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Publication guidelines for quality improvement in health care: evolution of the SQUIRE project
  1. F Davidoff1,
  2. P Batalden2,
  3. D Stevens2,
  4. G Ogrinc2,
  5. S Mooney2
  1. 1
    Institute for Healthcare Improvement, New Hampshire, USA
  2. 2
    Dartmouth Institute for Health Policy and Clinical Practice, Center for Leadership and Improvement, Dartmouth College, Hanover, New Hampshire, USA
  1. Dr F Davidoff, 143 Garden Street, Wethersfield, CT 06109, USA; fdavidoff{at}


In 2005, draft guidelines were published for reporting studies of quality improvement interventions as the initial step in a consensus process for development of a more definitive version. This article contains the full revised version of the guidelines, which the authors refer to as SQUIRE (Standards for QUality Improvement Reporting Excellence). This paper also describes the consensus process, which included informal feedback from authors, editors and peer reviewers who used the guidelines; formal written commentaries; input from a group of publication guideline developers; ongoing review of the literature on the epistemology of improvement and methods for evaluating complex social programmes; a two-day meeting of stakeholders for critical discussion and debate of the guidelines’ content and wording; and commentary on sequential versions of the guidelines from an expert consultant group. Finally, the authors consider the major differences between SQUIRE and the initial draft guidelines; limitations of and unresolved questions about SQUIRE; ancillary supporting documents and alternative versions that are under development; and plans for dissemination, testing and further development of SQUIRE.

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A great deal of meaningful and effective work is now done in clinical settings to improve the quality and safety of care. Unfortunately, relatively little of that work is reported in the biomedical literature, and much of what is published could be more effectively presented. Failure to publish is potentially a serious barrier to the development of improvement in health and medical care and improvement science generally, since public sharing of concepts, methods and findings is essential to the progress of all scientific work, both theoretical and applied. In an effort to strengthen the evidence base for improvement in health care, in 2005 we proposed draft guidelines for reporting planned original studies of improvement interventions.1 Our ultimate aims were to stimulate the publication of high-calibre improvement studies, and to increase the completeness, accuracy and transparency of published reports of that work.

Inadequate reporting of work in clinical improvement has been documented in several ways.2 3 For example, a recent meta-regression analysis of improvement strategies for diabetes control concluded that “complexity of the intervention … compounded by the paucity of descriptive detail in most studies, may have resulted in misclassification of interventions”.3 Moreover, an informal study carried out following publication of the draft guidelines found that only 12–68% of 30 published original reports of quality improvement projects provided full information on the individual guideline items we had identified,1 while individual guideline items were not addressed at all in 4–44% of those reports (Mooney S, Ogrinc G, unpublished).

Our initial draft guidelines were, of course, not a tested approach to judging the quality of the improvement literature, since that draft was based largely on the authors’ personal experience with improvement work, and was intended only as an initial step towards an established standard. We have now refined and extended that draft, as planned. In the current article we present a revised version, which we refer to as the Standard for QUality Improvement Reporting Excellence, or SQUIRE (table 1). We also describe the SQUIRE consensus development process; the major differences between the current version of SQUIRE and the initial draft guidelines; limitations of and questions about SQUIRE; ancillary supporting documents and variant versions that are under development; and plans for dissemination, testing and further development of the SQUIRE guidelines.

Table 1 SQUIRE guidelines (Standards for QUality Improvement Reporting Excellence)*


The SQUIRE development process proceeded along six general lines. First, we obtained informal feedback on the utility, strengths and limitations of the initial draft guidelines by using them in seminars with potential authors in both the United States and other countries; others have gathered similar information from journal reviewers.4 We obtained additional comment at the organisational meeting of the EQUATOR Network, a group of experienced publication guideline developers, in June 2006.5 Second, journal editors and authors “road tested” the draft guidelines as an aid to writing and editing submitted manuscripts. In that connection, at the time of writing this paper the 2005 article1 has been cited in approximately 40 subsequent publications, and full text or PDF copies have been downloaded from the journal website over 15 000 times. Third, we solicited formal commentaries by several knowledgeable authors on the initial version of the guidelines.610 Fourth, we conducted an ongoing review of the relevant literature on epistemology, methodology and evaluation of complex interventions, particularly in social sciences and the evaluation of social programmes. Fifth, in April 2007 we subjected the draft guidelines to intensive analysis, comment and recommendations for change at a two-day meeting of 30 stakeholders. Finally, following that meeting, we obtained further critical assessment and suggestions through three cycles of a Delphi process involving an international group of more than 50 consultants.

