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Chronic thromboembolic pulmonary hypertension

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Chronic thromboembolic pulmonary hypertension
Other namesCTEPH
SpecialtyPulmonology, cardiology
Usual onset63 years (median)[1]
DurationLong term
Risk factorsSplenectomy, inflammatory bowel disease, chronic thyroid hormone replacement, blood types other than O, malignancy, infected ventriculo-atrial shunt, permanent intravenous leads [1][2][3][4][5]
Diagnostic methodInvasively measured mean pulmonary arterial pressure combined with specialist imaging [6]
TreatmentPulmonary endarterectomy, Balloon pulmonary angioplasty, medical treatment [6]
Frequency5 cases per million[7]

Chronic thromboembolic pulmonary hypertension (CTEPH) is a long-term disease caused by a blockage in the blood vessels that deliver blood from the heart to the lungs (the pulmonary arterial tree). These blockages cause increased resistance to flow in the pulmonary arterial tree which in turn leads to rise in pressure in these arteries (pulmonary hypertension). The blockages either result from organised (or hardened) blood clots that usually originate from the deep veins of the lower limbs of the body (thromboembolism) and lodge in the pulmonary arterial tree after passing through the right side of the heart. The blockages may also result from scar tissue that forms at the site where the clot has damaged the endothelial lining of the pulmonary arteries, causing permanent fibrous obstruction (blood flow blockage).[8] Most patients have a combination of microvascular (small vessel) and macrovascular (large vessel) obstruction. Some patients may present with normal or near-normal pulmonary pressures at rest despite symptomatic disease. These patients are labelled as having chronic thromboembolic disease (CTED).[6]

Diagnosis is made after at least three months of effective blood thinning to discern this condition from subacute pulmonary embolism. Diagnostic findings for CTEPH are:[6]

  1. Invasively (i.e., in the blood) measured mean pulmonary arterial pressure (mPAP) ≥25 mmHg;
  2. Mismatched perfusion defects on lung ventilation/perfusion (V/Q) scan and specific diagnostic signs for CTEPH seen by multidetector computed tomography angiography (MDCT), magnetic resonance imaging (MRI) or conventional pulmonary cineangiography (PAG), such as ring-like stenoses, webs/slits, chronic total occlusions (pouch lesions, or tapered lesions) and tortuous lesions.

Signs and symptoms

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Clinical symptoms and signs are often non-specific or absent in early CTEPH, with signs of right heart failure only in advanced disease. The main symptom of CTEPH is exertional breathlessness (shortness of breath during exertion such as exercise), which is unspecific and may often be attributed to other, more common, diseases by physicians. When present, the clinical symptoms of CTEPH may resemble those of acute PE, or of idiopathic pulmonary arterial hypertension (iPAH). Leg oedema (swelling) and haemoptysis (blood in mucus) occur more often in CTEPH, while syncope (fainting) is more common in iPAH.[5]

Pathogenesis

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People with CTEPH lack traditional thrombosis risk factors.[1][2][3][4][5] Current understanding is that CTEPH is a result of “inflammatory thrombosis”:[5] When pro-thrombotic (blood-clot forming) conditions combine with chronic inflammation and infection, non-resolution of thrombus may ensue. Risk factors for CTEPH include splenectomy, inflammatory bowel disease, chronic thyroid hormone replacement, blood types other than 0, malignancy, infected ventriculo-atrial shunt and permanent intravenous leads.[4][5]

Diagnosis

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Example of a side-selective pulmonary artery angiogram (A and B right pulmonary artery, C and D left pulmonary artery) in digital subtraction technique of a patient with CTEPH. Panels A and C represent anterior-posterior projections, panels B and D represent lateral projections. 

