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CASE PRESENTATION A 37-year-old Caucasian woman presented to the emergency department with a two-day history of fevers, conjunctival hyperemia, abdominal cramps, myalgias, vaginal discharge and diffuse erythroderma prominent on her upper thorax, inner thighs and perineum. She had a history of Hashimoto’s thyroiditis and chronic menorrhagia. Ten days before her presentation, she began using The DivaCup (Diva International Inc, USA), a brand of menstrual cup for menstrual blood collection (Figure 1). She used appropriate hygiene when handling and changing the cup, but retrospectively reported causing a small abrasion during one of her initial insertions. Her subsequent menses became heavier and longer than normal. By day 7, she noticed an episode of black vaginal discharge followed two days later by yellow purulent discharge along with subjective fevers, at which point she stopped using the menstrual cup. She presented to the emergency department the following day, after continuing to feel unwell.

heavier and longer than normal. By day 7, she noticed an episode of black vaginal discharge followed two days later by yellow purulent discharge along with subjective fevers, at which point she stopped using the menstrual cup. She presented to the emergency department the following day, after continuing to feel unwell. On initial examination, she looked unwell and had an oral temperature of 37.2°C, blood pressure of 98/65 mmHg and a heart rate of 132 beats/min. No other obvious source of sepsis was found during physical examination. Despite receiving aggressive intravenous fluid resuscitation and antibiotic therapy, including linezolid and piperacillintazobactam, she remained hypotensive for the next 24 h. Vaginal examination revealed yellow discharge and mild menstrual bleeding, but no cervical motion tenderness. The menstrual cup was not present because it had been removed before presenting to hospital. Her blood and urine cultures, methicillin-resistant Staphylococcus aureus screening, Clostridium difficile toxin assay and nasopharyngeal swab for respiratory viruses were negative (Table 1).

but no cervical motion tenderness. The menstrual cup was not present because it had been removed before presenting to hospital. Her blood and urine cultures, methicillin-resistant Staphylococcus aureus screening, Clostridium difficile toxin assay and nasopharyngeal swab for respiratory viruses were negative (Table 1). During the next 24 h, the patient clinically deteriorated; she had a temperature of 39.1°C, a blood pressure of 76/45 mmHg and a heart rate of 137 beats/min. She continued to receive aggressive intravenous fluids and was transferred to a high-acuity observational unit. Postadmission day 2, the patient developed a generalized morbilliform rash. The Infectious Diseases services were consulted. Subsequently, intravenous clindamycin was added to her antibiotic regimen with probable diagnosis of menstrual toxic shock syndrome (TSS). Within 24 h of receiving clindamycin, her blood pressure had significantly improved. Desquamation of her skin rash began on postadmission day 4. The patient remained stable on her antibiotic regimen, ultimately being discharged in good health eight days postadmission. She remained stable for the next two weeks, at which point she was seen at the Infectious Diseases Outpatient Clinic at University Hospital, London Health Sciences Centre (London, Ontario). Control cultures including nasal swab for S aureus remained negative.

ly being discharged in good health eight days postadmission. She remained stable for the next two weeks, at which point she was seen at the Infectious Diseases Outpatient Clinic at University Hospital, London Health Sciences Centre (London, Ontario). Control cultures including nasal swab for S aureus remained negative. DISCUSSION Menstrual TSS The term ‘toxic shock syndrome’ was first coined in 1978 in a Lancet publication describing the symptom complex in children eight to 17 years of age with an acute febrile illness (1). It did not come to public attention until 1980, when an association between TSS and young menstruating women using tampons was discovered (2). Risk factors included the use of high-absorbency tampons and prolonged, continual usage (3). Cases occurring in men and nonmenstruating women were thereafter identified and it was recognized that TSS can occur in any population. There has been a recently published report of recurrent TSS in a 15-year-old girl even after she ceased to use tampons (4). Increased public awareness and change in the composition of tampons to less-absorbent materials led to a substantial decrease in the incidence of menstrual TSS over the next decade (3). Menstrual TSS is a severe, multisystem, toxin-mediated disease associated with multiorgan failure (Table 2) (5). Considering these criteria, the clinical findings of our patient and her laboratory data fulfill the criteria of a ‘confirmed’ case.

Increased public awareness and change in the composition of tampons to less-absorbent materials led to a substantial decrease in the incidence of menstrual TSS over the next decade (3). Menstrual TSS is a severe, multisystem, toxin-mediated disease associated with multiorgan failure (Table 2) (5). Considering these criteria, the clinical findings of our patient and her laboratory data fulfill the criteria of a ‘confirmed’ case. S aureus TSS toxin 1 (TSST-1) is responsible for multiorgan failure in nearly all (95%) patients with menstrual TSS. (6). This toxin acts as a superantigen, stimulating excessive and nonconventional T cell activation and, subsequently, cytokine expression (7). Superantigens bypass normal major histocompatibility complex-restricted antigen recognition and activate 30% of host T cells, while conventional antigen presentation activates only approximately 0.01% of the host T cell population (8). Eventually, significant cytokine release causes multiorgan failure. Detection of TSST-1 is not required for the diagnosis of TSS and this test is only available in some research laboratories.