Informal feedback

Informal input about the draft guidelines from authors and peer reviewers generally recognised their practical value, in comments such as “These guidelines … can guide the writing of the article, so it may be prudent to distribute [them] to the authors of papers,” and “I … have used them and find them most helpful”.4 These users also raised several relevant issues, including (1) uncertainty as to when (that is, to which studies) the guidelines apply, (2) the possibility their use might force QI reports into a rigid, narrow format, (3) the concern that their slavish application might result in unduly lengthy reports that were indiscriminately laden with detail and (4) difficulty for authors in knowing whether, and how, other guidelines (such as the CONSORT guidelines for reporting randomised trials) should be used in conjunction with guidelines for reporting studies of improvement and safety.

Deciding when to use the guidelines

Publications on improvement in health care appear to be emerging in four general categories: empirical studies on development and testing of quality improvement interventions; stories, theories and frameworks; literature reviews and syntheses; and the development and testing of improvement-related tools (Rubenstein L, et al, unpublished). Within that context, our consensus process has made it clear that the SQUIRE guidelines can and should apply to reporting in the first category: formal planned empirical studies on the development and testing of improvement interventions.

Forcing articles into a rigid format

Publication guidelines are often referred to as checklists, since they serve the function of “aides-memoires” whose value in managing information in highly complex systems is increasingly appreciated.11 Like all constraints, checklists can of course be rigidly applied, a form of misuse that prevents rather than helps to make sense of what is being reported.12 13 Paradoxically, constraints also serve as a crucial driver for creativity; as stated by the 19th century English writer and designer William Morris: “You can’t have art without resistance in the materials”. The SQUIRE guidelines, like all form and structure, must therefore always be understood and used as signposts, not shackles.14 This caution probably translates best into practice if authors simply keep the guidelines in mind as a general framework while writing their initial draft, and then use them for detailed critical appraisal of what they’ve written while they revise the text.

Creating longer articles

Improvement is a complex undertaking, and its evaluation can produce substantial amounts of qualitative and quantitive information. Added length can therefore meet a principal aim of SQUIRE if it makes reports of improvement studies more complete, coherent, usable, and systematic; of course, adding irrelevant information simply to “cover” guideline items distorts that purpose. Publishing portions of improvement studies electronically is one important way to make the content of long papers publicly available while preserving the scarce resource of print publication.

Conjoint use with other publication guidelines

Most other biomedical publication guidelines apply to the reporting of specific study designs (for example, randomised trials or observational studies). The SQUIRE guidelines, in contrast, are concerned with reporting studies in a defined content area—improvement and safety. The two guideline types are therefore complementary; when appropriate, other specific design-related guidelines can and should therefore be used in conjunction with SQUIRE.

Road testing

The editors of the journal Quality and Safety in Health Care gained experience with the initial draft guidelines by using them to help judge the completeness and transparency of submitted manuscripts, and encouraging their use by authors in revising their papers.1518 The guidelines were also used by authors participating in the Academy for Healthcare Improvement’s 2007 scientific symposium in preparing their abstracts for subsequent publication.