Early diagnosis still remains a challenge in CTEPH, with a median time of 14 months between symptom onset and diagnosis in expert centres.[7] A suspicion of PH is often raised by echocardiography, but an invasive right heart catheterisation is required to confirm it.[6] Once PH is diagnosed, the presence of thromboembolic disease requires imaging. The recommended diagnostic algorithm stresses the importance of initial investigation using an echocardiogram and V/Q scan and confirmation with right heart catheter and pulmonary angiography (PA).[8]

Both V/Q scanning and modern multidetector CT angiography (CTPA) may be accurate methods for the detection of CTEPH, with excellent diagnostic efficacy in expert hands (sensitivity, specificity, and accuracy of 100%, 93.7%, and 96.5% for V/Q and 96.1%, 95.2%, and 95.6% for CTPA).[9] CTPA alone cannot exclude the disease, but may help identify pulmonary artery distension resulting in left main coronary artery compression, pulmonary parenchymal lesions (e.g. as complications from previous pulmonary infarctions), and bleeding from bronchial collateral arteries.[10]

Treatment

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Decision making for patients with CTEPH can be complex and needs to be managed by CTEPH teams in expert centres. CTEPH teams comprise cardiologists and pulmonologists with specialist PH training, radiologists, experienced PEA surgeons with a significant caseload of CTEPH patients per year and physicians with percutaneous interventional expertise. Currently, there are three recognised targeted treatment options available including the standard treatment of pulmonary endarterectomy (PEA). Balloon pulmonary angioplasty (BPA) and pulmonary vasodilator drug treatment may be considered for those people that are not suitable for surgery.[11]

Specialist imaging using either magnetic resonance or invasive PA is necessary to determine risks and benefits of interventional treatment with PEA or BPA.[8]

Medical therapy

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Standard medical treatment consists of anticoagulants (blood thinners), diuretics, and oxygen. Lifelong anticoagulation is recommended, even after PEA. Routine inferior vena cava filter placement is not recommended.[6]

In patients with non-operable CTEPH or persistent/recurrent PH after PEA, there is evidence for benefit from pulmonary vasodilator drug treatment.[12] The microvascular disease component in CTEPH has provided the rationale for off-label use of drugs approved for PAH.[1] Currently, only riociguat (a stimulator of soluble guanylate cyclase) is approved for treatment of adults with inoperable CTEPH or persistent or recurrent CTEPH after surgical treatment.[13] Other drug trials are ongoing in patients with inoperable CTEPH, with macitentan recently proving efficacy and safety in MERIT[14]

Pulmonary endarterectomy

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Typical specimen harvested during the surgical procedure of pulmonary endarterectomy in a patient with chronic thromboembolic pulmonary hypertension.

Pulmonary endarterectomy (PEA) is the gold standard treatment for suitable CTEPH patients. Operability of patients with CTEPH is determined by multiple factors among which surgical accessibility of thrombi and the patient-determined risk-benefit ratio are most important. There is no haemodynamic (e.g., considering pulmonary pressure) or age threshold that should exclude patients from surgery, and concomitant cardiac procedures can be included if necessary. About 60% of patients are classified as operable across Europe and Canada.[15]

In contrast to surgical embolectomy for acute PE, treatment of CTEPH necessitates a true bilateral endarterectomy (removal of blockage from the blood vessels) through the medial layer of the pulmonary arteries, which is performed under deep hypothermia (lowering of body temperature) and circulatory arrest (temporary stoppage of blood flow),[16] which is not complicated by cognitive dysfunction.[17] The majority of patients experience substantial relief from symptoms and improvement in haemodynamics after PEA.[16][18][19] In Europe, in-hospital mortality during PEA is currently 4.7% or lower in high volume single centres.[16][18]

Up to 35% of patients may have persistent/recurrent CTEPH following surgery.[12] The definition of post-PEA PH is still not clear, but some data suggest that 500–590 dynes·s·cm−5 may represent a pulmonary vascular resistance (PVR) threshold for poor long-term outcome.[20][21] Recent data from National UK PEA cohort suggests residual PH post PEA only impacts on longer term survival when mPAP is >38 mmHg or PVR >425 dynes·s·cm−5.[22]

Bridging therapy with PAH-targeted drugs, complications and additional procedures during PEA, and residual PH after PEA are associated with worse outcomes. Immediate postoperative PVR is a long-term predictor of prognosis.[20]

