Urinary catecholamine excretion, cardiovascular variability, and outcomes in tetanus.

Autonomic nervous system dysfunction Cardiovascular Catecholamine Infectious diseases Intensive care Mechanical ventilation Tetanus

Journal

Tropical medicine and health
ISSN: 1348-8945
Titre abrégé: Trop Med Health
Pays: Japan
ID NLM: 101215093

Informations de publication

Date de publication:
30 Mar 2023
Historique:
received: 04 11 2022
accepted: 17 03 2023
medline: 31 3 2023
entrez: 30 3 2023
pubmed: 31 3 2023
Statut: epublish

Résumé

Severe tetanus is characterized by muscle spasm and cardiovascular system disturbance. The pathophysiology of muscle spasm is relatively well understood and involves inhibition of central inhibitory synapses by tetanus toxin. That of cardiovascular disturbance is less clear, but is believed to relate to disinhibition of the autonomic nervous system. The clinical syndrome of autonomic nervous system dysfunction (ANSD) seen in severe tetanus is characterized principally by changes in heart rate and blood pressure which have been linked to increased circulating catecholamines. Previous studies have described varying relationships between catecholamines and signs of ANSD in tetanus, but are limited by confounders and assays used. In this study, we aimed to perform detailed characterization of the relationship between catecholamines (adrenaline and noradrenaline), cardiovascular parameters (heart rate and blood pressure) and clinical outcomes (ANSD, mechanical ventilation required, and length of intensive care unit stay) in adults with tetanus, as well as examine whether intrathecal antitoxin administration affected subsequent catecholamine excretion. Noradrenaline and adrenaline were measured by ELISA from 24-h urine collections taken on day 5 of hospitalization in 272 patients enrolled in a 2 × 2 factorial-blinded randomized controlled trial in a Vietnamese hospital. Catecholamine results measured from 263 patients were available for analysis. After adjustment for potential confounders (i.e., age, sex, intervention treatment, and medications), there were indications of non-linear relationships between urinary catecholamines and heart rate. Adrenaline and noradrenaline were associated with subsequent development of ANSD, and length of ICU stay.

Identifiants

pubmed: 36998027
doi: 10.1186/s41182-023-00512-0
pii: 10.1186/s41182-023-00512-0
pmc: PMC10061701
doi:

Types de publication

Journal Article

Langues

eng

Pagination

20

Subventions

Organisme : Wellcome Trust
ID : 107367/Z/15/Z
Pays : United Kingdom
Organisme : Wellcome Trust
ID : 204904/Z/16/Z
Pays : United Kingdom

Informations de copyright

© 2023. The Author(s).

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Auteurs

Duc Hong Du (DH)

Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam. ducdh@oucru.org.

Nguyen Quan Nhu Hao (NQN)

Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
University Medical Center, Ho Chi Minh City, Vietnam.

Nguyen Van Hao (N)

University Medical Center, Ho Chi Minh City, Vietnam.
Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.

Tran Tan Thanh (TT)

Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.

Huynh Thi Loan (HT)

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.

Lam Minh Yen (LM)

Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.

Tran Thi Diem Thuy (TTD)

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.

Duong Bich Thuy (DB)

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.

Nguyen Thanh Nguyen (NT)

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.

Nguyen Thi Phuong Dung (NTP)

Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.

Evelyne Kestelyn (E)

Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, UK.

Ha Thi Hai Duong (HTH)

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.

Nguyen Thanh Phong (NT)

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.

Pham Thi Tuyen (PT)

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.

Nguyen Hoan Phu (NH)

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.

Ho Dang Trung Nghia (HDT)

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Pham Ngoc, Thach Medicine University, Ho Chi Minh City, Vietnam.

Bui Thi Bich Hanh (BTB)

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.
Pham Ngoc, Thach Medicine University, Ho Chi Minh City, Vietnam.

Pham Kieu Nguyet Oanh (PKN)

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.

Phan Vinh Tho (PV)

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.

Phung Tran Huy Nhat (PTH)

Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.

Phan Nguyen Quoc Khanh (PNQ)

Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.

Duncan Wyncoll (D)

Guys and St, Thomas' Hospitals, London, UK.

Nicholas P J Day (NPJ)

Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, UK.
Mahidol Oxford Research Unit, Bangkok, Thailand.

Nguyen Van Vinh Chau (N)

Hospital for Tropical Diseases, Ho Chi Minh City, Vietnam.

H Rogier van Doorn (HR)

Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, UK.

Le Van Tan (L)

Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.

Ronald B Geskus (RB)

Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, UK.

C Louise Thwaites (CL)

Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Centre for Tropical Medicine and Global Health, University of Oxford, Oxford, UK.

Classifications MeSH