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A more recent article on acute pelvic pain in women is available.

Am Fam Physician. 2016;93(1):41-48A

Patient information: See related handout on acute pelvic pain in women.

Author disclosure: No relevant financial affiliations.

Acute pelvic pain is defined as lower abdominal or pelvic pain of less than three months' duration. It is a common presentation in primary care. Evaluation can be challenging because of a broad differential diagnosis and because many associated signs and symptoms are nonspecific. The most common diagnoses in reproductive-aged women with acute pelvic pain are idiopathic pelvic pain, pelvic inflammatory disease, acute appendicitis, ovarian cysts, ectopic pregnancy, and endometriosis. Among postmenopausal women, cancer must be considered. Findings from the history and physical examination can point to likely diagnoses, and laboratory testing and imaging can help confirm. Women of reproductive age should take a pregnancy test. In early pregnancy, transvaginal ultrasonography and beta human chorionic gonadotropin levels can help identify ectopic pregnancy and spontaneous abortion. For nonpregnant women, ultrasonography or computed tomography is indicated, depending on the possible diagnosis (e.g., ultrasonography is preferred when ovarian pathology is suspected). If ultrasonography results are nondiagnostic, magnetic resonance imaging can be helpful in pregnant women when acute appendicitis is suspected. If magnetic resonance imaging is unavailable, computed tomography may be indicated.

Acute pelvic pain is often defined as lower abdominal or pelvic pain lasting less than three months.1 Although most patients with acute pelvic pain are diagnosed with one of a few common conditions, the differential diagnosis is broad. Many case studies describe acute pelvic pain caused by conditions that are uncommon but clinically important.

WHAT IS NEW ON THIS TOPIC: ACUTE PELVIC PAIN

C-reactive protein measurement is not recommended in the routine evaluation of acute pelvic pain because of a high false-negative rate for acute conditions.

If computed tomography has already been performed and is unrevealing, follow-up transvaginal ultrasonography is unlikely to provide additional useful information.

Clinical recommendationsEvidence ratingReferences
When patients have adnexal tenderness with cervical motion tenderness, pelvic inflammatory disease should be considered as a likely diagnosis.C13
A normal transvaginal ultrasonography with Doppler flow study does not necessarily rule out ovarian torsion. Although it has a high positive predictive value for detecting ovarian torsion, it also has a high false-negative rate.C26
Transvaginal ultrasonography should be the initial imaging test in pregnant women presenting with acute pelvic pain.C31
If transvaginal ultrasonography is nondiagnostic in pregnant patients and additional imaging is required, magnetic resonance imaging should be used instead of computed tomography.C3234

Acute pelvic pain is a common presentation in primary care. Although well-designed studies on the prevalence of pelvic pain are lacking, one study estimated that up to 39% of reproductive-aged women who presented to their primary care physician had symptoms related to pelvic pain, and one in seven women has acute or chronic pelvic pain at some point.2,3 The consequence of a missed diagnosis can be serious. For example, delay in diagnosis of an ectopic pregnancy can result in rupture and life-threatening hemorrhage. Untreated sexually transmitted infections and pelvic inflammatory disease (PID) can lead to long-term sequelae, such as infertility and chronic pain.

The workup of acute pelvic pain in the office setting can be challenging. This article provides an evidence-based framework to narrow the differential diagnosis while assuring that serious conditions are not missed.

How Do Physicians Narrow the Differential Diagnosis to Focus on Important Common Conditions?

Physicians should first categorize the patient according to age (e.g., is she in her reproductive years or postmenopausal?). If the patient is of reproductive age, possible diagnoses are next categorized by whether she is pregnant or attempting pregnancy.

NONPREGNANT REPRODUCTIVE-AGED WOMEN

The typical diagnoses made in nonpregnant reproductive-aged women who present with acute pelvic pain include the following (from most to least common): idiopathic pelvic pain, PID, acute appendicitis, conditions related to ovarian cysts, and endometriosis.4,5 Other less common causes of acute pelvic pain in this population are listed in Table 1.69

