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Volume 25, Number 5—May 2019
Research

Management of Central Nervous System Infections, Vientiane, Laos, 2003–2011

Audrey Dubot-PérèsComments to Author , Mayfong Mayxay, Rattanaphone Phetsouvanh1, Sue J. Lee, Sayaphet Rattanavong, Manivanh Vongsouvath, Viengmon Davong, Vilada Chansamouth, Koukeo Phommasone, Catrin Moore, Sabine Dittrich, Olay Lattana, Joy Sirisouk, Phonelavanh Phoumin, Phonepasith Panyanivong, Amphonesavanh Sengduangphachanh, Bountoy Sibounheuang, Anisone Chanthongthip, Manivone Simmalavong, Davanh Sengdatka, Amphaivanh Seubsanith, Valy Keoluangkot, Prasith Phimmasone, Kongkham Sisout, Khamsai Detleuxay, Khonesavanh Luangxay, Inpanh Phouangsouvanh, Scott B. Craig, Suhella M. Tulsiani, Mary-Anne Burns, David A.B. Dance, Stuart D. Blacksell, Xavier de Lamballerie, and Paul N. Newton
Author affiliations: Lao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit, Mahosot Hospital, Vientiane, Laos (A. Dubot-Pérès, M. Mayxay, R. Phetsouvanh, S. Rattanavong, M. Vongsouvath, V. Davong, V. Chansamouth, K. Phommasone, C. Moore, S. Dittrich, O. Lattana, J. Sirisouk, P. Phoumin, P. Panyanivong, A. Sengduangphachanh, B. Sibounheuang, A. Chanthongthip, M. Simmalavong, D. Sengdatka, A. Seubsanith, D.A.B. Dance, P.N. Newton); University of Oxford Nuffield Department of Clinical Medicine Center for Tropical Medicine and Global Health, Oxford, UK (A. Dubot-Pérès, S.J. Lee, C. Moore, S. Dittrich, D.A.B. Dance, S.D. Blacksell, P.N. Newton); Unité des Virus Émergents (UVE: Aix-Marseille Univ-IRD 190-INSERM 1207-IHU Méditerranée Infection), Marseille, France (A. Dubot-Pérès, X. de Lamballerie); University of Health Sciences Institute of Research and Education Development, Vientiane (M. Mayxay); Mahidol University Faculty of Tropical Medicine Mahidol– Oxford Tropical Medicine Research Unit, Bangkok, Thailand (S.J. Lee, S.D. Blacksell); Mahosot Hospital, Vientiane (V. Keoluangkot, P. Phimmasone, K. Sisout, K. Detleuxay, K. Luangxay, I. Phouangsouvanh); Queensland Health Forensic and Scientific Service World Health Organization Collaborating Centre for Reference and Research on Leptospirosis, Brisbane, Queensland, Australia (S.B. Craig, S.M. Tulsiani, M.-A. Burns); London School of Hygiene and Tropical Medicine Faculty of Infectious and Tropical Diseases, London, UK (D.A.B. Dance, P.N. Newton)

Main Article

Table 4

Characteristics of peripheral blood and cerebrospinal fluid at admission of patients with suspected central nervous system infection, by age group and etiology, Laos, January 2003–August 2011*