% of host T cells, while conventional antigen presentation activates only approximately 0.01% of the host T cell population (8). Eventually, significant cytokine release causes multiorgan failure. Detection of TSST-1 is not required for the diagnosis of TSS and this test is only available in some research laboratories. Treatment includes active fluid resuscitation, early use of vasopressors and appropriate antimicrobial therapy. Clindamycin has been demonstrated to reduce the expression of superantigens (9). Theoretically, clindamycin suppresses the protein synthesis and, as a result, more effectively inhibits toxin production compared with vancomycin, which inhibits cell wall synthesis. Linezolid has also been successfully used to treat nonmenstrual TSS and has been shown to decrease TSST-1 production (10). To our knowledge, we report the first case of menstrual TSS that was successfully treated with combination of linezolid and clindamycin. Although rapid clinical improvement has been previously described with the use of linezolid in TSST-1-producing S aureus, our patient remained hypotensive while receiving linezolid (10). Her blood pressure significantly improved only after the addition of clindamycin. She did not require intravenous immunoglobulin. Although both clindamycin and linezolid inhibit bacterial protein synthesis and, therefore, toxin production, our patient remained hypotensive until clindamycin was included in her antibiotic regimen. Further experimental and comparative studies are required to determine the inhibitory effects of these two medications against TSST-1.

lindamycin and linezolid inhibit bacterial protein synthesis and, therefore, toxin production, our patient remained hypotensive until clindamycin was included in her antibiotic regimen. Further experimental and comparative studies are required to determine the inhibitory effects of these two medications against TSST-1. Menstrual cups Menstrual cups are a reusable alternative to conventional tampons. Designed to collect rather than absorb menstrual flow, they are made of silicone and worn internally (Figure 1). In a recent multicentre randomized controlled trial by Howard et al (11), the use of tampons was compared with The DivaCup in a total of 110 women. The results demonstrated that overall satisfaction was higher among users of The DivaCup, with 91% of users stating they would continue using it. The present case report identified increased vaginal irritation with The DivaCup compared with tampons, but was not powered to detect a difference in infectious complications (11). Tierno (12) explained the probable reasons for the association between hyperabsorbable tampons and TSS as follows: Accumulation of blood in the polyester foam cubes and chips of carboxymethylcellulose. Increase of vaginal pH in menstruation from 4.2 to around 7.4. Existence of both oxygen and carbon dioxide in the vagina during menstruation.

Tierno (12) explained the probable reasons for the association between hyperabsorbable tampons and TSS as follows: Accumulation of blood in the polyester foam cubes and chips of carboxymethylcellulose. Increase of vaginal pH in menstruation from 4.2 to around 7.4. Existence of both oxygen and carbon dioxide in the vagina during menstruation. These three main factors provide a condition for S aureus growth. In a narrative review, Vostral (13), concluded that the gelled carboxymethylcellulose, in essence, acted like agar in a petri dish, providing a medium on which the bacteria may grow. Menstrual cups are made of silicone or rubber, and carboxymethylcellulose is not used in their structure. Silicone itself does not support microbiological growth. However, because of accumulation of blood, menstrual cups appear to provide a medium for bacterial growth with the same three conditions mentioned above. Menstrual blood in the uterine environment is sufficient to promote the growth of S aureus in the lower genital tract. As such, the menstrual cup appears to provide a necessary milieu for S aureus growth during menstruation. Our patient began using the menstrual cup approximately 10 days before presentation. This duration appears to be sufficient for S aureus growth. High placement of a previously handled cup, an abundant volume of menstrual blood and mucosal irritation within the vagina may be considered as other probable contributing factors.

atient began using the menstrual cup approximately 10 days before presentation. This duration appears to be sufficient for S aureus growth. High placement of a previously handled cup, an abundant volume of menstrual blood and mucosal irritation within the vagina may be considered as other probable contributing factors. To our knowledge, the present report is the first to detail the association between a menstrual cup and menstrual TSS. We present here a rare case in a 37-year-old woman who met all six Centers for Disease Control and Prevention (Georgia, USA) criteria (5) for confirmed TSS after wearing a menstrual cup for the first time. DISCLOSURES: The authors have no financial disclosures or conflicts of interest to declare. Figure 1) The DivaCup (Diva International Inc, USA) (a brand of menstrual cup) TABLE 1 Laboratory results from initial assessment

