Your new experience awaits. Try the new design now and help us make it even better

CASE REPORT article

Front. Med., 01 August 2025

Sec. Pulmonary Medicine

Volume 12 - 2025 | https://doi.org/10.3389/fmed.2025.1555471

Polyinfection secondary to exogenous lipoid pneumonia caused by aspiration of paraffin oil: a Case Report


Xiaoru Yan&#x;Xiaoru YanXun Chen&#x;Xun ChenYanan Zhu&#x;Yanan ZhuShu ChenShu ChenXiangrui MengXiangrui MengJie LiJie LiYufeng TangYufeng TangWei ZhangWei ZhangLiang YiLiang YiYan Fu*Yan Fu*
  • Xiyuan Hospital of China Academy of Chinese Medical Sciences, Beijing, China

Background: Exogenous lipoid pneumonia is a rare condition caused by the aspiration of lipid-containing substances. Its diagnosis can be challenging due to non-specific respiratory symptoms and imaging findings. Complications, such as secondary infections, may exacerbate the clinical course, particularly in immunocompromised or elderly patients. No cases of ELP complicated by concurrent viral (SARS-CoV-2), bacterial, and fungal infections have been reported in recent literature.

Case Presentation: We present the case of a 90-year-old female who developed ELP following the use of oral paraffin oil for ileus management. Initial symptoms included fever, cough, and respiratory distress, with rapidly worsening dyspnea. A chest CT revealed fat-density consolidations. Lipid droplets and lipid-laden macrophages were found in the bronchoalveolar lavage fluid. Her condition was further complicated by polymicrobial infections, including SARS-CoV-2, Mycobacterium abscessus, Klebsiella pneumoniae, and Candida albicans. A comprehensive treatment approach combining antibiotics, antifungals, antivirals, and corticosteroids resulted in significant clinical and radiological improvement over 1 week.

Conclusion: This case underscores the importance of early recognition of ELP, particularly in high-risk populations, and highlights the need for a multidisciplinary approach to manage secondary infections. Systemic corticosteroids and tailored antimicrobial therapy proved effective in this critically ill patient.

Background

Exogenous lipoid pneumonia is a condition caused by the aspiration of oily substances into the lungs. It leads to symptoms such as acute and chronic lung inflammation, local pulmonary fibrosis, and granuloma formation, all of which can impair gas exchange and, in severe cases, result in respiratory failure or death (1). While these pathological features are useful for diagnosing ELP, respiratory symptoms and imaging findings lack specificity. Additionally, due to its rarity, many clinicians are unfamiliar with ELP, leading to a high rate of misdiagnosis.

In ELP patients with rapid disease progression or poor response to treatment, clinicians should consider the possibility of secondary infections caused by other microorganisms, as these may complicate the clinical course and require additional interventions to manage effectively. Although there have been some reports of secondary infections in ELP, the pathogens involved are generally uncomplicated (2, 3). We hereby report a case of mixed infections following the diagnosis of ELP, including viral (SARS-CoV-2), bacterial, and fungal infections. Triple infections with bacteria, fungi, and viruses in ELP have been reported in children (4), while adult cases are extremely rare. To our knowledge, this is the first reported case of triple infection identified in a PubMed literature review spanning the last 5 years.

Case presentation

A 90-year-old Chinese female with a significant medical history of ischemic stroke presented to the gastroenterology department following 3 weeks of altered mental status and recurrent vomiting. Initial diagnostic considerations included intestinal obstruction. She was administered oral paraffin oil (50 mL tid) for 3 days starting October 26, 2024, as part of the management. There were no significant respiratory symptoms until the night of October 29, when the patient developed fever (maximum temperature 37.6°C), coughing with a small amount of white sticky phlegm. A complete blood count was almost normal, but with elevated neutrophil percentage, and procalcitonin level was 0.224 ng/ml. She was preliminarily diagnosed with a pulmonary infection and started on intravenous etimicin sulfate 0.1 g qd. On November 1, the patient suddenly experienced chest tightness, dyspnea, and profuse sweating, unable to lie flat. Examination revealed a heart rate of 136 beats/min, blood pressure of 200/110 mmHg, widespread dry wheezing sound, and few moist rales in both lungs. Echocardiography indicated reduced left ventricular diastolic function, and she was treated with diuretics and bronchodilators.

