Skip to main content

Outcomes of surgery for different types of chronic pulmonary aspergillosis: results from a single-center, retrospective cohort study

Abstract

Background

The reported experience of surgical treatment for chronic pulmonary aspergillosis (CPA) mainly focused on simple aspergilloma (SA), few about other types of CPA. The present study aims to evaluate the outcomes of surgical treatment for different types of CPA.

Methods

We performed a retrospective analysis of 85 patients with CPA who underwent surgery from 2014 to 2020 at Shandong Provincial Chest Hospital. The patients were divided into four types, including SA, chronic cavitary pulmonary aspergillosis (CCPA), chronic fibrosing pulmonary aspergillosis (CFPA), aspergillus nodule (AN). We collected and analyzed the preoperative, perioperative, and postoperative data to evaluate the outcomes of surgical treatment of different types of CPA.

Results

The four groups had similar age (p = 0.22), symptoms (p = 0.36), lesion location (p = 0.09), VATS rate (p = 0.08), recurrence rate (p = 0.95), and had significant difference in surgical procedures (p < 0.01), time of surgery (p < 0.01), intraoperative blood loss (p < 0.01), postoperative complication (p = 0.01). CFPA (P = 0.01), longer surgical time (P = 0.001), and more intraoperative blood loss (P = 0.004) were risk factors of postoperative complication, more intraoperative blood loss (> 400 ml) was the independent risk factor (OR 13.5, 95% CI 1.6–112.1, P = 0.02). 6 patients relapsed after surgery with a recurrence rate of 7.1%. The mean time to relapse was 14.8 months (2–30 months) after surgery. Relapse occurred in 2 SA patients, 3 CCPA, and 1 CFPA, respectively, while none of the AN patients relapsed. No risk factor for recurrence was found.

Conclusions

Surgical resection seems safe and effective in the treatment of SA, AN, CCPA with a low complication and recurrence rate, while surgery for CFPA should be limited to selected patients because of its higher complication rate.

Peer Review reports

Background

Chronic pulmonary aspergillosis is a pulmonary infection caused by caused by Aspergillus species [1]. Recent reports have shown an increased incidence of CPA in recent years [2,3,4]. The European Society for Clinical Microbiology and Infectious Diseases (ESCMID) and the European Respiratory Society (ERS) reached an agreement on the rationale and clinical guidelines for diagnosis and management for CPA in 2015 [5]. CPA is categorised as single (simple) pulmonary aspergilloma (SA), chronic cavitary pulmonary aspergillosis (CCPA), chronic fibrosing pulmonary aspergillosis (CFPA), aspergillus nodule (AN), subacute invasive aspergillosis (SAIA).

SA with symptoms is recommended for surgical treatment, while close follow-up with observation is recommended for asymptomatic SA. Treatment for AN differs from clinical symptoms and relevant examinations. Other types of CPA are all first treated by antifungal therapy usually [5, 6]. However, some patients are not sensitive to antifungal therapy and need to use drugs for a long time. Side effects, drug resistance, inevitable recurrence after drug withdrawal, and other problems also come along with them. Surgery offers a chance of cure, but this is limited to selected patients with localized lesions. The reported experience mainly focused on simple aspergilloma, few about other types of CPA.

We believe that surgery is beneficial for certain CPA patients, no matter what type of CPA. What’s more, we have performed surgery for different types of CPA in recent years. Herein, we reviewed our experience with the surgical management of 85 CPA patients in the present study, to evaluate the surgical outcomes of different types of CPA.

Methods

From 2014 to 2020, 85 patients with CPA underwent surgery at Shandong Provincial Chest Hospital in China. The clinical data were collected retrospectively, including gender, age, comorbidities, symptoms, location and CPA classification, preoperative bronchial artery embolization, preoperative and postoperative antifungal therapy, surgical procedures, intraoperative blood loss, and postoperative complications.

The diagnosis of CPA was based on the criteria of ERS and ESCMID: one or more cavities with or without a fungal ball or nodules present on thoracic imaging for ≥ 3 months, direct evidence of Aspergillus infection (sputum culture), or immunological response to Aspergillus spp. (GM (galactomannan) assay, Megazyme Co.), and exclusion of alternative diagnoses. Once diagnosed, voriconazole was administered for at least 2 weeks, except for drug-intolerance or fatal massive hemoptysis.

