Cargando…
The negative effect of initial high-dose methylprednisolone and tapering regimen for acute respiratory distress syndrome: a retrospective propensity matched cohort study
BACKGROUND: The efficacy of corticosteroid use in acute respiratory distress syndrome (ARDS) remains controversial. Generally, short-term high-dose corticosteroid therapy is considered to be ineffective in ARDS. On the other hand, low-dose, long-term use of corticosteroids has been reported to be ef...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5463340/ https://www.ncbi.nlm.nih.gov/pubmed/28592332 http://dx.doi.org/10.1186/s13054-017-1723-0 |
_version_ | 1783242686944247808 |
---|---|
author | Takaki, Makoto Ichikado, Kazuya Kawamura, Kodai Gushima, Yasuhiro Suga, Moritaka |
author_facet | Takaki, Makoto Ichikado, Kazuya Kawamura, Kodai Gushima, Yasuhiro Suga, Moritaka |
author_sort | Takaki, Makoto |
collection | PubMed |
description | BACKGROUND: The efficacy of corticosteroid use in acute respiratory distress syndrome (ARDS) remains controversial. Generally, short-term high-dose corticosteroid therapy is considered to be ineffective in ARDS. On the other hand, low-dose, long-term use of corticosteroids has been reported to be effective since they provide continued inhibition of the systemic inflammatory response syndrome (SIRS) that accompanies ARDS. Thus far, no reports have been published on the efficacy of initiating treatment with a high-dose corticosteroid regimen with tapering. METHODS: We conducted a retrospective observational study involving 186 patients treated at a teaching hospital (68% had sepsis, pneumonia, or aspiration pneumonia). ARDS was diagnosed according to the Berlin definition. Patients were divided into a high-dose (n = 21) or low-dose corticosteroid group (n = 165) to compare the effectiveness of a down-titration regimen. The primary medical team chose which treatment a patient would receive. We were careful to conduct a differential diagnosis of interstitial pneumonia (e.g., acute eosinophilic pneumonia) since corticosteroid treatment has been proven effective in that patient population. The primary outcome was the 60-day mortality rate. The secondary outcome was the number of ventilator-free days (VFD). RESULTS: Those started on a high-dose regimen had a significantly higher 60-day mortality rate (P = 0.031) with significantly fewer VFD (P = 0.021). Propensity scores were used to adjust patient backgrounds in a variable analysis that also showed the high-dose regimen was a factor in decreasing VFD (OR, 95.63; 95% CI, 1.74–5271.07; P = 0.026) and worsening the 60-day mortality rate (OR, 2.54; 95% CI, 0.92–7.02; P = 0.072). CONCLUSIONS: A tapering regimen after high-dose corticosteroids is likely to increase ventilator dependency and might aggravate the prognosis of patients with ARDS diagnosed according to the Berlin definition. |
format | Online Article Text |
id | pubmed-5463340 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54633402017-06-08 The negative effect of initial high-dose methylprednisolone and tapering regimen for acute respiratory distress syndrome: a retrospective propensity matched cohort study Takaki, Makoto Ichikado, Kazuya Kawamura, Kodai Gushima, Yasuhiro Suga, Moritaka Crit Care Research BACKGROUND: The efficacy of corticosteroid use in acute respiratory distress syndrome (ARDS) remains controversial. Generally, short-term high-dose corticosteroid therapy is considered to be ineffective in ARDS. On the other hand, low-dose, long-term use of corticosteroids has been reported to be effective since they provide continued inhibition of the systemic inflammatory response syndrome (SIRS) that accompanies ARDS. Thus far, no reports have been published on the efficacy of initiating treatment with a high-dose corticosteroid regimen with tapering. METHODS: We conducted a retrospective observational study involving 186 patients treated at a teaching hospital (68% had sepsis, pneumonia, or aspiration pneumonia). ARDS was diagnosed according to the Berlin definition. Patients were divided into a high-dose (n = 21) or low-dose corticosteroid group (n = 165) to compare the effectiveness of a down-titration regimen. The primary medical team chose which treatment a patient would receive. We