| Literature DB >> 26890854 |
Martin Hoenigl, Nella Green, Martha Camacho, Sara Gianella, Sanjay R Mehta, Davey M Smith, Susan J Little.
Abstract
We analyzed signs and symptoms in 90 patients diagnosed with acute HIV infection in a community-based program that offered universal HIV-1 nucleic acid amplification testing. Forty-seven (52%) patients reported ongoing signs or symptoms at the time of testing. Another 25 (28%) reported signs or symptoms that had occurred during the 14 days before testing.Entities:
Keywords: HIV/AIDS and other retroviruses; MSM; NAT; acute HIV infection; acute retroviral syndrome; men who have sex with men; nucleic acid amplification; screening; seroconversion; signs; symptoms; testing; typical acute retroviral syndrome; viruses
Mesh:
Year: 2016 PMID: 26890854 PMCID: PMC4766914 DOI: 10.3201/eid2203.151607
Source DB: PubMed Journal: Emerg Infect Dis ISSN: 1080-6040 Impact factor: 6.883
Comparison of AHI stage, characteristics of signs or symptoms, CD4+ cell count, and viral load between persons with signs or symptoms before and at the time of NAT versus persons without, San Diego, California, USA, 2007–2014*
| Characteristic | Total no. persons | Symptoms before NAT† | Asymptomatic before NAT | p value | Ongoing symptoms at NAT | Absence of symptoms at NAT | p value |
|---|---|---|---|---|---|---|---|
| No. persons | 90 | 72 | 18 | 47 | 43 | ||
| Overall no. signs/symptoms in those symptomatic, median (IQR) | 5 (3–7); n = 84 | 5 (4–7) | 5 (2–6); n = 12 | NS | 6 (4–8) | 5 (3–6); n = 37 | NS |
| Duration of symptoms, d, median (IQR) | 9 (5–13); n = 79 | 10 (6–13); n = 67 | 4 (3–7); n = 12 | <0.01 | 11 (8–14); n = 43 | 6 (3–9); n = 36 | <0.01 |
| CD4+ cell count, cells/μL, median (IQR) | 435 (298–597) | 435 (302–586) | 448 (257–615) | NS | 424 (299–592) | 445 (295–610) | NS |
| Viral load, log10 RNA, median (IQR) | 5.4 (4.5–6.3) | 5.8 (4.8–6.4) | 4.5 (3.2–5.0) | <0.01 | 5.6 (4.8–6.4) | 5.0 (3.8–6.1) | 0.07 |
*AHI, acute HIV infection; IQR, interquartile range; NAT, nucleic acid amplification testing; NS, not significant. †Most frequently observed signs or symptoms that occurred during the 14 days before NAT or were ongoing at the time of NAT were fatigue (53 persons, 59% of the study population), fever (51, 57%), myalgia (48, 53%), headache (41, 46%), night sweats (35, 39%), pharyngitis (32, 36%), and gastrointestinal symptoms (29, 32%).
Signs or symptoms occurring in 69 persons with AHI, San Diego, California, USA, 2007–2014*
| Characteristic | Signs/symptoms | p value | Signs/symptoms | p value | |||
|---|---|---|---|---|---|---|---|
| Compatible with AHI† | Resolved before NAT | Ongoing at NAT | Persons seeking medical attention | Persons not seeking medical attention | |||
| No. persons reporting symptoms | 69 | 16 | 41 | 10 | 22 | ||
| Duration of symptoms, d, median (IQR) | 8 (5–11) | 7 (4–8) | 11 (7–13) | <0.01 | 13 (10–17) | 10 (4–11) | 0.01 |
| No. (%) persons with typical AHI | 64 (93) | 15 (94) | 36 (86) | NS | 10 (100) | 18 (82) | NS |
| Signs or symptoms, no. (%) | |||||||
| Fever | 53 (77) | 11 (69) | 34 (83) | NS | 9 (90) | 16 (73) | NS |
| Myalgia | 48 (70) | 13 (81) | 28 (68) | NS | 8 (80) | 12 (55) | NS |
| Fatigue | 48 (70) | 13(81) | 29 (71) | NS | 9 (90) | 13 (59) | NS |
| Headache | 42 (61) | 10 (63) | 27 (66) | NS | 8 (80) | 11 (50) | NS |
| Night sweats | 38 (55) | 5 (31) | 26 (63) | 0.04 | 7 (70) | 9 (41) | NS |
| Pharyngitis | 34 (49) | 9 (56) | 17 (41) | NS | 4 (40) | 11 (50) | NS |
| GI symptoms‡ | 29 (42) | 3 (19) | 22 (54) | 0.02 | 5 (50) | 7 (32) | NS |
| Rash | 19 (28) | 6 (38) | 12 (29) | NS | 5 (50) | 5 (23) | NS |
| Weight loss§ | 15 (22) | 2 (13) | 12 (29) | NS | 6 (60) | 3 (14) | 0.01 |
| Arthralgia | 14 (20) | 3 (19) | 8 (20) | NS | 4 (40) | 1 (5) | 0.02 |
*AHI, acute HIV infection; GI, gastrointestinal; IQR, interquartile range; NAT, nucleic acid amplification testing; NS, not significant. †Defined as having started <4 days before estimated date of infection or after the estimated date of infection. ‡General GI symptoms (e.g., nausea, vomiting, and diarrhea). §Weight loss >2.5 kg.