| Literature DB >> 32426111 |
John J Ryan1, Lana Melendres-Groves2, Roham T Zamanian3, Ronald J Oudiz4, Murali Chakinala5, Erika B Rosenzweig6, Mardi Gomberg-Maitland7.
Abstract
The COVID-19 pandemic presents many unique challenges when caring for patients with pulmonary hypertension. The COVID-19 pandemic has altered routine standard of care practice and the acute management particularly for those patients with pulmonary arterial hypertension, where pulmonary arterial hypertension-specific treatments are used. It is important to balance the ongoing care and evaluation of pulmonary arterial hypertension patients with "exposure risk" to COVID-19 for patients coming to clinic or the hospital. If there is a morbidity and mortality benefit from starting pulmonary arterial hypertension therapies, for example in a patient with high-likelihood of pulmonary arterial hypertension, then it remains important to complete the thorough evaluation. However, the COVID-19 outbreak may also represent a unique time when pulmonary hypertension experts have to weigh the risks and benefits of the diagnostic work-up including potential exposure to COVID-19 versus initiating targeted pulmonary arterial hypertension therapy in a select high-risk, high likelihood World Symposium Pulmonary Hypertension Group 1 pulmonary arterial hypertension patients. This document will highlight some of the issues facing providers, patients, and the pulmonary arterial hypertension community in real-time as the COVID-19 pandemic is evolving and is intended to share expected common clinical scenarios and best clinical practices to help the community at-large.Entities:
Keywords: clinical trials; mechanical ventilation; prostacyclin; pulmonary hypertension; right heart failure; therapeutics
Year: 2020 PMID: 32426111 PMCID: PMC7222260 DOI: 10.1177/2045894020920153
Source DB: PubMed Journal: Pulm Circ ISSN: 2045-8932 Impact factor: 3.017
Considerations for pulmonary hypertension programs during COVID-19 pandemic.
| Adopt a temporary visit (new and returning) schedule to balance exposure risk with benefit of evaluation. Consider telemedicine visits as an alternate, as long as patient accessibility is addressed. |
| Establish protocols for PAH work-up and evaluation to decrease the risk of exposure or transmission of COVID-19. For example, consider less frequent echocardiography and 6MWT testing on stable patients and avoid pulmonary function or V/Q testing if possible. |
| Airway management and oxygenation is challenging in PAH with respiratory failure. Best practice should be shared throughout the PAH community regarding use of BiPAP/CPAP, intubation, ventilators, and even home nitric oxide delivery systems. |
| Stratify need for right heart catheterization based on pre-test probability of group 1 PAH and risk profile of new or returning patients who require augmentation of PAH therapy. |
| Follow NIH, FDA, Sponsor, and institutional guidance on limiting and/or halting enrolment in PAH clinical trials. |
PAH: pulmonary arterial hypertension; COVID-19: coronavirus disease of 2019; 6MWT: six-minute walk test; NIH: National Institutes of Health; FDA: Food and Drug administration.
Updated clinical classification of pulmonary hypertension (PH).
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| 1.1 Idiopathic PAH |
| 1.2 Heritable PAH |
| 1.3 Drug- and toxin-induced PAH |
| 1.4 PAH associated with: |
| 1.4.1 Connective tissue disease |
| 1.4.2 HIV infection |
| 1.4.3 Portal hypertension |
| 1.4.4 Congenital heart disease |
| 1.4.5 Schistosomiasis |
| 1.5 PAH long-term responders to calcium channel blockers |
| 1.6 PAH with overt features of venous/capillaries (PVOD/PCH) involvement |
| 1.7 Persistent PH of the newborn syndrome |
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| 2.1 PH due to heart failure with preserved LVEF |
| 2.2 PH due to heart failure with reduced LVEF |
| 2.3 Valvular heart disease |
| 2.4 Congenital/acquired cardiovascular conditions leading to post-capillary PH |
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| 3.1 Obstructive lung disease |
| 3.2 Restrictive lung disease |
| 3.3 Other lung disease with mixed restrictive/obstructive pattern |
| 3.4 Hypoxia without lung disease |
| 3.5 Developmental lung disorders |
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| 4.1 Chronic thromboembolic PH |
| 4.2 Other pulmonary artery obstructions |
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| 5.1 Haematological disorders |
| 5.2 Systemic and metabolic disorders |
| 5.3 Others |
| 5.4 Complex congenital heart disease |
PAH: pulmonary arterial hypertension; PH: pulmonary hypertension; PVOD: pulmonary veno-occlusive disease; PCH: pulmonary capillary hemangiomatosis; LVEF: left ventricular ejection fraction.
Source: reproduced with permission from Simonneau et al.[32]