Page 853 - Hall et al (2015) Principles of Critical Care-McGraw-Hill
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584     PART 5: Infectious Disorders


                 unique chest x-ray pattern of rounded cavitary infiltrates along the   HCAP patient is more frequent in large academic medical centers with
                 bronchovascular bundle (Fig. 65-2). However, extensive workup for   active oncology and transplant programs.  The availability of home
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                 endocarditis is overwhelmingly negative.              wound care and antibiotic infusion services also varies tremendously by
                                                                       locale. In these settings, HCAP may be more common than traditional
                 Acute Cardiac Events:  Patients with CAP in severe sepsis or septic shock   CAP.  In smaller hospitals, the relative frequency is dramatically lower
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                 are prone to multiorgan system failure, including septic cardiomyopa-  and the number of patients with MDR pathogens is extremely small. 97
                 thy, similar to other serious infections. However, acute cardiovascular   Missing from the original description, the recent use of antibiotics is
                 complications appear to be more common in CAP patients than in other   also a major predictor of the risk of MDR pathogens. As broader spectrum
                 types of sepsis. Up to 20% of patients with pneumococcal pneumonia   oral antibiotics have become available, the selective pressure for MDR
                 can develop acute myocardial infarction, new onset congestive heart   pathogens has increased. This is best illustrated by a study of NHAP, which
                 failure, or new onset arrhythmia when hospitalized for pneumonia. 77,78     demonstrated that the risk of MDR pathogens was primarily determined
                 This increased risk of cardiovascular complications extends past the   by recent antibiotic use and secondarily by dependence in activities of daily
                 duration of hospitalization and may be related to persistent procoagu-  living.  Therefore, nursing home patients who have not been recently hos-
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                 lant cytokine elevation even at the time of discharge. 92  pitalized or given broad-spectrum antibiotics and who are independently
                     ■  PREVENTION                                     functioning can be treated safely with traditional CAP drugs.
                                                                         Surprisingly, the most common risk factor for HCAP is consistently
                 Secondary prevention of CAP in patients who have been admitted to   recent hospitalization, with nursing home residence constituting a
                 the ICU with one episode of SCAP has not been specifically studied.   smaller proportion of patients in all studies. 96,97,99-101  Many patients have
                 However, patients with one episode of bacteremic pneumococcal   multiple risk factors, with the most common overlap again being recent
                 pneumonia are 50 times more likely to develop recurrent disease than   hospitalization. The  risk  of MDR  pathogens in  stable nursing home
                 is the general population to develop a first episode.  This is likely due   patients, chronic hemodialysis patients, or even patients receiving che-
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                 to genetic risk factors for severe infection, especially in patients who   motherapy is unclear if they have not been recently hospitalized.
                 do not have hematologic malignancies or HIV disease. Therefore, both   Because many of the early studies were based on retrospective analysis
                 pneumococcal vaccination and yearly influenza vaccination are prob-  of large administrative databases, the analysis was limited to culture-
                 ably indicated even if the patient is not otherwise in a high-risk group.   positive cases.  Prospective studies demonstrate both a lower incidence
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                 Efficacy of vaccination at the end of the original hospitalization or even   of HCAP and a lower frequency of MDR pathogens.  A recent com-
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                 subsequent to recovery is unclear in this population if indeed they have   parison demonstrated that culture-negative HCAP patients can be safely
                 a form of immunocompromise.                           treated with  CAP antibiotic regimens with good  success.  However,
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                                                                       risk factors for culture positive HCAP include ICU admission. 103,104
                 HEALTH CARE–ASSOCIATED PNEUMONIA                      Therefore, patients with HCAP risk factors admitted to the ICU are at
                                                                       increased risk for MDR pathogens.