Formal commentaries

Written commentaries on the draft guidelines raised several additional major points. On the one hand, the guidelines’ focus on “pragmatic science” was seen as an important complement to traditional experimental clinical science.6 They were also seen as a valuable instrument for strengthening the design and conduct of improvement research, potentially leading to greater synergy with improvement practice,9 and for increasing the feasibility of combining improvement studies in systematic reviews. On the other hand, the commentaries identified a number of potential difficulties: the draft guidelines were seen as being inattentive to racial and ethnic disparities in care8; their IMRaD structure (Introduction, Methods, Results and Discussion) was judged to be incompatible with the reality that improvement interventions, by design, change over time7; and there was concern that their use could result in a “dumbing down” of improvement science.10

Health disparities

In our view, it would not be useful (even if it were possible) to address every relevant content issue in a concise set of guidelines for reporting improvement studies. We do agree, however, that disparities in care are not considered often enough in improvement work, and that improvement initiatives should address this important issue whenever possible. We have therefore specifically cited the issue of care disparities among important outcomes to consider (table 1, item 13(b)(ii)).

The IMRaD structure

The Methods sections of scientific reports traditionally describe study protocols that are rigidly fixed, as required by the dictates of experimental design.19 Improvement, in contrast, is a “reflexive” learning process—that is, improvement interventions are most effective when they are modified over time in response to outcome feedback. On those grounds, it has been suggested that reporting improvement interventions in the IMRaD format requires multiple sequential Methods sections, one for each iteration of the evolving intervention.7 This apparent lack of fit between the realities of improvement practice and the traditional reporting structure for experimental studies has generated considerable debate, which remains unresolved since a reasonable case can be made both for and against use of the IMRaD structure. However, we continue to argue that, as is true for all reports of scholarly inquiry,20 reports of improvement studies need to answer A Bradford Hill’s four fundamental questions: Why did you start? What did you do? What did you find? And what does it mean? In our view, that generic requirement justifies using a single Methods section to describe the initial improvement plan and the theory on which it is based; the changes in interventions over time and the learning that comes from making those changes then belong in the Results section rather appearing than in a series of separate Methods sections, since they are themselves important improvement outcomes.1

“Dumbing down” improvement reports

The main declared purpose of all publication guidelines is to improve the completeness and transparency of reporting. Since it is precisely those characteristics of reporting that make it possible to detect weak, sloppy, or poorly designed studies, it is difficult to understand how use of the draft guidelines might lead to a “dumbing down” of improvement science. The underlying concern here apparently has less to do with transparency, therefore, than with the inference that the draft guidelines were seen as failing to require the rigorous standards of evidence associated with true experimental and quasi-experimental design.19 We recognise the importance of those standards in protecting the integrity of outcome measurements, primarily by reducing selection bias19 21; those standards, however, fail to take into account the unique purpose and characteristics of the improvement process.

Unlike the “conceptually neat and procedurally unambiguous” interventions—drugs, tests and procedures—whose efficacy is traditionally studied in clinical research, improvement is essentially a social process. Its immediate purpose is to change human performance, and it is driven primarily by experiential learning.22 23 It is therefore inherently context dependent and, as noted, reflexive; it is unstable; and it generally involves complex, multi-component interventions. Although traditional experimental and quasi-experimental methods are clearly important for learning whether improvement interventions change behaviour, they do not address the crucial pragmatic (or “realist”) questions about improvement: what is it about the mechanism of a particular intervention that works, for whom and under what circumstances?2426 Using methods that will simultaneously answer all of these questions is not an easy task, since the experimental and pragmatic approaches can work at cross purposes. The SQUIRE guidelines attempt to maintain an appropriate balance between these two crucial methodologies.

Consensus meeting of editors and research scholars

With generous support from the Robert Wood Johnson Foundation we undertook a critical appraisal of the draft guidelines at a two-day meeting in April 2007. Thirty people, including clinicians, improvement professionals, epidemiologists, clinical researchers and journal editors attended, several from outside the United States. Before the meeting we sent participants a reading list and a concept paper on the epistemology of improvement. In plenary and small group sessions, participants at the meeting critically discussed and debated the content and wording of every item in the draft guidelines, recommended changes and provided input on plans for dissemination, adoption and future uses of the guidelines. Working from transcribed audiorecordings of all meeting sessions and flip charts listing the key discussion points, a coordinating group (the authors of this paper, with important administrative support from Joy McAvoy) then revised, refined and expanded the draft guidelines.

