Skip to main content

CASE REPORT article

Front. Med., 17 July 2024
Sec. Pulmonary Medicine
This article is part of the Research Topic Case Reports in Pulmonary Medicine 2024 View all 7 articles

Case report: From oral infection to life-threatening pneumonia: clinical considerations in Nocardia infection from a case

Kang Chen&#x;Kang Chen1Ying Wang&#x;Ying Wang2Jing Dong&#x;Jing Dong3Ping-Shang WuPing-Shang Wu1Jun Yang
Jun Yang4*Guo-Ping Ai
Guo-Ping Ai5*
  • 1Department of Thoracic Cardiovascular Surgery, The Third Hospital of Wuhan, Wuhan, China
  • 2Department of Otolaryngology, Qingdao Hospital, University of Health and Rehabilitation Sciences (Qingdao Municipal Hospital), Qingdao, China
  • 3Department of Endocrinology, General Hospital of Central Theater Command of the People's Liberation Army, Wuhan, China
  • 4Department of Stomatology, General Hospital of Central Theater Command of the People's Liberation Army, Wuhan, China
  • 5Department of Radiology, General Hospital of Central Theater Command of the People's Liberation Army, Wuhan, China

Nocardia is an anthropozoonotic bacteria that occurs widely in the natural environment. However, because it is a gram-positive aerobic opportunistic pathogen, it rarely occurs in patients with no prior history of immune function disease. Since the symptoms are nonspecific the diagnosis of Nocardia pneumonia is challenging. Previous studies have not reported that this anthropozoonotic bacteria colonizing the human body could cause severe pneumonia by gingival pain and pharyngeal discomfort. This case report describes a previously healthy 60-year-old female farmer who presented to the doctor with gingival pain and pharyngeal discomfort. She was treated with a dental cleaning and oral metronidazole. The patient rapidly progressed to breathing difficulties. Lung shadow was found by computerized tomography examination. The radiologist diagnosed pulmonary tuberculosis as image-based. Through laboratory examination and culture of pathogenic microorganisms in the sputum and blood of the patient, no obvious positive findings were found. The disease progressed rapidly to tracheal intubation ventilator assisted breathing. Subsequently, the patient underwent alveolar lavatory examination under endotracheal intubation fiberbronchoscopy, and the culture of alveolar lavage fluid indicated Nocardia. According to this result, the patient’s disease was quickly controlled after selecting the targeted drug compound sulfamethoxazole and intravenous meropenem for treatment. In view of the reason for the high misdiagnosis rate due to the low positive rate of Nocardia culture in most cases, the clinical thinking of diagnosis and treatment from oral infection symptoms to fatal pneumonia reported in this case has certain clinical popularization and enlighten significance, not only improved the diagnosis and treatment of rare diseases, but also be reduced medical disputes.

Introduction

The clinical manifestations and imaging examinations of pulmonary nocardiosis were nonspecific (1). In addition to the detection of pathogens by culture or next-generation sequencing (NGS) analysis of species, source, and drug sensitivity of pathogens, general laboratory tests also had no specificity and/or sensitivity indicators (2, 3). However, Nocardia pneumophila grew very slowly in in vitro medium and was easily covered by other fast-growing bacteria, which made it difficult to be detected (4, 5). Nocardia, as an opportunistic anthropozoonotic bacteria pathogen, is resistant to general antibiotics (6). As a result, infection of the lungs of even healthy people with this organism can lead to rapid progression and catastrophic consequences (7). We report a case of pulmonary nocardiosis with rapid progression from oral symptoms in order to promote the attention of clinicians to this disease.