were careful to conduct a differential diagnosis of interstitial pneumonia (e.g., acute eosinophilic pneumonia) since corticosteroid treatment has been proven effective in that patient population. The primary outcome was the 60-day mortality rate. The secondary outcome was the number of ventilator-free days (VFD). RESULTS: Those started on a high-dose regimen had a significantly higher 60-day mortality rate (P = 0.031) with significantly fewer VFD (P = 0.021). Propensity scores were used to adjust patient backgrounds in a variable analysis that also showed the high-dose regimen was a factor in decreasing VFD (OR, 95.63; 95% CI, 1.74–5271.07; P = 0.026) and worsening the 60-day mortality rate (OR, 2.54; 95% CI, 0.92–7.02; P = 0.072). CONCLUSIONS: A tapering regimen after high-dose corticosteroids is likely to increase ventilator dependency and might aggravate the prognosis of patients with ARDS diagnosed according to the Berlin definition. BioMed Central 2017-06-08 /pmc/articles/PMC5463340/ /pubmed/28592332 http://dx.doi.org/10.1186/s13054-017-1723-0 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Takaki, Makoto Ichikado, Kazuya Kawamura, Kodai Gushima, Yasuhiro Suga, Moritaka The negative effect of initial high-dose methylprednisolone and tapering regimen for acute respiratory distress syndrome: a retrospective propensity matched cohort study |
title | The negative effect of initial high-dose methylprednisolone and tapering regimen for acute respiratory distress syndrome: a retrospective propensity matched cohort study |
title_full | The negative effect of initial high-dose methylprednisolone and tapering regimen for acute respiratory distress syndrome: a retrospective propensity matched cohort study |
title_fullStr | The negative effect of initial high-dose methylprednisolone and tapering regimen for acute respiratory distress syndrome: a retrospective propensity matched cohort study |
title_full_unstemmed | The negative effect of initial high-dose methylprednisolone and tapering regimen for acute respiratory distress syndrome: a retrospective propensity matched cohort study |
title_short | The negative effect of initial high-dose methylprednisolone and tapering regimen for acute respiratory distress syndrome: a retrospective propensity matched cohort study |
title_sort | negative effect of initial high-dose methylprednisolone and tapering regimen for acute respiratory distress syndrome: a retrospective propensity matched cohort study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5463340/ https://www.ncbi.nlm.nih.gov/pubmed/28592332 http://dx.doi.org/10.1186/s13054-017-1723-0 |
work_keys_str_mv | AT takakimakoto thenegativeeffectofinitialhighdosemethylprednisoloneandtaperingregimenforacuterespiratorydistresssyndromearetrospectivepropensitymatchedcohortstudy AT ichikadokazuya thenegativeeffectofinitialhighdosemethylprednisoloneandtaperingregimenforacuterespiratorydistresssyndromearetrospectivepropensitymatchedcohortstudy AT kawamurakodai thenegativeeffectofinitialhighdosemethylprednisoloneandtaperingregimenforacuterespiratorydistresssyndromearetrospectivepropensitymatchedcohortstudy AT gushimayasuhiro thenegativeeffectofinitialhighdosemethylprednisoloneandtaperingregimenforacuterespiratorydistresssyndromearetrospectivepropensitymatchedcohortstudy AT sugamoritaka thenegativeeffectofinitialhighdosemethylprednisoloneandtaperingregimenforacuterespiratorydistresssyndromearetrospectivepropensitymatchedcohortstudy AT takakimakoto negativeeffectofinitialhighdosemethylprednisoloneandtaperingregimenforacuterespiratorydistresssyndromearetrospectivepropensitymatchedcohortstudy AT ichikadokazuya negativeeffectofinitialhighdosemethylprednisoloneandtaperingregimenforacuterespiratorydistresssyndromearetrospectivepropensitymatchedcohortstudy AT kawamurakodai negativeeffectofinitialhighdosemethylprednisoloneandtaperingregimenforacuterespiratorydistresssyndromearetrospectivepropensitymatchedcohortstudy AT gushimayasuhiro negativeeffectofinitialhighdosemethylprednisoloneandtaperingregimenforacuterespiratorydistresssyndromearetrospectivepropensitymatchedcohortstudy AT sugamoritaka negativeeffectofinitialhighdosemethylprednisoloneandtaperingregimenforacuterespiratorydistresssyndromearetrospectivepropensitymatchedcohortstudy |