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. 2022 Aug 12;51(2):483–487. doi: 10.1007/s15010-022-01896-7

Monkeypox in-patients with severe anal pain

Frieder Pfäfflin 1, Daniel Wendisch 1, Roland Scherer 2, Linda Jürgens 1, Gisèle Godzick-Njomgang 1, Eva Tranter 3, Pinkus Tober-Lau 1, Miriam Songa Stegemann 1, Victor Max Corman 4, Florian Kurth 1,✉,#, Dirk Schürmann 1,#
PMCID: PMC10042938  PMID: 35960457

Abstract

Berlin is amongst the cities most affected by the current monkeypox outbreak. Here, we report clinical characteristics of the first patients with confirmed monkeypox admitted to our center. We analyzed anamnestic, clinical, and laboratory data. Within a period of 2 weeks, six patients were hospitalized in our unit. All were MSM and had practiced condomless receptive anal intercourse in the weeks preceding admission. The chief complaint in all patients but one was severe anal pain unprecedented in severity. Investigations revealed proctitis, as well as anal and rectal ulcers with detection of monkeypox virus. Our findings support the hypothesis that sexual transmission plays a role in the current outbreak.

Keywords: Monkeypox, MPX, MPXV, Germany, MSM, HIV

Introduction

In May 2022, the United Kingdom Health Security Agency reported patients with monkeypox (MPX) in the UK, followed by increasing case numbers in several cities in Europe and the U.S. [1, 2]. Berlin is amongst the cities most affected by the current global MPX outbreak with 617 of a total of 874 cases reported in Germany as of June 29, 2022 [3, 4]. Here, we report clinical characteristics of the first six patients with confirmed MPX admitted to the Department of Infectious Diseases of Charité—Universitätsmedizin Berlin, Germany, the regional referral center for patients with MPX needing hospitalization.

Methods

The patients described in this case series are the first six patients included in an ongoing prospective clinical cohort study, with the aim to analyze clinical and laboratory characteristics of MPX. Patients were included from May 27 to June 10, 2022, after written informed consent had been obtained. Treatment of patients, clinical sampling, investigations and documentation were carried out according to clinical necessity. The study is approved by the ethics committee of Charité—Universitätsmedizin Berlin (EA2/139/22) and is performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments. All patients provided written informed consent to publication of their data and one patient additionally to publication of a photograph.

Results

From May 27 to June 10, 2022, six patients with non-travel related monkeypox detected by PCR in fluid from cutaneous blisters were hospitalized in our unit (GenBank: ON813251.2). Details of the clinical courses are summarized in the Table 1. All patients self-identified as men who have sex with men (MSM) and had practiced condomless receptive anal sexual intercourse with different partners in the weeks preceding admission. None of the patients was immunocompromised. Two patients were living with HIV and on anti-retroviral therapy (ART) with well controlled infection, three patients were on pre-exposure prophylaxis (PrEP). Prodromal symptoms were mild and had subsided spontaneously before admission. The number of concurrent lesions ranged from three on one arm to a maximum of 36 with a wide distribution over the body surface. Concurrent STDs were detected in three patients: two patients with gonorrhea, both detected with PCR (COBAS®, Roche, Basel, Switzerland), and one patient with gonorrhea, Ureaplasma and Mycoplasma hominis, each detected with PCR (COBAS® for gonococci and RIDA® GENE STI, R-Biopharm, Darmstadt, Germany for Ureaplasma and Mycoplasma hominis). The general condition was good in all but one patient who had extended inflammation of the sigmoid, rectum, and anus. One patient suffered from a perianal abscess, which was treated by incision and drainage. The abscess had appeared prior to the onset of prodromal symptoms and the other skin lesions and was thus considered not to be related to monkeypox. The chief complaint of all other patients was intense anal pain. These patients rated the pain as 9–10/10 on the numerical rating scale (NRS, with zero representing 'no pain at all' and ten representing 'the worst pain possible’). The character of the pain was mostly described as unprecedented in severity (although all patients had experienced anal disorders in the past), stabbing, burning, and unbearable on defecation. Three of these patients underwent proctoscopy under spinal anesthesia to rule out anal abscess. Proctoscopic findings were severe proctitis, anal and rectal ulcers (Fig. 1). Computer tomography (CT) of the pelvis was performed in one patient. CT scans showed severe inflammation of the sigmoid, rectum, and anus. Anal lesions were positive for monkeypox DNA in all three cases where swabs were obtained. All patients were treated with systemic and local analgesics (some doses of the systemic analgesics were administered intravenously). Stool softeners were given to ease the aggravated pain during defecation. The intense pain lessened within a couple of days in all patients. The duration of hospital stay ranged from 3 to 6 days. All symptoms from all patients had much alleviated at hospital discharge.

