Small gauge vitrectomy for vitreous amyloidosis and subsequent management of secondary glaucoma in patients with hereditary transthyretin amyloidosis

被引:16
|
作者
Kakihara, Shinji [1 ]
Hirano, Takao [1 ]
Imai, Akira [1 ]
Miyahara, Teruyoshi [1 ]
Murata, Toshinori [1 ]
机构
[1] Shinshu Univ, Dept Ophthalmol, Sch Med, 3-1-1 Asahi, Matsumoto, Nagano 3908621, Japan
关键词
OCULAR MANIFESTATIONS; LIVER-TRANSPLANTATION; POLYNEUROPATHY; SURGERY; IMPACT;
D O I
10.1038/s41598-020-62559-x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We conducted a retrospective observational study including 31 eyes of 20 patients in order to investigate the efficacy of 25-gauge vitrectomy for vitreous opacity with minimal conjunctival invasion and subsequent management of intraocular pressure (IOP) secondary to hereditary transthyretin amyloidosis. We followed up these patients for an average of 44.7 +/- 32.6 months. The primary outcome was best corrected visual acuity (BCVA) at 1 month after surgery and at the final follow-up visit, with management of subsequent IOP elevation. Secondary outcomes included the post-vitrectomy IOP survival rate, to determine the frequency of IOP elevation requiring glaucoma surgery. Mean age at vitrectomy was 55.4 +/- 9.1 years. Logarithm of the Minimum Angle of Resolution (LogMAR) BCVA showed immediate improvement from 0.73 +/- 0.62 to 0.00 +/- 0.22 at 1 month (p=4.1 x 10(-7)), an improvement that was maintained up to the final follow-up visit, when IOP was maintained at 13.1 +/- 5.2mmHg. The survival rate of post-vitrectomy IOP control was 0.51, 0.38, and 0.23 at 12, 24, and 60 months, respectively. A poor post-vitrectomy IOP survival rate suggests that removing vitreous amyloid via 25-gauge vitrectomy is not sufficient to guarantee good visual function; subsequent careful follow-up and proper glaucoma management is also required in order to achieve this goal.
引用
收藏
页数:8
相关论文
共 50 条
  • [31] THE IMPACT OF HEREDITARY TRANSTHYRETIN AMYLOIDOSIS (HATTR) ON WORK: THE PATIENTS' PERSPECTIVES
    Raymond, K.
    White, M. K.
    Guthrie, S. D.
    Pollock, M.
    VALUE IN HEALTH, 2018, 21 : S355 - S355
  • [32] Treatment characteristics of patients with hereditary transthyretin amyloidosis: a cohort study
    Qarni, Taha N.
    Jones, Felipe J. S.
    Drachman, Brian
    Khella, Sami
    Pieretti, Janice
    Bustamante, Nicolas Sarmiento
    Karam, Chafic
    ORPHANET JOURNAL OF RARE DISEASES, 2024, 19 (01)
  • [33] Unreliable pupillary light reflex in hereditary transthyretin amyloidosis patients
    Marques, J.
    Malheiro, L.
    Oliveira, L.
    Meneres, M.
    Melo Beirao, J.
    EUROPEAN JOURNAL OF NEUROLOGY, 2021, 28 : 433 - 433
  • [34] BURDEN OF ILLNESS AMONG PATIENTS WITH HEREDITARY TRANSTHYRETIN (HATTR) AMYLOIDOSIS
    Reddy, S. R.
    Guthrie, S.
    Chang, E.
    Tieu, R. S.
    Tarbox, M.
    Pollock, M.
    VALUE IN HEALTH, 2019, 22 : S848 - S848
  • [35] Implantable Cardioverter Defibrillators in Patients With Hereditary Transthyretin Cardiac Amyloidosis
    Yalamanchili, Sreeram
    Brown, Matthew T.
    Blank, Evan A.
    Lyle, Melissa A.
    Bhatt, Kunal N.
    CIRCULATION, 2020, 142
  • [36] Occupational practice in patients with hereditary transthyretin amyloidosis, a qualitative study
    Aina Gayà-Barroso
    Juan González-Moreno
    Adrián Rodríguez
    Tomás Ripoll-Vera
    Inés Losada-López
    Margarita Gili
    Milena Paneque
    Sara Pérez-Martínez
    Eugenia Cisneros-Barroso
    Orphanet Journal of Rare Diseases, 18
  • [37] The Impact of Hereditary Transthyretin Amyloidosis (hATTR) on Work: The Patients' Perspectives
    Raymond, Kimberly
    White, Michelle K.
    Guthrie, Spencer
    Pollock, Michael
    NEUROLOGY, 2019, 92 (15)
  • [38] Occupational practice in patients with hereditary transthyretin amyloidosis, a qualitative study
    Gaya-Barroso, Aina
    Gonzalez-Moreno, Juan
    Rodriguez, Adrian
    Ripoll-Vera, Tomas
    Losada-Lopez, Ines
    Gili, Margarita
    Paneque, Milena
    Perez-Martinez, Sara
    Cisneros-Barroso, Eugenia
    ORPHANET JOURNAL OF RARE DISEASES, 2023, 18 (01)
  • [39] NEUROPATHIC IMPAIRMENT SCORE IN PATIENTS WITH HEREDITARY TRANSTHYRETIN AMYLOIDOSIS WITH POLYNEUROPATHY
    Yarlas, Aaron
    Lovley, Andrew
    Brown, Duncan
    Llonch, Montserrat Vera
    Khella, Sami
    Karam, Chafic
    MUSCLE & NERVE, 2021, 64 : S61 - S61
  • [40] THAOS - The Transthyretin Amyloidosis Outcomes Survey: initial report on clinical manifestations in patients with hereditary and wild-type transthyretin amyloidosis
    Coelho, Teresa
    Maurer, Mathew S.
    Suhr, Ole B.
    CURRENT MEDICAL RESEARCH AND OPINION, 2013, 29 (01) : 63 - 76