Delphi process

Following the consensus meeting, we circulated sequential revisions of the guidelines for further comments and suggestions in three cycles of a Delphi process. The group involved in that process included the meeting participants plus roughly 20 additional expert consultants. All participants in this process were then asked whether they would be willing to endorse the final consensus version (SQUIRE).

Several features of SQUIRE are worth noting in particular. First, it distinguishes clearly between the practice of improvement (that is, the complex process of planning and implementing improvement interventions) and the evaluation of those interventions (that is, the equally complex process of designing and executing formal studies to assess whether those interventions work, and why they do or do not work). Second, SQUIRE highlights the essential and unique properties of improvement interventions, particularly their social nature, focus on changing performance, context-dependence, complexity, non-linearity, adaptation and reflexiveness. Third, this version specifies both the elements of study design that assess whether improvement interventions work (by minimising bias and confounding) and the elements of methods that assess why interventions are or are not effective (by marking out contexts and mechanisms of change). And fourth, this version explicitly addresses the ethical dimensions of improvement and improvement studies. Further differences between the initial draft guidelines and the SQUIRE guidelines are provided in table 2.

Table 2 Key features of the SQUIRE guidelines that differ from the initial draft


The SQUIRE guidelines have been characterised as providing both too little and too much information: too little, because they fail to represent adequately the many unique and nuanced issues in the practice of improvement (for example, matching system changes with the type of healthcare problem: simple, complicated or complex),27 or the details of experimental and realist study methods19 21 2426; too much, because the detail and density of the item descriptions can seem intimidating to authors. Recognising the impossibility of characterising adequately all the essentials of a specific study design or a domain of inquiry in the item descriptions themselves, the developers of several publication guidelines have created accompanying “Explanation and Elaboration” (E & E) documents that provide much of the depth and detail that are missing from the guidelines.2830 Building on this concept, the Medical Journal of Australia published a series of analytical articles, each devoted to an individual CONSORT guideline item, which were later collected into a book.31

That said, we recognise that the SQUIRE item descriptions are significantly more detailed than those of some other publication guidelines. In our view, the complexity of the improvement process, plus the relative unfamiliarity of improvement interventions and of the methods for evaluating them, justifies that level of detail, particularly in light of the enormously diverse backgrounds of people working to improve health care. Moreover, the level of detail in the SQUIRE guidelines closely resembles that in the guidelines for reporting observational studies, which also involve substantial complexities of study design.32 To minimise the difficulty of understanding and using the SQUIRE guidelines we do plan, however, to make available a shortened electronic version, accompanied by a glossary of terms that may be unfamiliar to potential users.


In this supplement, we advance an E & E document that provides the rationale for including the item in SQUIRE, as well as examples of reporting practice for each guideline item, with commentary on strengths and weaknesses of the examples.33 To increase the awareness of SQUIRE we are pursuing simultaneous print publication of the present article, as well as editorial commentary on the article, in several journals, along with links to an electronic version, as has been the practice with the public release of other reporting guidelines. We are also promoting the adoption of SQUIRE as journal editorial policy, and its use in peer review and the editorial process.

The SQUIRE website ( will provide an authentic electronic home for the guidelines themselves, a medium for their progressive refinement and an electronic community for authors, students, teachers, reviewers and editors who are interested in the emerging body of knowledge on improvement. Plans for the site include full and short versions of SQUIRE; its accompanying E & E document; commentaries; background readings on the epistemology and science of improvement; a listserve; links to related sites (for example, sites for other publication guidelines, articles that have cited the initial draft guidelines or the SQUIRE version and the like); an edited Wiki section made up of topic areas anchored in SQUIRE; and perhaps a section where authors can post drafts of manuscripts of improvement studies for critical peer review and assessment before journal submission.

Although the primary purpose of SQUIRE is to improve the reporting of original, data-driven improvement studies, we believe the guidelines can also serve useful educational purposes, particularly as a framework for understanding the epistemology of improvement and the methodologies for evaluating improvement work. We believe, similarly, that they can be helpful in planning improvement interventions and studies of those interventions, and therefore plan to support SQUIRE-related educational efforts in those areas.

