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PULMONARY TOXICITY OF DRUGS USED TO TREAT SYSTEMIC AUTOIMMUNE DISEASES

Identifieur interne : 002738 ( Main/Exploration ); précédent : 002737; suivant : 002739

PULMONARY TOXICITY OF DRUGS USED TO TREAT SYSTEMIC AUTOIMMUNE DISEASES

Auteurs : Daniel Libby [États-Unis] ; Dorothy A. White [États-Unis]

Source :

RBID : ISTEX:7052B35C605A66D89EA33CD3BB8772E88F1A0797

English descriptors

Abstract

A large number of drugs are now used to treat systemic autoimmune diseases. These include cytotoxic drugs, antimetabolites, antimalarial agents, gold, penicillamine, nonsteroidal anti-inflammatory drugs (NSAIDs), antihyperuricemic drugs, and immune modulators, such as corticosteroids and cyclosporin. In the last few decades, it has been recognized that many of these agents cause pulmonary toxic manifestations. Recognition of a respiratory complication in a patient with a systemic autoimmune disease as being caused by drug toxicity rather than other causes can be problematic. First, these disorders themselves involve the lung in patterns that can be indistinguishable from drug toxicity. Bronchospasm, pleural effusions, pulmonary infiltrates with eosinophilia, interstitial pneumonitis, and pulmonary fibrosis can all be manifestations of drug toxicity or the underlying autoimmune disease. From a histopathologic viewpoint, the lung tends to respond to injury in a limited number of ways, so that there are no pathologic findings that are pathognomonic of antirheumatic drug toxicity. Similarly, radiologic and pulmonary function findings of drug toxicity are often nonspecific. Additionally, in systemic autoimmune disorders, particularly in rheumatoid arthritis (RA), it is common to use more than one disease-modifying agent at a time, and therefore, even if drug toxicity is suspected it may be difficult to ascertain the precise offending agent. Recognition of pulmonary toxicity of antirheumatic drugs then depends on a careful clinical assessment and requires knowledge of the manifestations of the underlying rheumatologic disorder and the type and time course of pulmonary toxicity associated with the antirheumatic drugs being used. This article reviews the most important of the antirheumatic drug-related pulmonary complications, discusses difficulties with their diagnosis, and where known, gives proposed mechanisms of toxicity.

Url:
DOI: 10.1016/S0272-5231(05)70118-0


Affiliations:


