E-ISSN: 1308-5263
Management of Primary Immune Thrombocytopenia: Turkish Modified Delphi-Based Consensus Statement for Special Considerations [Turk J Hematol]
Turk J Hematol. 2024; 41(3): 141-145 | DOI: 10.4274/tjh.galenos.2024.2024.0101  

Management of Primary Immune Thrombocytopenia: Turkish Modified Delphi-Based Consensus Statement for Special Considerations

Elif Ümit1, Ahmet Muzaffer Demir1, Muhlis Cem Ar2, Mesut Ayer3, Meltem Aylı4, Volkan Karakuş5, Emin Kaya6, Fahir Özkalemkaş7, Nilgün Sayınalp8, Mehmet Sönmez9, Fahri Şahin10, Selami Koçak Toprak11, Tayfur Toptaş12, İrfan Yavaşoğlu13, Ümran Çalış14
1Trakya University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, Edirne, Türkiye
2İstanbul University-Cerrahpaşa, Cerrahpaşa Faculty of Medicine, Department of Internal Medicine, Division of Hematology, İstanbul, Türkiye
3University of Health Sciences Türkiye, Başakşehir Çam and Sakura City Hospital, Clinic of Hematology, İstanbul, Türkiye
4University of Health Sciences Türkiye, Gülhane Faculty of Medicine, Department of Internal Medicine, Division of Hematology, Ankara, Türkiye
5University of Health Sciences Türkiye, Antalya Training and Research Hospital, Clinic of Hematology, Antalya, Türkiye
6İnönü University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, Malatya, Türkiye
7Bursa Uludağ University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, Bursa, Türkiye
8Hacettepe University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, Ankara, Türkiye
9Karadeniz Technical University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, Trabzon, Türkiye
10Ege University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, İzmir, Türkiye
11Ankara University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, Ankara, Türkiye
12Marmara University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, İstanbul, Türkiye
13Aydın Adnan Menderes University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, Aydın, Türkiye
14Abdi İbrahim İlaç Sanayi ve Tic. A.Ş., Senior Medical Manager, İstanbul, Türkiye

Objective: Primary immune thrombocytopenia (ITP) is an acquired disorder of platelets with a complex and unclear mechanism of increased immune destruction or impaired production of platelets. While the management of ITP is evolving, there is still a need for guidance, particularly in certain circumstances such as pregnancy, emergencies, or patients requiring co-medications. We aimed to determine the tendencies of hematologists in Türkiye in the event of such special considerations.
Materials and Methods: Applying a modified Delphi method, the Turkish National ITP Working Group, founded under the auspices of the Turkish Society of Hematology, developed a questionnaire consisting of statements regarding pregnancy, emergencies, and circumstances requiring co-treatment with antiaggregants or anticoagulants. A total of 107 hematologists working in university or state hospitals voted for their agreement or disagreement with the statements for two sequential rounds.
Results: The participating hematologists reached an agreement on starting treatment for pregnant patients with platelets of less than 30x109/L and delivery either vaginally or by cesarean section being safe at platelet counts above 50x109/L. For emergencies and the rescue management of ITP, the panel agreed against the use of high-dose corticosteroids alone, preferring combinations with transfusions or intravenous immunoglobulin. For patients who require interventions, platelet counts of >50x109/L were regarded as safe for low-risk procedures as well as co-treatment with antiplatelets or anticoagulants.
Conclusion: As the National ITP Study Group, we have observed the need to increase the practice guidance regarding patients with primary ITP requiring additional treatments including invasive interventions and co-treatments for coagulation. Decisions on the management of ITP during pregnancy should be individualized. There is a lack of consensus on the thresholds of platelet counts as well as co-morbidities and co-medications. This lack of consensus may be due to variations in practices.

Keywords: Adult primary immune thrombocytopenia, Management, Delphi method, Special considerations


Primer İmmün Trombositopeni Yönetimi: Özel Durumlar için Düzenlenmiş Türkiye Delphi Temelli Konsensus Bildirisi

