TY - JOUR
T1 - Comment on:
Management of Hyperglycemia in Type 2 Diabetes: A
Patient-Centered Approach. Position Statement of the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD)
AU - Giaccari, Andrea
PY - 2012
Y1 - 2012
N2 - Management of hyperglycaemia in type 2 diabetes is certainly one the most debated field in
medicine (1). While poor possibilities in drug choice kept for years the discussion on what
glucose target should be reached, the recent introduction of new drugs, playing on different
mechanisms of action, compelled the debate on what drug should be chosen. Unfortunately,
most drugs share similar efficacy, and this generated several comments and recommendations
usually based on experts’ opinion rather than on evidence-based medicine (2,3). A clear
demonstration of the subjectivity of the previous EASD/ADA, and the present, consensus
statements are the profound changes observed between them (1-3). For example, DPP-4
inhibitors, previously excluded (3) for lower efficacy, are now included in the flow-chart (1);
certainly their efficacy was known since their market launch. Glyburide (European
glibenclamide) was banned for increased risk of severe hypoglycaemia (3); in this last
consensus it is included again, with the suggestion of particular care in prescribing it in
patients with moderate to severe renal insufficiency (strange again, such contraindication is
shared by almost all sulfonylureas). Strong evidences can hardly change in such a short period
of time.
The two Italian scientific diabetes societies (SID: Società Italiana di Diabetologia, and AMD:
Associazione Medici Diabetologi) have provided specific recommendations (4) for the diagnosis
and treatment of diabetes and its complications, including recommendations for oral
medications for type 2 diabetes mellitus. An original processing system was used to create
these recommendations: the document prepared by the editorial team was published online for
20 days, and the suggestions and criticisms of all of the members were evaluated and
integrated with those from a panel of specialists and members of other health care professions
Page 1 of 3 Diabetes Care
CONFIDENTIAL-For Peer Review Onlycommitted to diabetes care, as well as lay members, including patient representatives. More
importantly, each statement is accompanied by a pre-defined 6-scale grade of force and
evidence for the recommendation, which helps the reader in distinguishing between opinion
and proof.
We hereby recognize that the last (1) consensus statement is based on evidences more than
the previous ones. Actually, we are glad to observe that the proposed flow-chart is almost
identical to what has been proposed in the Italian document (4). Further, the choice between
different therapeutic opportunities is predominantly based on well-known possible side-effects
(or absence of side-effects) instead of pathophysiologic wishes, with an attempt to cope with
the patients’ needs. Nevertheless, the absence of any grade of evidence (the only grade is the
eventual presence of a question mark) still leaves the readers too free of interpreting,
enforcing the belief of acting following the EASD/ADA proposed consensus. Guidelines should
serve as reference (5); a non-expert practitioner can be particularly puzzled by the
unexplained mix of evidences and opinions, especially if the latter change profoundly between
the various consensus versions; the experts will read these consensus just to stimulate
(successful) debates.
We hope, for the future, that other models of reporting graded evidences, as ours (4), will be
taken into account.
AB - Management of hyperglycaemia in type 2 diabetes is certainly one the most debated field in
medicine (1). While poor possibilities in drug choice kept for years the discussion on what
glucose target should be reached, the recent introduction of new drugs, playing on different
mechanisms of action, compelled the debate on what drug should be chosen. Unfortunately,
most drugs share similar efficacy, and this generated several comments and recommendations
usually based on experts’ opinion rather than on evidence-based medicine (2,3). A clear
demonstration of the subjectivity of the previous EASD/ADA, and the present, consensus
statements are the profound changes observed between them (1-3). For example, DPP-4
inhibitors, previously excluded (3) for lower efficacy, are now included in the flow-chart (1);
certainly their efficacy was known since their market launch. Glyburide (European
glibenclamide) was banned for increased risk of severe hypoglycaemia (3); in this last
consensus it is included again, with the suggestion of particular care in prescribing it in
patients with moderate to severe renal insufficiency (strange again, such contraindication is
shared by almost all sulfonylureas). Strong evidences can hardly change in such a short period
of time.
The two Italian scientific diabetes societies (SID: Società Italiana di Diabetologia, and AMD:
Associazione Medici Diabetologi) have provided specific recommendations (4) for the diagnosis
and treatment of diabetes and its complications, including recommendations for oral
medications for type 2 diabetes mellitus. An original processing system was used to create
these recommendations: the document prepared by the editorial team was published online for
20 days, and the suggestions and criticisms of all of the members were evaluated and
integrated with those from a panel of specialists and members of other health care professions
Page 1 of 3 Diabetes Care
CONFIDENTIAL-For Peer Review Onlycommitted to diabetes care, as well as lay members, including patient representatives. More
importantly, each statement is accompanied by a pre-defined 6-scale grade of force and
evidence for the recommendation, which helps the reader in distinguishing between opinion
and proof.
We hereby recognize that the last (1) consensus statement is based on evidences more than
the previous ones. Actually, we are glad to observe that the proposed flow-chart is almost
identical to what has been proposed in the Italian document (4). Further, the choice between
different therapeutic opportunities is predominantly based on well-known possible side-effects
(or absence of side-effects) instead of pathophysiologic wishes, with an attempt to cope with
the patients’ needs. Nevertheless, the absence of any grade of evidence (the only grade is the
eventual presence of a question mark) still leaves the readers too free of interpreting,
enforcing the belief of acting following the EASD/ADA proposed consensus. Guidelines should
serve as reference (5); a non-expert practitioner can be particularly puzzled by the
unexplained mix of evidences and opinions, especially if the latter change profoundly between
the various consensus versions; the experts will read these consensus just to stimulate
(successful) debates.
We hope, for the future, that other models of reporting graded evidences, as ours (4), will be
taken into account.
KW - diabetes
KW - guidelines
KW - diabetes
KW - guidelines
UR - http://hdl.handle.net/10807/24701
UR - http://care.diabetesjournals.org/
U2 - 10.2337/dc12-0413
DO - 10.2337/dc12-0413
M3 - Article
SN - 0149-5992
SP - N/A-N/A
JO - Diabetes Care
JF - Diabetes Care
ER -