TY - JOUR
T1 - Real-world application of Short Term Psychodynamic Psychotherapy (STPP) as chronic migraine preventive therapy
T2 - Profiling responders and predictive factors
AU - Viganò, Alessandro
AU - Petolicchio, Barbara
AU - Toscano, Massimiliano
AU - Ruggero, Sonia
AU - Di Giambattista, Romina
AU - Puma, Marta
AU - Lanzone, Jacopo
AU - Bellinvia, Angelo
AU - Diani, Nicholas
AU - Castaldo, Matteo
AU - Valota, Chiara
AU - De Sanctis, Rita
AU - Tiberio, Paola
AU - Altieri, Marta
AU - Gilliéron, Edmond
AU - Di Piero, Vittorio
N1 - © 2025. Fondazione Società Italiana di Neurologia.
PY - 2025/6
Y1 - 2025/6
N2 - INTRODUCTION: Among non-pharmacological approach for chronic migraine (CM), Short-Term Psychodynamic Psychotherapy (STPP) is suggested in CM and, particularly, in interrupting medication overuse (MO). In this study, we aim at identifying clinical predictive factors to identify CM patients who could more likely respond to STPP.METHODS: We designed a prospective real-world observational study on CM patients undergoing STPP. We collected clinical data related to migraine burden (baseline headache days, number of acute medications used, MIDAS, HIT-6), as well as psychiatric comorbidities (though MINI) and mentalization level obtained by the STPP first interview phase (called BPI) to use them as predictive factors by univariate and discriminant function analysis at 3 (early) and 6 months (only sustained response).RESULTS: We recruited 119 patients (mean age 39.90 ± 14.4, F = 102); 113(94%) completed the STPP treatment. All patients presented a low-to-intermediate mentalization level. After stand-alone STPP, we observed a reduction in monthly headache days and MO at 3 months. Mentalization level didn't affect the STPP outcome (p = 0.40). Early response was directly related to a higher baseline headache days number, the previous used of alternative therapies, and higher Hamilton Depression scale scores. Sustained response was predicted by current use of preventive therapy, pain intensity, HIT-6 score, hypomania, and dysthymia.CONCLUSION: This real-world study showed that STPP could represent a valid therapeutic option in complex CM patients with a high number of headache days and comorbid depression.
AB - INTRODUCTION: Among non-pharmacological approach for chronic migraine (CM), Short-Term Psychodynamic Psychotherapy (STPP) is suggested in CM and, particularly, in interrupting medication overuse (MO). In this study, we aim at identifying clinical predictive factors to identify CM patients who could more likely respond to STPP.METHODS: We designed a prospective real-world observational study on CM patients undergoing STPP. We collected clinical data related to migraine burden (baseline headache days, number of acute medications used, MIDAS, HIT-6), as well as psychiatric comorbidities (though MINI) and mentalization level obtained by the STPP first interview phase (called BPI) to use them as predictive factors by univariate and discriminant function analysis at 3 (early) and 6 months (only sustained response).RESULTS: We recruited 119 patients (mean age 39.90 ± 14.4, F = 102); 113(94%) completed the STPP treatment. All patients presented a low-to-intermediate mentalization level. After stand-alone STPP, we observed a reduction in monthly headache days and MO at 3 months. Mentalization level didn't affect the STPP outcome (p = 0.40). Early response was directly related to a higher baseline headache days number, the previous used of alternative therapies, and higher Hamilton Depression scale scores. Sustained response was predicted by current use of preventive therapy, pain intensity, HIT-6 score, hypomania, and dysthymia.CONCLUSION: This real-world study showed that STPP could represent a valid therapeutic option in complex CM patients with a high number of headache days and comorbid depression.
KW - Chronic migraine
KW - Mentalization
KW - Predictive model
KW - Preventive therapy
KW - Psychotherapy
UR - http://www.scopus.com/inward/record.url?scp=86000520637&partnerID=8YFLogxK
U2 - 10.1007/s10072-025-08075-0
DO - 10.1007/s10072-025-08075-0
M3 - Journal article
C2 - 40048115
SN - 1590-1874
VL - 46
SP - 2727
EP - 2736
JO - Neurological Sciences
JF - Neurological Sciences
IS - 6
ER -