Table 1.

Clinical and laboratory characteristics of six patients with monkeypox

Patient 1 Patient 2 Patient 3 Patient 4 Patient 5 Patient 6
Sex Male Male Male Male Male Male
Age range 41–50 21–30 31–40 31–40 21–30 31–40
Mode of infection (sexual preference) MSM (insertive anal, receptive anal) MSM (insertive anal, receptive anal, oral) MSM (receptive anal) MSM (receptive anal) MSM (receptive anal) MSM (receptive anal)
Prodrome Fever Fever, malaise None Fatigue Fever, malaise, myalgia, sweats Myalgia, fever, malaise
Lymphadenopathy Left inguinal None None Left inguinal None none
Number of concurrent lesions 15 5 7 ≈ 20 36 3
Distribution of lesions Limbs Left arm Limbs Arms, trunk, genital Head, neck, trunk, limbs Legs
HIV status Positive Negative Negative Negative Negative Positive
CD4 count (if HIV positive) 870/µl  > 500/µl
Concurrent STD (site of diagnostic sample) None None None Syphilis (blood), gonorrhea (rectal) Gonorrhea, Ureaplasma, Mycoplasma hominis (all urethral) Gonorrhea (rectal)
Treatment of concurrent STD Penicillin G benzathine, ceftriaxone Ceftriaxone, azithromycin Cefriaxone, azithromycin
Chief clinical complaint Perianal pain Anal pain Anal pain Anal pain Anal pain Anal pain
Maximum severity of anal pain 5/10 10/10 9/10 10/10 10/10 10/10
Character of anal pain Stabbing, pressing Unprecedented in severity, stabbing, burning, aggravation on defecation Unprecedented in severity, pressing, stabbing, burning, aggravation on defecation Aggravation on defecation Unprecedented in severity, burning, stabbing, aggravation on defecation Burning
Anal investigation for specific causes Proctoscopy under spinal anesthesia Proctoscopy under spinal anesthesia CT scan of pelvis Proctoscopy under spinal anesthesia
Finding on ano-rectal investigation Anal abscess Anal fissure Rectal ulcer, proctitis Anal ulcer Inflammation of sigmoid, rectum and anal canal Anal ulcer, proctitis
Other findings Histology from anal abscess: extensive suppurative, partially hemorrhagic- necrotizing inflammation of corium and subcutis Histology from ulcer: rectal ulcer with crypt hyperplasia and interstitial stromal fibrosis
Specific management of complications Incision and drainage
Analgesia (per os if not indicated differently) Ibuprofen 600 mg q8h Metamizole 500 mg q6h, tramadol 50 mg q12h, lidocaine 50 mg/g topical Ibuprofen 600 mg q8h, metamizole 500 mg q6h intravenously, lidocaine 50 mg/g topical Metamizole 500 mg q6h, lidocaine 50 mg/g topical Metamizole 500 mg q6h intravenously, lidocaine 50 mg/g topical Metamizole 500 mg q6h, lidocaine 50 mg/g topical
Other supportive care Macrogol, rinsing with polyhexanide Macrogol Macrogol Macrogol Macrogol Macrogol
Duration of clinical course prior to admission 14 d 9 d 11 d 5 d 2 d 5 d
Duration of hospital stay 4 d 3 d 3 d 3 d 6 d 3d
Outcome at hospital discharge Improved Improved Improved Improved Improved Improved

MSM, men who have sex with men; STD, sexually transmitted disease; CT, computer tomography

Fig. 1.