Case report

A 60-year-old female farmer, previously healthy, with no immune-related diseases. The patient visited the hospital due to gingival pain and pharyngeal discomfort. The body temperature was 38.6°C, the gums were red and swollen (Figure 1A), the pharynx was congested, and the tonsils were bilateral II degree enlarged. A diagnosis of tonsillitis and gingivitis was made by the community doctor. She was treated with dental cleaning and oral metronidazole. However, the symptoms did not relieve. Three days later, the patient developed dyspnea. Physical examination revealed tachypnea (42 beats/min), moist rales in both lungs, low breath sounds in the right lower lung, a regular heart rate of 131 beats /min, and no obvious heart murmur. The abdomen was soft and non-tender. The patient underwent chest CT, which revealed multiple solid opacities in the right lung (Figures 1BD). The radiologist believes that pulmonary tuberculosis should be the preferred consideration. The patient’s hemocyte, blood biochemical, and blood tuberculosis laboratory tests are shown in Table 1. After multidisciplinary team (MDT) discussion based on the medical history, the diagnosis of this case should be considered pulmonary infection firstly, and the possibility of tuberculosis cannot be excluded. Therefore, the patient was treated with intravenous ceftriaxone sodium, an intravenous anti-inflammatory therapy. After 3 days of treatment, the patient’s symptoms worsened tachypnea developed. A repeat CT scan of the chest was performed, which revealed a markedly enlarged area of patchy hyperdensity in the right lung and spread to the left lung (Figures 1EG). In cases where respiration could not be maintained, the patient was placed a ventilator assisted respiration with endotracheal intubation. Blood and sputum cultures were obtained, and both were negative. After MDT discussion again, G test, GM test and cryptococcus detection should be improved, and fiberoptic bronchoscopy should be improved if conditions permit. Pulmonary fungal infection combined with bacterial infection should be considered in the diagnosis. Intravenous meropenem combined with voriconazole was given as anti-inflammatory treatment. Subsequent tests, G test, GM test, cryptococcal antigen were all negative. No abnormalities were found in the bronchi except for thick sputum. No tumor or severe inflammation was found in the trachea by fiberoptic bronchoscopy (Figures 2AC). As an unexpected bonus, Nocardia was found the bronchoalveolar lavage fluid smear and a week of culture (Figures 2DG). At this point, the patient was diagnosed multisite infection by Nocardia. Based on the drug susceptibility analysis of bacterial culture, compound sulfamethoxazole 1.5 g every 6 h was given nasal feeding combined with intravenous meropenem. Two days later, the patient’s temperature got normalized, her spirits got improved gradually. The symptoms of gingival pain, pharyngeal discomfort and dyspnea with her did relieve also. Two weeks after treatment, the patient underwent a repeat CT scan of the chest, which revealed a reduction in the extent of bilateral lung shadow. The patient was scheduled to be discharged with oral trimethoprim-sulfamethoxazole for another 3 months. Subsequent follow-up chest CT showed that the lesions in both lungs were basically absorbed (Figures 3AC). The symptoms of the oral and respiratory with her completely disappeared, and she was very satisfied with the treatment.

Figure 1
www.frontiersin.org

Figure 1. The timeline of the patient’ disease progression. Gingivitis and oral hygiene of the patients (A); 16-slice computerized tomography images of the chest at initial diagnosis of the patient, neck (B), upper lobe (C), lower lobe (D); 16-slice computerized tomography images of the chest in the advanced stage of the patient, neck (E), upper lobe (F), lower lobe (G).

Table 1
www.frontiersin.org

Table 1. Laboratory test results of the patient.

Figure 2
www.frontiersin.org

Figure 2. Picture of the bronchus of the right lung of the patient under a fiberoptic bronchoscope (A, main bronchus; B, lower lobe bronchus; C, basal segment bronchus) and microbe detected by fiberoptic bronchoscopic lavage fluid smear (D, culture original; E, micrograph of pathogenic bacteria; F, the standard acid-fast stain; G, the modified weakly acid-fast).

Figure 3
www.frontiersin.org

Figure 3. 16-slice computerized tomography images of the chest during follow-up after the patient was cured. (A) Neck; (B) upper lobe; (C) lower lobe.