The surgical indication of CPA was that the main lesions were confined to the ipsilateral lung with the following conditions: massive hemoptysis; persistent or recurrent small amount of hemoptysis; antifungal treatment was ineffective or intolerable; suspected to be lung cancer.

The CPA diagnosis in these patients was pathologically confirmed after surgery (Fig. 1). Voriconazole was administered for at least 2 weeks for SA and AN patients, 3 months for CCPA, and 6 months for CFPA, except for drug-intolerance.

Fig. 1
figure 1

Postoperative pathological images of CPA. a Hematoxylin–Eosin staining. b Gomori's Methenamine Silver staining

Being a retrospective study, ethics review and patients’ informed consent were waived.

Statistical analyses and data management were performed using SPSS 21.0. Continuous variable data was expressed as the mean ± SD, whereas categorical data was presented as number or percentage. The Pearson chi-square test or continuous correction Chi-square test or Fisher's precision probability test was used to compare categorical variables. Binary logistic regression analysis was used to assess risk factors for postoperative complication and recurrence. Comparisons were considered to be statistically significant when P < 0.05.

Results

85 patients were enrolled in this study with a mean age of 46.6 years (range 7–74 years), including 50 men (58.8%) and 35 women (41.2%). The general clinical characteristics of the four types of CPA are shown in Table 1. CCPA was the most common type, accounting for 41.2% of CPA, while the percentage of SA was 29.4%, CFPA 15.3%, AN 14.1%. The most common underlying pulmonary disease was pulmonary tuberculosis (n = 44, 51.8%), followed by pulmonary cyst (n = 20, 23.5%). The less common diseases included bronchiectasis (n = 6, 7.1%), tuberculous empyema (n = 3, 3.5%), lung cancer (n = 2, 2.4%), pulmonary bullae (n = 1, 1.2%), and lung abscess (n = 1, 1.2%). 8 patients (9.4%) showed no respiratory disease. The main symptoms included cough and sputum, hemoptysis, which are shown in Table 1.

Table 1 Baseline clinical characteristics of CPA

The main indications for surgery included hemoptysis (n = 56, 65.9%), failure or intolerance of antifungal therapy (n = 22, 25.9%), suspicion of lung cancer (n = 7, 8.2%). Of the 56 patients with persistent hemoptysis, 2 received emergency surgery because of massive hemoptysis, and 11 suffered from persistent small amount of hemoptysis. And recurrent hemoptysis appeared in 43 patients, of whom 9 accepted bronchial artery embolization to control hemorrhage. However, hemoptysis occurred again in a short time. The mean duration of hemoptysis was 17.3 months (range 4 days–204 months). 7 patients were suspected to have lung cancer, whereas only 2 were confirmed to have lung cancer combined with aspergillosis (1 squamous cell carcinoma, 1 neuroendocrine carcinoma), another 4 were AN, 1 was SA. CPA lesions were most often found in the right upper lobe, and no lesions were found in the right middle lobe.

The surgical procedures are listed in Table 2. More than half of the 85 patients accepted lobectomy (n = 43, 50.6%), and wedge resection (n = 14, 16.5%) was the second most frequent procedure, followed by segmentectomy (n = 13, 15.3%). 4 patients received pleural strip with lobectomy or segmentectomy because of empyema or pleural thickening, and the pneumonectomy was performed for 1 SA patient and 1 CFPA patient. Video-assisted thoracoscopy (VATS) was performed in 37 patients (43.5%).

Table 2 Surgical outcomes of CPA

The amount of intraoperative blood loss and time of surgery are shown in Table 1. The SA patients consumed the shortest operation time among the four group’s patients (P = 0.01, P < 0.01, P < 0.01, respectively), while the CFPA patients had the most blood loss (P < 0.01, P < 0.01, P < 0.01, respectively).

Sixteen complications developed in 10 patients (11.8%), including pleural effusion, pyothorax, pneumonia, acute respiratory failure, bronchopleural fistula, prolonged air leak, and persistent chest distress. Pleural effusion appeared in 1 SA patient. Pleural effusion and pyothorax were observed in 1 CCPA patient, while another CCPA patient experienced prolonged air leak for 3 weeks. 5 CFPA patients suffered from complications, which makes the highest incidence of postoperative complications, including prolonged air leak, pneumonia (n = 2), pneumonia and pyothorax, acute respiratory failure and pneumonia, bronchopleural fistula. Pneumonia and pleural effusion, and prolonged air leak were observed in 2 AN patients, respectively. No perioperative mortality occurred. Univariable risk factor analyses reveal that CFPA (P = 0.01), longer surgical time (P = 0.001), and more intraoperative blood loss (P = 0.004) were the risk factors of postoperative complication. Logistic analyses show that more intraoperative blood loss (> 400 ml) was the independent risk factor (Table 3).