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<term>Adverse effects</term>
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<term>American review</term>
<term>Antihyperuricemic drugs</term>
<term>Antirheumatic</term>
<term>Antirheumatic agent</term>
<term>Antirheumatic drugs</term>
<term>Arch intern</term>
<term>Arthritis</term>
<term>Arthritis rheum</term>
<term>Aspirin</term>
<term>Bridge therapy</term>
<term>Bronchiolitis</term>
<term>Bronchiolitis obliterans</term>
<term>Bronchoalveolar lavage</term>
<term>Bronchospasm</term>
<term>Bronchovascular bundles</term>
<term>Carinii</term>
<term>Carinii pneumonia</term>
<term>Cause noncardiogenic</term>
<term>Chest radiograph</term>
<term>Clin</term>
<term>Clin rheumatol</term>
<term>Clinical features</term>
<term>Complication</term>
<term>Connective tissue disease</term>
<term>Corticosteroid</term>
<term>Cyclophosphamide</term>
<term>Cytotoxic drugs</term>
<term>Cytotoxic therapy</term>
<term>Diffuse alveolitis</term>
<term>Distress syndrome</term>
<term>Dos</term>
<term>Dose methotrexate</term>
<term>Drug toxicity</term>
<term>Dyspnea</term>
<term>Edema</term>
<term>Eosinophilia</term>
<term>Erythematosus</term>
<term>Fungal infection</term>
<term>Gastric mucosa</term>
<term>Glucocorticoid</term>
<term>Gold lung</term>
<term>Gold pneumonitis</term>
<term>Gold therapy</term>
<term>Gold toxicity</term>
<term>Granulocyte macrophage colony</term>
<term>Gravis</term>
<term>Hypersensitivity</term>
<term>Hypersensitivity pneumonitis</term>
<term>Infiltrates</term>
<term>Intern</term>
<term>Interstitial</term>
<term>Interstitial pneumonia</term>
<term>Interstitial pneumonitis</term>
<term>Intravenous cyclophosphamide</term>
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<term>Lung tissue</term>
<term>Lung toxicity</term>
<term>Lupus</term>
<term>Lymphocyte</term>
<term>Malignant diseases</term>
<term>Many patients</term>
<term>Methotrexate</term>
<term>Methotrexate pneumonitis</term>
<term>Methotrexate therapy</term>
<term>Myasthenia</term>
<term>Myasthenia gravis</term>
<term>Noncardiogenic</term>
<term>Nonsteroidal</term>
<term>Nonsteroidal drugs</term>
<term>Nsaid</term>
<term>Obliterans</term>
<term>Obliterative bronchiolitis</term>
<term>Opportunistic infections</term>
<term>Other cases</term>
<term>Other settings</term>
<term>Penicillamine</term>
<term>Penicillamine therapy</term>
<term>Pleural effusions</term>
<term>Pneumocystis</term>
<term>Pneumocystis carinii pneumonia</term>
<term>Pneumonia</term>
<term>Pneumonitis</term>
<term>Positive lymphocyte stimulation test</term>
<term>Psoriatic arthritis</term>
<term>Pulmonary capillary</term>
<term>Pulmonary disease</term>
<term>Pulmonary dysfunction</term>
<term>Pulmonary edema</term>
<term>Pulmonary function</term>
<term>Pulmonary function tests</term>
<term>Pulmonary function tests show</term>
<term>Pulmonary infiltrates</term>
<term>Pulmonary toxicity</term>
<term>Relapsing polychondritis</term>
<term>Respir crit care</term>
<term>Respiratory diseases</term>
<term>Restrictive ventilatory defect</term>
<term>Rheum</term>
<term>Rheumatic diseases</term>
<term>Rheumatoid</term>
<term>Rheumatoid arthritis</term>
<term>Rheumatoid arthritis patients</term>
<term>Rheumatol</term>
<term>Rheumatologic</term>
<term>Rheumatologic disorder</term>
<term>Rheumatologic disorders</term>
<term>Risk factors</term>
<term>Salicylate</term>
<term>Salicylate toxicity</term>
<term>Semin arthritis rheum</term>
<term>Successful treatment</term>
<term>Syndrome</term>
<term>Systemic</term>
<term>Systemic lupus erythematosus</term>
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<div type="abstract">A large number of drugs are now used to treat systemic autoimmune diseases. These include cytotoxic drugs, antimetabolites, antimalarial agents, gold, penicillamine, nonsteroidal anti-inflammatory drugs (NSAIDs), antihyperuricemic drugs, and immune modulators, such as corticosteroids and cyclosporin. In the last few decades, it has been recognized that many of these agents cause pulmonary toxic manifestations. Recognition of a respiratory complication in a patient with a systemic autoimmune disease as being caused by drug toxicity rather than other causes can be problematic. First, these disorders themselves involve the lung in patterns that can be indistinguishable from drug toxicity. Bronchospasm, pleural effusions, pulmonary infiltrates with eosinophilia, interstitial pneumonitis, and pulmonary fibrosis can all be manifestations of drug toxicity or the underlying autoimmune disease. From a histopathologic viewpoint, the lung tends to respond to injury in a limited number of ways, so that there are no pathologic findings that are pathognomonic of antirheumatic drug toxicity. Similarly, radiologic and pulmonary function findings of drug toxicity are often nonspecific. Additionally, in systemic autoimmune disorders, particularly in rheumatoid arthritis (RA), it is common to use more than one disease-modifying agent at a time, and therefore, even if drug toxicity is suspected it may be difficult to ascertain the precise offending agent. Recognition of pulmonary toxicity of antirheumatic drugs then depends on a careful clinical assessment and requires knowledge of the manifestations of the underlying rheumatologic disorder and the type and time course of pulmonary toxicity associated with the antirheumatic drugs being used. This article reviews the most important of the antirheumatic drug-related pulmonary complications, discusses difficulties with their diagnosis, and where known, gives proposed mechanisms of toxicity.</div>
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