<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">CRCM</journal-id><journal-title-group><journal-title>Case Reports in Clinical Medicine</journal-title></journal-title-group><issn pub-type="epub">2325-7075</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/crcm.2016.59051</article-id><article-id pub-id-type="publisher-id">CRCM-71013</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  &lt;i&gt;Pseudomonas aeruginosa&lt;/i&gt; Community Acquired Pneumonia with Septicemia in a Previously Healthy Woman
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Yoshiro</surname><given-names>Imai</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Ryo</surname><given-names>Iida</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Masahiko</surname><given-names>Nitta</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Akira</surname><given-names>Takasu</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Emergency Medicine, Osaka Medical College, Osaka, Japan</addr-line></aff><pub-date pub-type="epub"><day>26</day><month>09</month><year>2016</year></pub-date><volume>05</volume><issue>09</issue><fpage>335</fpage><lpage>341</lpage><history><date date-type="received"><day>August</day>	<month>11,</month>	<year>2016</year></date><date date-type="rev-recd"><day>Accepted:</day>	<month>September</month>	<year>26,</year>	</date><date date-type="accepted"><day>September</day>	<month>29,</month>	<year>2016</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  A previously healthy 53-year-old woman was urgently hospitalized due to septic shock. She was diagnosed with bacterial pneumonia based on chest radiograph and computed tomography findings of right upper lobe consolidation. Sputum Gramstain at the time of admission showed gram-negative rods with phagocytosis. Intravenous meropenem was immediately initiated as empiric antibacterial therapy. Bacterial culture specimens from sputum and blood were positive for 
  Pseudomonas aeruginosa. Following appropriate antibiotic therapies, the patient recovered from a shock state and gradually became well. There has been no evidence of recurrence at 6 months after discharge. 
  P. aeruginosa community acquired pneumonia with septicemia is rapidly progressive and often fatal. The choice of initial empiric antibiotic treatment that is active against 
  P. aeruginosa is critical in improving outcome.
 
</p></abstract><kwd-group><kwd>&lt;i&gt;Pseudomonas aeruginosa&lt;/i&gt;</kwd><kwd> Community Acquired Pneumonia</kwd><kwd> Septicemia</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>P. aeruginosa is a frequent pathogen causing hospital-acquired pneumonia and healthcare-associated pneumonia, but is a rare cause of Community Acquired Pneumonia (CAP) in an immune competent host [<xref ref-type="bibr" rid="scirp.71013-ref1">1</xref>] . However, P. aeruginosa CAP is prone to develop septicemia, is often rapidly progressive, and may be fatal [<xref ref-type="bibr" rid="scirp.71013-ref2">2</xref>] . Appropriate initial empiric antibiotic treatment is crucial in improving outcomes. We herein report a case of P. aeruginosa CAP with septicemia in a previously healthy woman who was successfully treated by appropriate antibiotic treatment.</p></sec><sec id="s2"><title>2. Case Report</title><p>A 53-year-old woman was brought by ambulance to the emergency department of our hospital due to fever and right shoulder pain for a few hours. She had no pertinent past medical history, family history, or recent history of overseas travel. However, she had been a smoker of 20 cigarettes per day for 30 years. On examination, her body temperature was 36.3˚C, blood pressure was 90/40 mmHg, pulse rate was 100 beats/min, respiratory rate was 22 breaths/min, and oxygen saturation was 97% at an oxygen support of 10 L/min by face mask. Auscultation of the chest revealed coarse crackles on the right upper lobe. Initial laboratory tests revealed white blood cell (WBC) count of 6740 cells/&#181;L, and elevations of C-reactive protein (CRP; 2.94 mg/dl), procalcitonin (PCT; 37.73 ng/ml). And arterial blood gas revealed lactic acidosis (pH; 7.363, base excess; -0.5 mmol/L, lactate; 22.6 mg/dl). Chest radiograph showed right upper lobe consolidation and computed tomography (CT) scan showed air space consolidation in the posterior segment of the right upper lobe (<xref ref-type="fig" rid="fig1">Figure 1</xref>).</p><p><xref ref-type="fig" rid="fig2">Figure 2</xref> summarizes her clinical course in the hospital. She was diagnosed as septic shock due to lobar pneumonia. Treatment with bolus infusion of lactated Ringer’s solution and norepinephrine (0.3 &#181;g/kg/min) was started at the emergency room. She did not require emergency intubation, but she was transferred to the intensive care unit. Sputum Gramstain on admission showed Gram-negative rods with phagocytosis. At the emergency room, empiric antibiotic treatment with intravenous meropenem (MEPM) at 3 g/day was immediately started. The results of blood and sputum cultures were positive for P. aeruginosa. An acid-fast stain of the sputum was negative. After the 4th day of hospitalization, cardiovascular stabilization was achieved and norepinephrine drip was discontinued. Subsequently, her clinical symptoms and the level of CRP improved and her body temperature normalized. On the 7thday of hospitalization, antibiotic treatment was de-escalated to intravenous ciprofloxacin (CPFX) at 0.6 g/day.</p><p>A repeat chest CT scan on the 11th hospital day showed reduction of air space consolidation, but anew cavity formation was observed (<xref ref-type="fig" rid="fig3">Figure 3</xref>). Although not detected in any of the specimens, co-infection with an anaerobe was suspected and intravenous clindamycin (CLDM) at 2.4 g/day was added and continued for 10 days. Follow-up chest radiograph and CT scan on the 24th hospital day revealed further improvement of the consolidation and resolution of the cavity (<xref ref-type="fig" rid="fig4">Figure 4</xref>). Intravenous CPFX was continued until discharge on the 28th hospital day and oral CPFX was prescribed for one more week after discharge. Six months after discharge, there were no clinical symptoms of recurrence and follow-up chest radiograph revealed resolution of the infiltrates (<xref ref-type="fig" rid="fig5">Figure 5</xref>).</p></sec>