Table 3 The Binary logistic regression analysis for risk factors of complications in CPA patients

The majority of patients (n = 66, 77.6%) received antifungal treatment postoperatively, and the length of the medication varied from 2 weeks to 6 months. Voriconazole was the most commonly used antifungal medication.

The median follow-up time after surgery was 47 months. Overall, 6 patients relapsed after surgery with a recurrence rate of 7.1%, all of whom accepted postoperative antifungal treatment without postoperative complications. The mean time to relapse was 14.8 months (2–30 months) after surgery. Relapse occurred in 2 SA patients, 3 CCPA, and 1 CFPA, respectively, while none of the AN patients relapsed. The characteristics of the 6 patients are shown in Additional file 1: Table S1. No risk factor of relapse was found in univariable analyses.

Discussion

Generally, medical treatment with oral azole drugs is the first choice when CPA is diagnosed. Sometimes the drug course is long and the effect is not ideal. Some authors reported that a considerable proportion of patients do not respond to antifungal therapy, the effective rate ranges from 32 to 76% [7,8,9,10,11]. Relapses occur often after treatment is stopped, in approximately one-third of cases. Many patients may require long-term or even lifelong antifungal therapy [12]. Surgery offers a chance of cure, which has been confirmed by many analyses [13]. However, it is associated with high morbidity and mortality rates due to severe pleural adhesion and infection in the underlying lung. There is general agreement that surgery is limited to patients with a single aspergilloma or with nonprogressive CPA, localized disease, and no significant comorbidities, especially for those with recurrent hemoptysis despite bronchial artery embolization or with azole-resistant disease [3, 14, 15]. Nevertheless, most experience of surgical treatment for CPA is derived from patients with simple pulmonary aspergilloma, with rare studies involving other types of CPA. In this study, we analyzed the surgical treatment of different types of CPA according to the 2015 ESCMID/ERS guidelines [5].

As antifungal treatment is ineffective for SA usually, asymptomatic SA patients should be observed under computed tomography at regular intervals. And surgery should be selected without hesitation when occurring recurrent hemoptysis. Chen reported that 96 SA patients received surgical treatment carrying a complication rate of 8.3% [16]. Complications occurred in 4% of SA patients in our study, the complication rate is lower than others’ [15]. We believe that surgical treatment for SA is safe and effective.

Patients with CCPA without clinical symptoms can also be observed without antifungal therapy and followed every 3–6 months, and should be treated with a minimum of 6 months of antifungal therapy when the disease is developed [17]. Surgery can be considered in CCPA with severe hemoptysis or failed therapy, and studies have reported higher postoperative complication rates in patients with CCPA. In our study, 24 CCPA patients (68.6%) received surgery because of persistent or repeated hemoptysis, 5 of whom experienced life-threaten hemoptysis and accepted bronchial artery embolization before surgery. The postoperative complication rate and recurrence rate were 5.7% and 8.6%, respectively. Some articles have reported that the postoperative outcomes of CCPA are less favorable than those with single aspergilloma, which is not consistent with ours, and we get a similar postoperative complication and recurrence rate [13, 15, 18].

CFPA is the terminal fibrosing evolution of CCPA, and the optimal treatment is not yet known. Continuous antifungal therapy is usually required to delay disease progression or alleviate symptoms. Surgical outcomes are uncertain, and there are only a few reports on the surgical treatment of CFPA [19,20,21], which may be because of the high postoperative complication rate and mortality. 13 patients accepted surgery in the present study, and 5 (38.5%) suffered postoperative complications, 1 relapsed. We also found CFPA was the risk factor for postoperative complications. CFPA patients usually tend to have more severe thoracic adhesions, more difficult dissections in our experience, and more intraoperative bleeding, meanwhile, we found more intraoperative blood loss (> 400 ml) was the independent risk factor of complication. This may explain why CFPA patients had a higher complication rate.

