Hypothalamic Pituitary Adrenocortical Axis Suppression following a Single Epidural Injection of Methylprednisolone Acetate

被引:3
作者
Abdul, Aleem Jameel [1 ]
Ghai, Babita [1 ]
Bansal, Dipika [2 ]
Sachdeva, Naresh [3 ]
Bhansali, Anil [3 ]
Dhatt, Saravdeep Singh [4 ]
机构
[1] Postgrad Inst Med Educ & Res, Dept Anesthesia, Chandigarh, India
[2] Natl Inst Pharmaceut Educ & Res, Dept Pharm Practice Clin Res, Sas Nagar, Mohali, India
[3] Postgrad Inst Med Educ & Res, Dept Endocrinol, Chandigarh, India
[4] Post Grad Inst Med Educ & Res, Dept Orthoped, Chandigarh, India
关键词
Epidural injections; steroids; HPA; suppression; cortisol; ACTH; ACTIVE-CONTROL TRIAL; INTERVENTIONAL PAIN MANAGEMENT; LOW-BACK-PAIN; DOUBLE-BLIND; STEROID INJECTIONS; ADRENAL AXIS; CORTICOSTEROID INJECTIONS; SALIVARY CORTISOL; CUSHINGS-SYNDROME; DISC HERNIATION;
D O I
暂无
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: Epidural injections (EIs) are the most commonly performed minimally invasive intervention in managing chronic low back pain (CLBP). There is inconsistency in data to accurately predict the degree of hypothalamic-piuitary-adrenal (HPA) axis suppression in patients receiving exogenous steroid therapy, especially in the form of epidural steroid injections (ESIs). Objective: We aim to quantify the degree and duration of HPA axis suppression after a single ESI of 80 mg methyl prednisolone acetate in patients with CLBP. Study Design: A single open-label prospective study. Setting: An operating room of a tertiary care hospital. Methods: Patients with CLBP and unilateral radicular pain were included in this study. An ESI of 80 mg of methylprednisolone acetate was administered in each patient. Blood samples for cortisol and adrenocorticotropic hormone (ACTH) were collected before the ESI and on days 7, 14, and 28 after the ESI. The patients' pain levels were graded on the numeric rating scale (NRS) at baseline and on days 7, 14, 28, and 60 after the ESI in the pain clinic. Results: A total of 30 patients were enrolled in this study. The median with interquartile range (IQR) serum cortisol level at baseline and on days 7, 14, and 28 after intervention were found to be 329.55 (208.49 -399.48) nmol/L, 72.99 (52.95 -119.82) nmol/L, 194.45 (73.88 - 292.52) nmol/L, and 302.56 (257.68 - 357.43) nmol/L, respectively. A significant discrease in the serum cortisol levels was observed on days 7 (P < 0.001) and 14 (P < 0.001). Twenty-six (87%), 13 (43%), and 2 (7%) patients had serum cortisol levels below normal (< 170 nmol/L) on days 7, 14, and 28, respectively. HPA axis suppression was observed in all of the patients for a median (IQR) period of 14 days (range: 11-17 days). Limitations: This study was an unblinded observational study. The effect of a single ESI was studied and the sample collection of day 21 serum cortisol and ACTH were passed over. Conclusions: HPA axis function was suppressed after the ESI until day 14 and returned to the normal range by postoperative week 4.
引用
收藏
页码:E991 / E1001
页数:11
相关论文
共 50 条
  • [31] Maternal prenatal licorice consumption alters hypothalamic-pituitary-adrenocortical axis function in children
    Raikkonen, Katri
    Seckl, Jonathan R.
    Heinonen, Kati
    Pyhala, Riikka
    Feldt, Kimmo
    Jones, Alexander
    Pesonen, Anu-Katriina
    Phillips, David I. W.
    Lahti, Jari
    Jarvenpaa, Anna-Liisa
    Eriksson, Johan G.
    Matthews, Karen A.
    Strandberg, Timo E.
    Kajantie, Eero
    PSYCHONEUROENDOCRINOLOGY, 2010, 35 (10) : 1587 - 1593
  • [32] Effect of Chronic Administration of Selective Glucocorticoid Receptor Antagonists on the Rat Hypothalamic–Pituitary–Adrenocortical Axis
    Cornelius G Bachmann
    Astrid C E Linthorst
    Florian Holsboer
    Johannes M H M Reul
    Neuropsychopharmacology, 2003, 28 : 1056 - 1067
  • [33] Central nitric oxide regulation of the hypothalamic-pituitary-adrenocortical axis in adult male rats
    Givalois, L
    Li, SY
    Pelletier, G
    MOLECULAR BRAIN RESEARCH, 2002, 102 (1-2): : 1 - 8
  • [34] Blunted hypothalamic-pituitary-adrenocortical axis responsivity to stress in persons with a family history of alcoholism
    Sorocco, KH
    Lovallo, WR
    Vincent, AS
    Collins, FL
    INTERNATIONAL JOURNAL OF PSYCHOPHYSIOLOGY, 2006, 59 (03) : 210 - 217
  • [35] The effect of long-term stress on the hypothalamic-pituitary-adrenocortical axis and the role of the stressor
    Jensen, KH
    Hansen, SW
    Pedersen, LJ
    ACTA AGRICULTURAE SCANDINAVICA SECTION A-ANIMAL SCIENCE, 1996, : 40 - 45
  • [36] Hypothalamic-pituitary-adrenocortical axis responses to physostigmine: Effects of Alzheimer's disease and gender
    Peskind, ER
    Raskind, MA
    Wingerson, D
    Pascualy, M
    BIOLOGICAL PSYCHIATRY, 1996, 40 (01) : 61 - 68
  • [37] Hypothalamic-pituitary-adrenocortical axis function in premenopausal women with rheumatoid arthritis not treated with glucocorticoids
    Cutolo, M
    Foppiani, L
    Prete, C
    Ballarino, P
    Sulli, A
    Villaggio, B
    Seriolo, B
    Giusti, M
    Accardo, S
    JOURNAL OF RHEUMATOLOGY, 1999, 26 (02) : 282 - 288
  • [38] Endocannabinoid signaling in hypothalamic-pituitary-adrenocortical axis recovery following stress: Effects of indirect agonists and comparison of male and female mice
    Roberts, Christopher J.
    Stuhr, Kara L.
    Hutz, Michael J.
    Raff, Hershel
    Hillard, Cecilia J.
    PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2014, 117 : 17 - 24
  • [39] Activation in the Hypothalamic-Pituitary-Adrenocortical Axis and Sympathetic Nervous System in Women with Carpal Tunnel Syndrome
    Fernandez-de-las-Penas, Cesar
    Diaz-Rodriguez, Lourdes
    Salom-Moreno, Jaime
    Galiano-Castillo, Noelia
    Valverde-Herreros, Lis
    Martinez-Martin, Javier
    Pareja, Juan A.
    PAIN MEDICINE, 2014, 15 (08) : 1373 - 1378
  • [40] Hair Loss and Hypothalamic-Pituitary-Adrenocortical Axis Activity in Captive Rhesus Macaques (Macaca mulatta)
    Novak, Melinda A.
    Hamel, Amanda F.
    Coleman, Kris
    Lutz, Corrine K.
    Worlein, Julie
    Menard, Mark
    Ryan, Amy
    Rosenberg, Kendra
    Meyer, Jerrold S.
    JOURNAL OF THE AMERICAN ASSOCIATION FOR LABORATORY ANIMAL SCIENCE, 2014, 53 (03): : 261 - 266