By November 3, 2024, her respiratory distress markedly worsened, leading to coma, and she was subsequently transferred to the ICU for treatment. Lung sounds were coarse with evident rhonchi and rales. Laboratory tests showed significantly elevated infection markers (procalcitonin 5.480 ng/ml, CRP 158.54 mg/L), a remarkable rise in white blood cells and neutrophil percentage, and arterial blood gas analysis indicated metabolic acidosis and hypoxemia. A chest CT scan performed on November 4 revealed multiple patchy, confluent, and ill-defined infiltrates with areas of consolidation in both lungs. Notably, the consolidation areas showed fat density on CT, raising high suspicion for exogenous lipoid pneumonia (ELP) (Figure 1). Given the clinical findings, the patient underwent bronchoalveolar lavage (BAL) for diagnostic confirmation. On the morning of November 6, bronchoscopic examination revealed significant hyperemia and edema of the airway mucosa, with erythematous walls and numerous scattered petechial hemorrhages. Copious brownish-red secretions were noted in the left and right main bronchi, which were suctioned and collected for culture. The right middle lobe bronchus exhibited marked edema. 50 ml of bronchoalveolar lavage (BAL) fluid were obtained, with one aliquot submitted for pathological analysis and the other for metagenomics next-generation sequencing (mNGS) (Shengting Medical, utilizing MultiCapX coupled with a third-generation nanopore sequencing platform, covering the entire genome of bacteria, fungi, and viruses). In response, the patient was initiated on low-dose corticosteroid therapy with hydrocortisone (100 mg every 12 h) to alleviate edema and reduce inflammation. Concurrently, the patient was started on empirical antibiotic therapy with moxifloxacin and piperacillin/tazobactam, considering the possibility of a worsening pulmonary infection.

FIGURE 1
CT scan image showing a cross-sectional view of the chest, highlighting both lungs with visible dark areas indicating possible lung abnormalities. The surrounding tissues and bone structures are also visible.

Figure 1. 2024-11-4 chest CT shows multiple patchy and consolidated shadows in both lungs, with the CT value within the consolidated areas consistent with fat density.

On November 7, the pathology report confirmed the presence of scattered fat droplets in the BAL fluid, which were positive for Oil Red O staining, confirming the diagnosis of exogenous lipoid pneumonia (Figure 2). Then mNGS results revealed a polymicrobial infection, including Mycobacterium abscessus, Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii, Enterococcus faecium, Candida albicans, cytomegalovirus (CMV), parvovirus B19, and SARS-CoV-2. Sputum culture results indicated the presence of Candida albicans, Acinetobacter baumannii, and Enterococcus faecium, while BAL microscopy revealed a large number of hyphae. And the patient’s nucleic acid test for SARS-CoV-2 was positive. Given the multiple identified pathogens, the treatment regimen was adjusted to include a combination of piperacillin/tazobactam, levofloxacin, fosfomycin, ritonavir/nirmatrelvir, and liposomal amphotericin B for fungal coverage. Methylprednisolone was added to control potential cytokine storms in the setting of viral and bacterial co-infections. The patient’s clinical condition progressively improved with this combined therapy. A follow-up chest CT on November 11 showed marked improvement, with significant resolution of the patchy and consolidative opacities in both lungs (Figure 3).

FIGURE 2
Panel A shows a light microscopy image of single-celled parasites in a clear background. Panel B depicts cystic structures and small red-stained areas. Panel C displays various blue and red-stained cellular structures on a pale background, indicating potential histological analysis.

Figure 2. (A) Microscopic examination reveals fat droplets of varying sizes. (B) The bronchoalveolar lavage fluid shows positive Oil Red O staining. Microscopically, red-stained particles of varying sizes are observed. (C) Macrophages phagocytosing lipids are observed under the microscope.

FIGURE 3
CT scan of a chest showing lung tissue with irregular, dense areas in both lungs, suggesting possible abnormalities or infection. The scan includes visible structures such as the spine and ribs.

