Tubo Ovarian Abscess: Ultrasound Findings

Rapid Communication

Austin J Obstet Gynecol. 2019; 6(3): 1142.

Tubo Ovarian Abscess: Ultrasound Findings

El-Agwany AS*

Department of Obstetrics and Gynecology, Faculty of Medicine, Alexandria University, Egypt

*Corresponding author: Ahmed S El-Agwany, Department of Obstetrics and Gynecology, El-shatby Maternity University Hospital, Faculty of Medicine, Alexandria University, Alexandria, Egypt

Received: April 18, 2019; Accepted: May 22, 2019; Published: May 29, 2019

Abstract

Tubo Ovarian Abscesses (TOAs) are common pelvic infections requiring inpatient admission in opposite to complex. We discuss here the different ultrasound findings related to be aware of by different physicians.

Keywords: Pelvic Inflammatory Disease; Tubo ovarian Abscess

Introduction

Pelvic Inflammatory Disease (PID) is a polymicrobial ascending infection that causes inflammation of the upper genital tract, including endometritis, salpingitis, pelvic peritonitis, and occasionally leading to Tubo Ovarian Abscess (TOA) and complex formation [1]. The healthcare burden of PID is generally underestimated because of cases of undiagnosed subclinical PID [2]. The incidence of PID correlates with the incidence of sexually transmitted diseases [3]. It is unclear why some women with PID develop TOA, whereas the majority of women do not. Formation of TOA may be related to prior PID infection, delay in treatment, or virulence factors of the pathogens. Among hospitalized patients with PID approximately one third have TOA [4]. TOAs are caused by an ascending infection to the fallopian tube causing endothelial damage and edema of the infundibulum resulting in tubal blockage. The ovary may become involved presumably by invasion of organisms through the ovulation site. Eventually the separation between the ovary and fallopian tube is lost. Necrosis inside this complex mass may result in 1 or more abscess cavities and an anaerobic growth environment [4]. The adherence of adjacent pelvic structures, such as the omentum and bowel, might serve a host defense mechanism to contain the inflammatory process within the pelvis. This could be a reason that some women with TOA are not overtly sick with an elevated white cell count or fever. PID has been determined to be polymicrobial in nature [5]. Sexually transmitted infections, such as N. gonorrhoeae, Chlamydia trichomatis, and Mycoplasma genitalium, have all been identified from the cervix, endometrium, and fallopian tubes from women with acute sapingitis [6]. However, endogenous, bacterial vaginosis-associated lower genital tract organisms, such as Prevotella species, Peptostreptococci sp., Gardnerella vaginitis, Escherichia coli, Haemophilus influenza, and aerobic streptococci are found in a high percentage of PID cases [7]. The most common organisms isolated for TOAs are E. coli, Bacteriodes fragilis, Bacteriodes species, Peptostreptococcus, Peptococcus, and aerobic streptococcus [8]. Importantly, E. coli is a common isolate in women with ruptured TOAs and a frequent cause of Gramnegative sepsis. TOAs that occur in women with long-term use of an IUD are often associated with Actinomyces israelii [8]. Acute PID is difficult to diagnose because of the wide variation of signs and symptoms [9]. Empiric treatment should be initiated in women at risk for sexually transmitted diseases if they are experiencing pelvic or lower abdominal pain, if other illnesses have been ruled out and if they have cervical motion tenderness, uterine tenderness, or adnexal tenderness. In addition (1) or more of the following criteria enhances the specificity of the diagnosis: fever, abnormal cervical or vaginal mucopurulent discharge, presence of abundant white blood cells on saline microscopy, elevated erythrocyte sedimentation rate, elevated C-reactive protein, and cervical infection with N. gonorrhoeae or C. trichomatis. Transvaginal ultrasound and pelvic Computed Tomography (CT) are the most common imaging modalities used to detect TOA. Transvaginal ultrasound is considered the first-line imaging modality because it provides excellent imaging of the upper genital tract, is relatively inexpensive, and does not expose the patient to radiation. Ultrasound finding suggestive of PID includes enlarged ovarian volumes or polycystic ovaries, thickened fluid-filled ovaries with incomplete septum or the “cog wheel” sign, and complex free fluid in the cul-de-sac. With more severe or progressive PID, the anatomic distinction between the ovary and the fallopian tube can no longer be identified, forming a TOA [7]. TOAs are characterized by a complex multilocular cystic mass with thick irregular walls, partitions, and internal echoes (Figure 1-5). Pelvic CT is preferred for women where the diagnosis is uncertain and there is concern for a coexisting malignancy or gastrointestinal pathology, such as appendicitis or diverticulitis [7]. Women with mild or moderate PID achieved clinical outcomes with outpatient oral antibiotics similar to those with inpatient IV antibiotics. The decision for hospitalization should be Surgical emergencies cannot be excluded; Pregnancy; Lack of response to oral antibiotics; Inability to follow or tolerate an outpatient oral regimen; Severe illness, nausea and vomiting, or high fever; Presence of TOA. Women with TOA should have direct inpatient observation for 24 hours because of risk of abscess rupture and sepsis. In acute PID: IV cefotetan or IV cefoxitin plus oral or IV doxycycline IV clindamycin plus IV gentamicin, Alternative: ampicillin/sulbactam plus doxycycline [8]. These regimens provide broad coverage for not only N. gonorrhoeae, C. trichomatis, and M. genitalium, but also for streptococcus, Gram-negative enteric bacteria (E. coli, Klebsiella spp., and Proteus spp.), and bacteria vaginosisassociated anaerobic organisms [8]. The cephalosporin based regimen is preferred because of improved tolerability. In the case of a severe penicillin allergy, clindamycin plus gentamicin is recommended. For the treatment of TOA, when comparing the first-line parenteral antibiotic regimens, none of the regimens have been shown to be superior [9]. Amnioglycosides have reduced activity in acidic, anaerobic environments with purulent debris. For the treatment of TOA, an extended-spectrum cephalosporin for the coverage of Gram-negative organisms (rather than an aminoglycoside) combined with clindamycin or metronidazole is a good option. Guidelines for the treatment of intraabdominal infections have recommended that when resistance for a specific antibiotic exceeds >10% to 20% of all isolates, then a change in the recommended antibiotic should occur. For this reason, ampicillin-sulbactam is no longer recommended for treatment of community-acquired intra-abdominal infections because of significant increased resistance in E. coli [9]. Antibiotic therapy can be switched from parenteral to oral route of administration after 24 hours of clinical improvement, resolution of nausea and vomiting and severe pain. Patients should complete an entire 14-day course of antibiotics with oral doxycycline. When a TOA is present or when the illness was preceded by gynecologic procedure greater anaerobic coverage is required, thus we recommend the addition of clindamycin or metronidazole to doxycycline. We prefer to use metronidazole because of the increased risk of Clostridium difficile colitis with clindamycin. Intrauterine Contraceptive Device (IUCD) In Situ When PID occurs with an IUCD in place removal of the IUCD is not required [10]. When the IUCD is removed, it should not be replaced until 3 months after the PID has resolved. Surgical Management and Drainage of TOAs In general, the decision to combine antimicrobial therapy with drainage or surgical excision of the TOA depends on the status of the patient and the size of the abscess. Signs of sepsis, such as hypotension, tachycardia, and tachypnea, and an acute abdomen are indicative of rupture, and such patients should immediately proceed to the operating room for surgical exploration. TOAs usually present without evidence of rupture and in these cases the role for drainage or operative management of TOA is less clear.