Discussion

Nocardia is an aerobic prokaryotic actinomycete, widely exists in soil, air, decaying plants and other organic matter (8). It is an opportunistic pathogen of human, livestock and poultry. So far, a total of 791 nocardia isolates have been identified, of which 119 Nocardia species with effective names have been confirmed in literature, and 54 Nocardia species are related to human infection (9). It does not belong to the normal flora of human body, so it is not an endogenous infection. So, if this bacterium is detected in laboratory culture or NGS, it must be pathogenic. Unlike Candida, which can colonize the human body (10). Nocardia species often invade the human body from respiratory tract, oral mucosa lesions and skin lesions, and spread to lung, brain and other organs through respiratory tract and blood, which is easy to cause infection (11). Nocardial is aerobic, and the colonies were smooth and moist when cultured at 37° with general medium, grows into macroscopic colonies within 2–6 days, obtain satisfactory culture results requiring 4–6 weeks (12, 13). The colonies varied in color, including cheese, yellow, pink, coral red, and orange red (14, 15).

Besides, Nocardia belongs to the order actinomycetes, which was first isolated by Nocard in 1888 (16). It is similar to that of Mycobacterium tuberculosis (17). However, Nocardial mycelial ends did not show club-like expansion, different concentrations of decolorization solution were used for acid-fast staining, and the lower the concentration of decolorization solution used, the higher the positive rate of acid-fast staining (18). Mycobacterium tuberculosis has strong acid resistance and is not easy to decolorize. Therefore, the weakly acid-fast staining method can be used to distinguish Nocardia from Mycobacteria.

Nocardia pneumonia should be differentiated from actinomyces pneumonia and aspergillus pneumonia in chest imaging (19). Sulfur particles can be found in actinomyces pneumonia, and aspergillus pneumonia is the most common pulmonary fungal disease (20). The typical clinical manifestations of Nocardia pneumonia in the early stage were nodules or masses with halo sign around them, and crescent sign could be seen when cavitation was formed (20). However, their imaging identification is complicated and difficult in clinical practice (21).

These specific factors determine the complexity of the diagnosis of Nocardia, which is why the patient in this case was not diagnosed for days. It is difficult to culture Nocardia from sputum, for one thing, it is difficult to detect by smear staining, which is often misinterpreted by other bacteria and causes false positive results (15). On the other hand, it is because of the rapid growth of oral flora during sputum culture, which often leads to the suppression of nocardia. In addition, the commonly used media and culture conditions are not conducive to the cultivation of Nocardia, which will also lead to false negative results. In addition, the growth of Nocardia is slow, and the culture time is short in most laboratories, resulting in the missed detection of some nocardia. Nocardia is not the normal flora of the human body, so it is very important to detect the pathogen from tissue or body fluid secretions. Although the next generation sequencing (NGS) analysis testing of species, source, and drug sensitivity of pathogens has the advantages of fast speed and high sensitivity, the price is relatively expensive. In China, this testing has not been routinely carried out in hospital, can be shipped to commercial biological companies, so it is not very convenient. Bronchoalveolar lavage fluid obtained from fiberoptic bronchoscopy can obtain pathogenic bacteria in the lower respiratory tract, and it is rarely contaminated by other bacteria, which is a valuable sampling material for pathogenic bacteria in clinical work (22, 23).

Previous studies showed that nocardial pneumonia accounted for 85% of all nocardiosis cases and the in-hospital mortality rate was 15.0% (6). Delays in diagnosis and treatment are the most common reasons. The diagnosis and treatment of this case was also tortuous. She started with gums inflammation by the unclean mouth, and it is understandable that metronidazole was given to the dentist. Then, the inflammation rapidly progressed to the lungs. After ruling out mycoplasma and chlamydia pneumonia, the patient was treated empiric with ceftriaxone. However, Nocardia is sensitive to sulfonamides, aminoglycosides, some cephalosporins, carbapenems and quinolones, and sulfonamides are the first choice for treatment (20, 24). The advantages of this drug are its good oral bioavailability and its good permeability into tissues and cerebrospinal fluid. The dosage should be adequate and the course of treatment should be long. Six weeks for immunocompetent patients with localized pulmonary nocardiosis and at least 6 months for immunocompromised patients (20). For patients with central nervous system spread, this should be extended to 12 months. For people with AIDS, 12 months or more (25).

