Should analyses of large, national palliative care data sets with patient reported outcomes (PROs) be restricted to services with high patient participation? A register-based study

Peer Review reports

Original Submission
8 Apr 2019	Submitted	Original manuscript
14 Dec 2019	Reviewed	Reviewer Report - Fliss Murtagh
10 Mar 2020	Reviewed	Reviewer Report - Research Square Reviewer 1
11 May 2020	Author responded	Author comments - Maiken Bang Hansen
Resubmission - Version 2
11 May 2020	Submitted	Manuscript version 2
17 May 2020	Reviewed	Reviewer Report - Fliss Murtagh
18 May 2020	Reviewed	Reviewer Report - Research Square Reviewer 1
11 Jun 2020	Author responded	Author comments - Maiken Bang Hansen
Resubmission - Version 3
11 Jun 2020	Submitted	Manuscript version 3
Publishing
17 Jun 2020	Editorially accepted
23 Jun 2020	Article published	10.1186/s12904-020-00596-z

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