Elif Ümit1, Ahmet Muzaffer Demir1, Muhlis Cem Ar2, Mesut Ayer3, Meltem Aylı4, Volkan Karakuş5, Emin Kaya6, Fahir Özkalemkaş7, Nilgün Sayınalp8, Mehmet Sönmez9, Fahri Şahin10, Selami Koçak Toprak11, Tayfur Toptaş12, İrfan Yavaşoğlu13, Ümran Çalış14
1Trakya University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, Edirne, Türkiye
2İstanbul University-Cerrahpaşa, Cerrahpaşa Faculty of Medicine, Department of Internal Medicine, Division of Hematology, İstanbul, Türkiye
3University of Health Sciences Türkiye, Başakşehir Çam and Sakura City Hospital, Clinic of Hematology, İstanbul, Türkiye
4University of Health Sciences Türkiye, Gülhane Faculty of Medicine, Department of Internal Medicine, Division of Hematology, Ankara, Türkiye
5University of Health Sciences Türkiye, Antalya Training and Research Hospital, Clinic of Hematology, Antalya, Türkiye
6İnönü University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, Malatya, Türkiye
7Bursa Uludağ University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, Bursa, Türkiye
8Hacettepe University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, Ankara, Türkiye
9Karadeniz Technical University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, Trabzon, Türkiye
10Ege University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, İzmir, Türkiye
11Ankara University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, Ankara, Türkiye
12Marmara University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, İstanbul, Türkiye
13Aydın Adnan Menderes University Faculty of Medicine, Department of Internal Medicine, Division of Hematology, Aydın, Türkiye
14Abdi İbrahim İlaç Sanayi ve Tic. A.Ş., Senior Medical Manager, İstanbul, Türkiyec

Amaç: Primer immün trombositopeni (ITP), trombositlerin karmaşık ve tam aydınlanmamış bir mekanizma ile artmış immün yıkım ya da azalmış yapımına bağlı olarak azaldığı edinsel bir hastalıktır. ITP tedavisi gelişmek ile birlikte, gebelik, acil durumlar ve ek tedavi gereksinimi gibi özel durumların yönetimi için rehberlere ihtiyaç vardır. Çalışmamızdaki amaç, Türkiye’deki hematologların bu özel durumlara yaklaşımını belirlemektir.
Gereç ve Yöntem: Türk Hematoloji Derneği altında kurulan Ulusal ITP Çalışma Grubu tarafından oluşturulan bir anket ile modifiye bir Delphi metodu kullanılarak, gebelik, acil ve ek tedavi gereksiniminde ITP’ye yaklaşım hedeflenmiştir. Üniversite ve devlet hastanelerinde görev yapmakta olan 107 hematoloji uzmanına iki tur halinde bu sorular yöneltilmiştir.
Bulgular: Katılımcı hematologlar, gebelikte trombositin 30x109/L altına inmesi ile tedavi başlanması gerektiği ve 50x109/L üzerindeki değerlerde normal ya da sezaryen doğumun güvenli olacağı konusunda görüş birliğine varmıştır. Acil ve kurtarma tedavilerine ilişkin olarak katılımcıların tek başına yüksek doz kortikosteroidden ziyade transfüzyon ya da intravenöz immünoglobulin ile kombine kullanımını tercih ettikleri gözlenmiştir. Düşük kanama riskli girişimsel işlemler ya da antiagregan veya antikoagulan gibi ek tedavi gereksiniminde 50x109/L üzerindeki trombosit değerlerinin güvenli olabileceği konusunda fikir birliği gözlenmiştir.
Sonuç: Ulusal ITP çalışma grubu olarak girişimsel işlemler ve pıhtılaşma sistemine yönelik ek tedavilerin gerektiği özel durumlarda ITP yönetimine ilişkin uygulama rehberlerine ihtiyaç olduğunu gözlemledik. Gebelikte ITP’nin yönetimine ilişkin kararlar bireyselleştirilmelidir. Trombosit sayısı eşikleri, eşlik eden hastalıklar ve birlikte kullanılan ilaçlar konusunda bir fikir birliği eksikliği vardır. Bu fikir birliği eksikliği klinik pratikteki farklılıklardan kaynaklanıyor olabilir.

Anahtar Kelimeler: Erişkin primer immün trombositopeni, Hastalık yönetimi, Delphi metodu, Özel durumlar


Elif Ümit, Ahmet Muzaffer Demir, Muhlis Cem Ar, Mesut Ayer, Meltem Aylı, Volkan Karakuş, Emin Kaya, Fahir Özkalemkaş, Nilgün Sayınalp, Mehmet Sönmez, Fahri Şahin, Selami Koçak Toprak, Tayfur Toptaş, İrfan Yavaşoğlu, Ümran Çalış. Management of Primary Immune Thrombocytopenia: Turkish Modified Delphi-Based Consensus Statement for Special Considerations. Turk J Hematol. 2024; 41(3): 141-145

Corresponding Author: Elif Ümit


TOOLS
Full Text PDF
Print
Download citation
RIS
EndNote
BibTex
Medlars
Procite
Reference Manager
Share with email
Share


Similar articles
PubMed
Google Scholar