![]() Moreover, the current view in the United Kingdom is that access to palliative care should be based on patients’ needs instead of a diagnosis. By contrast, there are guidelines on palliative care for ILD patients based on collaboration between several medical societies. In addition, the guidelines from the Japanese Respiratory Society (JRS) only contain recommendations on the diagnosis and treatment of ILD, which may account for why ILD patients are infrequently provided palliative care. Less ILD patients receive morphine even if they suffer from dyspnea than LC patients. ILD patients generally do not receive adequate palliative care in Japan. These signs and symptoms, in the end, stage are similar to those of patients with lung cancer (LC). Moreover, most end-stage patients with ILD have dyspnea, hypoxemia, and cough. The mean survival time of patients with IPF in Japan is 61 months. Interstitial lung disease (ILD), especially idiopathic pulmonary fibrosis (IPF), is a fatal disease with a poor prognosis, and the therapeutic options are limited.
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