Aspergillus nodules are usually incidentally discovered on thoracic CT examination, which are very similar in appearance to malignancy and can only be definitively diagnosed through histology [5, 22]. However, only 2 patients were asymptomatic, while 3 had cough and sputum, and 7 suffered hemoptysis. It is not very clear if surgery or other treatment are needed when they are asymptomatic. We performed surgery for 4 patients because of suspicion of lung cancer. Usually, serial follow-up with low dose chest CT scan is suggested for asymptomatic patients in our department.

Open thoracic surgery is often the first choice before, while more and more VATS are performed recently. We performed VATS for 43.6% of patients, and the SA and AN patients were the preferred choices for VATS. The present study confirmed that the VATS surgery was safe and effective and not associated with a higher complication rate and recurrence rate, which is consistent with the previous report [23]. In our opinion, the possible reason is that VATS is often performed for selected patients whose operations are considered to be not very difficult.

Hemoptysis is the most common symptom associated with CPA. In our study, 65.9% of patients suffered from hemoptysis. Life-threatening hemoptysis requires emergency surgery or catheter embolization of bronchial arteries [24, 25]. Bronchial artery embolization is believed to be life-saving for severe hemoptysis, prior to surgery. However, it’s rarely completely effective with a high recurrence rate, it is rather a bridge towards elective surgery [5]. In our present study, 2 received emergency surgery because of massive hemoptysis, while 9 accepted bronchial artery embolization, all of whom relapsed and finally received surgery. This conforms with previous literature [26]. There was no difference among the four groups about hemoptysis and interventional therapy, meanwhile, we didn’t confirm that preoperative bronchial artery embolization would increase or decrease the complication rate and recurrence rate.

The role of antifungal therapy following surgery for CPA cases is controversial [27]. Various studies about antifungal therapy have shown no positive findings regarding antifungal therapy and surgery outcomes [23, 28]. We also didn’t find relationship between antifungal therapy and recurrence in this study. 6 patients who received antifungal therapy relapsed, while none relapsed among the 18 patients who didn’t receive antifungal therapy. However, Setianingrum F analyzed three different time points of antifungal therapy (before, in, and after surgery) correlated with the clinical outcomes of patients, and concluded that antifungal therapy at any point before surgery was highly protective of relapse (P = 0.002), in contrast to a lack of significant benefit if only given after surgery (P = 0.15) [29]. Another study also found the benefit of antifungal therapy given 2 weeks before surgery and 3 months after surgery, but the number of patients was limited [30].

In our view, CPA, as a benign disease, is operated on to eliminate symptoms and preserve more lung function, rather than radical resection as a malignant tumor. So, we resected the main lesion only without secondary lesions in the adjacent lobes for some CFPA and CCPA patients. In the present study, 1 CFPA patient who received lobectomy, 1 CCPA patient who received wedge resection, and 1 SA patient who received wedge resection relapsed. Insufficient surgical resection may be a risk factor for relapse. In addition, high aspergillus spore density may be another risk factor for relapse. However, we cannot quantify these risks precisely because of the lack of relevant data in this retrospective study.

Its retrospective nature and the limited sample size which inevitably introduced bias in the study. We didn’t conclude the risk factor of recurrence perhaps because of its small size. Further large sample studies are required to extend the knowledge on surgical treatment for CPA.

Conclusion

In conclusion, Surgical resection seems safe and effective in the treatment of SA, AN, CCPA with a low complication and recurrence rate, while surgery for CFPA should be limited to selected patients because of its higher complication rate. We advocate early surgical intervention for SA, AN, CCPA if the patient is a suitable candidate for operation and the lesion could be resected completely, even if the patient has minor hemoptysis. Surgery offers the only chance of cure, whereas non-operative treatment is only considered in the patient who is not suitable for surgical resection. VATS is safe for selected patients.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

CPA:

Chronic pulmonary aspergillosis

SA:

Single (simple) pulmonary aspergilloma

CCPA:

Chronic cavitary pulmonary aspergillosis

CFPA:

Chronic fibrosing pulmonary aspergillosis

AN:

Aspergillus nodule

SAIA:

Subacute invasive aspergillosis

References

  1. Garcia-Vidal C, Peghin M, Cervera C, Gudiol C, Ruiz-Camps I, Moreno A, et al. Causes of death in a contemporary cohort of patients with invasive aspergillosis. PLoS ONE. 2015;10(3):e0120370.

    Article  Google Scholar 

  2. Olum R, Osaigbovo II, Baluku JB, Stemler J, Kwizera R, Bongomin F. Mapping of chronic pulmonary aspergillosis in Africa. J Fungi (Basel). 2021;7(10):790.

