CC BY 4.0 · The Arab Journal of Interventional Radiology 2023; 07(01): 026-030
DOI: 10.1055/s-0043-1763496
Original Article

Bronchial Artery Embolization in Management of Hemoptysis in a Developing Country: An Initial Experience

Puneet Garg
1   Department of Radiodiagnosis, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India
,
1   Department of Radiodiagnosis, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India
,
Krishna Bhardwaj
1   Department of Radiodiagnosis, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India
,
2   Department of Pulmonary, Critical Care and Sleep Medicine, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India
,
Rajat Khurana
1   Department of Radiodiagnosis, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India
,
1   Department of Radiodiagnosis, Vardhman Mahavir Medical College and Safdarjung Hospital, New Delhi, India
› Author Affiliations
Funding None.
 

Abstract

Objectives This article evaluates the immediate success, recurrence rate, complications, and the culprit vessel of bronchial artery embolization (BAE) in patients presenting with hemoptysis.

Materials and Methods All patients who underwent BAE from July 1, 2018 to August 31, 2021 were included. BAE was done for moderate to severe hemoptysis or for mild hemoptysis which was recurrent and not controlled by medical management. Patients referred for surgical intervention and hemoptysis controlled on medical management were excluded.

Results One hundred and thirty patients underwent BAE in the study period. Mean age was 41.5 years and majority (73.1%) was male. Forty-three (33.1%) patients had mild, 46 (35.4%) had moderate, and 41 (31.5%) with the duration of symptoms ranging from 3 days to 25 years. Most common culprit vessel was posterior intercostal artery closely followed by the intercostobronchial artery. Hypervascularity was the most common angiographic abnormality encountered. On an average, 2.75 vessels were embolized per BAE with a wide range of 1 to 8 vessels. Hemoptysis control was seen in 96.1% patients immediately, 90.7 % at 1 month, 82.3 % at 3 months, and 66.9 % at 6 months. Overall recurrence was seen in 43 patients (33.1%). Chest pain was the most common minor side effect occurring in 77.1% cases.

Conclusion BAE is a safe and effective procedure that can be performed routinely in patients presenting with moderate to massive hemoptysis or with mild hemoptysis refractory to medical management.


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Introduction

Hemoptysis is defined as expectoration of blood in sputum. Massive hemoptysis has been defined by various researchers as expectorant volume varying from 100 mL to more than 1,000 ml in 24 hours; however, nowadays the focus is being shifted to other clinical risks like hemodynamic instability, shock, and hypoxic respiratory failure rather than absolute volume quantifications.[1] Nonetheless, massive hemoptysis is life threatening if left untreated.[2] In the majority of cases, the culprit arteries are the bronchial arteries and nonbronchial systemic collaterals (NBSCs).[3]

Some of the common causes of hemoptysis in our country include tuberculosis, aspergilloma, bronchiectasis, chronic bronchitis, and malignancy among the noncardiac causes.[4]

The bronchial arteries usually originate from the proximal descending thoracic aorta and are termed orthotopic if the origin is between the superior endplate of the T5 vertebral body and the inferior endplate of the T6 vertebral body. Angiographic landmark for the same is 1 cm below or above the level of left main bronchus, where it is seen to cross the descending thoracic aorta.[5] These arteries are called ectopic if the origin is from any other vertebral level or other artery. Multiple variations of bronchial arteries are seen with the most common being origin of right bronchial artery as intercostobronchial trunk and two left bronchial arteries.[6]

NBSCs include vessels from the inferior aortic arch, distal descending thoracic aorta, subclavian artery, brachiocephalic trunk, thyrocervical trunk, and internal mammary artery and even a coronary artery and they can also contribute to hemoptysis. These can also be the sources of ectopic bronchial arteries if they are seen to follow the course of bronchus.[7]

Bronchial artery embolization (BAE) involves selective catheterization and angiography of bronchial arteries followed by embolization of abnormal vessels. BAE has been used for control of hemoptysis in variety of clinical conditions ranging from active pulmonary tuberculosis, aspergilloma, bronchiectasis, fibrocavitary lung disease, and even malignancy. It has undergone widespread use in Indian subcontinent especially in view of high burden of persistent hemoptysis due to tuberculosis or post-tubercular sequelae. Even in surgical candidates like unilateral localized disease, aspergilloma, benign lesions, etc., BAE can serve to control life-threatening hemoptysis and decrease the size of the lesion preoperatively.

