Updated: Feb 29, 2008
Patients who come to the ED after sexual assault present several challenges to the physician.
The patient may be ashamed and unwilling to give a clear history of the assault, at precisely the time when such history is critical for timely treatment and forensic documentation. The need for both treatment and evidence collection means that clinicians find themselves simultaneously advocates for the patient and assistants to state and local law enforcement.
It is vital to both the health of the patient and the well-being of society that the ED physician know how to proceed in such cases.
Sexual assaults are distinguished from other assaults by forcible, inappropriate sexual behavior. Sexual assault is an act of violence, not of sexual gratification. Sex is the weapon; it is a means, not the end.
A myriad of different psychological classifications have been proposed to characterize the sexual assailant, but the psychodynamics involved in all such schema involve feelings of inadequacy, unchanneled rage (eg, impulse control disorders), or other aberrant character disorders.
The National Crime Victimization Survey for 2006 reported more than 272,350 sexual assaults — "rape, attempted rape or sexual assaults" — in the United States. It is certain that many more assaults occur than are reported due to postassault stress and misplaced shame levied against the victim. Current best estimates indicate that 1 in 6 women and 1 in 33 men will be the victim of a sexual assault at least once in their lifetime.
In the course of a sexual assault, any injury may be inflicted on the victim, up to and including life-threatening multiorgan system trauma.
Sexual assault victims come from all socioeconomic and racial groups.
Most sexual assaults involve women. However, men may also present to EDs as victims of sexual assault. Societal attitudes and myths about male victims of sexual assault discourage them from coming forward; it is altogether likely that such assaults are even more underreported than female victim assaults.
All ages are potential victims of sexual assault, from toddlers to elderly individuals.
| Abdominal Trauma, Blunt | Cervical Strain |
| Abdominal Trauma, Penetrating | Chancroid |
| Abruptio Placentae | Compartment Syndrome, Extremity |
| Acute Coronary Syndrome | Corneal Abrasion |
| Alcohol and Substance Abuse Evaluation | Corneal Laceration |
| Ankle Injury, Soft Tissue | Costochondritis |
| Anxiety | Depression and Suicide |
| Asthma | Diaphragmatic Injuries |
| Back Pain, Mechanical | Dislocations, Ankle |
| Bartholin Gland Diseases | Dislocations, Elbow |
| Bites, Human | Dislocations, Foot |
| Burns, Thermal | Dislocations, Hand |
| Candidiasis | Dislocations, Hip |
| Cellulitis | Dislocations, Interphalangeal |
The above list, protean in its extent, reflects the overwhelming number of co-injuries that can occur during sexual assault, as well as the potential sequelae of such assaults.
If EMS is involved in transporting the patient, their primary focus should be on stabilization of life-threatening injuries and providing emotional support for the victim. Evidence collection and crisis intervention should be handled by the ED team.
The responsibilities of the ED physician are more complex than in routine patients. The examiner must provide psychological support and referral to the appropriate resources, treat physical injuries, collect legal evidence, document pertinent history, perform a thorough head-to-toe physical examination, give prevention of unwanted pregnancy, and provide prevention of and screening for STDs.
Medical intervention in sexual assault is focused on prevention of unwanted pregnancy and STDs. The recommendations below follow the most recent CDC guidelines, dated August 2006.
Empiric antimicrobial therapy must be comprehensive and should cover all likely pathogens in the context of the clinical setting.
Current DOC for prophylaxis against gonorrheal infection. Third-generation cephalosporin with broad-spectrum, gram-negative activity; lower efficacy against gram-positive organisms; higher efficacy against resistant organisms. Bactericidal activity results from inhibiting cell wall synthesis by binding to 1 or more penicillin-binding proteins. Exerts antimicrobial effect by interfering with synthesis of peptidoglycan, a major structural component of the bacterial cell wall. Bacteria eventually lyse because of the ongoing activity of cell wall autolytic enzymes while cell wall assembly is arrested.
Highly stable in presence of beta-lactamases and both penicillinase and cephalosporinase of gram-negative and gram-positive bacteria. Approximately 33-67% of dose is excreted unchanged in urine and remainder is secreted in bile and ultimately in feces as microbiologically inactive compounds. Reversibly binds to human plasma proteins and bindings have been reported to decrease from 95% bound at plasma concentrations <25 mcg/mL to 85% bound at 300 mcg/mL.
125 mg IM once
25-50 mg/kg IM as single dose (maximum 125 mg)
Probenecid may increase levels; coadministration with ethacrynic acid, furosemide, and aminoglycosides may increase nephrotoxicity
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Adjust dose in severe renal insufficiency (high doses may cause CNS toxicity); superinfections and promotion of nonsusceptible organisms may occur with prolonged use or repeated therapy; caution in breastfeeding women
Former DOC for broad-spectrum prophylaxis of gonorrhea and syphilis. Inhibits bacterial cell wall synthesis, and the bacteria eventually lyse because of ongoing activity of cell wall autolytic enzymes while cell wall assembly is arrested. No longer readily available; hence, no longer CDC recommended. FDA has approved Lupin Ltd to renew production, but they have yet to do so.
400 mg PO once
Administer as in adults
Coadministration of aminoglycosides increase nephrotoxicity; probenecid may increase effects of cefixime
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Adjust dose with renal impairment
Active against various anaerobic bacteria and protozoa. Appears to be absorbed into cells. Intermediate-metabolized compounds formed bind DNA and inhibit protein synthesis, causing cell death.
