Strengthening the use of artificial intelligence within healthcare delivery organizations: balancing regulatory compliance and patient safety.
PMID: 38767890 ·
M, a, r, k, , P, , S, e, n, d, a, k, ;, , V, i, n, c, e, n, t, , X, , L, i, u, ;, , A, s, h, l, e, y, , B, e, e, c, y, ;, , D, a, v, i, d, , E, , V, i, d, a, l, ;, , K, e, o, , S, h, a, w, ;, , M, a, r, k, , A, , L, i, f, s, o, n, ;, , D, a, n, n, y, , T, o, b, e, y, ;, , A, l, e, x, a, n, d, r, a, , V, a, l, l, a, d, a, r, e, s, ;, , B, r, e, n, n, a, , L, o, u, f, e, k, ;, , M, u, r, t, a, z, a, , M, o, g, r, i, ;, , S, u, r, e, s, h, , B, a, l, u
Publicidade
Resumo
Surface the urgent dilemma that healthcare delivery organizations (HDOs) face navigating the US Food and Drug Administration (FDA) final guidance on the use of clinical decision support (CDS) software. We use sepsis as a case study to highlight the patient safety and regulatory compliance tradeoffs that 6129 hospitals in the United States must navigate. Sepsis CDS remains in broad, routine use. There is no commercially available sepsis CDS system that is FDA cleared as a medical device. There is
Publicidade
Fonte oficial
Ver no PubMed →Dados provenientes do PubMed / NCBI. Para consultar o texto integral e as informações mais recentes, recorra sempre ao registo oficial.