Besides, low-dose maintenance therapy is recommended for immunosuppressed patients. At present, due to the high drug resistance rate of sulfonamides, the total drug resistance rate is more than 40%, and the combination therapy is advocated (20, 25). Carbapenems and linezolid are the two drugs with high sensitivity. Linezolid is the first to be sensitive to almost all nocardial species and is indicated for severe infections, disseminated nocardiosis, and sulfonamides allergy. It is suggested that the above drugs can be preferentially selected according to the condition of the patient in the treatment of refractory pulmonary nocardiosis. If the diagnosis is delayed, the mortality rate may reach 30–50% (6, 20, 26, 27). Therefore, early and rapid diagnosis and treatment are of great significance for the prognosis of patients.

Conclusion

This case illustrates the tortuous course of physician’s diagnosis and treatment of a healthy peasant woman with typical infection progression from oral infection to life-threatening pneumonia. From this tortuous process, we can learn the harmfulness of nocardiosis and the difficulty of diagnosis. It can provide some clinical thoughts for explaining a class of infectious diseases with common clinical symptoms but catastrophic outcomes, reduce medical disputes, and improve the diagnosis and treatment of rare diseases.

Data availability statement

The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding authors.

Ethics statement

Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.

Author contributions

KC: Data curation, Methodology, Project administration, Funding acquisition, Writing – review & editing. YW: Conceptualization, Formal analysis, Methodology, Resources, Software, Writing – original draft. JD: Data curation, Formal analysis, Investigation, Methodology, Software, Writing – original draft. P-SW: Conceptualization, Data curation, Formal analysis, Methodology, Writing – original draft. JY: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – original draft, Writing – review & editing. G-PA: Conceptualization, Data curation, Formal analysis, Funding acquisition, Investigation, Methodology, Project administration, Resources, Software, Supervision, Validation, Visualization, Writing – review & editing.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Acknowledgments

The authors thank the patient who agreed to be included in this report for her cooperation and support in academic communication.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

1. Wang, X, Liang, Y, Cheng, Q, Nong, W, and Hu, L. Abdominal abscesses caused by Nocardia farcinica in an immunocompromised patient: a case report and literature review. Infect Drug Resist. (2023) 16:7447–54. doi: 10.2147/IDR.S441117

PubMed Abstract | Crossref Full Text | Google Scholar

2. Tajima, Y, Tashiro, T, Furukawa, T, Murata, K, Takaki, A, Sugahara, K, et al. Pulmonary Nocardiosis with Endobronchial involvement caused by Nocardiaaraoensis. Chest. (2024) 165:e1–4. doi: 10.1016/j.chest.2023.07.067

PubMed Abstract | Crossref Full Text | Google Scholar

3. Weng, SS, Zhang, HY, Ai, JW, Gao, Y, Liu, YY, Xu, B, et al. Rapid detection of Nocardia by next-generation sequencing. Front Cell Infect Microbiol. (2020) 10:13. doi: 10.3389/fcimb.2020.00013

PubMed Abstract | Crossref Full Text | Google Scholar

4. Besteiro, B, Coutinho, D, Fragoso, J, Figueiredo, C, Nunes, S, Azevedo, C, et al. Nocardiosis: a single-center experience and literature review. Braz J Infect Dis. (2023) 27:102806. doi: 10.1016/j.bjid.2023.102806

PubMed Abstract | Crossref Full Text | Google Scholar

5. Miyamoto, M, Sasaki, Y, and Ohta, K. Pulmonary nocardiosis caused by Nocardia exalbida mimicking lung cancer. Respirol Case Rep. (2019) 7:e00458. doi: 10.1002/rcr2.458

PubMed Abstract | Crossref Full Text | Google Scholar

6. Yang, M, Xu, M, Wei, W, Gao, H, Zhang, X, Zhao, H, et al. Clinical findings of 40 patients with nocardiosis: a retrospective analysis in a tertiary hospital. Exp Ther Med. (2014) 8:25–30. doi: 10.3892/etm.2014.1715

