Publications by authors named "Eija-Riitta Salomaa"

Article Synopsis
  • The study analyzed the real-world use of antifibrotic drugs in idiopathic pulmonary fibrosis (IPF) patients, using data from Finnish registries.
  • Half of the 263 patients started antifibrotic treatment from 2011-2018, with a mean delay of about 367 days post-diagnosis.
  • Factors like younger age and lower lung capacity were linked to earlier medication initiation, while a significant number discontinued treatment within the first year, highlighting the need for better understanding of treatment adherence.
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Idiopathic pulmonary fibrosis (IPF) is characterised by unpredictable disease course and poor survival. After the introduction of novel antifibrotic drugs, the prognosis of patients with IPF is probably changing. FinnishIPF, a nationwide registry of carefully characterised patients, was initiated in Finland in 2011.

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: The early diagnosis of idiopathic pulmonary fibrosis (IPF) has become increasingly important due to evolving treatment options. IPF patients experience a significant delay in receiving an accurate diagnosis, thus delayed access to tertiary care is associated with higher mortality independently from disease severity. : The aims were to evaluate whether there had been a delay in the referral process, and to determine whether the referring doctors had suspected IPF or other interstitial lung disease (ILD) already during the time of referral.

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Background: The survival of lung cancer patients is still poor; 10-15% are alive five years after diagnosis.

Material And Methods: We evaluated 1 542 patients with new lung cancer diagnosis in 2004-2011.

Results: The one-, two- and five-year survival rate was 37.

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Background: We evaluated the changes in nasal CPAP treatment and adherence in patients with sleep-disordered breathing (SDB).

Material And Methods: Information from the clinic database of 4,385 patients commencing CPAP treatment during 2002-2009.

Results: Average CPAP adherence was 74%.

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Article Synopsis
  • The study investigates the rising incidence of idiopathic pulmonary fibrosis (IPF) and highlights the lack of consistent epidemiological data on the disease.
  • Recent research methods were reviewed, focusing on identifying trends in IPF prevalence and incidence through a systematic database search of articles published after 2000.
  • It concluded that three main methodologies are used in IPF studies, with findings showing varying prevalence and incidence rates, and suggests that contrasting methods could pave the way for better future research.
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Introduction: Pemetrexed has emerged as standard chemotherapy for malignant pleural mesothelioma (MPM).

Objectives: MPMs at two Finnish University Hospitals during 7 years (2000-2006) were reviewed in order to evaluate the treatments, survival and prognostic factors. The results in two periods (before pemetrexed use in 2000-2002 and with pemetrexed in 2003-2006) were compared.

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Treatment of advanced or metastatic non-small cell lung cancer with current cytotoxic agents is at its best able to only slow down the progression of the disease, while no curative treatment is known. Novel antiangiogenetic agents such as Bevacizumab have been expected to bring about a change in the treatment and prognosis of this disease. Two randomized studies have been conducted with Bevacizumab, whereby it was observed to make the therapeutic results more effective when combined with a cytotoxic platinum agent in a selected patient group.

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Study Objectives: This study was undertaken to measure delays of diagnosis and to assess the causes for those delays in patients with lung cancer. In addition, the relation of delay times and survival was analyzed.

Design: A retrospective study based on patient records.

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Background: A causal relationship between gastroesophageal reflux (GER) and asthma has been suggested. Should this be the case, one could expect treatment of GER to diminish bronchial sensitivity. There has been a lack of trials evaluating the efficacy of antireflux surgery on airway reactivity.

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