Figure 3. After 1 week of treatment, the patient’s chest CT shows significant improvement in the patchy shadows and consolidated areas in both lungs.

Discussion

The patient in this case presented with acute respiratory distress, progressive dyspnea, and hypoxemia, and was ultimately diagnosed with ELP. This rare pulmonary condition is typically caused by the inhalation of lipid-containing substances, such as mineral oil, which is commonly used in the management of chronic constipation in elderly patients. The high suspicion for ELP in this case was supported by imaging and laboratory findings, including characteristic lung CT findings, fat droplets and lipid-laden macrophages in the bronchoalveolar lavage (BAL). The diagnosis of ELP was further complicated by the presence of multiple concurrent infections, including viral (SARS-CoV-2), bacterial (Klebsiella pneumoniae, Acinetobacter baumannii, and Enterococcus faecium), and fungal (Candida albicans) infections.

Exogenous lipoid pneumonia primarily affects populations with aspiration risks, including elderly individuals, children, or patients with dysphagia. It is well-documented that aspiration of exogenous lipids triggers an inflammatory cascade leading to chronic granulomatous reactions, alveolar hemorrhage, and pulmonary fibrosis in severe cases (5). The patient’s history of dysphagia and prolonged use of mineral oil for constipation placed her at high risk. This aligns with findings in prior studies, where mineral oil aspiration has been associated with extensive lung consolidation and poor prognosis in geriatric populations with compromised immunityated with extensive lung consolidation and poor prognosis in geriatric populations with compromised immunity.

The diagnosis of exogenous lipoid pneumonia (ELP) is primarily based on chest CT findings, supplemented by relevant exposure history and bronchoalveolar lavage (BAL). Chest CT often reveals features such as ground-glass opacities (GGO), interlobular septal thickening, crazy paving, and bronchial dilatation. Areas of consolidation may show fat attenuation foci (<−30 Hu), which is a characteristic CT finding. We recommend routine chest CT screening for high-risk populations. BAL may demonstrate lipid-laden macrophages, which can exhibit large vacuoles and be positive for Oil Red O staining. Treatment focuses on discontinuing exposure to the lipid source. For more severe cases, systemic corticosteroid therapy (e.g., prednisolone, methylprednisolone) can be considered (610). The patient’s clinical response, as reflected by the improvement in inflammatory markers and the reduction in imaging abnormalities, confirms the potential benefits of corticosteroid therapy.

Therapeutic lung lavage might be an effective and safe therapy with long-term benefits for ELP (11). The whole lung lavage (WLL) is particularly useful in patients who fail to respond to conservative measures or systemic corticosteroid therapy (12). By physically removing lipid-laden material from the alveoli, WLL may improve lung function and oxygenation. However, this procedure carries inherent risks, especially in critically ill patients with poor cardiorespiratory reserve. In the present case, the risk-benefit analysis, considering the patient’s fragile condition and multiple infections, led to the decision to prioritize medical therapy over invasive interventions.

Most ELP cases secondary to single or mixed infections occur in children. A systematic review (4) showed that the predominant pathogens include Mycobacterium fortuitum, M. fortuitum/chelonei, M. smegmatis, and M. abscessus complex. Other reported infections encompass Branhamella catarrhalis; Pseudomonas, Acinetobacter, and Klebsiella spp.; respiratory viruses (e.g., adenovirus, human metapneumovirus, bocavirus, rhinovirus, parainfluenza, RSV A/B, coronavirus); various bacteria and fungi; Chlamydia (serologically confirmed); and peritoneal isolates such as Enterococcus, Escherichia coli, Klebsiella, coagulase-positive Staphylococcus, and Clostridium. Secondary infections in adult ELP are predominantly caused by bacteria or fungi. Bacterial pathogens include non-tuberculous mycobacteria (2, 3), Acinetobacter baumannii (9) and Klebsiella pneumoniae (8), while fungal pathogens are mostly Candida (8, 9). Relevant literature on this topic remains limited. Triple infections involving viruses, bacteria, and fungi are extremely rare. A search of PubMed literature over the past 5 years revealed that this case represents the first reported case of such multiple infections. Multiple infections are more common in immunocompromised populations such as children (4). The patient in this case had no history of definite immunodeficiency, and the multiple infections may be associated with advanced age (90 years), repeated hospitalizations, and recurrent aspiration due to swallowing dysfunction.