PubMed Abstract | Crossref Full Text | Google Scholar

7. Al Umairi, RS, Pandak, N, and Al, BM. The findings of pulmonary Nocardiosis on chest high resolution computed tomography: single Centre experience and review of literature. Sultan Qaboos Univ Med J. (2022) 22:357–61. doi: 10.18295/squmj.9.2021.131

PubMed Abstract | Crossref Full Text | Google Scholar

8. Yuan, D, Shen, L, Qin, BE, Xu, X, Su, Z, Liu, J, et al. Central nervous system nocardiosis diagnosed by metagenomic next-generation sequencing: a case series and literature review. Adv Clin Exp Med. (2023) 32:1453–63. doi: 10.17219/acem/175818

PubMed Abstract | Crossref Full Text | Google Scholar

9. Wang, H, Zhu, Y, Cui, Q, Wu, W, Li, G, Chen, D, et al. Epidemiology and antimicrobial resistance profiles of the Nocardia species in China, 2009 to 2021. Microbiol Spectr. (2022) 10:e0156021. doi: 10.1128/spectrum.01560-21

PubMed Abstract | Crossref Full Text | Google Scholar

10. Miramón, P, Pountain, AW, and Lorenz, MC. Candida auris-macrophage cellular interactions and transcriptional response. Infect Immun. (2023) 91:e0027423. doi: 10.1128/iai.00274-23

PubMed Abstract | Crossref Full Text | Google Scholar

11. Sun, H, Goolam Mahomed, M, and Patel, J. Brain metastasis or nocardiosis? A case report of central nervous system Nocardiosis with a review of the literature. J Community Hosp Intern Med Perspect. (2021) 11:258–62. doi: 10.1080/20009666.2021.1877399

PubMed Abstract | Crossref Full Text | Google Scholar

12. Choquet, E, Rodriguez-Nava, V, Peltier, F, Wankap-Mogo, R, Bergeron, E, Joseph, C, et al. Nocardia neocaledoniensis as rare cause of spondylodiscitis. Emerg Infect Dis. (2023) 29:444–6. doi: 10.3201/eid2902.221389

PubMed Abstract | Crossref Full Text | Google Scholar

13. Nouioui, I, Pötter, G, Jando, M, and Goodfellow, M. Nocardia noduli sp. nov., a novel actinobacterium with biotechnological potential. Arch Microbiol. (2022) 204:260. doi: 10.1007/s00203-022-02878-x

PubMed Abstract | Crossref Full Text | Google Scholar

14. Liang, Y, Lin, M, Qiu, L, Chen, M, Tan, C, Tu, C, et al. Clinical characteristics of hospitalized patients with Nocardia genus detection by metagenomic next generation sequencing in a tertiary hospital from southern China. BMC Infect Dis. (2023) 23:772. doi: 10.1186/s12879-023-08615-z

Crossref Full Text | Google Scholar

15. Toyokawa, M, Taniguchi, M, Uesaka, K, and Nishimura, K. Complete genome sequence of multidrug-resistant strain Nocardia wallacei FMUON74, isolated from a sputum culture. Microbiol Resour Announc. (2020) 9:e01022–05. doi: 10.1128/MRA.01022-20

PubMed Abstract | Crossref Full Text | Google Scholar

16. McNeil, MM, and Brown, JM. The medically important aerobic actinomycetes: epidemiology and microbiology. Clin Microbiol Rev. (1994) 7:357–417. doi: 10.1128/CMR.7.3.357

PubMed Abstract | Crossref Full Text | Google Scholar

17. Chen, Y, and Hu, W. Co-infection with Mycobacterium tuberculosis and Nocardia farcinica in a COPD patient: a case report. BMC Pulm Med. (2023) 23:136. doi: 10.1186/s12890-023-02434-3

PubMed Abstract | Crossref Full Text | Google Scholar

18. Muricy, EC, Lemes, RA, Bombarda, S, Ferrazoli, L, and Chimara, E. Differentiation between Nocardia spp. and Mycobacterium spp.: critical aspects for bacteriological diagnosis. Rev Inst Med Trop São Paulo. (2014) 56:397–401. doi: 10.1590/s0036-46652014000500005

