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Table 1.  

Category Site of diagnosis   Transplant recipient Total, n = 268
MN, n = 129 AZ, n = 87 FL, n = 52 No, n = 186 Yes, n = 82
Demographics
   Age, mean (SD) 63.4 (16.3) 65.9 (15.0) 61.2 (11.7)   66.1 (15.7) 58.6 (12.4) 63.8 (15.1)
   Sex
      M 61 (47.3) 41 (47.1) 37 (71.2)   83 (44.6) 56 (68.3) 139 (51.9)
      F 68 (52.7) 46 (52.9) 15 (28.8)   103 (55.4) 26 (31.7) 129 (48.1)
   White 121 (97.6) 71 (84.5) 39 (76.5)   173 (96.6) 58 (72.5) 231 (89.2)
   Hispanic 0 (0.0) 12 (14.0) 3 (5.9)   4 (2.2) 11 (13.4) 15 (5.7)
Coexisting conditions
   Diabetes 7 (5.4) 18 (20.7) 23 (44.2)   12 (6.5) 36 (43.9) 48 (17.9)
   Liver failure 4 (3.1) 1 (1.1) 2 (3.8)   1 (0.5) 6 (7.3) 7 (2.6)
   Renal failure/dialysis 6 (4.7) 4 (4.6) 17 (32.7)   2 (1.1) 25 (30.5) 27 (10.1)
   Active malignancy 16 (12.5) 12 (13.8) 13 (25.0)   26 (14.0) 15 (18.5) 41 (15.4)
   Rheumatologic conditions 21 (16.4) 5 (5.7) 7 (13.5)   28 (15.1) 5 (6.2) 33 (12.4)
   Chronic lung disease 95 (74.8) 34 (39.1) 27 (51.9)   130 (69.9) 26 (32.5) 156 (58.6)
   Transplant recipient 14 (10.9) 35 (40.2) 33 (63.5)   NA NA 82 (30.6)
Transplanted organs
   Kidney 2 (14.3) 18 (51.4) 13 (39.4)   NA 33 (40.2) 33 (40.2)
   Liver 2 (14.3) 2 (5.7) 1 (3.0)   NA 5 (6.1) 5 (6.1)
   Pancreas 1 (7.1) 0 0   NA 1 (1.2) 1 (1.2)
   Lung 1 (7.1) 0† 12 (36.4)   NA 13 (15.9) 13 (15.9)
   Heart 2 (14.3) 9 (25.7) 2 (6.1)   NA 13 (15.9) 13 (15.9)
   Kidney and liver 1 (7.1) 0 1 (3.0)   NA 2 (2.4) 2 (2.4)
   Kidney and pancreas 0 0 3 (9.1)   NA 3 (3.7) 3 (3.7)
   HSCT 5 (35.7) 6 (17.1) 1 (3.0)   NA 12 (14.6) 12 (14.6)

Table 1. Patient demographics and coexisting conditions by site of diagnosis and transplant status in study of invasive Nocardia infections across 3 distinct geographic regions, United States*

*Values are no. (%) patients except at indicated. AZ, Mayo Clinic Arizona, Phoenix/Scottsdale, Arizona, USA; FL, Mayo Clinic Florida, Jacksonville, Florida, USA; HSCT, hematopoietic stem cell transplant; MN, Mayo Clinic Rochester, Rochester, Minnesota, USA; NA, not applicable. †Lung transplantations not performed at Mayo Clinic Arizona during study period.

Table 2.  