In recent years, metagenomic next-generation sequencing (mNGS) has been increasingly integrated into clinical pathogen detection workflows (13, 14). Distinguished by its enhanced efficiency, superior sensitivity, rapid turnaround time, and broad-spectrum coverage, mNGS enables simultaneous identification of bacteria, fungi, viruses, mycobacteria, parasites, and atypical pathogens (13, 15). A proof-of-concept study (16) has demonstrated the technical feasibility and clinical utility of metagenomic next-generation sequencing (mNGS) for diagnosing hospital-acquired pneumonia (HAP) and ventilator-associated pneumonia (VAP) in intensive care unit (ICU) settings. The findings showed strong concordance with culture-based diagnostics and enabled the identification of pathogens in pneumonia cases with initially undetermined etiology. Another study (17) has demonstrated that metagenomic next-generation sequencing (mNGS) provides clinical utility in guiding the management of severe hospital-acquired pneumonia (HAP). For this patient, we adopted a combined approach of sputum culture and bronchoalveolar lavage (BAL) mNGS for pathogen detection.

Sputum culture and mNGS revealed multiple pathogens, among which Candida albicans and Klebsiella pneumoniae are common colonizers of the upper respiratory tract, potentially aspirated into the lungs with paraffin oil due to swallowing dysfunction to form local infection foci. The infection of Mycobacterium abscessus may be associated with changes in the pulmonary microenvironment, and disinfection management loopholes of medical devices cannot be excluded. Acinetobacter baumannii and Enterococcus faecium are common drug-resistant bacteria in the ICU, and the patient was highly likely infected after transfer to the ICU. SARS-CoV-2 infection was considered cross-transmission during hospitalization. To this end, the patient was isolated in a single-room ward to prevent the transmission of multidrug-resistant bacteria and viruses. Antimicrobial therapy was tailored accordingly, including piperacillin-tazobactam, levofloxacin, caspofungin, and inhaled liposomal amphotericin B, in conjunction with antiviral agents nirmatrelvir/ritonavirnjunction. The multidisciplinary approach ensured comprehensive coverage of the infectious spectrum while closely monitoring inflammatory markers such as CRP and IL-6. Due to the partially similar imaging manifestations of ELP and pulmonary infections, it is challenging to differentiate between the two in a timely manner. Furthermore, ELP often leads to secondary infections due to compromised lung function. Therefore, the empirical use of antibiotics is essential (18).

Exogenous lipoid pneumonia typically has a benign prognosis when diagnosed early and treated appropriately. Once ELP is identified, immediate discontinuation of lipid substances can reduce intrapulmonary lipid deposition and avoid inflammatory cascade reactions. As reported in the literature, early administration of glucocorticoids (such as methylprednisolone) can significantly improve patients’ symptoms (6). In this case, the patient initiated glucocorticoid therapy immediately upon diagnosis, and the infection was observed to be controlled, indicating that early intervention yields better outcomes. ELP patients are predisposed to secondary infections due to alveolar lipid deposition disrupting the local immune barrier. Early diagnosis allows for close monitoring of infection markers and respiratory pathogen screening, enabling timely initiation of empirical anti-infective therapy to prevent single infections from progressing to mixed infections with multidrug-resistant bacteria (1).

However, delayed diagnosis, comorbid conditions, and severe infections may contribute to poor outcomes. This case underscores the multifactorial nature of ELP management, including early identification of lipid exposure, radiological confirmation, anti-inflammatory therapy, and aggressive management of secondary infections. Further studies are needed to establish optimal treatment protocols and clarify the role of interventions such as WLL in critically ill patients. Clinicians should maintain a high index of suspicion for ELP in patients presenting with unexplained respiratory symptoms and a history of oil ingestion.

