5.3.0.0 Nonin­sulin Ther­a­pies

The safe­ty and efficacy of nonin­sulin an­ti­hy­per­glycemic ther­a­pies in the hos­pi­tal set­ting is an area of ac­tive re­search. A few re­cent ran­dom­ized pilot tri­als in gen­er­al medicine and surg­ery pa­tients re­port­ed that a dipep­tidyl pep­ti­dase 4 in­hibitor alone or in com­bi­na­tion with basal in­sulin was well tol­er­at­ed and re­sulted in sim­i­lar glu­cose con­trol and fre­quen­cy of hy­po­glycemia com­pared with a basal-‍bolus reg­i­men (46-48). How­ev­er, an FDA bul­letin states that pro­viders should con­sid­er dis­con­tin­u­ing saxagliptin and alogliptin in peo­ple who de­vel­op heart fail­ure (49). A re­view of an­ti­hy­per­glycemic med­i­ca­tions con­clud­ed that glucagon-‍like pep­tide 1 re­cep­tor ag­o­nists show promise in the in­pa­tient set­ting (50); how­ev­er, proof of safe­ty and efficacy awaits the re­sults of ran­dom­ized con­trolled tri­als (51).

More­over, the gas­troin­testi­nal symp­toms as­so­ci­at­ed with the glucagon-‍like pep­tide 1 re­cep­tor ag­o­nists may be prob­lem­at­ic in the in­pa­tient set­ting.

Re­gard­ing the sodi­um–glu­cose trans­porter 2 (SGLT2) in­hibitors, the FDA in­cludes warn­ings about di­a­bet­ic keto-‍aci­do­sis (DKA) and urosep­sis (52), uri­nary tract in­fec­tions, and kid­ney in­jury (53) on the drug la­bels. A re­cent re­view sug­gest­ed SGLT2 in­hibitors be avoid­ed in se­vere ill­ness, when ke­tone bod­ies are pre­sent, and dur­ing pro­longed fast­ing and sur­gi­cal pro­ce­dures (3). Until safe­ty and ef­fec­tiveness are es­tab­lished, SGLT2 in­hibitors can­not be rec­om­mend­ed for rou­tine in-‍hos­pi­tal use.