2 g PO once
40 mg/kg PO once
May increase toxicity of anticoagulants, lithium, and phenytoin; cimetidine may increase toxicity of metronidazole; disulfiram reaction may occur with orally ingested ethanol
Documented hypersensitivity
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Adjust dose in hepatic disease; monitor for seizures and development of peripheral neuropathy
Treats mild to moderate infections caused by susceptible strains of microorganisms. Indicated for prophylaxis of chlamydial infections of the genital tract.
1 g PO once
5-12 mg/kg/d PO for 15 d
May increase toxicity of theophylline, warfarin, and digoxin; effects are reduced with coadministration of aluminum and/or magnesium antacids; nephrotoxicity and neurotoxicity may occur when coadministered with cyclosporine
Documented hypersensitivity; hepatic impairment; do not administer with pimozide
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Site reactions can occur with IV route; bacterial or fungal overgrowth may result with prolonged antibiotic use; may increase hepatic enzymes and cholestatic jaundice; caution in patients with impaired hepatic function, prolonged QT intervals, or pneumonia; caution in hospitalized, geriatric, or debilitated patients
Alternate to azithromycin in STD prophylaxis regimens. Broad-spectrum, synthetically derived bacteriostatic antibiotic in the tetracycline class. Almost completely absorbed, concentrates in bile, and is excreted in urine and feces as a biologically active metabolite in high concentrations.
Inhibits protein synthesis and, thus, bacterial growth by binding to 30S and possibly 50S ribosomal subunits of susceptible bacteria. May block dissociation of peptidyl tRNA from ribosomes, causing RNA-dependent protein synthesis to arrest.
100 mg PO bid for 7 d
<8 years: Not recommended
>8 years: Administer as in adults
Bioavailability decreases with antacids containing aluminum, calcium, magnesium, iron, or bismuth subsalicylate; tetracyclines can increase hypoprothrombinemic effects of anticoagulants; tetracyclines can decrease effects of oral contraceptives, causing breakthrough bleeding and increased risk of pregnancy
Documented hypersensitivity; severe hepatic dysfunction
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
Photosensitivity may occur with prolonged exposure to sunlight or tanning equipment; reduce dose in renal impairment; consider drug serum level determinations in prolonged therapy; tetracycline use during tooth development (last one half of pregnancy through age 8 y) can cause permanent discoloration of teeth; Fanconilike syndrome may occur with outdated tetracyclines
These agents are used to prevent unwanted pregnancies after sexual assault.
Inhibits ovulation by suppressing FSH and LH. Alterations that take place in the genital tract, including cervical mucus and the endometrium, may contribute to the effects of contraceptives.
2 tab PO in ED, then 2 tab PO 12 h after first dose
Administer as in adults
Onset of acetaminophen effect may be delayed or decreased slightly; hepatic metabolism of TCAs, caffeine, corticosteroids, benzodiazepines, beta-blockers, and theophylline may be decreased with increased therapeutic effects
Documented hypersensitivity; thrombophlebitis; known or suspected breast carcinoma or estrogen-dependent neoplasia; thromboembolic disorders; myocardial infarction; coronary artery disease; carcinoma of the endometrium; other hepatic adenomas/carcinomas
X - Contraindicated; benefit does not outweigh risk
Caution in hepatic impairment, migraine, seizure disorders, cerebrovascular disorders, breast cancer, or thromboembolic disease; progestins may elevate LDL levels and decrease HDL levels, making hyperlipidemia control more difficult; depression may occur, attributed to a deficiency in pyridoxine; caution in patients with conditions that may be aggravated by fluid retention
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da Silva DA, Goes AC, de Carvalho JJ, de Carvalho EF. DNA typing from vaginal smear slides in suspected rape cases. Sao Paulo Med J. Mar 4 2004;122(2):70-2. [Medline].
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Sachs CJ. How To Convict A Rapist: Sexual Assault Response Teams. ACEP Scientific Assembly Proceedings. 1999.
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sexual assault, domestic violence, rape, impulse control disorders, post-assault emotional stress, posttraumatic stress disorder, post-traumatic stress disorder, PTSD, pregnancy, sexually transmitted diseases, STDs, male victims of sexual assault, female victims of sexual assault, Sexual Assault Nurse Examiner, SANE, Trichomonas vaginalis, T vaginalis
William Ernoehazy Jr, MD, FACEP, Medical Director, Emergency Department, Ed Fraser Memorial Hospital, Florida
William Ernoehazy Jr, MD, FACEP is a member of the following medical societies: American College of Emergency Physicians
Disclosure: Nothing to disclose.
Heather Murphy-Lavoie, MD, FAAEM, Assistant Professor, Section of Emergency Medicine and Hyperbaric Medicine, Louisiana State University School of Medicine, New Orleans; Clinical Instructor, Department of Surgery, Tulane University School of Medicine
Heather Murphy-Lavoie, MD, FAAEM is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, American Medical Association, and Undersea and Hyperbaric Medical Society
Disclosure: Nothing to disclose.
Francis Counselman, MD, Program Director, Chair, Professor, Department of Emergency Medicine, Eastern Virginia Medical School
Francis Counselman, MD is a member of the following medical societies: American College of Emergency Physicians and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.
Robert C Harwood, MD, MPH, Program Director, Chair, Department of Emergency Medicine, Christ Hospital and Medical Center; Assistant Professor, Department of Emergency Medicine, University of Illinois at Chicago Medical School
Robert C Harwood, MD, MPH is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, American Medical Association, Council of Emergency Medicine Residency Directors, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center
John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.
Pamela L Dyne, MD, Associate Professor, Program Director, Department of Medicine, Division of Emergency Medicine, University of California at Los Angeles School of Medicine
Pamela L Dyne, MD is a member of the following medical societies: American College of Emergency Physicians and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.