PubMed Abstract | Crossref Full Text | Google Scholar

19. Jouneau, S, Ménard, C, and Lederlin, M. Pulmonary alveolar proteinosis. Respirology. (2020) 25:816–26. doi: 10.1111/resp.13831

Crossref Full Text | Google Scholar

20. Lafont, E, Conan, PL, Rodriguez-Nava, V, and Lebeaux, D. Invasive Nocardiosis: disease presentation, diagnosis and treatment - old questions, new answers? Infect Drug Resist. (2020) 13:4601–13. doi: 10.2147/IDR.S249761

PubMed Abstract | Crossref Full Text | Google Scholar

21. Zhu, J, Huang, WC, Huang, B, Zhu, Y, Jiang, XJ, Zou, JN, et al. Clinical characteristics and prognosis of COVID-19 patients with initial presentation of lung lesions confined to a single pulmonary lobe. Am J Transl Res. (2020) 12:7501–9.

PubMed Abstract | Google Scholar

22. Wang, L, Lu, S, Guo, Y, Liu, J, Wu, P, and Yang, S. Comparative study of diagnostic efficacy of sputum and bronchoalveolar lavage fluid specimens in community-acquired pneumonia children treated with fiberoptic bronchoscopy. BMC Infect Dis. (2023) 23:565. doi: 10.1186/s12879-023-08522-3

PubMed Abstract | Crossref Full Text | Google Scholar

23. Li, L, Li, MJ, Sun, L, Jiang, YL, and Zhu, J. Neglected foreign body aspiration mimicking lung Cancer recurrence. Risk Manag Healthc Policy. (2022) 15:491–6. doi: 10.2147/RMHP.S361081

PubMed Abstract | Crossref Full Text | Google Scholar

24. Benndorf, R, Schwitalla, JW, Martin, K, de Beer, ZW, Vollmers, J, Kaster, AK, et al. Nocardia macrotermitis sp. nov. and Nocardia aurantia sp. nov., isolated from the gut of the fungus-growing termite Macrotermes natalensis. Int J Syst Evol Microbiol. (2020) 70:5226–34. doi: 10.1099/ijsem.0.004398

PubMed Abstract | Crossref Full Text | Google Scholar

25. Stefaniak, J . HIV/AIDS presenting with stroke-like features caused by cerebral Nocardia abscesses: a case report. BMC Neurol. (2015) 15:183. doi: 10.1186/s12883-015-0437-7

PubMed Abstract | Crossref Full Text | Google Scholar

26. Haussaire, D, Fournier, PE, Djiguiba, K, Moal, V, Legris, T, Purgus, R, et al. Nocardiosis in the south of France over a 10-years period, 2004-2014. Int J Infect Dis. (2017) 57:13–20. doi: 10.1016/j.ijid.2017.01.005

PubMed Abstract | Crossref Full Text | Google Scholar

27. Zhong, C, Huang, P, Zhan, Y, Yao, Y, Ye, J, and Zhou, H. Clinical features of pulmonary Nocardiosis in patients with different underlying diseases: a case series study. Infect Drug Resist. (2022) 15:1167–74. doi: 10.2147/IDR.S359596

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: Nocardia, severe acute diseaseintensive care, immunocompetent patient, pulmonary coinfection, case report

Citation: Chen K, Wang Y, Dong J, Wu P-S, Yang J and Ai G-P (2024) Case report: From oral infection to life-threatening pneumonia: clinical considerations in Nocardia infection from a case. Front. Med. 11:1424564. doi: 10.3389/fmed.2024.1424564

Received: 28 April 2024; Accepted: 01 July 2024;
Published: 17 July 2024.

Edited by:

Giuseppe Fiorentino, Hospital of the Hills, Italy

Reviewed by:

Serkan Surme, Istanbul University-Cerrahpasa, Türkiye
Tohru Gonoi, Chiba University, Japan

Copyright © 2024 Chen, Wang, Dong, Wu, Yang and Ai. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Jun Yang, 705500524@qq.com; Guo-Ping Ai, zbzqzyyagp@126.com

These authors have contributed equally to this work and share first authorship

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.