Characteristic | Frequency, no. (%) |
---|---|
Shigella spp. infection | |
S. flexneri | 71 (55) |
S. sonnei | 57 (45) |
Sex | |
M | 104 (81.3) |
F | 21 (16.4) |
Transgender, male-to-female | 3 (2.3) |
Ethnicity | |
Hispanic/Latin | 28 (21.9) |
Mixed race/other | 16 (12.5) |
Native Hawaiian/Pacific Islander | 1 (0.8) |
Non-Hispanic Black | 12 (9.4) |
Non-Hispanic White | 69 (53.9) |
Unknown | 2 (1.6) |
Sexual orientation | |
GBM/transgender | 71 (55.5) |
Not GBM | 20 (15.6) |
Unknown | 37 (28.9) |
HIV status | |
Positive | 65 (50.8) |
Negative | 49 (38.3) |
Unknown | 14 (10.9) |
HAART use by persons living with HIV | |
Yes | 55/65 (84.6) |
No | 10/65 (15.4) |
PrEP use among persons at risk for HIV | |
Yes | 8/12 (66.7) |
No | 4/12 (33.3) |
Unhoused | |
Yes | 29/128 (22.7) |
No | 99/128 (77.3) |
Methamphetamine use | |
Yes | 42/128 (32.8) |
GBM/transgender | 24/42 (57) |
Unhoused | 24/42 (57) |
HIV positive | 23/42 (55) |
No | 86/128 (67.2) |
Travel history (international and domestic travel) | |
Yes | 20/128 (15.6) |
No | 67/128 (52.3) |
Unknown | 41/128 (32.0) |
Table 1. General characteristics of persons with diarrheal disease and Shigella spp. isolated from stool culture, San Diego, California, USA, March 1, 2017–May 31, 2020*
*Patient age range 15–79 y, mean age 47 y. GBM, gay and bisexual man; HAART, highly active antiretroviral therapy; PrEP, preexposure prophylaxis.
Patient variable | Shigella flexneri, no. (%) | Shigella sonnei, no. (%) | p value |
---|---|---|---|
HIV positive | 44 (68) | 21 (43) | 0.008 |
Sexual orientation, GBM/transgender woman | 45 (85) | 26 (68) | 0.061 |
HAART use by persons living with HIV | 40 (91) | 15 (71) | 0.065 |
PrEP use among HIV-negative | 4 (80) | 4 (57) | 0.408 |
Unhoused | 6 (8) | 23 (40) | <0.001 |
Methamphetamine use | 16 (23) | 26 (46) | 0.006 |
Travel | 11 (15) | 9 (20) | 0.008 |
Table 2. Variables associated with Shigella flexneri and Shigella sonnei Infection, San Diego, California, USA, March 1, 2017–May 31, 2020*
*GBM, gay and bisexual man; HAART, highly active antiretroviral therapy; PrEP, preexposure prophylaxis.
Physicians - maximum of 1.00 AMA PRA Category 1 Credit(s)™
ABIM Diplomates - maximum of 1.00 ABIM MOC points
This activity is intended for primary care physicians, infectious disease specialists, and other physicians who care for patients at risk for Shigella spp. infection.
The goal of this activity is to evaluate variables associated with Shigella spp. infection and antimicrobial resistance.
Upon completion of this activity, participants will:
Medscape, LLC requires every individual in a position to control educational content to disclose all financial relationships with ineligible companies that have occurred within the past 24 months. Ineligible companies are organizations whose primary business is producing, marketing, selling, re-selling, or distributing healthcare products used by or on patients.
All relevant financial relationships for anyone with the ability to control the content of this educational activity are listed below and have been mitigated according to Medscape policies. Others involved in the planning of this activity have no relevant financial relationships.
Medscape, LLC designates this Journal-based CME for a maximum of 1.0
AMA PRA Category 1 Credit(s)™
. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to 1.0 MOC points in the American Board of Internal Medicine's (ABIM) Maintenance of Certification (MOC) program. Participants will earn MOC points equivalent to the amount of CME credits claimed for the activity. It is the CME activity provider's responsibility to submit participant completion information to ACCME for the purpose of granting ABIM MOC credit.