Disease characteristics Site of diagnosis   Transplant recipient Total, n = 268
MN, n = 129 AZ, n = 87 FL, n = 52   No, n = 186 Yes, n = 82
Diseased organ
   Lung only 106 (82.2) 80 (92.0) 31 (59.6)   157 (84.4) 60 (73.2) 217 (81.0)
   Skin/soft tissue only 8 (6.2) 0 (0.0) 10 (19.2)   11 (5.9) 7 (8.5) 18 (6.7)
   Disseminated 15 (11.6) 7 (8.0) 11 (21.2)   18 (9.7) 15 (18.3) 33 (12.3)
      Any CNS involvement 6 (4.7) 5 (5.7) 5 (9.6)   6 (3.2) 10 (12.2) 16 (6.0)
Nocardia spp.
   N. abscessus 13 (10.1) 1 (1.1) 3 (5.8)   14 (7.5) 3 (3.7) 17 (6.3)
   N. brevicatena/N. paucivorans 3 (2.3) 2 (2.3) 0   2 (1.1) 3 (3.7) 5 (1.9)
   N. cyriacigeorgica 24 (18.6) 36 (41.4) 8 (15.4)   52 (28.0) 16 (19.5) 68 (25.4)
   N. farcinica 26 (20.2) 13 (14.9) 8 (15.4)   30 (16.1) 17 (20.7) 47 (17.5)
   N. nova complex 43 (33.3) 2 (2.3) 6 (11.5)   44 (23.7) 7 (8.5) 51 (19.0)
   N. transvalensis complex 1 (0.8) 10 (11.5) 1 (1.9)   10 (5.4) 2 (2.4) 12 (4.5)
   N. brasiliensis 2 (1.6) 2 (2.3) 9 (17.3)   8 (4.3) 5 (6.1) 13 (4.9)
   N. wallacei 0 12 (13.8) 1 (1.9)   7 (3.8) 6 (7.3) 13 (4.9)
   N. veterana 1 (0.8) 2 (2.3) 2 (3.8)   0 5 (6.1) 5 (1.9)
   Other† 16 (12.4) 7 (8.0) 14 (26.9)   19 (10.2) 18 (22.0) 37 (13.8)
Outcomes
   Alive after 1 y 108 (91.5) 69 (83.1) 44 (84.6)   155 (90.6) 66 (80.5) 221 (87.4)
   Died within 1 y 21 (8.5) 18 (16.9) 8 (15.4)   31 (9.4) 16 (19.5) 47 (12.6)

Table 2. Disease characteristics and outcomes by site of diagnosis and transplant status in study of invasive Nocardia infections across 3 distinct geographic regions, United States*

*Values are no. (%) patients. AZ, Mayo Clinic Arizona, Phoenix/Scottsdale, Arizona, USA; CNS, central nervous system; FL, Mayo Clinic Florida, Jacksonville, Florida, USA; MN, Mayo Clinic Rochester, Rochester, Minnesota, USA. †Other species (n<5 each): N. amikacinitolerans (1), N. asiatica (1), N. asteroides (3), N. beijingensis (3), N. carnea (1), N. cerradoensis (1), N. exalbida (1), N. flavorosea (1), N. kruczakiae (1), N. niwae (2), N. otitidiscaviarum (1), N. pseudobrasiliensis (4), N. puris (1), N. takedensis (3), N. vermiculata (1), N. vinacea (1), N. yamanashiensis (1); no species identified (9).

Table 3.  

Species No.
isolates
Susceptibility
AM/CL CEF CTX IMP CIP MOX CLA AMI TOB DOX MIN TMP/SMX LIN
N. abscessus 17 82 82 94 59 0 14 41 100 94 88 88 94 100
N. brevicatena/N. paucivorans 5 50 75 100 100 100 100 100 100 100 100 100 100 100
N. cyriacigeorgica 68 6 28 60 97 2 3 2 99 99 6 9 100 100
N. farcinica 47 96 4 4 87 57 88 4 100 0 0 6 100 100
N. nova complex 51 4 51 12 98 4 7 100 98 6 2 18 100 100
N. transvalensis complex 12 92 17 58 8 58 100 0 8 0 0 17 100 100
N. brasiliensis 13 100 0 0 15 0 46 0 100 100 8 0 100 100
N. wallacei 13 92 8 67 0 58 100 0 25 0 17 50 100 100
N. veterana 5 0 60 20 100 0 0 100 100 20 0 20 100 100
Other† 37 11 44 61 78 42 61 50 94 86 47 67 92 97
Total 268 40 33 40 78 24 40 33 91 51 17 27 99 100

Table 3. Antimicrobial susceptibilities based on Nocardia spp. in study of invasive Nocardia infections across 3 distinct geographic regions, United States*

*AM/CL, amoxicillin/clavulanic acid; CEF, cefepime; CTX, ceftriaxone; IMP, imipenem; CIP, ciprofloxacin; MOX, moxifloxacin; CLA, clarithromycin; AMI, amikacin; TOB, tobramycin; DOX, doxycycline; MIN, minocycline; TMP/SMX, trimethoprim/sulfamethoxazole; LIN, linezolid †Other species (n<5 each): N. amikacinitolerans (1), N. asiatica (1), N. asteroides complex (3), N. beijingensis (3), N. carnea (1), N. cerradoensis (1), N. exalbida (1), N. flavorosea (1), N. kruczakiae (1), N. niwae (2), N. otitidiscaviarum (1), N. pseudobrasiliensis (4), N. puris (1), N. takedensis (3), N. vermiculata (1), N. vinacea (1), and N. yamanashiensis (1); no species identified (9)

Table 4.  