Patient categoryCommon diagnosesLess common diagnosesRare diagnoses
Reproductive age (not pregnant)Endometriosis (ruptured endometrioma)AdenomyosisEndosalpingiosis
Idiopathic (no cause identified)DysmenorrheaRound ligament mass (lipoma, teratoma)
Ovarian cyst, rupturedEndometritis (postprocedure)Transverse vaginal septum
Ovarian torsionImperforate hymen
PID, tubo-ovarian abscessIntrauterine device perforation
Leiomyoma (degenerating)
Mittelschmerz
Reproductive age (pregnancy related)Corpus luteum cystLeiomyoma (degenerating)Incarcerated gravid uterus
Ectopic pregnancyPubic symphysis separationOvarian vein thrombosis
Endometritis (postpartum)Subchorionic hemorrhagePID (rare after first trimester)
Normal laborUterine rupture
Ovarian torsion
PID (first trimester)
Placental abruption
Preterm labor
Spontaneous abortion
Reproductive age (undergoing fertility treatment)Ectopic pregnancyHeterotopic pregnancy
Ovarian follicular cyst
Ovarian hyperstimulation syndrome
Ovarian torsion
PostmenopausalMalignancyIschemic colitisEndometriosis
PID, tubo-ovarian abscess
Retained intrauterine device
All groupsAppendicitisBowel obstructionMesenteric adenitis
DiverticulitisInguinal hernia
Inflammatory bowel diseaseInterstitial cystitis
Irritable bowel syndromePelvic adhesive disease (postoperative scarring)
Musculoskeletal (abdominal wall) painPerirectal abscess
Urinary tract infectionUrethral diverticulum
UrolithiasisUrinary retention

REPRODUCTIVE-AGED WOMEN WHO ARE PREGNANT OR ATTEMPTING PREGNANCY

Women who are pregnant or attempting pregnancy through fertility treatments have other common causes of acute pelvic pain (Table 169 ). For pregnant women, the clinical scenario narrows the list of possible causes, but it is critical to detect serious or life-threatening conditions, such as ectopic pregnancy in the early weeks of pregnancy and placental abruption in the later stages of pregnancy. Nongynecologic conditions, such as appendicitis, can also occur during pregnancy.

Women undergoing infertility treatments through ovarian stimulation or in vitro fertilization have unique risks, such as ovarian hyperstimulation syndrome (i.e., ovarian enlargement with multiple ovarian cysts and leakage of fluid from the ovary into the abdominal/pelvic space), ovarian torsion, and heterotopic pregnancy (i.e., simultaneous ectopic and intrauterine pregnancy).6

POSTMENOPAUSAL WOMEN

Cancer must be primarily considered in a postmenopausal woman with acute pelvic pain. Other rare causes are postmenopausal endometriosis10 and, on occasion, a retained intrauterine device that the patient had forgotten to remove.11

Which History and Physical Examination Findings Are Most Helpful in Evaluating Acute Pelvic Pain?

HISTORY

Several findings in the patient's history can help guide laboratory testing and imaging to confirm a suspected diagnosis (Table 26,7,9 ). Relevant historical features include whether the patient is sexually active (e.g., pain related to a complication of pregnancy), specific symptoms (e.g., description of the pain; changes in menstrual pattern; the presence of vaginal discharge, dysuria, hematuria, or nausea), and whether she has had intra-uterine instrumentation or pelvic surgery. A recent study reported rare occurrences of PID in women who denied ever having sexual intercourse, illustrating the need for a high index of suspicion for this condition.12

