002, 1003 equipment. Do not administer medications from a syringe to multiple patients, even if the needle or cannula on the syringe is changed. Needles, cannulae and syringes are sterile, single-use items; they should not be reused for another patient nor to access a medication or solution 453, 919, 1004, 1005 that might be used for a subsequent patient. Consider a syringe or needle/cannula contaminated once it has been used to enter or connect to a 453 patients intravenous infusion bag or administration set. Do not administer medications from single-dose vials or ampules to 369 453, multiple patients or combine leftover contents for later use 1005. If multidose vials must be used, both the needle or cannula and 453, 1002 syringe used to access the multidose vial must be sterile. Do not keep multidose vials in the immediate patient treatment area and store in accordance with the manufacturers recommendations; 453, 1003 discard if sterility is compromised or questionable. Do not use bags or bottles of intravenous solution as a common 453, 1006 source of supply for multiple patients. Infection control practices for special lumbar puncture procedures Wear a surgical mask when placing a catheter or injecting material into the spinal canal or subdural space. Worker safety Adhere to federal and state requirements for protection of healthcare 739 personnel from exposure to bloodborne pathogens. In addition to Standard Precautions, use Transmission-Based Precautions for patients with documented or suspected infection or colonization with highly transmissible or epidemiologically-important pathogens for which additional precautions are needed to prevent 24, 93, 126, 141, 306, 806, 1008 transmission (see Appendix A). Use Contact Precautions as recommended in Appendix A for patients with known or suspected infections or evidence of syndromes that represent an increased risk for contact transmission. Draw the privacy curtain between beds to minimize opportunities for direct contact. In long-term care and other residential settings, make decisions regarding patient placement on a case-by-case basis, balancing infection risks to other patients in the room, the presence of risk factors that increase the likelihood of transmission, and the 84 potential adverse psychological impact on the infected or 920, 921 colonized patient. In ambulatory settings, place patients who require Contact Precautions in an examination room or cubicle as soon as 20 possible. Gloves 24, 89, 134, 559, Wear gloves whenever touching the patients intact skin 746, 837 or surfaces and articles in close proximity to the patient. Wear a gown whenever anticipating that clothing will have direct contact with the patient or potentially contaminated environmental surfaces or equipment in close proximity to the patient. Remove gown and observe hand 24, 88, hygiene before leaving the patient-care environment 134, 745, 837. After gown removal, ensure that clothing and skin do not contact potentially contaminated environmental surfaces that could result in possible transfer of microorganism to 72, 73 other patients or environmental surfaces. When transport or movement in any healthcare setting is necessary, ensure that infected or colonized areas of the patients body are contained and covered. Handle patient-care equipment and instruments/devices 739, 836 according to Standard Precautions. In acute care hospitals and long-term care and other residential settings, use disposable noncritical patient-care equipment. If common use of equipment for multiple patients is unavoidable, clean and disinfect such equipment 24, 88, 796, 836, 837, 854, 1016 before use on another patient. Limit the amount of non-disposable patient-care equipment brought into the home of patients on Contact Precautions. Whenever possible, leave patient-care equipment in the home until discharge from home care services. Alternatively, place contaminated reusable items in a plastic bag for transport and subsequent cleaning and disinfection. In ambulatory settings, place contaminated reusable noncritical patient-care equipment in a plastic bag for transport to a soiled utility area for reprocessing. Environmental measures Ensure that rooms of patients on Contact Precautions are prioritized for frequent cleaning and disinfection. Discontinue Contact Precautions after signs and symptoms of the infection have resolved or according to pathogen-specific recommendations in Appendix A. Use Droplet Precautions as recommended in Appendix A for patients known or suspected to be infected with pathogens transmitted by respiratory droplets. Draw the privacy curtain between 103, 104 410 beds to minimize opportunities for close contact. In long-term care and other residential settings, make decisions regarding patient placement on a case-by-case basis after considering infection risks to other patients in the room and 410 available alternatives. In ambulatory settings, place patients who require Droplet Precautions in an examination room or cubicle as soon as possible. Instruct patients to follow recommendations for 447, 448 9, 828 Respiratory Hygiene/Cough Etiquette. In acute care hospitals and long-term care and other residential settings, limit transport and movement of patients outside of the room to medically-necessary purposes. If transport or movement in any healthcare setting is necessary, instruct patient to wear a mask and follow Respiratory Hygiene/Cough Etiquette Discontinue Droplet Precautions after signs and symptoms have resolved or according to pathogen-specific recommendations in Appendix A. Use Airborne Precautions as recommended in Appendix A for patients known or suspected to be infected with infectious agents transmitted person-to-person by the airborne route. Provide at least six (existing facility) or 12 (new construction/renovation) air changes per hour. Once the patient leaves, the room should remain vacant for the appropriate time, generally one hour, to allow for a full 11, 12, 122 exchange of air. Instruct patients with a known or suspected airborne infection to wear a surgical mask and observe Respiratory Hygiene/Cough Etiquette. Personnel restrictions Restrict susceptible healthcare personnel from entering the rooms of patients known or suspected to have measles (rubeola), varicella (chickenpox), disseminated zoster, or smallpox if other immune 17, 775 healthcare personnel are available. Respiratory protection is recommended for all healthcare personnel, including those with a documented take after smallpox vaccination due to the risk of a genetically engineered virus against which the vaccine may not provide protection, or of exposure to a very large viral load. For patients with skin lesions associated with varicella or smallpox or draining skin lesions caused by M. Healthcare personnel transporting patients who are on Airborne Precautions do not need to wear a mask or respirator during transport if the patient is wearing a mask and infectious skin lesions are covered. Exposure management Immunize or provide the appropriate immune globulin to susceptible persons as soon as possible following unprotected contact. Discontinue Airborne Precautions according to pathogen-specific recommendations in Appendix A. The environmental recommendations in these guidelines may be applied to patients with other infections that require Airborne Precautions. No recommendation for placing patients with other medical conditions that are associated with increased risk for environmental fungal infections 11. Directed room airflow with the air supply on one side of the room that moves air across the patient bed and out through an 13 exhaust on the opposite side of the room. Positive air pressure in room relative to the corridor (pressure 13 differential of >12. Lower dust levels by using smooth, nonporous surfaces and finishes that can be scrubbed, rather than textured material. Wet dust horizontal surfaces whenever dust detected and routinely clean crevices and sprinkler heads where dust may 940, 941 accumulate. Minimize the length of time that patients who require a Protective Environment are outside their rooms for diagnostic procedures and other 11, 158, 945 activities. During periods of construction, to prevent inhalation of respirable particles that could contain infectious spores, provide respiratory protection. No recommendation for use of particulate respirators when leaving the Protective Environment in the absence of construction. Implement Droplet and Contact Precautions as recommended for diseases listed in Appendix A. Transmission-Based precautions for viral infections may need to be prolonged because of the patients 930 immunocompromised state and prolonged shedding of viruses 1010 928, 932 1011. Implement Airborne Precautions for patients who require a Protective Environment room and who also have an airborne infectious disease. Ensure that the Protective Environment is designed to maintain 13 positive pressure. Principlesourcesconsultedforthedevelopm entof disease-specific recom m endationsforAppendix A includedinfectious 833,1043,1044 diseasem anualsandtex tbooks.
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