The value of publication guidelines has been assessed primarily by measuring their impact on the completeness and transparency of relevant publications.34 35 Although such studies are difficult, we will encourage and support efforts to evaluate the impact of SQUIRE on the quality of the published improvement literature. And, finally, since publication guidelines are only as strong as their constituent items, we will in addition support efforts to provide empirical evidence that individual guideline items contribute materially to the validity and value of published information in improvement science.


  • Published reports of medical quality improvement are relatively few, and reporting is often inadequate.

  • The SQUIRE guidelines presented here were developed to encourage more and better reporting of formal improvement studies.

  • This paper describes the consensus process used to develop the SQUIRE guidelines.

  • The current paper also considers limitations, questions and future directions of the SQUIRE project.

Linked information


We are grateful to R Gibson and L Leviton for their unflagging support of this project, and to J McAvoy for her invaluable administrative work in coordinating the entire SQUIRE development process. The following people contributed critical input to the guidelines during their development: K Dickersin, D Goldmann, P Goetzsche, G Guyatt, H Luft, K McPherson, V Montori, D Needham, D Neuhauser, K Shojania, V Snow, E Wagner, V Weber.

The following participants in the consensus process also provided critical input on the guidelines, and endorsed the final version. Their endorsements are personal, and do not imply endorsement by any group, organisation or agency: D Aron, V Barbour, J Berlin, S Berman, D Berwick, M Bisognano, A Booth, I Boutron, P Buerhaus, M Chin, B Crabtree, L Cronenwett, M Dixon-Woods, B Doebbling, D Dougherty, M Eccles, S Ellenberg, W Garrity, L Green, T Greenhalgh, L Headrick, S Horn, J Johnson, K Koplan, D Korn, U Kotegal, S Landefield, E Loder, J Lynn, S Mallett, P Margolis, D Mason, D Minckler, B Mittman, C Mulrow, E Nelson, P Plsek, P Pronovost, L Provost, P Ravaud, R Resar, J Roessner, J-A Røttingen, L Rubenstein, H Sox, T Speroff, R Thomson, E von Elm, E Wager, D Wakefield, B Weeks, H Williams, S Williams.

All authors contributed substantively to the ideas developed in the SQUIRE project, and provided critical input on the guidelines themselves. FD, PB and DS were co-principal investigators for the RWJF components of the project. FD drafted the paper, and serves as the guarantor. All authors reviewed, commented on and approved the final version of the paper.



  • Funding: The SQUIRE project was supported in part by a grant from the Robert Wood Johnson Foundation (RWJF grant number 58073).

  • Competing interests: FD is editor emeritus of Annals of Internal Medicine and serves currently as executive editor for the Institute for Healthcare Improvement, Cambridge, Massachusetts, USA. PB is director of the Center for Leadership and Improvement at the Dartmouth Institute for Health Policy and Clinical Practice at Dartmouth College, Hanover, New Hampshire, USA; DS formerly served as vice president for healthcare improvement and director of the Institute for Improving Clinical Care within the Association of American Medical Colleges, Washington, DC, USA; he is currently director of the Quality Literature Program at the Center for Leadership and Improvement at the Dartmouth Institute for Health Policy and Clinical Practice; he is also editor of the journal Quality and Safety in Health Care. GO is associate director of the Quality Literature Program in the Center for Leadership and Improvement at the Dartmouth Institute for Health Policy and Clinical Practice and director of the Office of Research and Innovation at Medical Education at Dartmouth Medical School; he is also on the clinical staff of the White River Junction Veterans Administration Hospital, White River Junction, Vermont, USA. SM is medical director for quality improvement at the Alice Peck Day Memorial Hospital, Lebanon, New Hampshire, and a member of the staff of the Center for Leadership and Improvement in the Dartmouth Institute for Health Policy and Clinical Practice, New Hampshire, USA.

  • Some of the work reported in this paper was done at the SQUIRE Advisory Committee Meeting, 3–5 April 2007, which was supported in part by a grant from the Robert Wood Johnson Foundation (RWJF grant number 58073).

  • This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.