Balloon pulmonary angioplasty

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Although BPA technique is still evolving, it may currently be considered for CTEPH patients who are technically non-operable or carry an unfavourable risk-benefit ratio for PEA.[6] The technique has been refined in Japan[23] and initial reports have confirmed the safety and efficacy of the technique, based on data showing haemodynamic improvement and recovery of right ventricular function.[24] Research is ongoing.[11][25]

Prognosis

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Historically the prognosis for patients with untreated CTEPH was poor, with a 5-year survival of <40% if the mPAP was >40 mmHg at presentation.[26] More contemporary data from the European CTEPH registry have demonstrated a 70% 3-year survival in patients with CTEPH who do not undergo the surgical procedure of pulmonary endarterectomy (PEA).[15] Recent data from an international CTEPH registry demonstrate that mortality in CTEPH is associated with New York Heart Association (NYHA) functional class IV, increased right atrial pressure, and a history of cancer. Furthermore, comorbidities such as coronary disease, left heart failure, and chronic obstructive pulmonary disease (COPD) are risk factors for mortality.[15]

Epidemiology

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CTEPH is an orphan disease with an estimated incidence of 5 cases per million,[7] but it is likely that CTEPH is under-diagnosed as symptoms are non-specific. Although a cumulative incidence of CTEPH between 0.1% and 9.1% within the first 2 years after a symptomatic PE has been reported,[27] it is currently unclear whether acute symptomatic PE begets CTEPH. Routine screening for CTEPH after PE is not recommended because a significant number of CTEPH cases develops in the absence of previous acute symptomatic PE.[6] In addition, approximately 25% of patients with CTEPH do not present with a clinical history of acute PE.[1] The median age of patients at diagnosis is 63 years (there is a wide age range, but paediatric cases are rare), and both genders are equally affected.[1][28][29]