Sample type and parameter Age group
Etiology
All, n = 1,065 Children, n = 358 Adults, n = 707 Confirmed, n = 450 None confirmed, n = 615 Confirmed viral, n = 172 Confirmed bacterial, n = 175
Peripheral blood
Elevated white cell count,† n = 952 449 (47.2) 150 (47.9) 299 (46.8) 198 (49.0) 251 (45.8) 84 (53.9) 84 (53.5)
Low white cell count, n = 952 45 (4.7) 22 (7.0) 23 (3.6) 22 (5.5) 23 (4.2) 6 (3.9) 7 (4.5)
Anemia, n = 948 355 (37.5) 112 (35.7) 243 (38.3) 160 (39.8) 195 (35.7) 44 (28.2) 68 (43.9)
Thrombocytopenia, n = 649 55 (8.5) 16 (6.8) 39 (9.4) 22 (7.8) 33 (9.0) 4 (3.5) 12 (10.6)
Elevated C-reactive protein, n = 868 547 (63.0) 145 (51.6) 402 (68.5) 265 (69.2) 282 (58.1) 98 (64.9) 114 (79.7)
Hyperglycemia,† n = 991 237 (23.9) 81 (25.8) 156 (23.0) 105 (24.5) 132 (23.5) 40 (24.0) 53 (32.3)
Severe hyperglycemia,† n = 991 72 (7.3) 26 (8.3) 46 (6.8) 35 (8.2) 37 (6.6) 12 (7.2) 22 (13.4)
Elevated serum sodium,‡ n = 807 225 (27.9) 45 (17.8) 180 (32.5) 82 (22.8) 143 (31.9) 40 (28.6) 26 (19.4)
Low serum sodium,‡ n = 807
63 (7.8)
31 (12.3)
32 (5.8)

31 (8.6)
32 (7.1)
8 (5.7)
16 (11.9)
Cerebrospinal fluid
Turbid, n = 999 145 (14.5) 40 (12.2) 105 (15.7) 80 (18.4) 65 (11.5) 21 (12.4) 38 (23.2)
Elevated opening pressure, n = 977 334 (34.2) 86 (27.6) 248 (37.3) 155 (36.4) 179 (32.5) 42 (24.9) 60 (37.3)
Elevated white cell count,§ n = 975 729 (74.8) 237 (74.8) 492 (74.8) 341 (80.2) 388 (70.6) 141 (84.9) 129 (80.1)
Elevated lymphocyte count, n = 890 467 (52.5) 149 (51.2) 318 (53.1) 234 (59.5) 233 (46.9) 106 (68.4) 91 (62.3)
Elevated neutrophil count, n = 889 644 (72.4) 213 (73.5) 431 (72.0) 309 (78.8) 335 (67.4) 130 (83.9) 116 (80.0)
Elevated eosinophil count,¶ n = 1,001 46 (4.6) 7 (2.1) 39 (5.8) 11 (2.5) 35 (6.2) 9 (5.3) 2 (1.2)
Elevated protein, n = 955 601 (62.9) 177 (57.3) 424 (65.6) 281 (66.9) 320 (59.8) 112 (66.3) 108 (69.7)
Decreased glucose, n = 957 280 (29.3) 58 (18.8) 222 (34.3) 138 (32.8) 142 (26.5) 45 (26.6) 51 (32.9)
Decreased cerebrospinal fluid:venous glucose ratio, n = 929 540 (58.1) 159 (54.8) 381 (59.6) 253 (61.7) 287 (55.3) 97 (58.8) 97 (64.2)
Elevated lactate, n = 985 650 (66.0) 217 (67.8) 433 (65.1) 298 (69.8) 352 (63.1) 93 (56.0) 132 (80.5)

*Values are no. (%). We defined children as patients <15 years of age and adults >15 years of age. The confirmed viral group includes patients infected with multiple viruses, and the confirmed bacterial group includes patients infected with multiple bacteria. Elevated and low parameters mean above or below reference ranges. Anemia is defined as hematocrit below reference range. Thrombocytopenia is defined as platelet count below reference range. See Appendix Table 3 for reference ranges. CSF, cerebrospinal fluid.
†Hyperglycemia was defined as a blood glucose level of >7.7 mmol/L and severe hyperglycemia as a blood glucose level >11.1 mmol/L.
‡Serum sodium levels >150 mmol/L were considered elevated and <130 mmol/L considered low; 5 patients (0.6%) had serum sodium <115 mmol/L.
§Samples with high turbidity could not be counted and were thus not included.
¶An eosinophil count >10% was considered elevated.

Main Article

1Deceased.

Page created: April 17, 2019
Page updated: April 17, 2019
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