<sec id="s3">
<title>3. Discussion</title>
<p>P. aeruginosa is a frequent pathogen causing hospital-acquired pneumonia and healthcare-associated pneumonia [<xref ref-type="bibr" rid="scirp.71013-ref1">1</xref>] [<xref ref-type="bibr" rid="scirp.71013-ref3">3</xref>] . However, CAP secondary to P. aeruginosa is uncommon, with an incidence of only 0.6%, as shown in Sibila’s cohort study on 62,689 pneumonia patients aged ≥65 years old [<xref ref-type="bibr" rid="scirp.71013-ref4">4</xref>] . It is often rapidly progressive and may be fatal [<xref ref-type="bibr" rid="scirp.71013-ref4">4</xref>] , with a 30-day mortality rate of 17.4% [<xref ref-type="bibr" rid="scirp.71013-ref4">4</xref>] .</p><p>There have been only 12 case reports found in PubMed on P. aeruginosa CAP with septicemia in patients without comorbidities (<xref ref-type="table" rid="table1">Table 1</xref>) [<xref ref-type="bibr" rid="scirp.71013-ref3">3</xref>] [<xref ref-type="bibr" rid="scirp.71013-ref5">5</xref>] - [<xref ref-type="bibr" rid="scirp.71013-ref13">13</xref>] . The clinical characteristics of these cases were pleuritic chest pain and right upper lobe predilection; in</p><p>addition, mortality rate was high. The outcome was shown to be dependent on initiation of appropriate antibiotic therapy against P. aeruginosa within the first 48 hours of</p><fig id="fig1"  position="float"><label><xref ref-type="fig" rid="fig1">Figure 1</xref></label><caption><title> Chest radiograph and computed tomography (CT) scan of the chest. (a) Chest radiograph obtained at the emergency room shows right upper lobe consolidation (red arrow); (b) CT scan of the chest showed air space consolidation in the posterior segment of the right upper lobe (red arrow)</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-2770707x2.png"/></fig><fig id="fig2"  position="float"><label><xref ref-type="fig" rid="fig2">Figure 2</xref></label><caption><title> Course of treatment. The level of C-reactive protein (CRP) improved and her body temperature normalized MEPM: meropenem, CPFX: ciprofloxacin, CLDM: clindamycin, NA: norepinephrine</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-2770707x3.png"/></fig><p>admission [<xref ref-type="bibr" rid="scirp.71013-ref14">14</xref>] , therefore, timely appropriate empiric antibiotic treatment is crucial [<xref ref-type="bibr" rid="scirp.71013-ref14">14</xref>] . For this patient, we chose MEPM because the main target of treatment was septicemia due to lobar pneumonia and based on the presence of gram-negative rods on sputum. Gramstain is the most commonly performed microbiology test that can immediately identify the cause of a bacterial infection. Henderson et al. [<xref ref-type="bibr" rid="scirp.71013-ref10">10</xref>] suggest that P. aeruginosa CAP should be suspected in any patient who has gram-negative bacilli seen on sputum sample. Gram-negative bacteria include P. aeruginosa, which is reported to be one of the risk factors for death in CAP patients [<xref ref-type="bibr" rid="scirp.71013-ref15">15</xref>] .</p><p>P. aeruginosa CAP may sometimes progressive to cavitary pneumonia [<xref ref-type="bibr" rid="scirp.71013-ref2">2</xref>] [<xref ref-type="bibr" rid="scirp.71013-ref3">3</xref>] or lung abscess; for the latter, anaerobes are the major pathogens involved and may co-infect</p><fig-group id="fig3"><label><xref ref-type="fig" rid="fig3">Figure 3</xref></label><caption><title> Follow-up chest radiograph and CT scan of the chest. (a) Follow-up chest radiograph on the 15th day of hospitalization shows improvement of the right upper lobe consolidation (red arrow); (b) Follow-up CT scan of the chest on the 15th day of hospitalization showed improvement of air space consolidation, but a new cavity on the right upper lobe (red arrow).</title></caption><fig id ="fig3_1"><label> (b)</label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-2770707x4.png"/></fig></fig-group><fig-group id="fig4"><label><xref ref-type="fig" rid="fig4">Figure 4</xref></label><caption><title> Follow-up chest radiograph and CT scan of the chest. (a) Follow-up chest radiograph on the 24th day of hospitalization shows further improvement of the right upper lobe consolidation (red arrow); (b) Follow-up CT scan of the chest on the 24th day of hospitalization showed stability of the air space consolidation, but resolution of the cavitation (red arrow).</title></caption><fig id ="fig4_1"><label> (b)</label><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-2770707x5.png"/></fig></fig-group><fig id="fig5"  position="float"><label><xref ref-type="fig" rid="fig5">Figure 5</xref></label><caption><title> Follow-up chest radiograph. Follow- up chest radiograph 6 months after discharge revealed almost complete resolution of the infiltrates</title></caption><graphic mimetype="image"   position="float"  xlink:type="simple"  xlink:href="http://html.scirp.org/file/5-2770707x6.png"/></fig></sec></body>
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