FindingSuggested diagnosesFurther diagnostic considerations
History of intrauterine instrumentation, multiple cesarean deliveries, or other uterine surgeriesAdenomyosis (endometrial tissue grown into the uterine wall)Magnetic resonance imaging
Pelvic adhesionsConsider nonurgent referral to gynecologist or general surgeon in absence of other findings
Menstrual abnormalities
AmenorrheaImperforate hymenPelvic examination
Transverse vaginal septumPelvic ultrasonography
DysmenorrheaEndometriosis, ovarian cystPelvic ultrasonography (to assess for ovarian cyst)
Nausea and vomitingAppendicitis, ovarian torsionIf appendicitis is more likely: proceed with contrast CT
If ovarian torsion is more likely: proceed with pelvic ultrasonography with Doppler flow study
Early urgent referral for surgical evaluation and treatment is recommended
Pain symptoms
Bilateral pain, particularly if associated with mucopurulent vaginal dischargePelvic inflammatory diseaseTesting for sexually transmitted infections
Complete blood count to test for leukocytosis or left shift
Dull, unilateral adnexal pain that is constant or intermittentOvarian torsionPresence of risk factors (nausea, vomiting, pregnancy)
Pelvic ultrasonography with Doppler flow study
Consider urgent referral for surgical evaluation and treatment
Right lower quadrant painAcute appendicitisComplete blood count demonstrating leukocytosis
Contrast CT of the abdomen and pelvis
Ectopic pregnancyQualitative urine β-hCG can detect a pregnancy at four weeks' gestation
Quantitative serum β-hCG can determine if pregnancy is above the discriminatory level such that an intrauterine pregnancy should be visible on pelvic ultrasonography to rule out ectopic gestation (Figure 2)
Blood type to determine Rh status; if bleeding and pregnant, will need Rho(D) immune globulin (RhoGam)
Pelvic ultrasonography
Ovarian torsionPelvic ultrasonography with Doppler flow study
Sexually active; pregnancy possibleEctopic pregnancy, spontaneous abortionQualitative urine β-hCG can detect a pregnancy at four weeks' gestation
Quantitative serum β-hCG can determine if pregnancy is above the discriminatory level such that an intrauterine pregnancy should be visible on pelvic ultrasonography to rule out ectopic gestation (Figure 2)
Blood type to determine Rh status; if bleeding and pregnant, will need Rho(D) immune globulin
Pelvic ultrasonography
Urinary symptoms
DysuriaUrinary tract infectionUrinalysis demonstrating white blood cells, bacteria, leukocyte esterase, or nitrites
Gross hematuriaUrolithiasisAbdominal ultrasonography

PHYSICAL EXAMINATION

The physical examination should focus on vital signs, abdominal examination, bimanual pelvic examination, and speculum examination (Table 36,7,9 and eTable A). Hypotension, tachycardia, or evidence of guarding or rebound on abdominal examination could indicate a surgical emergency (e.g., ruptured ectopic pregnancy, ovarian torsion, ruptured appendix) and should prompt immediate referral.

FindingSuggested diagnosesFurther diagnostic considerations
Carnett sign (increased pain to palpation when the abdominal wall musculature is voluntarily contracted)Musculoskeletal (abdominal wall) painNo further testing needed in the absence of other historical or physical examination findings that might suggest intrapelvic or intra-abdominal conditions
Cervical motion tendernessPelvic inflammatory diseaseConsider testing for sexually transmitted infections
FeverAppendicitisUltrasonography or contrast CT of the abdomen and pelvis
Complete blood count demonstrating leukocytosis
Pelvic inflammatory diseaseConsider testing for sexually transmitted infections
PyelonephritisUrinalysis demonstrating evidence of urinary tract infection (white blood cells, bacteria, leukocyte esterase, or nitrites)
Complete blood count demonstrating leukocytosis, left shift
Tubo-ovarian abscessPelvic ultrasonography
Complete blood count demonstrating leukocytosis, left shift
Pelvic massEctopic pregnancySee Table 2
Fibroid uterusPelvic ultrasonography
Ovarian cancerPelvic ultrasonography
Consider CT of the chest, abdomen, and pelvis if metastatic disease is suspected
Ovarian cystPelvic ultrasonography
Tubo-ovarian abscessPelvic ultrasonography
Rovsing sign (palpation in the left lower quadrant causes pain in the right lower quadrant)AppendicitisContrast CT of the abdomen and pelvis
Complete blood count demonstrating leukocytosis
Tachycardia, hypotensionRuptured ectopic pregnancyConsider urgent referral to facility with immediate surgical
Ruptured hemorrhagic cyst capability
Posttest probability* (5% pretest probability)Posttest probability* (25% pretest probability)

FindingLR+LR−Finding presentFinding absentFinding presentFinding absent
Pelvic inflammatory disease
Purulent endocervical discharge3.30.81545221
Abdominal rebound tenderness2.50.81244521
Fever1.30.8643021
Leukocyte count > 10,500 per mm3 (10.50 × 109 per L)1.30.9653023
Erythrocyte sedimentation rate > 15 mm per hour1.20.6632917
Cervical motion tenderness1.10.9552723
Pelvic organ tenderness1.01.0552525
Ectopic pregnancy
Finding of any noncystic, extraovarian adnexal mass on ultrasonography27.00.01590900
β-hCG < 1,000 mIU per mL (1,000 IU per L)§3.60.71645519
Indeterminate ultrasonography and β-hCG < 1,000 mIU per mL§2.60.41224612
Appendicitis
Right lower quadrant abdominal pain8.40.2311746
Pain migration from periumbilical area to the right lower quadrant of the abdomen3.60.41625413
Fever3.20.41425112
Psoas sign3.20.91445223
Rebound tenderness2.00.51034015
Rigidity1.60.9953823