    Article  Google Scholar 

  3. Alastruey-Izquierdo A, Cadranel J, Flick H, Godet C, Hennequin C, Hoenigl M, et al. Treatment of chronic pulmonary aspergillosis: current standards and future perspectives. Respiration. 2018;96(2):159–70.

    Article  CAS  Google Scholar 

  4. Godet C, Alastruey-Izquierdo A, Flick H, Hennequin C, Mikilps-Mikgelbs R, Munteanu O, et al. A CPAnet consensus statement on research priorities for chronic pulmonary aspergillosis: a neglected fungal infection that requires attention. J Antimicrob Chemother. 2018;73(2):280–6.

    Article  CAS  Google Scholar 

  5. Denning DW, Cadranel J, Beigelman-Aubry C, Ader F, Chakrabarti A, Blot S, et al. Chronic pulmonary aspergillosis: rationale and clinical guidelines for diagnosis and management. Eur Respir J. 2016;47(1):45–68.

    Article  CAS  Google Scholar 

  6. Gao Y, Soubani A. Advances in the diagnosis and management of pulmonary aspergillosis. Adv Respir Med. 2019;87(6):231–43.

    Article  Google Scholar 

  7. Al-Shair K, Atherton GT, Harris C, Ratcliffe L, Newton PJ, Denning DW. Long-term antifungal treatment improves health status in patients with chronic pulmonary aspergillosis: a longitudinal analysis. Clin Infect Dis. 2013;57(6):828–35.

    Article  Google Scholar 

  8. Felton TW, Baxter C, Moore CB, Roberts SA, Hope WW, Denning DW. Efficacy and safety of posaconazole for chronic pulmonary aspergillosis. Clin Infect Dis. 2010;51(12):1383–91.

    Article  CAS  Google Scholar 

  9. Camuset J, Nunes H, Dombret MC, Bergeron A, Henno P, Philippe B, et al. Treatment of chronic pulmonary aspergillosis by voriconazole in nonimmunocompromised patients. Chest. 2007;131(5):1435–41.

    Article  Google Scholar 

  10. Agarwal R, Vishwanath G, Aggarwal AN, Garg M, Gupta D, Chakrabarti A. Itraconazole in chronic cavitary pulmonary aspergillosis: a randomised controlled trial and systematic review of literature. Mycoses. 2013;56(5):559–70.

    Article  CAS  Google Scholar 

  11. Cadranel J, Philippe B, Hennequin C, Bergeron A, Bergot E, Bourdin A, et al. Voriconazole for chronic pulmonary aspergillosis: a prospective multicenter trial. Eur J Clin Microbiol Infect Dis. 2012;31(11):3231–9.

    Article  CAS  Google Scholar 

  12. Koyama K, Ohshima N, Suzuki J, Kawashima M, Takeda K, Ando T, et al. Recurrence of chronic pulmonary aspergillosis after discontinuation of maintenance treatment by antifungal triazoles. J Infect Chemother. 2014;20(6):375–9.

    Article  CAS  Google Scholar 

  13. He B, Wan C, Zhou W, Rui Y, Shi Y, Su X. Clinical profile and surgical outcome for different types of chronic pulmonary aspergillosis. Am J Transl Res. 2019;11(6):3671–9.

    PubMed  PubMed Central  Google Scholar 

  14. Farid S, Mohamed S, Devbhandari M, Kneale M, Richardson M, Soon SY, et al. Results of surgery for chronic pulmonary Aspergillosis, optimal antifungal therapy and proposed high risk factors for recurrence—a National Centre’s experience. J Cardiothorac Surg. 2013;8:180.

    Article  Google Scholar 

  15. Muniappan A, Tapias LF, Butala P, Wain JC, Wright CD, Donahue DM, et al. Surgical therapy of pulmonary aspergillomas: a 30-year North American experience. Ann Thorac Surg. 2014;97(2):432–8.

    Article  Google Scholar 

  16. Chen QK, Jiang GN, Ding JA. Surgical treatment for pulmonary aspergilloma: a 35-year experience in the Chinese population. Interact Cardiovasc Thorac Surg. 2012;15(1):77–80.

    Article  CAS  Google Scholar 

  17. Patterson TF, Thompson GR 3rd, Denning DW, Fishman JA, Hadley S, Herbrecht R, et al. Practice guidelines for the diagnosis and management of aspergillosis: 2016 update by the Infectious Diseases Society of America. Clin Infect Dis. 2016;63(4):e1–60.