BAE has undergone a lot of advancements including superselective catheterization to minimize complications and use of polyvinyl alcohol (PVA) particles instead of gelatin or coils to achieve a greater success. These advancements have made BAE a safe, minimally invasive, and highly effective procedure with low complication rate and decreased recurrence rate.

This study was carried out to evaluate the culprit vessels responsible for hemoptysis and study their angiographic signs, and to evaluate the immediate success rate and eventually recurrence rate of hemoptysis following BAE.


#

Methods

All patients undergoing BAE from July 1, 2018 to August 31, 2021 for hemoptysis were included. The inclusion criteria were moderate to severe hemoptysis or mild hemoptysis which was recurrent and not controlled by medical management. Patients referred for surgical intervention or controlled on medical management were excluded.

A collaborative effort between department of radiodiagnosis and pulmonary medicine was sought. All eligible patients were admitted in the pulmonary medicine department, procedure done in the radiology department and interventional radiology after taking informed written consent, and the patients were observed for 24 hours postprocedure and subsequently discharged; the patients were serially followed up in the pulmonary medicine department at 1, 3, and 6 months. All such patients who had undergone BAE were analyzed retrospectively.

Hemoptysis was defined as mild if < 100 mL/day, moderate if 100 to 300 mL/day, and severe/massive if > 300 mL/day. Patients having a hemoglobin fall by 1 g %, hypoxemic respiratory failure after hemoptysis (pO2 < 60 mm Hg), or developing hypotension (systolic blood pressure < 90 mm Hg) were also classified under severe/massive hemoptysis.[8]

The vessels embolized included both bronchial and NBSCs depending on a pre-BAE computed tomography bronchial angiography with an aortic run to identify hypertrophy (> 2 mm), tortuosity, blush, pseudoaneurysm, and venous and pulmonary artery shunting.

We used 60 to 80 mL of contrast at flow rate of 4 mL/sec followed by saline chase and obtained arterial phase and venous phase images. Axial sections were scrutinized for hypertrophied bronchial and nonbronchial systemic feeders to the area of lung pathology. Number, ostial location, vertebral level, and parent artery origin were noted for each suspicious culprit vessel. Maximum intensity projection and multiplanar reconstruction images were scrutinized.

This was followed by the procedure of BAE in Digital subtraction angiography (DSA) lab. Prior to the procedure, informed consent was obtained and basic investigations checked including complete blood count, kidney function test, and coagulation profile. Under local anesthesia, arterial access was obtained thorough transfemoral route and secured using vascular sheath. This was followed by selective catheterization and angiography of bronchial vessels and NBSCs done using nonionic iodinated contrast material. Abnormal angiographic signs like hypertrophy, tortuosity, parenchymal blush, shunting, or aneurysms were looked for and then superselective catheterization done using microcatheter (2.7Fr) followed by embolization using PVA particles of size varying from 200 to 500 μm. Post-embolization runs were obtained to look for any residual abnormal signs.

Immediate success was defined as cessation of hemoptysis in the same admission or within 24 hours. Recurrence was defined as hemoptysis of any degree occurring after complete cessation of hemoptysis post-BAE and occurring after discharge requiring either hospital admission, medical management, or repeat intervention either as bronchoscopy, repeat embolization, or surgery.[8]

Major complications were defined as sequelae, which were permanent or a cause of death, requiring treatment or prolonged hospitalization. Minor complications were complication that did not require treatment and were self-limited.[9]


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Results

One hundred and thirty patients underwent BAE in the study period. Mean age was 41.5 years (16–70 years) and 95 (73.1%) of them were males while 35 (26.9%) were females. Forty-three patients had mild, 46 had moderate, and 41 had severe hemoptysis with the duration of symptoms ranging from 3 days to 25 years. The major symptoms were hemoptysis in all cases (100%) followed by cough in 15.3%, chest pain (3.8%), and dyspnea (2.3%). Underlying condition was found to be active tuberculosis in 11 patients (8.46%), post-tuberculosis sequelae in 65 patients (50%), tuberculosis with aspergilloma in 9 patients (6.9 %), aspergilloma in 1 patient (0.76%), and bronchiectasis in 36 patients (27.69%) while 8 patients had no coexisting condition.