If vital signs are unremarkable and there is no evidence of an acute abdomen, vaginal and pelvic examinations are the next steps. A mucopurulent cervical discharge, especially if accompanied by fever and leukocytosis, is suggestive of PID. When cervical discharge is combined with diffuse tenderness (cervical motion tenderness and bilateral adnexal tenderness) on pelvic examination, the likelihood of PID increases. However, cervical motion tenderness alone is not specific to PID; it is present in 25% of cases of appendicitis and 50% of ectopic pregnancies.13,14

When tenderness is unilateral or an adnexal mass is palpated, the cause of pain is more likely to be a localized process, such as an ovarian cyst, ovarian torsion, or ectopic pregnancy. However, pelvic examination has a sensitivity of only 15% to 36% for detecting adnexal masses,15 so the absence of a palpable mass should not preclude consideration of these conditions.

Appendicitis often presents with right lower quadrant pain over McBurney point with nausea, vomiting, and occasionally fever. Rovsing sign, which is less well known, involves palpation in the left lower quadrant that causes pain in the right lower quadrant. Although not specific, it has a sensitivity of greater than 90% for appendicitis.16 Right lower quadrant tenderness with digital rectal examination was shown to be only 49% sensitive and 61% specific for appendicitis, and thus may only add to patient discomfort without providing useful information.17

Finally, musculoskeletal pain often causes pelvic pain and can mimic visceral pelvic pain. This is usually a diagnosis of exclusion after ruling out intrapelvic and intra-abdominal causes. Carnett sign, which is the presence of increased pain on palpation of the lower abdominal wall when the abdominal wall musculature is voluntarily contracted, can indicate a musculoskeletal cause. Although first proposed in 1926, a more recent study validated use of the Carnett sign and found a sensitivity and specificity of 78% and 88%, respectively, for identifying pain originating in the abdominal wall.18,19

An algorithm for using physical examination findings to evaluate selected common causes of pelvic pain in nonpregnant women is shown in Figure 1.20

What Are the Roles of Laboratory Tests and Imaging Studies in Evaluating Acute Pelvic Pain?

Laboratory tests and imaging studies are largely guided by history and physical examination findings to identify possible causes of pelvic pain (Tables 26,7,9 and 36,7,9 ).

LABORATORY TESTS

A qualitative pregnancy test should be performed in all women of reproductive age to determine if pregnancy-related conditions are causing pelvic pain. Other commonly performed initial laboratory tests include a complete blood count, urinalysis, and nucleic acid amplification testing for gonococcal and chlamydial cervicitis.

C-reactive protein is a possible marker to discriminate acute processes requiring urgent intervention from chronic conditions. A recent study, however, demonstrated that C-reactive protein measurement has a high false-negative rate for detecting acute conditions21; therefore, it is not recommended in the routine evaluation of acute pelvic pain.

IMAGING

Although plain radiography of the abdomen and pelvis is widely available, it lacks sensitivity and diagnostic accuracy compared with other modalities (e.g., ultrasonography, computed tomography [CT]) in the evaluation of acute pelvic pain.22 For this reason, plain radiography is not indicated in the routine workup of acute pelvic pain.

Pelvic ultrasonography, consisting of transabdominal combined with transvaginal ultrasonography, is usually the imaging modality of choice because of a lack of radiation exposure and high sensitivity.23 It should be performed in most cases and is the initial imaging modality of choice in children.24,25 When ovarian torsion is suspected, Doppler venous flow studies should be part of the ultrasonography examination. Absent venous flow to the ovary has a 94% positive predictive value for ovarian torsion.7 However, transvaginal ultrasonography with Doppler flow studies also has a high false-negative rate for ovarian torsion because of the dual blood supply from the ovarian artery and the utero-ovarian vessels. Flow can be demonstrated even when torsion is present. Therefore, if the Doppler study result is negative, ovarian torsion should still be considered if the patient has peritoneal signs and risk factors for torsion, such as nausea and vomiting, an adnexal mass greater than 5 cm, or pregnancy.26,27