    Article  Google Scholar 

  18. Farid S, Mohamed S, Devbhandari M, Kneale M, Richardson M, Soon SY, et al. Results of surgery for chronic pulmonary Aspergillosis, optimal antifungal therapy and proposed high risk factors for recurrence–a National Centre’s experience. J Cardiothorac Surg. 2013;8:180.

    Article  Google Scholar 

  19. Kosmidis C, Newton P, Muldoon EG, Denning DW. Chronic fibrosing pulmonary aspergillosis: a cause of “destroyed lung” syndrome. Infect Dis (Lond). 2017;49(4):296–301.

    Article  Google Scholar 

  20. Denning DW. Chronic pulmonary aspergillosis commonly complicates treated pulmonary tuberculosis with residual cavitation. Eur Respir J. 2019;53(3):1801184.

    Article  Google Scholar 

  21. Ruan H, Gong C, Wang J. The efficacy and safety of surgical treatment for patients with tuberculosis destroyed lung with or without chronic pulmonary aspergillosis. World J Surg. 2021;45(5):1595–601.

    Article  Google Scholar 

  22. Kosmidis C, Denning DW. The clinical spectrum of pulmonary aspergillosis. Thorax. 2015;70(3):270–7.

    Article  Google Scholar 

  23. Zheng S, Li X, Hu B, Li H. Is adjuvant antifungal therapy after video-assisted thoracic surgery for pulmonary aspergilloma necessary? J Thorac Dis. 2018;10(11):6060–5.

    Article  Google Scholar 

  24. Brik A, Salem AM, Kamal AR, Abdel-Sadek M, Essa M, El Sharawy M, et al. Surgical outcome of pulmonary aspergilloma. Eur J Cardiothorac Surg. 2008;34(4):882–5.

    Article  Google Scholar 

  25. Lee JG, Lee CY, Park IK, Kim DJ, Chang J, Kim SK, et al. Pulmonary aspergilloma: analysis of prognosis in relation to symptoms and treatment. J Thorac Cardiovasc Surg. 2009;138(4):820–5.

    Article  Google Scholar 

  26. Corr P. Management of severe hemoptysis from pulmonary aspergilloma using endovascular embolization. Cardiovasc Intervent Radiol. 2006;29(5):807–10.

    Article  Google Scholar 

  27. Benhamed L, Woelffle D. Adjuvant antifungal therapy after pulmonary surgery for aspergilloma: is it useful? Interact Cardiovasc Thorac Surg. 2014;18(6):835–7.

    Article  Google Scholar 

  28. Sagan D, Goździuk K. Surgery for pulmonary aspergilloma in immunocompetent patients: no benefit from adjuvant antifungal pharmacotherapy. Ann Thorac Surg. 2010;89(5):1603–10.

    Article  Google Scholar 

  29. Setianingrum F, Rautemaa-Richardson R, Shah R, Denning DW. Clinical outcomes of patients with chronic pulmonary aspergillosis managed surgically. Eur J Cardiothorac Surg. 2020;58(5):997–1003.

    Article  Google Scholar 

  30. Gebitekin C, Sami Bayram A, Akin S. Complex pulmonary aspergilloma treated with single stage cavernostomy and myoplasty. Eur J Cardiothorac Surg. 2005;27(5):737–40.

    Article  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

The authors declare that there is no funding in the present study.

Author information

Authors and Affiliations

Authors

Contributions

CMS: Data curation; Formal analysis; Investigation; Methodology; Writing original draft. GFQ: Data curation; Methodology; Writing review and editing. CW and FJ: Methodology; Validation; Writing-review. YZZ: Conceptualization; Methodology; Supervision; Writing editing; Supervision. All authors read and approved the final manuscript.

Corresponding author

Correspondence to YunZeng Zhang.

Ethics declarations

Ethics approval and consent to participate

The retrospective data analysis was approved by the ethics board of Shandong Public Health Clinical Center. The need for patient consent was waived because of the retrospective nature of the study.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Table S1

. Characteristics of 6 relapsed patients.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Shen, C., Qiao, G., Wang, C. et al. Outcomes of surgery for different types of chronic pulmonary aspergillosis: results from a single-center, retrospective cohort study. BMC Pulm Med 22, 40 (2022). https://doi.org/10.1186/s12890-022-01836-z

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12890-022-01836-z

Keywords