Most common culprit bronchial vessel was intercostobronchial artery (50.8 % cases) followed by left bronchial artery (39.2%), while posterior intercostal artery was the most common NBSC involved (51.5%) followed by internal mammary artery (50 %) ([Table 1]). A total of 381 vessels were found to be abnormal, out of which 358 were embolized.

Table 1

Frequency of involvement of individual arteries in 130 patients

Vessel

Frequency of involvement (n = 130)

Intercostobronchial trunk

66 (50.8%)

Right bronchial

20 (15.3%)

Left bronchial

51 (39.2%)

Common bronchial

41 (31.5%)

Posterior intercostal artery

67 (51.5%)

Internal mammary artery

65 (50 %)

Others

 • Thyrocervical trunk

 • Costocervical trunk

 • Inferior phrenic

 • Lateral thoracic

 • Superior thoracic

 • Supreme Intercostal

71

5 (3.8%)

15 (11.5%)

9 (6.9%)

23 (17.7%)

16 (12.3%)

3 (2.3%)

The most common angiographic finding was hypertrophy seen in 259 vessels followed by tortuosity in 243 vessels ([Table 2]).

Table 2

Distribution of angiographic finding of abnormal vessels in bronchial artery embolization

Angiographic findings

Frequency

Hypertrophy/hypervascularity

259

Tortuosity

243

Parenchymal blush

208

Shunting

61

All abnormal vessels were embolized using PVA particles of sizes varying from 300 to 700 μm. On an average, 2.75 vessels were embolized per BAE with a wide range of 1 to 8 vessels with a total of 358 vessels embolized. In 23 (17.7%) patients, there was technical difficulty in the form of inability to catheterize the abnormal artery. More than one session was required in 16 cases (12.4%). [Figs. 1] and [2] show the digital subtraction angiographic findings seen in our study.

Zoom Image
Fig. 1 (AD) Angiographic images showing abnormal tortuous, hypertrophic left bronchial artery before (A) and after embolization using polyvinyl alcohol (PVA) particles (B). Another image showing abnormal tortuous and hypertrophic nonbronchial systemic collateral from left internal mammary artery before (C) and after PVA embolization (D).
Zoom Image
Fig. 2 (AD) Angiographic images show hypertrophic, tortuous right intercostobronchial trunk with parenchymal blush before (A) and after embolization (B). Another image showing abnormal hypertrophic and tortuous posterior intercostal artery before (C) and after polyvinyl alcohol (PVA) embolization (D).

Immediate success was seen in 125 patients (96.1 %). At 1-month follow-up, 7 patients had hemoptysis with only 4 having moderate amount for which a repeat BAE was done. At 3 months' follow-up, 11 patients had hemoptysis while at 6 months, 20 patients had recurrence. Overall, recurrence was seen in 43 patients (33.1%) while 87 patients (66.9%) remained symptom-free in our period of follow-up of 6 months.

Immediate complications in the form of chest pain (27 patients), fever (16 patients), and dyspnea (1 patient) were seen which resolved gradually and spontaneously. No chronic complications were seen during the course of our study. Two patients expired during the course of study due to hemoptysis.


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Discussion

The airways and supporting structures of the lung are supplied by bronchial arteries, while the lung, parenchyma, and respiratory bronchioles are supplied by pulmonary arteries. Bronchial circulation is the source of massive hemoptysis in 90% of cases.[3] Remy et al first described BAE for the treatment of hemoptysis in 1973.[10]

Since its initial descriptions in 1973, BAE has evolved in terms of indications, technique, and efficacy of hemoptysis control. BAE has been used for treatment for all grades of hemoptysis arising from both benign and malignant causes.