Initial treatment No. (%) Treatment after species confirmation and antimicrobial susceptibility testing results
AM/
CL
CEF CTX IMP CIP MOX CLA AMI TOB DOX MIN TMP/
SMX
LIN SUL Other†
AM/CL 7 (2.6) 57 0 0 14 14 14 14 0 0 0 0 57 0 0 0
CEF 3 (1.1) 0 100 0 0 0 0 0 0 33 33 0 67 0 0 0
CTX 22 (8.2) 14 0 27 5 5 18 9 5 0 9 14 45 5 9 5
IMP 49 (18.3) 16 0 8 22 0 22 8 2 0 4 31 69 0 4 2
CIP 7 (2.6) 14 0 0 0 86 0 0 0 0 0 14 43 14 0 29
MOX 19 (7.1) 11 0 11 16 0 74 11 0 0 5 16 37 0 0 0
CLA 10 (3.7) 0 0 0 0 10 20 80 10 0 0 10 20 0 0 10
AMI 8 (3.0) 25 0 0 0 13 13 25 13 0 0 13 75 0 13 0
TOB 2 (0.8) 0 50 0 0 0 0 0 0 50 0 0 50 0 0 0
DOX 15 (5.6) 20 7 0 20 7 13 0 0 0 33 0 73 0 7 0
MIN 27 (10.1) 11 0 7 7 4 30 7 0 0 4 37 52 0 0 0
TMP/SMX 153 (57.1) 6 1 7 5 5 5 17 3 1 4 10 82 2 3 3
LIN 21 (7.8) 19 0 10 19 5 33 5 0 0 5 38 57 5 10 0
SUL 4 (1.5) 25 0 50   0 25 0 0 0 0 25 0 0 75 0
Other 15 (5.6) 7 0 7 7 13 0 0 0 0 13 13 60 0 0 13

Table 4. Choice of initial/empiric antimicrobials and subsequent antimicrobials after susceptibilities were reported in study of invasive Nocardia infections across 3 distinct geographic regions, United States*

*Gray shaded cells show percentages of patients in which initial antimicrobial was retained as part of subsequent therapy. AM/CL, amoxicillin/clavulanic acid; CEF, cefepime; CTX, ceftriaxone; IMP, imipenem; CIP, ciprofloxacin; MOX, moxifloxacin; CLA, clarithromycin; AMI, amikacin; TOB, tobramycin; DOX, doxycycline; MIN, minocycline; TMP/SMX, trimethoprim/sulfamethoxazole; LIN, linezolid, SUL, sulfadiazine †Other species (n<5 each): N. amikacinitolerans (1), N. asiatica (1), N. asteroides complex (3), N. beijingensis (3), N. carnea (1), N. cerradoensis (1), N. exalbida (1), N. flavorosea (1), N. kruczakiae (1), N. niwae (2), N. otitidiscaviarum (1), N. pseudobrasiliensis (4), N. puris (1), N. takedensis (3), N. vermiculata (1), N. vinacea (1), and N. yamanashiensis (1); no species identified (9).

CME / ABIM MOC

Invasive Nocardia Infections Across Distinct Geographic Regions, United States

  • Authors: Simran Gupta, MD; Leah M. Grant, MD; Harry R. Powers, MD; Kathryn E. Kimes, DO; Ahmed Hamdi, MD; Richard J. Butterfield, MA; Juan Gea-Banacloche, MD; Prakhar Vijayvargiya, MBBSD; D. Jane Hata, PhD; Diana M. Meza Villegas, MS; Adrian C. Dumitrascu, MD; Dana M. Harris, MD; Razvan M. Chirila, MD; Nan Zhang, PhD; Raymund R. Razonable, MD; Shimon Kusne, MD; Salvador Alvarez, MD; Holenarasipur R. Vikram, MD
  • CME / ABIM MOC Released: 11/17/2023
  • Valid for credit through: 11/17/2024, 11:59 PM EST
Start Activity

  • Credits Available

    Physicians - maximum of 1.00 AMA PRA Category 1 Credit(s)™

    ABIM Diplomates - maximum of 1.00 ABIM MOC points

    You Are Eligible For

    • Letter of Completion
    • ABIM MOC points

Target Audience and Goal Statement

This activity is intended for primary care clinicians, infectious disease specialists, and other healthcare professionals who treat and manage patients with Nocardia infection.

