{
  "abstract": "Background: Phenylketonuria (PKU) is a rare inherited metabolic disorder requiring lifelong dietary management and regular monitoring to maintain metabolic control. Although international guidelines provide clear recommendations, their implementation in real-world clinical practice may be limited by structural and patient-related factors. This study aimed to evaluate clinician-reported PKU management practices across multiple centers in Turkiye and to identify key barriers to guideline implementation.\n\nMethods: A descriptive cross-sectional survey was conducted among metabolic specialists from multiple centers across Turkiye during a scientific meeting. The questionnaire, developed based on international PKU guidelines, assessed monitoring practices, dietary management, and barriers to implementation. Participants reported both theoretically recommended and clinician-reported monitoring frequencies across different age groups. Data were analyzed using descriptive statistics, and differences between recommended and reported practices were evaluated using the Stuart–Maxwell test.\n\nResults: Sixteen metabolic specialists from 16 centers participated. While 69% of clinicians recommended weekly monitoring in infants, only 25% reported achieving this in practice (p = 0.018). Similar discrepancies were observed in adolescents and adults (p = 0.009 and p = 0.043, respectively), whereas no significant difference was found in children aged 1–12 years (p = 0.122). Home-based dried blood spot monitoring was not routinely used in 69% of centers. The most important barriers to optimal monitoring included lack of home sampling systems, geographical distance, and work or school-related constraints. Substantial variability was also observed in dietary management practices, including protein prescription and protein substitute use.\n\nConclusions: PKU management in Turkiye is characterized by a clear gap between guideline recommendations and clinician-reported practices, primarily driven by structural and implementation-related barriers. These findings highlight the importance of strengthening healthcare infrastructure, improving access to monitoring tools, and integrating patient-centered strategies to enhance the real-world implementation of evidence-based care in rare diseases.\n\nSupplementary Information: The online version contains supplementary material available at https://doi.org/10.1186/s13023-026-04536-7.",
  "abstract_shown": true,
  "affiliations": [
    "Department of Pediatric Metabolism, Ankara University Faculty of Medicine, Ankara, Türkiye",
    "Department of Pediatric Metabolism, Yıldırım Beyazıt University, Ankara, Türkiye",
    "Department of Pediatric Metabolism, Etlik City Hospital, Ankara, Türkiye",
    "Department of Pediatric Metabolism, Mardin Training and Research Hospital, Mardin, Türkiye",
    "Department of Pediatric Metabolism, Şanlıurfa Training and Research Hospital, Şanlıurfa, Türkiye",
    "Department of Pediatric Metabolism, Dr. Behçet Uz Children’s Hospital, University of Health Sciences, İzmir, Türkiye",
    "Department of Pediatric Metabolism, Dokuz Eylül University Faculty of Medicine, İzmir, Türkiye",
    "Department of Pediatric Metabolism, Ümraniye Training and Research Hospital, İstanbul, Türkiye",
    "Department of Pediatric Metabolism, Çukurova University Faculty of Medicine, Adana, Türkiye",
    "Department of Pediatric Metabolism, Adana City Hospital, Adana, Türkiye",
    "Department of Pediatric Metabolism, Uludağ University Faculty of Medicine, Bursa, Türkiye"
  ],
  "article_type": "research article",
  "arxiv": null,
  "author_total": 11,
  "authors": [
    {
      "affs": [
        0
      ],
      "name": "Engin Köse"
    },
    {
      "affs": [
        1
      ],
      "name": "Berrak Bilginer Gürbüz"
    },
    {
      "affs": [
        2
      ],
      "name": "Halil Tuna Akar"
    },
    {
      "affs": [
        3
      ],
      "name": "Tuğba Akbey Koçak"
    },
    {
      "affs": [
        4
      ],
      "name": "Merve Aslantaş"
    },
    {
      "affs": [
        5
      ],
      "name": "Esra Er"
    },
    {
      "affs": [
        6
      ],
      "name": "Pelin Teke Kısa"
    },
    {
      "affs": [
        7
      ],
      "name": "İbrahim Taş"
    },
    {
      "affs": [
        8
      ],
      "name": "Nazmiye Tüzel Gündüz"
    },
    {
      "affs": [
        9
      ],
      "name": "Merve Yoldaş Çelik"
    },
    {
      "affs": [
        10
      ],
      "name": "Şahin Erdöl"
    }
  ],
  "bibtex": "https://research.draconitic.com/paper/1cggcq7gtr08k.bib",
  "cited_by": 0,
  "doi": "10.1186/s13023-026-04536-7",
  "fulltext_url": "https://pmc.ncbi.nlm.nih.gov/articles/PMC13732954/",
  "id": "1cggcq7gtr08k",
  "issns": [
    "1750-1172"
  ],
  "landing_url": "https://doi.org/10.1186/s13023-026-04536-7",
  "language": "en",
  "licence": "CC-BY-4.0",
  "licence_label": "CC BY 4.0",
  "licence_source": "article",
  "licence_url": "https://creativecommons.org/licenses/by/4.0/",
  "metadata_licence": null,
  "native_subjects": [
    [
      "heading",
      "Research"
    ],
    [
      "openalex",
      "1308|Metabolism and Genetic Disorders"
    ]
  ],
  "openalex": "W7196993028",
  "pdf_url": null,
  "pmcid": "PMC13732954",
  "pmid": "42983856",
  "published": "2026-08-06",
  "publisher": "BMC",
  "ris": "https://research.draconitic.com/paper/1cggcq7gtr08k.ris",
  "sources": [
    {
      "first_seen": "2026-11-08T12:22:50Z",
      "native_id": "PMC13732954",
      "source": "pmc",
      "url": "https://doi.org/10.1186/s13023-026-04536-7"
    }
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  "subjects": [
    {
      "field": "medicine",
      "origin": "openalex:1308|Metabolism and Genetic Disorders",
      "subfield": "general"
    }
  ],
  "title": "Implementation gaps in phenylketonuria management: a multicenter clinician survey from Turkiye",
  "title_text": "Implementation gaps in phenylketonuria management: a multicenter clinician survey from Turkiye",
  "type": "peer-reviewed",
  "updated_at": "2026-11-08T12:22:50Z",
  "url": "https://research.draconitic.com/paper/1cggcq7gtr08k",
  "venue": "Orphanet Journal of Rare Diseases",
  "versions": []
}