Our results showed that moderate to massive hemoptysis was seen to be more associated with underlying chronic lung disease such as pulmonary tuberculosis and aspergilloma and accounted for 93.8% of our patients. This is in accordance with the study conducted by Chan et al in Hong Kong.[11]

Hypervascularity was the most reported angiographic abnormality in our study seen in 250 abnormal vessels. It refers to the increased caliber and branching of the vessel supplying the abnormal area of lung parenchyma. In our study, the most common culprit vessel was the posterior intercostal artery (51.5% cases) followed by intercostobronchial trunk (50.8% cases) with pulmonary arteries having no significant role. Similar findings were also reported by Mal et al.[12]

The process of embolization was well tolerated by the patients in our study. In literature, the immediate clinical success of BAE varied from 70 to 99%.[2] [3] [12] [13] [14] [15] [16] In our study, hemoptysis control was seen in 96.1% cases immediately, 90.7% cases at 1 month, 82.3% at 3 months, and 66.9% at 6 months. The recurrence rate of hemoptysis ranged between 9.8 and 57.5%. The high recurrence rate is not surprising as BAE is essentially a palliative procedure to manage hemoptysis in patients with diffuse or bilateral lung disease or poor pulmonary reserve who are otherwise unfit to undergo surgery.[13] [14] The overall recurrence rate in our study was 33.1%.

The plausible explanation for early recurrences were technically inadequate or incomplete embolization, lack of complete search for all offending vessels, or inability to embolize all arteries including nonbronchial systemic vessels in the first session due to presence of collateralization. However, the late recurrences were attributed to recanalization of previously embolized arteries or recruitment of new arteries, especially nonbronchial systemic arteries, due to underlying disease progression.[17] [18] [19] [20] In the present study technical difficulty to catheterize the abnormal vessel was seen in 23 arteries.

The most common complications after BAE included transient chest/back pain and dysphagia which were reported in 1.4 to 34.5% and 0.7 to 30%, respectively.[8] The present study reported chest pain as the most common complication. However, no patient had contrast media hypersensitivity, groin puncture hematomas, and femoral artery pseudoaneurysms at the puncture site as previously documented in literature.[8] The literature also has documented neurologic complications due to spinal cord ischemia leading to transient or permanent paraparesis or paraplegia occurring in 0.6 to 4.4%[8] This was attributed to inadvertent embolization of spinal arteries arising from bronchial or intercostobronchial arteries. This has not been observed in the present study, probably due to fewer number of cases. The potential limitations of the study include smaller sample size and evaluation of efficacy of BAE only under elective conditions. A review of the various studies done in relation to the management of hemoptysis by BAE is shown in [Table 3].

Table 3

BAE in the management of hemoptysis: literature review

Author

Year

Number of patients

Amount of hemoptysis

Immediate success rate

Recurrence rate

Singhal and Banode[21]

2011

11

Massive

91%

9.1%

Agmy et al[22]

2013

348

Moderate to massive

95%

9.6%

Bhalla et al[18]

2015

334

Mild, moderate, and massive

78.1%

7.5% (long term)

Mishra et al[23]

2018

52

Intractable hemoptysis or massive hemoptysis

92%

4.2% at 1 month

Hwang et al[24]

2021

233

Mild, moderate

Technical 96.1%

Clinical 94%

27.5% after 197 days

Dorji et al[25]

2021

145

Life-threatening hemoptysis

Technical 92.4%

Clinical 70.1%

48.9%

Present study

130

Mild, moderate, and massive

96.1%

33.1%

Abbreviation: BAE, bronchial artery embolization.



#

Conclusion

Our results revealed that hypervascularity of abnormal bronchial and nonbronchial systemic arteries were the most common vascular abnormality. BAE is a safe procedure for control of moderate/massive hemoptysis or those with mild hemoptysis but refractory to medical management, with high success and low recurrence rate.


#
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Conflict of Interest

None declared.

Ethical Approval Statement

Ethical approval was taken from the institute's ethics committee.


Consent for Publication

Written informed consent was taken from the patients.