Data availability statement

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

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

XY: Writing – original draft, Writing – review and editing. XC: Writing – original draft, Writing – review and editing. YZ: Writing – original draft, Writing – review and editing. SC: Conceptualization, Data curation, Investigation, Supervision, Validation, Writing – review and editing. XM: Conceptualization, Data curation, Investigation, Methodology, Resources, Supervision, Writing – review and editing. JL: Data curation, Investigation, Supervision, Writing – review and editing. YT: Data curation, Investigation, Methodology, Software, Validation, Writing – review and editing. WZ: Data curation, Investigation, Methodology, Resources, Validation, Writing – review and editing. LY: Conceptualization, Investigation, Methodology, Writing – review and editing. YF: Conceptualization, Data curation, Formal Analysis, Investigation, Methodology, Project administration, Software, Supervision, Validation, Visualization, Writing – review and editing.

Funding

The author(s) declare that financial support was received for the research and/or publication of this article. This Research was supported by the National Natural Science Foundation of China (No. 82204913), China Academy of Chinese Medical Sciences Outstanding Young Science and Technology Talent Training Program (No. ZZ16-YQ-012) and Haidian District Traditional Chinese Medicine Service System Construction Project (No. 010990015).

Acknowledgments

We would like to thank the Clinical Laboratory and Pathology Department of Xiyuan Hospital, China Academy of Chinese Medical Sciences.

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.

Generative AI statement

The authors declare that no Generative AI was used in the creation of this manuscript.

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. Marchiori E, Zanetti G, Mano C, Hochhegger B. Exogenous lipoid pneumonia. Clinical and radiological manifestations. Respir Med. (2011) 105:659–66. doi: 10.1016/j.rmed.2010.12.001

Crossref Full Text | Google Scholar

2. Wang H, Lu S, Li H, Wang Y. Mycobacterium infection secondary to exogenous lipoid pneumonia caused by nasal drops: A case report and literature review. BMC Pulm Med. (2023) 23:47. doi: 10.1186/s12890-022-02265-8

Crossref Full Text | Google Scholar

3. Pidcock W, Chau-Etchapare F, Murin S. A 65-year-old man with pulmonary opacities and worsening cough. Chest. (2019) 156:e117–20. doi: 10.1016/j.chest.2019.05.041

Crossref Full Text | Google Scholar

4. Marangu D, Gray D, Vanker A, Zampoli M. Exogenous lipoid pneumonia in children: A systematic review. Paediatr Respir Rev. (2020) 33:45–51. doi: 10.1016/j.prrv.2019.01.001

Crossref Full Text | Google Scholar

5. Szabo-Gay O, Benoit N, Doutrellot-Philippon C, Le Meunier F, Sevestre H, Jounieaux V. [Occupational lipid pneumonia induced by cutting fluids exposition]. Presse Med. (2011) 40:656–9. doi: 10.1016/j.lpm.2010.12.009

Crossref Full Text | Google Scholar

6. Yasui H, Yokomura K, Suda T. A severe case of acute exogenous lipoid pneumonia treated with systemic corticosteroid. Respir Med Case Rep. (2016) 17:64–7. doi: 10.1016/j.rmcr.2016.01.009

Crossref Full Text | Google Scholar

7. Park S, Park J, Lee J. A case of lipoid pneumonia associated with occupational exposure to solvents in a dry-cleaning worker. Respirol Case Rep. (2021) 9:e00762. doi: 10.1002/rcr2.762

Crossref Full Text | Google Scholar

8. Wang J, Wang B, Chen H, He L, Yang R, Lei F. One case of severe exogenous lipoid pneumonia complicated with lung abscess caused by diesel inhalation. Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi. (2023) 41:695–9. doi: 10.3760/cma.j.cn121094-20220420-00204

Crossref Full Text | Google Scholar

9. Zhang J, Lei J, Wu X, You H. A case of severe exogenous lipoid pneumonia caused by diesel inhalation. Linchuang Feike Zazhi. (2017) 22:1547–9. doi: 10.3969/j.issn.1009-6663.2017.08.056