References

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  1. ^ a b c d e f Pepke-Zaba, Joanna; Delcroix, Marion; Lang, Irene; Mayer, Eckhard; Jansa, Pavel; Ambroz, David; Treacy, Carmen; D'Armini, Andrea M.; Morsolini, Marco (2011-11-01). "Chronic thromboembolic pulmonary hypertension (CTEPH): results from an international prospective registry". Circulation. 124 (18): 1973–1981. doi:10.1161/CIRCULATIONAHA.110.015008. ISSN 1524-4539. PMID 21969018.
  2. ^ a b Bonderman, Diana; Jakowitsch, Johannes; Adlbrecht, Christopher; Schemper, Michael; Kyrle, Paul A.; Schönauer, Verena; Exner, Markus; Klepetko, Walter; Kneussl, Meinhard P. (March 2005). "Medical conditions increasing the risk of chronic thromboembolic pulmonary hypertension". Thrombosis and Haemostasis. 93 (3): 512–516. doi:10.1160/TH04-10-0657. ISSN 0340-6245. PMID 15735803. S2CID 21467287.
  3. ^ a b Bonderman, Diana; Skoro-Sajer, Nika; Jakowitsch, Johannes; Adlbrecht, Christopher; Dunkler, Daniela; Taghavi, Sharokh; Klepetko, Walter; Kneussl, Meinhard; Lang, Irene M. (2007-04-24). "Predictors of outcome in chronic thromboembolic pulmonary hypertension". Circulation. 115 (16): 2153–2158. doi:10.1161/CIRCULATIONAHA.106.661041. ISSN 1524-4539. PMID 17420352.
  4. ^ a b c Bonderman, D.; Wilkens, H.; Wakounig, S.; Schäfers, H.-J.; Jansa, P.; Lindner, J.; Simkova, I.; Martischnig, A. M.; Dudczak, J. (February 2009). "Risk factors for chronic thromboembolic pulmonary hypertension". The European Respiratory Journal. 33 (2): 325–331. doi:10.1183/09031936.00087608. ISSN 1399-3003. PMID 18799507.
  5. ^ a b c d e Lang, Irene M.; Simonneau, Gérald; Pepke-Zaba, Joanna W.; Mayer, Eckhard; Ambrož, David; Blanco, Isabel; Torbicki, Adam; Mellemkjaer, Sören; Yaici, Azzedine (July 2013). "Factors associated with diagnosis and operability of chronic thromboembolic pulmonary hypertension. A case-control study". Thrombosis and Haemostasis. 110 (1): 83–91. doi:10.1160/TH13-02-0097. ISSN 0340-6245. PMID 23677493. S2CID 36628315.
  6. ^ a b c d e f g h Galiè, Nazzareno; Humbert, Marc; Vachiery, Jean-Luc; Gibbs, Simon; Lang, Irene; Torbicki, Adam; Simonneau, Gérald; Peacock, Andrew; Vonk Noordegraaf, Anton (2016-01-01). "2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: The Joint Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS): Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC), International Society for Heart and Lung Transplantation (ISHLT)". European Heart Journal. 37 (1): 67–119. doi:10.1093/eurheartj/ehv317. ISSN 1522-9645. PMID 26320113.
  7. ^ a b c Pepke-Zaba, Joanna; Jansa, Pavel; Kim, Nick H.; Naeije, Robert; Simonneau, Gerald (April 2013). "Chronic thromboembolic pulmonary hypertension: role of medical therapy". The European Respiratory Journal. 41 (4): 985–990. doi:10.1183/09031936.00201612. ISSN 1399-3003. PMID 23397304.
  8. ^ a b c Kim, Nick H. (August 2016). "Group 4 Pulmonary Hypertension: Chronic Thromboembolic Pulmonary Hypertension: Epidemiology, Pathophysiology, and Treatment". Cardiology Clinics. 34 (3): 435–441. doi:10.1016/j.ccl.2016.04.011. ISSN 1558-2264. PMID 27443139.
  9. ^ He, Jia; Fang, Wei; Lv, Bin; He, Jian-Guo; Xiong, Chang-Ming; Liu, Zhi-Hong; He, Zuo-Xiang (May 2012). "Diagnosis of chronic thromboembolic pulmonary hypertension: comparison of ventilation/perfusion scanning and multidetector computed tomography pulmonary angiography with pulmonary angiography". Nuclear Medicine Communications. 33 (5): 459–463. doi:10.1097/MNM.0b013e32835085d9. ISSN 1473-5628. PMID 22262242. S2CID 22353466.