The goal of this activity is for members of the healthcare team to be better able to assess patterns of infection and outcomes of Nocardia infection.

Upon completion of this activity, participants will:

  • Analyze the bacteriology of Nocardia
  • Evaluate patterns of infection with Nocardia in the current study
  • Differentiate infection sites based on different Nocardia species among transplant recipients
  • Analyze antibiotic susceptibility and survival data in the current study of patients with Nocardia infection


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Medscape, LLC requires every individual in a position to control educational content to disclose all financial relationships with ineligible companies that have occurred within the past 24 months. Ineligible companies are organizations whose primary business is producing, marketing, selling, re-selling, or distributing healthcare products used by or on patients.

All relevant financial relationships for anyone with the ability to control the content of this educational activity are listed below and have been mitigated. Others involved in the planning of this activity have no relevant financial relationships.


Faculty

  • Simran Gupta, MD

    Internal Medicine
    Mayo Clinic Arizona
    Scottsdale, Arizona

  • Leah M. Grant, MD

    Infectious Diseases
    Mayo Clinic Arizona
    Scottsdale, Arizona

  • Harry R. Powers, MD

    Infectious Diseases
    Mayo Clinic in Florida
    Jacksonville, Florida

  • Kathryn E. Kimes, DO

    Infectious Diseases
    Mayo Clinic Arizona
    Scottsdale, Arizona

  • Ahmed Hamdi, MD

    Infectious Diseases
    Mayo Clinic
    Rochester, Minnesota

  • Richard J. Butterfield, MA

    Quantitative Health Sciences
    Mayo Clinic Arizona
    Scottsdale, Arizona

  • Juan Gea-Banacloche, MD

    Infectious Diseases
    Mayo Clinic Arizona
    Scottsdale, Arizona

  • Prakhar Vijayvargiya, MBBSD

    Infectious Diseases
    Mayo Clinic
    Rochester, Minnesota

  • D. Jane Hata, PhD

    Pathology and Laboratory Medicine
    Mayo Clinic in Florida
    Jacksonville, Florida

  • Diana M. Meza Villegas, MS

    Pathology and Laboratory Medicine
    Mayo Clinic in Florida
    Jacksonville, Florida

  • Adrian C. Dumitrascu, MD

    Internal Medicine
    Mayo Clinic in Florida
    Jacksonville, Florida

  • Dana M. Harris, MD

    Internal Medicine
    Mayo Clinic in Florida
    Jacksonville, Florida

  • Razvan M. Chirila, MD

    Internal Medicine
    Mayo Clinic in Florida
    Jacksonville, Florida

  • Nan Zhang, PhD

    Quantitative Health Sciences
    Mayo Clinic Arizona
    Scottsdale, Arizona

  • Raymund R. Razonable, MD

    Infectious Diseases
    Mayo Clinic
    Rochester, Minnesota

  • Shimon Kusne, MD

    Infectious Diseases
    Mayo Clinic Arizona
    Scottsdale, Arizona

  • Salvador Alvarez, MD

    Infectious Diseases
    Mayo Clinic in Florida
    Jacksonville, Florida

  • Holenarasipur R. Vikram, MD

    Infectious Diseases
    Mayo Clinic Arizona
    Scottsdale, Arizona

Editor

  • Tony Pearson-Clarke, MS

    Copyeditor
    Emerging Infectious Diseases

CME Author

  • Charles P. Vega, MD

    Health Sciences Clinical Professor of Family Medicine
    University of California, Irvine School of Medicine
    Irvine, California

    Disclosures

    Charles P. Vega, MD, has the following relevant financial relationships:
    Consultant or advisor for: Boehringer Ingelheim; GlaxoSmithKline; Johnson & Johnson

Compliance Reviewer

  • Maria Morales, MSN, RN, CLNC

    ​​Associate Director, Accreditation and Compliance, Medscape, LLC​ 

    Disclosures

    Maria Morales, MSN, RN, CLNC, has no relevant financial relationships. 