Fig. 1

Proctoscopy under spinal anesthesia in lithotomy position reveals severe proctitis with ulceration at 5–7 o’clock. A small monkeypox lesion can be seen at 6 o’clock in the anoderm (white arrow)

Discussion

We report on six monkeypox cases hospitalized in a single center. Notable seems the homogeneous clinical presentation with intense anal pain in all but one patients, which was described as unprecedented in severity, despite a history of anal disorders in the past. The pain is in contrast to findings from recent studies from Nigeria, the Democratic Republic of the Congo (DRC) and the UK prior to the current outbreak, where anal pain was not reported [57]. All patients had practiced condomless receptive anal intercourse in a time window compatible with time of infection. Seminal fluid has been shown to be positive for MPX DNA earlier [8] and MPX DNA was also detected in one sample we tested. Anal lesions were positive for MPX DNA in all three of our cases where swabs had been obtained, a finding also reflected in other reports [8]. Our findings therefore strengthen the hypothesis and current perception that sexual transmission plays a role in the current outbreak. In a recent study from the Democratic Republic of the Congo, the most common exposures to monkeypox were cleaning/dressing/consumption of wild game and handling uncooked, freshly butchered meat. The most common clinical complaints were rash, malaise, sore throat, lymphadenopathy (mostly cervical), and anorexia [7]. Thus, in the study from the DRC, exposure of skin and pharynx led to affection of the skin and the gastrointestinal tract. Contrary to that, our patients suffered from anal pain after receptive anal intercourse. We therefore hypothesize, that the route of transmission conditions the clinical course. The clinical presentation observed in our patients merely reflects the extreme end of anal involvement in monkeypox. Of note, positive anorectal MPX PCR results from asymptomatic persons have been described recently [9].

None of our patients was treated with tecovirimat. The availability of tecovirimat in Germany was limited to five treatment courses for the whole country. Requests for tecovirimat had to be discussed within the working group of competence and treatment centers for high-consequence infectious diseases (Ständiger Arbeitskreis der Kompetenz- und Behandlungszentren für Krankheiten durch hochpathogene Erreger (STAKOB) at the Robert Koch-Institute (RKI)). We did not request tecovirimat for our patients as none of them was immunocompromised and no immediate danger for critical organs was perceived. However, we do not know whether administration of tecovirimat would have alleviated the intense pain. We did neither request brincidofovir as this drug was not available in Germany and treatment can be associated with side effects, hepatotoxicity in particular [6]. The World Health Organization (WHO), in its interim rapid response guidance, recommends antivirals to be preferentially administered within randomized clinical trials [10].

From May 27, to June 10, 2022, six out of 120 patients with confirmed monkeypox in Berlin were hospitalized in our center. Further six of 497 patients were treated as in-patients as of June 29, 2022. The decreasing hospitalization rate may reflect growing competence with the management of monkeypox cases. Of note, no cases with critical or life-threatening clinical conditions have been reported so far. Although severe, the pain described by our patients responded to analgesics.

Author contributions

FP, FK, and DS conceived and designed the study. FK and DS led the study. All authors contributed or analyzed the data. The first draft of the manuscript was written by FP and FK and edited by all authors. All authors read and approved the final manuscript.

Funding

Open Access funding enabled and organized by Projekt DEAL. No funds, grants, or other support were received for conducting the study.

Declarations

Competing interest

On behalf of all authors, the corresponding author states that there is no conflict of interest.

Ethics approval

Informed consent was obtained from all individual participants included in the study. Patients signed informed consent regarding publishing their data and, where applicable, photograph.

Informed consent

The authors declare that they have no competing interests.

Footnotes

Florian Kurth and Dirk Schürmann co-led the study.

Change history

10/15/2022

Missing Open Access funding information has been added in the Funding Note.

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