For questions regarding the content of this activity, contact the accredited provider for this CME/CE activity noted above. For technical assistance, contact [email protected]
There are no fees for participating in or receiving credit for this online educational activity. For information on applicability
and acceptance of continuing education credit for this activity, please consult your professional licensing board.
This activity is designed to be completed within the time designated on the title page; physicians should claim only those
credits that reflect the time actually spent in the activity. To successfully earn credit, participants must complete the
activity online during the valid credit period that is noted on the title page. To receive
AMA PRA Category 1 Credit™, you must receive a minimum score of 75% on the post-test.
Follow these steps to earn CME/CE credit*:
You may now view or print the certificate from your CME/CE Tracker. You may print the certificate but you cannot alter it.
Credits will be tallied in your CME/CE Tracker and archived for 6 years; at any point within this time period you can print
out the tally as well as the certificates from the CME/CE Tracker.
*The credit that you receive is based on your user profile.
CME / ABIM MOC Released: 5/23/2022
Valid for credit through: 5/23/2023
processing....
Annually, Shigella spp. cause ≈188 million cases of diarrheal disease globally, including 500,000 cases in the United States; rates of antimicrobial resistance are increasing. To determine antimicrobial resistance and risk factors in San Diego, California, USA, we retrospectively reviewed cases of diarrheal disease caused by Shigella flexneri and S. sonnei diagnosed during 2017–2020. Of 128 evaluable cases, S. flexneri was slightly more common than S. sonnei; most cases were in persons who were gay or bisexual cisgender men, were living with HIV, were unhoused, or used methamphetamines. Overall, rates of resistance to azithromycin, fluoroquinolones, ampicillin, and trimethoprim/sulfamethoxazole (TMP/SMX) were comparable to the most recent national data reported from the Centers for Disease Control and Prevention; 55% of isolates were resistant to azithromycin, 23% to fluoroquinolones, 70% to ampicillin, and 83% to TMP/SMX. The rates that we found for TMP/SMX were slightly higher than those in national data.
Shigella bacteria are facultatively anaerobic, nonmotile, gram-negative bacilli and a common global cause of infectious diarrhea, especially in low-income settings[1]. They are relatively resistant to the high acidity of the stomach and can survive transit into the small intestine, where they multiply and pass into the colon, invading colonic cells and causing diarrhea. As few as 10–100 organisms are capable of causing disease[2]. This low infectious dose increases transmission by the fecal–oral route or via contaminated food and water. Globally, Shigella spp. cause an estimated 188 million cases of diarrheal disease annually and account for 164,000 deaths[1] particularly in children.
In the United States, ≈500,000 cases of shigellosis occur annually; 81% are caused by Shigella sonnei, followed by S. flexneri (12.6%), S. boydii (0.2%), and S. dysenteriae (0.1%)[3]. Most transmission occurs via the fecal–oral route, at locations such as daycare centers, but transmission can also occur after ingesting contaminated food or drinking water, after ingesting untreated recreational water[4], and among men who have sex with men (MSM). Among MSM, multiple outbreaks have been described in Montreal, Quebec, Canada[5,6], and Germany[7]; and in the United States[8,9] including Minnesota[10]; the Chicago, Illinois, and Minneapolis-St. Paul, Minnesota, regions[11]; and New York, New York[12].
For children and adults with symptomatic shigellosis, antimicrobial therapy is typically recommended because it shortens symptom duration and decreases the duration of bacterial shedding in adults[13] and children[14–17]. For children, antimicrobial therapy should be guided by local resistance profiles. For adults, empiric antimicrobial therapy selection should be guided by local resistance profiles as well as patient demographics. For example, in parts of Asia, widespread resistance to azithromycin, ceftriaxone, and ciprofloxacin has been reported[18,19]. In addition, increasing antimicrobial resistance has been found in certain groups, such as MSM, and has also been associated with travel[20] including increasing resistance to first-line agents such as fluoroquinolones[5,7] and azithromycin[8] Last, susceptibilities obtained from culture should be used in the event of treatment failure.
To determine antimicrobial resistance and risk factors in the San Diego, California, USA, area, we investigated cases of symptomatic shigellosis causing diarrheal disease at the University of California San Diego Health System and San Diego Veterans Affairs Medical Center over a 3-year period. The study was approved by the Human Research Protection Program at University of California San Diego Health and the San Diego Veterans Affairs Institutional Review Board.