Data Availability Statement

Written informed consent was taken from all study participants to share their clinical data.


Authors' Contribution

P.G., A.K., P.I. involved in conceptualization, literature search, writing the original draft of manuscript, literature search, planning, conduct, and editing. P.G., A.K., K.B., A.M., P.I., R.K. involved in review and editing. All the authors have agreed with the submitted manuscript.


  • References

  • 1 Ibrahim WH. Massive haemoptysis: the definition should be revised. Eur Respir J 2008; 32 (04) 1131-1132
  • 2 Jean-Baptiste E. Clinical assessment and management of massive hemoptysis. Crit Care Med 2000; 28 (05) 1642-1647
  • 3 Yoon W, Kim JK, Kim YH, Chung TW, Kang HK. Bronchial and nonbronchial systemic artery embolization for life-threatening hemoptysis: a comprehensive review. Radiographics 2002; 22 (06) 1395-1409
  • 4 Hirshberg B, Biran I, Glazer M, Kramer MR. Hemoptysis: etiology, evaluation, and outcome in a tertiary referral hospital. Chest 1997; 112 (02) 440-444
  • 5 Tanomkiat W, Tanisaro K. Radiographic relationship of the origin of the bronchial arteries to the left main bronchus. J Thorac Imaging 2003; 18 (01) 27-33
  • 6 Cauldwell EW, Siekert RG. et al. The bronchial arteries; an anatomic study of 150 human cadavers. Surg Gynecol Obstet 1948; 86 (04) 395-412
  • 7 Hartmann IJC, Remy-Jardin M, Menchini L, Teisseire A, Khalil C, Remy J. Ectopic origin of bronchial arteries: assessment with multidetector helical CT angiography. Eur Radiol 2007; 17 (08) 1943-1953
  • 8 Panda A, Bhalla AS, Goyal A. Bronchial artery embolization in hemoptysis: a systematic review. Diagn Interv Radiol 2017; 23 (04) 307-317
  • 9 Angle JF, Siddiqi NH, Wallace MJ. Quality improvement guidelines for percutaneous transcatheter embolization: Society of Interventional Radiology Standards of Practice Committee. J Vasc Interv Radiol 2010; 21 (10) 1479-1486
  • 10 Remy J, Voisin C, Ribet M. et al. Treatment, by embolization, of severe or repeated hemoptysis associated with systemic hypervascularization [in French]. Nouv Presse Med 1973; 2 (31) 2060
  • 11 Chan VL, So LKY, Lam JYM. et al. Major haemoptysis in Hong Kong: aetiologies, angiographic findings and outcomes of bronchial artery embolisation. Int J Tuberc Lung Dis 2009; 13 (09) 1167-1173
  • 12 Mal H, Rullon I, Mellot F. et al. Immediate and long-term results of bronchial artery embolization for life-threatening hemoptysis. Chest 1999; 115 (04) 996-1001
  • 13 Poyanli A, Acunas B, Rozanes I. et al. Endovascular therapy in the management of moderate and massive haemoptysis. Br J Radiol 2007; 80 (953) 331-336
  • 14 Antonelli M, Midulla F, Tancredi G. et al. Bronchial artery embolization for the management of nonmassive hemoptysis in cystic fibrosis. Chest 2002; 121 (03) 796-801
  • 15 Swanson KL, Johnson CM, Prakash UBS, McKusick MA, Andrews JC, Stanson AW. Bronchial artery embolization : experience with 54 patients. Chest 2002; 121 (03) 789-795
  • 16 Shao H, Wu J, Wu Q. et al. Bronchial artery embolization for hemoptysis: a retrospective observational study of 344 patients. Chin Med J (Engl) 2015; 128 (01) 58-62
  • 17 Uflacker R, Kaemmerer A, Picon PD. et al. Bronchial artery embolization in the management of hemoptysis: technical aspects and long-term results. Radiology 1985; 157 (03) 637-644
  • 18 Bhalla A, Kandasamy D, Veedu P, Mohan A, Gamanagatti S. A retrospective analysis of 334 cases of hemoptysis treated by bronchial artery embolization. Oman Med J 2015; 30 (02) 119-128
  • 19 Rabkin JE, Astafjev VI, Gothman LN, Grigorjev YG. Transcatheter embolization in the management of pulmonary hemorrhage. Radiology 1987; 163 (02) 361-365
  • 20 Lee S, Chan JWM, Chan SCH. et al. Bronchial artery embolisation can be equally safe and effective in the management of chronic recurrent haemoptysis. Hong Kong Med J 2008; 14 (01) 14-20
  • 21 Singhal S, Banode P. Bronchial artery embolization in patients presenting with massive hemoptysis: initial experience from a rural tertiary centre of central India. Int Sch Res Not 2011; 2011: 1-5
  • 22 Agmy GM, Wafy SM, Mohamed SA. et al. Bronchial and nonbronchial systemic artery embolization in management of hemoptysis: experience with 348 patients. Int Sch Res Not 2013; 26: e263259
  • 23 Mishra A, Mathur A, Pathak K, Katoch CD, Khera A. Bronchial artery embolization in treatment of hemoptysis: treatment efficacy and complications at a tertiary care chest centre. Med J Armed Forces India 2018; 74 (04) 352-357
  • 24 Hwang JH, Kim JH, Park S, Lee KH, Park SH. Feasibility and outcomes of bronchial artery embolization in patients with non-massive hemoptysis. Respir Res 2021; 22 (01) 221
  • 25 Dorji K, Hongsakul K, Jutidamrongphan W, Oofuvong M, Geater S. Bronchial artery embolization in life-threatening hemoptysis: outcome and predictive factors. J Belg Soc Radiol 2021; 105 (01) 5