Crossref Full Text | Google Scholar

10. Chin N, Hui K, Sinniah R, Chan T. Idiopathic lipoid pneumonia in an adult treated with prednisolone. Chest. (1994) 105:956–7. doi: 10.1378/chest.105.3.956

Crossref Full Text | Google Scholar

11. Shang L, Gu X, Du S, Wang Y, Cao B, Wang C, et al. The efficacy and safety of therapeutic lung lavage for exogenous lipoid pneumonia: A systematic review. Clin Respir J. (2021) 15:134–46. doi: 10.1111/crj.13273

Crossref Full Text | Google Scholar

12. Chang H, Chen C, Chen C, Hsuie T, Chen C, Lei W, et al. Successful treatment of diffuse lipoid pneumonitis with whole lung lavage. Thorax. (1993) 48:947–8. doi: 10.1136/thx.48.9.947

Crossref Full Text | Google Scholar

13. Hu X, Jiang L, Liu X, Chang H, Dong H, Yan J, et al. The diagnostic value of bronchoalveolar lavage fluid metagenomic next-generation sequencing in critically ill patients with respiratory tract infections. Microbiol Spectr. (2024) 12:e0045824. doi: 10.1128/spectrum.00458-24

Crossref Full Text | Google Scholar

14. Wu X, Sun T, He H, Xing L, Cheng Z, Geng S, et al. Effect of metagenomic next-generation sequencing on clinical outcomes of patients with severe community-acquired pneumonia in the ICU: A Multicenter. Randomized Controlled Trial. Chest. (2025) 167:362–73. doi: 10.1016/j.chest.2024.07.144

Crossref Full Text | Google Scholar

15. Diao Z, Han D, Zhang R, Li J. Metagenomics next-generation sequencing tests take the stage in the diagnosis of lower respiratory tract infections. J Adv Res. (2022) 38:201–12. doi: 10.1016/j.jare.2021.09.012

Crossref Full Text | Google Scholar

16. Heitz M, Levrat A, Lazarevic V, Barraud O, Bland S, Santiago-Allexant E, et al. Metagenomics for the microbiological diagnosis of hospital-acquired pneumonia and ventilator-associated pneumonia (HAP/VAP) in intensive care unit (ICU): A proof-of-concept study. Respir Res. (2023) 24:285. doi: 10.1186/s12931-023-02597-x

Crossref Full Text | Google Scholar

17. Yang T, Mei Q, Fang X, Zhu S, Wang Y, Li W, et al. Clinical value of metagenomics next-generation sequencing in bronchoalveolar lavage fluid for patients with severe hospital-acquired pneumonia: A nested case-control study. Infect Drug Resist. (2022) 15:1505–14. doi: 10.2147/IDR.S356662

Crossref Full Text | Google Scholar

18. Franzen D, Kohler M, Degrandi C, Kullak-Ublick G, Ceschi A. Fire eater’s lung: Retrospective analysis of 123 cases reported to a national poison center. Respiration. (2014) 87:98–104. doi: 10.1159/000350443

Crossref Full Text | Google Scholar

Keywords: exogenous lipoid pneumonia, paraffin oil aspiration, polymicrobial infections, corticosteroid therapy, bronchoalveolar lavage, SARS-CoV-2

Citation: Yan X, Chen X, Zhu Y, Chen S, Meng X, Li J, Tang Y, Zhang W, Yi L and Fu Y (2025) Polyinfection secondary to exogenous lipoid pneumonia caused by aspiration of paraffin oil: a Case Report. Front. Med. 12:1555471. doi: 10.3389/fmed.2025.1555471

Received: 04 January 2025; Accepted: 23 June 2025;
Published: 01 August 2025.

Edited by:

Narasaiah Kolliputi, University of South Florida, United States

Reviewed by:

Vinod Kumar Yata, Malla Reddy University, India
Keerthi Prakash, Government Sivagangai Medical College, India

Copyright © 2025 Yan, Chen, Zhu, Chen, Meng, Li, Tang, Zhang, Yi and Fu. 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: Yan Fu, YmVpc2VmZW5uaV83QGhvdG1haWwuY29t

These authors have contributed equally to this work

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.