                 HCAP is technically a subgroup of CAP. This category of pneumonia
                 was developed in response to the fairly consistent finding of patients   Mortality:  One justification for separating HCAP from CAP was that
                 who develop pneumonia while outside the hospital yet have patho-  the associated mortality in HCAP was much greater than in CAP and
                 gens traditionally associated with HAP, such as MRSA, Pseudomonas,   closer to that of HAP. This finding is not surprising given that the
                 and drug-resistant Enterobacteriaceae. 55,94  Initially, this appeared to be   most frequent risk factor is recent hospitalization. Subsequent studies
                 predominantly patients admitted from nursing homes and an exten-  suggest that this excess mortality is primarily due to the underlying
                 sive literature on nursing home–acquired pneumonia (NHAP) exists.   disease rather than the presence of MDR pathogens. 101
                 However, subsequently it became obvious that this criterion alone did     ■  ETIOLOGIC SPECTRUM AND RECOMMENDED ANTIBIOTIC THERAPY
                 not describe the spectrum of patients who presented with CAP due to
                 MDR pathogens. This entity is extremely controversial, in part because   The implication of separating HCAP from CAP is that the pathogens
                 the frequency truly differs between hospitals and health care systems.  are more similar to those of HAP and VAP (Table 65-8). However, the
                     ■  DEFINITION                                     patients receiving broad-spectrum antibiotics without a positive culture
                                                                       criteria for HCAP are consistently oversensitive and result in many
                 One cause of the HCAP controversy is that the risk factors were initially   for MDR pathogens. In addition, the risk for all MDR pathogens is
                                                                       not the same. While a case can be made that home infusion therapy or
                 adapted from a study of bacteremia.  The initial criteria for HCAP were   wound care and chronic hemodialysis may be risk factors for MRSA
                                           95
                 proposed in the ATS/IDSA guidelines for hospital-acquired pneumonia,     pneumonia, no evidence exists that they increase the risk of MDR gram-
                                                                    94
                 and are listed in Table 65-6. Subsequent studies have used variations on   negative pathogens such as  Pseudomonas and  Acinetobacter. In these
                 the criteria that affect both frequency and etiology. Probably the most   situations, anti-MRSA coverage can simply be added to the traditional
                 significant is the inclusion of immunocompromised patients in the   CAP antibiotic regimen.
                 HCAP category.  The  immunocompromised  patient  was technically   An accurate diagnosis is critical to management and is often avail-
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                 a separate category and not included in HCAP in the original guide-  able in ventilated HCAP patients via tracheal aspirates or BAL. Initial
                 lines. However, with the expansion of both the indications for immu-  empirical antibiotic therapy for patients truly at risk for MDR patho-
                 nosuppressive therapy and the types of immunosuppression, defining   gens is the same as described for HAP in Table 65-8. If HCAP patients
                 immunocompromise is no longer easy. In addition, the criterion for   are culture negative, they can be safely de-escalated to traditional CAP
                 prior hospitalization has been increased from 3 months to as much as   coverage, such as a fluoroquinolone.  No RCT is available for HCAP
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                 a year in some studies. Hospitalization within the previous month has   patients admitted to the ICU and retrospective studies often exclude
                 traditionally been considered hospital-acquired pneumonia. However,   ICU patients and have often been contradictory regarding the clinical
                 this has also been challenged and many of these patients are included   benefit of HAP-like versus traditional CAP treatment. 96,97,100,102
                 in the HCAP group.                                      Surprisingly, given the frequent concern regarding aspiration, patients
                   Clearly HCAP is a diagnosis in transition. Further refinements of the   with  NHAP who  developed respiratory failure  do  not have evidence
                 definition are expected in the future.                that anaerobes play a significant role.  Therefore, specific anaerobic
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                     ■  EPIDEMIOLOGY                                   coverage is not necessarily required. Conversely, poor infection control
                                                                       practices in nursing home patients, particularly those with skin break-
                 Several patterns have emerged as the database of HCAP has increased.   down, surgical wounds, tracheostomy, or who are incontinent, increase
                 The first is that HCAP is clearly a disease of medical progress. The   the risk of MDR gram-negative pathogens.








            section05_c61-73.indd   584                                                                                1/23/2015   12:47:56 PM
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