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Nursing Care of Dyspnea: The 6th Vital Sign in Individuals with ...

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<strong>Nurs<strong>in</strong>g</strong> Best Practice Guidel<strong>in</strong>eAntibioticsRam, Joppi and Barnes (2004), <strong>in</strong> a systematic review, <strong>in</strong>dicate that acute bacterial exacerbations <strong>of</strong> COPDare common, costly and difficult to manage. A number <strong>of</strong> researchers l<strong>in</strong>k AECOPD to bacterial <strong>in</strong>fectionby pathogens such as Streptococcus pneumoniae, Haemophilus <strong>in</strong>fluenzae, Pseudomonas aerug<strong>in</strong>osa andM. catarrhalis. <strong>The</strong>se bacteria may be associated <strong>with</strong> <strong>in</strong>creased sputum volume and purulence (Blanchard,2002; Eller, Ede, Schaberg, Niederman, Mauch & Lode, 1998; Grossman, 1998; Murphy, Sethi & Niederman, 2000; Ram et al.,2004). However, the use <strong>of</strong> antibiotics is <strong>of</strong>ten prescribed to alleviate and to treat the cough and <strong>in</strong>creasepurulent sputum production that leads to <strong>in</strong>crease breathlessness (Calverley & Walker, 2003). In these<strong>in</strong>stances, the use <strong>of</strong> antibiotics is controversial (Adams, Melo, Luther, & Anzueto, 2000; Anthonisen, Manfreda,Warren, Hershfield, Hard<strong>in</strong>g, & Nelson, 1987; Dewan, Rafique, Kanwar, Satpathy, Ryschon, Tillotson, et al., 2000; Grossman,1997; 1998; Murphy et al., 2000; Nicotra, Rivera & Awe, 1982; Niederman, 1997; Ram et al., 2004; Wilson, 1998). Ram andcolleagues (2004) suggest there is <strong>in</strong>creased recognition that exacerbations may be due to viral <strong>in</strong>fections<strong>of</strong> the upper respiratory tract or may be non-<strong>in</strong>fective, so that antibiotic treatment is not always warranted.Anthonisen et al. (1987) found statistically significant advantages <strong>of</strong> antibiotic therapy for exacerbationscompared to placebo and suggest that antibiotic use is favourable where <strong>in</strong>creased dyspnea, sputumproduction or <strong>in</strong>creased purulence <strong>of</strong> sputum is present <strong>in</strong> more severe exacerbations. A meta-analysis bySa<strong>in</strong>t, Bent, Vitt<strong>in</strong>gh<strong>of</strong>f & Grady (1995) attempted to estimate the effectiveness <strong>of</strong> antibiotics <strong>in</strong> treat<strong>in</strong>gAECOPD and demonstrated benefits from antibiotic therapy. Adams et al. (2000) assessed predictivefactors <strong>of</strong> relapse for patients <strong>with</strong> AECOPD and the f<strong>in</strong>d<strong>in</strong>gs suggest that patients treated <strong>with</strong> antibioticshad significantly lower relapse rates than those who did not receive antibiotics.Psychotropic DrugsRipamonti (1999) suggests that although benzodiazep<strong>in</strong>es are commonly used <strong>in</strong> the symptomatictreatment <strong>of</strong> cancer-related dyspnea, no cl<strong>in</strong>ical controlled trials have been performed <strong>in</strong> cancer patients.Buspirone, a nonbenzodiazeo<strong>in</strong>e anxiolytic and a seroton<strong>in</strong> agonist has been demonstrated to be effective<strong>in</strong> reliev<strong>in</strong>g dyspnea <strong>in</strong> patients <strong>with</strong> anxiety disorders and obstructive lung disease when given at doses <strong>of</strong>15-45 mg/day (Craven & Sutherland, 1991). Ripamonti (1999) suggests that chlorpromaz<strong>in</strong>e (Chlorpromanyl) issignificantly more effective than placebo <strong>in</strong> reduc<strong>in</strong>g dyspnea <strong>in</strong> patients <strong>with</strong> COPD.OpioidsCurrently available evidence does not support the cl<strong>in</strong>ical use <strong>of</strong> nebulized opioids; however, somecl<strong>in</strong>icians utilize opioids to treat the symptom <strong>of</strong> dyspnea <strong>in</strong> end-stage COPD. Controlled cl<strong>in</strong>ical trials onthe symptomatic effect <strong>of</strong> nebulized opioids <strong>in</strong> COPD have been carried out and the use is controversial(Ripamonti, 1999; Zebraski, Kochenasti & Raffa, 2000). Moreover, Zebraski et al. (2000) suggest that the effect <strong>of</strong>nebulized morph<strong>in</strong>e sulfate <strong>in</strong> COPD patients has not always been robust nor always reproducible.Foral, Malesker, Huerta and Hilleman (2004) exam<strong>in</strong>ed the literature related to the use <strong>of</strong> nebulized opioids<strong>in</strong> COPD. <strong>The</strong>y suggest that the evidence <strong>in</strong> the literature that suppots the use <strong>of</strong> nebulized opioids islack<strong>in</strong>g and studies varied considerably <strong>in</strong> dose, opioid used, adm<strong>in</strong>istration schedule and methodology.Moreover, they mentioned that as stated <strong>in</strong> the the Global Initiative for Lung Disease guidel<strong>in</strong>es, opioid use iscontra<strong>in</strong>dicated <strong>in</strong> COPD management due to the potential respiratory depression and worsen<strong>in</strong>g hypercapnia.37

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