  10. ^ Tunariu, Nina; Gibbs, Simon J. R.; Win, Zarni; Gin-Sing, Wendy; Graham, Alison; Gishen, Philip; Al-Nahhas, Adil (May 2007). "Ventilation-perfusion scintigraphy is more sensitive than multidetector CTPA in detecting chronic thromboembolic pulmonary disease as a treatable cause of pulmonary hypertension". Journal of Nuclear Medicine. 48 (5): 680–684. doi:10.2967/jnumed.106.039438. ISSN 0161-5505. PMID 17475953.
  11. ^ a b Brenot, Philippe; Mayer, Eckhard; Ghofrani, Hossein-Ardeschir; Kurzyna, Marcin; Matsubara, Hiromi; Ogo, Takeshi; Meyer, Bernhard C.; Lang, Irene (31 March 2017). "Balloon pulmonary angioplasty in chronic thromboembolic pulmonary hypertension". European Respiratory Review. 26 (143): 160119. doi:10.1183/16000617.0119-2016. ISSN 1600-0617. PMC 9489135. PMID 28356406.
  12. ^ a b Hoeper, Marius M. (June 2015). "Pharmacological therapy for patients with chronic thromboembolic pulmonary hypertension". European Respiratory Review. 24 (136): 272–282. doi:10.1183/16000617.00001015. ISSN 1600-0617. PMC 9487825. PMID 26028639.
  13. ^ Ghofrani, Hossein-Ardeschir; D'Armini, Andrea M.; Grimminger, Friedrich; Hoeper, Marius M.; Jansa, Pavel; Kim, Nick H.; Mayer, Eckhard; Simonneau, Gerald; Wilkins, Martin R. (2013-07-25). "Riociguat for the treatment of chronic thromboembolic pulmonary hypertension" (PDF). The New England Journal of Medicine. 369 (4): 319–329. doi:10.1056/NEJMoa1209657. hdl:10044/1/19669. ISSN 1533-4406. PMID 23883377.
  14. ^ "Clinical Study to Assess the Efficacy, Safety and Tolerability of Macitentan in Subjects With Inoperable Chronic Thromboembolic Pulmonary Hypertension - Full Text View - ClinicalTrials.gov". clinicaltrials.gov. Retrieved 2017-07-31.
  15. ^ a b c Delcroix, Marion; Lang, Irene; Pepke-Zaba, Joanna; Jansa, Pavel; D'Armini, Andrea M.; Snijder, Repke; Bresser, Paul; Torbicki, Adam; Mellemkjaer, Sören (2016-03-01). "Long-Term Outcome of Patients With Chronic Thromboembolic Pulmonary Hypertension: Results From an International Prospective Registry". Circulation. 133 (9): 859–871. doi:10.1161/CIRCULATIONAHA.115.016522. ISSN 1524-4539. PMID 26826181. S2CID 32395285.
  16. ^ a b c Madani, Michael M.; Auger, William R.; Pretorius, Victor; Sakakibara, Naohide; Kerr, Kim M.; Kim, Nick H.; Fedullo, Peter F.; Jamieson, Stuart W. (July 2012). "Pulmonary endarterectomy: recent changes in a single institution's experience of more than 2,700 patients". The Annals of Thoracic Surgery. 94 (1): 97–103. doi:10.1016/j.athoracsur.2012.04.004. ISSN 1552-6259. PMID 22626752.
  17. ^ Vuylsteke, Alain; Sharples, Linda; Charman, Gill; Kneeshaw, John; Tsui, Steven; Dunning, John; Wheaton, Ella; Klein, Andrew; Arrowsmith, Joseph (2011-10-15). "Circulatory arrest versus cerebral perfusion during pulmonary endarterectomy surgery (PEACOG): a randomised controlled trial". Lancet. 378 (9800): 1379–1387. doi:10.1016/S0140-6736(11)61144-6. ISSN 1474-547X. PMID 22000135. S2CID 31844211.
  18. ^ a b Mayer, Eckhard; Jenkins, David; Lindner, Jaroslav; D'Armini, Andrea; Kloek, Jaap; Meyns, Bart; Ilkjaer, Lars Bo; Klepetko, Walter; Delcroix, Marion (March 2011). "Surgical management and outcome of patients with chronic thromboembolic pulmonary hypertension: results from an international prospective registry". The Journal of Thoracic and Cardiovascular Surgery. 141 (3): 702–710. doi:10.1016/j.jtcvs.2010.11.024. ISSN 1097-685X. PMID 21335128.
  19. ^ Jenkins, D.; Mayer, E.; Screaton, N.; Madani, M. (2012-03-01). "State-of-the-art chronic thromboembolic pulmonary hypertension diagnosis and management". European Respiratory Review. 21 (123): 32–39. doi:10.1183/09059180.00009211. ISSN 1600-0617. PMC 9487476. PMID 22379172.