Address for correspondence

Pranav Ish, MD, DM
Department of Pulmonary, Critical Care and Sleep Medicine, Room Number 638, Superspeciality block, Vardhman Mahavir Medical College and& Safdarjung Hospital
New Delhi 110029
India   

Publication History

Article published online:
03 March 2023

© 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting unrestricted use, distribution, and reproduction so long as the original work is properly cited. (https://creativecommons.org/licenses/by/4.0/)

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  • References

  • 1 Ibrahim WH. Massive haemoptysis: the definition should be revised. Eur Respir J 2008; 32 (04) 1131-1132
  • 2 Jean-Baptiste E. Clinical assessment and management of massive hemoptysis. Crit Care Med 2000; 28 (05) 1642-1647
  • 3 Yoon W, Kim JK, Kim YH, Chung TW, Kang HK. Bronchial and nonbronchial systemic artery embolization for life-threatening hemoptysis: a comprehensive review. Radiographics 2002; 22 (06) 1395-1409
  • 4 Hirshberg B, Biran I, Glazer M, Kramer MR. Hemoptysis: etiology, evaluation, and outcome in a tertiary referral hospital. Chest 1997; 112 (02) 440-444
  • 5 Tanomkiat W, Tanisaro K. Radiographic relationship of the origin of the bronchial arteries to the left main bronchus. J Thorac Imaging 2003; 18 (01) 27-33
  • 6 Cauldwell EW, Siekert RG. et al. The bronchial arteries; an anatomic study of 150 human cadavers. Surg Gynecol Obstet 1948; 86 (04) 395-412
  • 7 Hartmann IJC, Remy-Jardin M, Menchini L, Teisseire A, Khalil C, Remy J. Ectopic origin of bronchial arteries: assessment with multidetector helical CT angiography. Eur Radiol 2007; 17 (08) 1943-1953
  • 8 Panda A, Bhalla AS, Goyal A. Bronchial artery embolization in hemoptysis: a systematic review. Diagn Interv Radiol 2017; 23 (04) 307-317
  • 9 Angle JF, Siddiqi NH, Wallace MJ. Quality improvement guidelines for percutaneous transcatheter embolization: Society of Interventional Radiology Standards of Practice Committee. J Vasc Interv Radiol 2010; 21 (10) 1479-1486
  • 10 Remy J, Voisin C, Ribet M. et al. Treatment, by embolization, of severe or repeated hemoptysis associated with systemic hypervascularization [in French]. Nouv Presse Med 1973; 2 (31) 2060
  • 11 Chan VL, So LKY, Lam JYM. et al. Major haemoptysis in Hong Kong: aetiologies, angiographic findings and outcomes of bronchial artery embolisation. Int J Tuberc Lung Dis 2009; 13 (09) 1167-1173
  • 12 Mal H, Rullon I, Mellot F. et al. Immediate and long-term results of bronchial artery embolization for life-threatening hemoptysis. Chest 1999; 115 (04) 996-1001
  • 13 Poyanli A, Acunas B, Rozanes I. et al. Endovascular therapy in the management of moderate and massive haemoptysis. Br J Radiol 2007; 80 (953) 331-336