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Interprofessional Continuing Education

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    Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to 1.0 MOC points in the American Board of Internal Medicine’s (ABIM) Maintenance of Certification (MOC) program. Participants will earn MOC points equivalent to the amount of CME credits claimed for the activity. It is the CME activity provider’s responsibility to submit participant completion information to ACCME for the purpose of granting ABIM MOC credit. Aggregate participant data will be shared with commercial supporters of this activity.

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CME / ABIM MOC

Invasive Nocardia Infections Across Distinct Geographic Regions, United States

Authors: Simran Gupta, MD; Leah M. Grant, MD; Harry R. Powers, MD; Kathryn E. Kimes, DO; Ahmed Hamdi, MD; Richard J. Butterfield, MA; Juan Gea-Banacloche, MD; Prakhar Vijayvargiya, MBBSD; D. Jane Hata, PhD; Diana M. Meza Villegas, MS; Adrian C. Dumitrascu, MD; Dana M. Harris, MD; Razvan M. Chirila, MD; Nan Zhang, PhD; Raymund R. Razonable, MD; Shimon Kusne, MD; Salvador Alvarez, MD; Holenarasipur R. Vikram, MDFaculty and Disclosures

CME / ABIM MOC Released: 11/17/2023

Valid for credit through: 11/17/2024, 11:59 PM EST

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Abstract and Introduction

Abstract

We reviewed invasive Nocardia infections in 3 noncontiguous geographic areas in the United States during 2011–2018. Among 268 patients with invasive nocardiosis, 48.2% were from Minnesota, 32.4% from Arizona, and 19.4% from Florida. Predominant species were N. nova complex in Minnesota (33.4%), N. cyriacigeorgica in Arizona (41.4%), and N. brasiliensis in Florida (17.3%). Transplant recipients accounted for 82/268 (30.6%) patients overall: 14 (10.9%) in Minnesota, 35 (40.2%) in Arizona, and 33 (63.5%) in Florida. Manifestations included isolated pulmonary nocardiosis among 73.2% of transplant and 84.4% of non–transplant patients and central nervous system involvement among 12.2% of transplant and 3.2% of non–transplant patients. N. farcinica (20.7%) and N. cyriacigeorgica (19.5%) were the most common isolates among transplant recipients and N. cyriacigeorgica (38.0%), N. nova complex (23.7%), and N. farcinica (16.1%) among non–transplant patients. Overall antimicrobial susceptibilities were similar across the 3 study sites.

Introduction

Nocardia is a genus of aerobic, filamentous, beaded, gram-positive bacteria ubiquitous in the environment, especially in soil, decomposing organic matter, and water. Nocardia spp. are opportunistic pathogens in immunocompromised hosts and immunocompetent persons with chronic lung disease[1]. The Centers for Disease Control and Prevention has estimated that the United States sees 500–1,000 new cases of Nocardia infection annually[2,3]. Pulmonary infections acquired by inhaling aerosolized organisms account for most Nocardia-associated illness[4]. Direct inoculation, which causes cutaneous infections, constitutes the second most common route of exposure[3,5]. Patients with defects in cell-mediated immunity are at highest risk for infection[6,7]. Other risk factors include systemic corticosteroid use, solid organ or hematopoietic stem cell transplantation, HIV infection, diabetes mellitus, and underlying malignancy being treated with chemotherapy[8]. The brain, skin, and soft tissues, and to a lesser degree bones and joints or other organs, comprise the most common sites of extrapulmonary dissemination[6,9].

Geographic distribution of various Nocardia spp. and their effect on human disease has not been described. Although N. cyriacigeorgica (formerly N. asteroides drug pattern type VI)[10,11] and N. farcinica are distributed evenly throughout the United States, distribution of other Nocardia spp. varies by geographic location. N. brasiliensis is associated with tropical and subtropical environments and has a higher prevalence in the southwestern and southeastern regions of the United States[4,12]. Because Mayo Clinic, headquartered in Rochester, Minnesota, USA, operates tertiary locations in the midwestern, southeastern, and southwestern United States, we had a unique opportunity to study Nocardia infections in those 3 distinct noncontiguous geographic areas.