Ultrasonography can be useful even when pain may have a nongynecologic cause. In one series of 500 cases, abdominal ultrasonography demonstrated a 76% sensitivity and 90% specificity for diagnosing appendicitis.28 A more recent study demonstrated higher sensitivity and specificity of 94% and 84%, respectively, albeit with a smaller study population.29 Currently, however, if acute appendicitis is suspected over gynecologic conditions (e.g., a nonpregnant woman with isolated right lower quadrant pain and nausea), or if ultrasonography does not clearly show a normal appendix, CT is still considered more accurate, with a sensitivity of 94% to 97% and specificity up to 100%.28,30 CT use has led to a decrease in laparotomies performed for suspected appendicitis in which the final pathology was negative for acute appendicitis. CT is also appropriate to evaluate acute pelvic pain if ultrasonography is not readily available.

What Is the Imaging Test of Choice for Pregnant Women with Acute Pelvic Pain?

In early pregnancy, the most important consideration is to identify the location of the gestation to exclude ectopic pregnancy. Transvaginal ultrasonography is the imaging modality of choice, but results must be correlated with beta human chorionic gonadotropin (β-hCG) levels and, in particular, the discriminatory level (the β-hCG level at which the gestation should be visible on ultrasonography).31 Figure 2 provides an algorithm for the evaluation and follow-up of patients with a positive β-hCG level and pelvic pain.20

In early pregnancy, if the β-hCG level is below the discriminatory level and an intrauterine gestation is not visible, the patient must have follow-up evaluations until ectopic pregnancy or a viable pregnancy is confirmed. If the β-hCG level is above the discriminatory level and the intrauterine gestational sac and yolk sac are not visible on ultrasonography, the pregnancy is likely ectopic and gynecologic consultation should be obtained.

If the diagnosis is still uncertain in the absence of ectopic pregnancy or spontaneous abortion, magnetic resonance imaging (MRI) can be used to further evaluate pelvic and abdominal structures.32 MRI provides high-quality images to assess the placenta and exclude abruption, and it has sensitivities and specificities close to 100% for acute appendicitis.33,34 MRI is also useful for detecting conditions such as inflammatory bowel disease, nephrolithiasis, adnexal masses, ovarian hemorrhagic cysts, and large uterine fibroids.

CT may be the only imaging option if MRI is unavailable, if ultrasonography is unavailable or inconclusive, and if the patient's condition requires imaging for diagnosis. The fetal exposure from a single pelvic CT is estimated to be 1.5 rad, or less if low-exposure techniques are used. This level of exposure is thought to increase the lifetime risk of leukemia in the exposed fetus by a factor of 1.5 to 2. The baseline lifetime incidence of childhood leukemia is low (one in 3,000), so a single CT increases the risk to only 1.5 to 2 per 3,000.35,36 Thus, in appropriate clinical scenarios, the benefit of diagnostic CT may outweigh the risk.

Is Additional Imaging Helpful if CT Results Are Inconclusive?

From a technical standpoint, transvaginal ultrasonography is superior for obtaining images of contrasting pelvic soft tissue, especially fluid-filled structures, and can reliably assess for adnexal masses, cysts, uterine fibroids, and the size and location of ovaries and luminal structures. It can also identify pelvic fluid or blood extravasation and provide Doppler flow studies.

If CT has already been performed and is unrevealing, follow-up ultrasonography is not likely to provide additional useful information. One small study showed that follow-up transvaginal ultrasonography did not provide information that changed the working diagnosis.8 In such cases, discussions with the radiologist can determine whether additional imaging studies may be helpful.

Data Sources: A PubMed search was performed using the terms acute and pelvic pain, differential diagnosis, and MeSH terms: diagnosis, differential, acute disease, genital diseases, female/diagnosis, pelvic girdle pain, and pelvic pain. Stat!Ref, Books@Ovid, and Clinical Key were searched using keywords pelvic pain, and age. Also searched was Essential Evidence Plus. Search dates: October and December 2014, and April and September 2015.

The opinions and assertions contained herein are the private views of the authors and are not to be construed as official or as reflecting the views of the U.S. Army Medical Department or the U.S. Army at large.

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