  • 14 Antonelli M, Midulla F, Tancredi G. et al. Bronchial artery embolization for the management of nonmassive hemoptysis in cystic fibrosis. Chest 2002; 121 (03) 796-801
  • 15 Swanson KL, Johnson CM, Prakash UBS, McKusick MA, Andrews JC, Stanson AW. Bronchial artery embolization : experience with 54 patients. Chest 2002; 121 (03) 789-795
  • 16 Shao H, Wu J, Wu Q. et al. Bronchial artery embolization for hemoptysis: a retrospective observational study of 344 patients. Chin Med J (Engl) 2015; 128 (01) 58-62
  • 17 Uflacker R, Kaemmerer A, Picon PD. et al. Bronchial artery embolization in the management of hemoptysis: technical aspects and long-term results. Radiology 1985; 157 (03) 637-644
  • 18 Bhalla A, Kandasamy D, Veedu P, Mohan A, Gamanagatti S. A retrospective analysis of 334 cases of hemoptysis treated by bronchial artery embolization. Oman Med J 2015; 30 (02) 119-128
  • 19 Rabkin JE, Astafjev VI, Gothman LN, Grigorjev YG. Transcatheter embolization in the management of pulmonary hemorrhage. Radiology 1987; 163 (02) 361-365
  • 20 Lee S, Chan JWM, Chan SCH. et al. Bronchial artery embolisation can be equally safe and effective in the management of chronic recurrent haemoptysis. Hong Kong Med J 2008; 14 (01) 14-20
  • 21 Singhal S, Banode P. Bronchial artery embolization in patients presenting with massive hemoptysis: initial experience from a rural tertiary centre of central India. Int Sch Res Not 2011; 2011: 1-5
  • 22 Agmy GM, Wafy SM, Mohamed SA. et al. Bronchial and nonbronchial systemic artery embolization in management of hemoptysis: experience with 348 patients. Int Sch Res Not 2013; 26: e263259
  • 23 Mishra A, Mathur A, Pathak K, Katoch CD, Khera A. Bronchial artery embolization in treatment of hemoptysis: treatment efficacy and complications at a tertiary care chest centre. Med J Armed Forces India 2018; 74 (04) 352-357
  • 24 Hwang JH, Kim JH, Park S, Lee KH, Park SH. Feasibility and outcomes of bronchial artery embolization in patients with non-massive hemoptysis. Respir Res 2021; 22 (01) 221
  • 25 Dorji K, Hongsakul K, Jutidamrongphan W, Oofuvong M, Geater S. Bronchial artery embolization in life-threatening hemoptysis: outcome and predictive factors. J Belg Soc Radiol 2021; 105 (01) 5

Zoom Image
Fig. 1 (AD) Angiographic images showing abnormal tortuous, hypertrophic left bronchial artery before (A) and after embolization using polyvinyl alcohol (PVA) particles (B). Another image showing abnormal tortuous and hypertrophic nonbronchial systemic collateral from left internal mammary artery before (C) and after PVA embolization (D).
Zoom Image
Fig. 2 (AD) Angiographic images show hypertrophic, tortuous right intercostobronchial trunk with parenchymal blush before (A) and after embolization (B). Another image showing abnormal hypertrophic and tortuous posterior intercostal artery before (C) and after polyvinyl alcohol (PVA) embolization (D).