To our knowledge, the present report is the first to detail the association between a menstrual cup and menstrual TSS. We present here a rare case in a 37-year-old woman who met all six Centers for Disease Control and Prevention (Georgia, USA) criteria (5) for confirmed TSS after wearing a menstrual cup for the first time. DISCLOSURES: The authors have no financial disclosures or conflicts of interest to declare. Figure 1) The DivaCup (Diva International Inc, USA) (a brand of menstrual cup) TABLE 1 Laboratory results from initial assessment Parameter (normal range) Result White blood cell count (4.0–10.0×109/L) 23.6×109/L Hemoglobin (115–160 g/L) 72 g/L Platelets 1(50–400×109/L) 107×109/L International normalized ratio (0.9–1.1) 1.8 Fibrinogen (2.0–4.0 g/L) 4.79 g/L Creatinine (<100 μmol/L) 106 μmol/L Creatine kinase (<167 U/L) 346 U/L Blood urea nitrogen (<8.3 mmol/L) 2.8 mmol/L Alanine aminotransferase (<33 U/L) 52 U/L Aspartate aminotransferase (<32 U/L) 72 U/L Total bilirubin (3.4–17.1 μmol/L) 61.3 μmol/L Potassium (3.5–5.0 mmol/L) 3.0 mmol/L Magnesium (0.65–1.05 mmol/L) 0.34 mmol/L Ionized calcium (1.09–1.30 mmol/L) 1.05 mmol/L Urinalysis 20–30 leukocytes/high power field Total beta human chorionic gonadotropin Negative (<1 IU/L) Blood cultures Negative ×2 Urine culture Negative TABLE 2 Centers for Disease Control and Prevention (Georgia, USA) 2011 case definition for toxic shock syndrome (other than Streptococcus) (5) Clinical criteria An illness with the following clinical manifestations: Fever: temperature ≥102.0°F (≥38.9°C) Rash: diffuse macular erythroderma

Parameter (normal range) Result White blood cell count (4.0–10.0×109/L) 23.6×109/L Hemoglobin (115–160 g/L) 72 g/L Platelets 1(50–400×109/L) 107×109/L International normalized ratio (0.9–1.1) 1.8 Fibrinogen (2.0–4.0 g/L) 4.79 g/L Creatinine (<100 μmol/L) 106 μmol/L Creatine kinase (<167 U/L) 346 U/L Blood urea nitrogen (<8.3 mmol/L) 2.8 mmol/L Alanine aminotransferase (<33 U/L) 52 U/L Aspartate aminotransferase (<32 U/L) 72 U/L Total bilirubin (3.4–17.1 μmol/L) 61.3 μmol/L Potassium (3.5–5.0 mmol/L) 3.0 mmol/L Magnesium (0.65–1.05 mmol/L) 0.34 mmol/L Ionized calcium (1.09–1.30 mmol/L) 1.05 mmol/L Urinalysis 20–30 leukocytes/high power field Total beta human chorionic gonadotropin Negative (<1 IU/L) Blood cultures Negative ×2 Urine culture Negative TABLE 2 Centers for Disease Control and Prevention (Georgia, USA) 2011 case definition for toxic shock syndrome (other than Streptococcus) (5) Clinical criteria An illness with the following clinical manifestations: Fever: temperature ≥102.0°F (≥38.9°C) Rash: diffuse macular erythroderma Desquamation: one to two weeks after onset of rash Hypotension: systolic blood pressure ≤90 mmHg for adults or less than fifth percentile for children <16 years of age Multisystem involvement (≥3 of the following organ systems): Gastrointestinal: vomiting or diarrhea at onset of illness Muscular: severe myalgia or creatine phosphokinase level at least twice the upper limit of normal Mucous membrane: vaginal, oropharyngeal or conjunctival hyperemia

Hypotension: systolic blood pressure ≤90 mmHg for adults or less than fifth percentile for children <16 years of age Multisystem involvement (≥3 of the following organ systems): Gastrointestinal: vomiting or diarrhea at onset of illness Muscular: severe myalgia or creatine phosphokinase level at least twice the upper limit of normal Mucous membrane: vaginal, oropharyngeal or conjunctival hyperemia Renal: blood urea nitrogen or creatinine at least twice the upper limit of normal for laboratory or urinary sediment with pyuria (≥5 leukocytes per high-power field) in the absence of urinary tract infection Hepatic: total bilirubin, alanine aminotransferase enzyme or asparate aminotransferase enzyme levels at least twice the upper limit of normal for laboratory Hematological: platelets <100,000/mm3 Central nervous system: disorientation or alterations in consciousness without focal neurological signs when fever and hypotension are absent Laboratory criteria for diagnosis Negative results on the following tests, if obtained: Blood or cerebrospinal fluid cultures blood culture may be positive for Staphylococcus aureus Negative serologies for Rocky Mountain spotted fever, leptospirosis or measles Case classification Probable A case that meets the laboratory criteria and in which four of the five clinical criteria described above are present Confirmed A case that meets the laboratory criteria and in which all five of the clinical criteria described above are present, including desquamation, unless the patient dies before desquamation occurs