  20. ^ a b Skoro-Sajer, Nika; Marta, Gabriel; Gerges, Christian; Hlavin, Gerald; Nierlich, Patrick; Taghavi, Shahrokh; Sadushi-Kolici, Roela; Klepetko, Walter; Lang, Irene Marthe (February 2014). "Surgical specimens, haemodynamics and long-term outcomes after pulmonary endarterectomy". Thorax. 69 (2): 116–122. doi:10.1136/thoraxjnl-2013-203746. ISSN 1468-3296. PMC 3913220. PMID 24052543.
  21. ^ Jamieson, Stuart W.; Kapelanski, David P.; Sakakibara, Naohide; Manecke, Gerard R.; Thistlethwaite, Patricia A.; Kerr, Kim M.; Channick, Richard N.; Fedullo, Peter F.; Auger, William R. (November 2003). "Pulmonary endarterectomy: experience and lessons learned in 1,500 cases". The Annals of Thoracic Surgery. 76 (5): 1457–1462. doi:10.1016/S0003-4975(03)00828-2. ISSN 0003-4975. PMID 14602267.
  22. ^ Cannon, John E.; Su, Li; Kiely, David G.; Page, Kathleen; Toshner, Mark; Swietlik, Emilia; Treacy, Carmen; Ponnaberanam, Anie; Condliffe, Robin (2016-05-03). "Dynamic Risk Stratification of Patient Long-Term Outcome After Pulmonary Endarterectomy: Results From the United Kingdom National Cohort". Circulation. 133 (18): 1761–1771. doi:10.1161/CIRCULATIONAHA.115.019470. ISSN 1524-4539. PMC 5860739. PMID 27052413.
  23. ^ Mizoguchi, Hiroki; Ogawa, Aiko; Munemasa, Mitsuru; Mikouchi, Hiroshi; Ito, Hiroshi; Matsubara, Hiromi (December 2012). "Refined balloon pulmonary angioplasty for inoperable patients with chronic thromboembolic pulmonary hypertension". Circulation: Cardiovascular Interventions. 5 (6): 748–755. doi:10.1161/CIRCINTERVENTIONS.112.971077. ISSN 1941-7632. PMID 23192917.
  24. ^ Fukui, Shigefumi; Ogo, Takeshi; Morita, Yoshiaki; Tsuji, Akihiro; Tateishi, Emi; Ozaki, Kumi; Sanda, Yoshihiro; Fukuda, Tetsuya; Yasuda, Satoshi (May 2014). "Right ventricular reverse remodelling after balloon pulmonary angioplasty". The European Respiratory Journal. 43 (5): 1394–1402. doi:10.1183/09031936.00012914. ISSN 1399-3003. PMID 24627536.
  25. ^ Lang, Irene Marthe; Madani, Michael (2014-08-05). "Update on chronic thromboembolic pulmonary hypertension". Circulation. 130 (6): 508–518. doi:10.1161/CIRCULATIONAHA.114.009309. ISSN 1524-4539. PMID 25092279.
  26. ^ Riedel, M.; Stanek, V.; Widimsky, J.; Prerovsky, I. (February 1982). "Longterm follow-up of patients with pulmonary thromboembolism. Late prognosis and evolution of hemodynamic and respiratory data". Chest. 81 (2): 151–158. doi:10.1378/chest.81.2.151. ISSN 0012-3692. PMID 7056079.
  27. ^ Pengo, Vittorio; Lensing, Anthonie W. A.; Prins, Martin H.; Marchiori, Antonio; Davidson, Bruce L.; Tiozzo, Francesca; Albanese, Paolo; Biasiolo, Alessandra; Pegoraro, Cinzia (2004-05-27). "Incidence of chronic thromboembolic pulmonary hypertension after pulmonary embolism". The New England Journal of Medicine. 350 (22): 2257–2264. doi:10.1056/NEJMoa032274. hdl:11577/2438406. ISSN 1533-4406. PMID 15163775.
  28. ^ Berger, Rolf M. F.; Beghetti, Maurice; Humpl, Tilman; Raskob, Gary E.; Ivy, D. Dunbar; Jing, Zhi-Cheng; Bonnet, Damien; Schulze-Neick, Ingram; Barst, Robyn J. (2012-02-11). "Clinical features of paediatric pulmonary hypertension: a registry study". Lancet. 379 (9815): 537–546. doi:10.1016/S0140-6736(11)61621-8. ISSN 1474-547X. PMC 3426911. PMID 22240409.
  29. ^ Madani, Michael M.; Wittine, Lara M.; Auger, William R.; Fedullo, Peter F.; Kerr, Kim M.; Kim, Nick H.; Test, Victor J.; Kriett, Jolene M.; Jamieson, Stuart W. (March 2011). "Chronic thromboembolic pulmonary hypertension in pediatric patients". The Journal of Thoracic and Cardiovascular Surgery. 141 (3): 624–630. doi:10.1016/j.jtcvs.2010.07.010. ISSN 1097-685X. PMID 20800245.
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