eMedicine Specialties > Emergency Medicine > Gastrointestinal

Perirectal Abscess: Treatment & Medication

Author: Drew Evan Fenton, MD, Hospitalist, Our Health Care Consultants
Contributor Information and Disclosures

Updated: Nov 20, 2009

Treatment

Emergency Department Care

Recognition of a perirectal abscess is the primary ED goal. Determination of the exact anatomic space or spaces involved is best left to the surgical consultant.

The isolated perianal abscess that is not associated with deeper, perirectal abscesses is the only type of anorectal abscess that can be adequately treated in an ED setting and is very rare.

Perirectal abscess must be treated in the operating suite, where optimal anesthesia can be achieved and the abscess and any fistula or other complication may be treated definitively. The "point" of a deep abscess must not be mistaken for a superficial perianal abscess. Inadequate ED debridement of a perirectal abscess may result in increased morbidity and even mortality. ED debridement of perirectal abscesses should not be performed. Because the ED lacks adequate anesthesia, ED treatment of perirectal abscesses is inhumane.

A simple (and, by definition, superficial) perianal abscess may be incised and drained in the ED. Adequate analgesia should be obtained by using the steps discussed in Procedures. Conscious sedation may be considered for pain control and to make the procedure as humane as possible. The patient may be discharged home after appropriate wound care with instructions for Sitz baths and routine follow-up care.

Superficial perianal abscesses are uncommon; thus, the provider should err on the side of assuming a deeper process exists if the diagnosis is in doubt.

  • As an example, optimal treatment of ischiorectal abscesses is incision and drainage often followed by fistulotomy under general anesthesia in the operating suite.  
    • The performance of an extensive and complete surgical procedure by a consultant with accurate anatomical knowledge of the region is imperative to avoid serious complications. Such treatment results in a lower recurrence rate.
    • The need for the routine use of antibiotics has not been established. Intravenous antibiotics may be used as preventive or therapeutic measures in patients who are immunocompromised, in those who appear septic, or in those who have heart valve abnormalities or prostheses.
    • Ascertain tetanus immunity. When acceptable immunity cannot be established, follow the currently recommended guidelines for high-risk wounds.
  • The goal in treating any abscess is to make an incision to surgically release pus and to remove any dead tissue, and then to keep the surgical incision open by the use of a drain, either (1) a Penrose drain, which may be sutured to the incisional margin and later removed, or (2) iodoform gauze stripping. In the case of perianal abscess, the procedure involves sterile preparation, adequate analgesia, incision and drainage often facilitated by irrigation of the abscess cavity, blunt disruption of any loculations (a gloved fingertip is ideal for this), debridement of any accessible necrotic tissue, and placement of a drain.
    • Do not pack the abscess full of iodoform gauze. The intent is to keep the surgical incision open so that pus and other material can drain. If iodoform gauze stripping is used, using a limited amount of gauze is important, that is, just enough to keep the wound open. Packing the wound full of iodoform gauze does not improve the outcome, and, in fact, it may worsen the prognosis by creating a large foreign body that may become a nidus of infection. This nidus could perpetuate the infection and cause the abscess to enlarge, spread to other areas, erode into vessels or into the peritoneal cavity, and, occasionally, it could cause sepsis and death.
    • In one pediatric case, an incision and drainage (I&D) and packing was performed on a large perirectal abscess in the ED. This packing was left in the wound for days. Shortly thereafter, sepsis and seeding of the myocardium developed with a resultant myocardial abscess. This myocardial abscess eventually ruptured into the pericardial sac, causing tamponade and sudden death.

Consultations

  • When the diagnosis of perirectal abscess is made or is being entertained, expeditious consultation with a surgeon is mandatory.
    • Timely and appropriate operative treatment prevents more serious complications such as extension of the abscess or serious systemic infection.
    • The appropriate surgical treatment of perirectal abscess is complex and painful and therefore should not be undertaken in the ED. General or spinal anesthesia is necessary to obtain the appropriate anesthetic result.
    • A newer technique includes endoscopic ultrasonographic-guided drainage of deep pelvic abscesses with stent placement for drainage of pus. In one study, this technique successfully treated most patients who underwent this treatment, requiring no further intervention. 

Medication

Antibiotics are unnecessary in otherwise healthy individuals. The practitioner should provide appropriate empiric intravenous antibiotic coverage for patients who are elderly or immunosuppressed, patients who have comorbidities, patients with a heart valve abnormality or prosthetic valve likely to benefit from antibiotic prophylaxis, or those in whom infection has become systemic. Predisposing or comorbid factors may guide empiric antibiotic selection.

Analgesia is necessary for pain control and may be given orally or via an intravenous route, in conjunction with anesthetics if needle aspiration or I&D of an abscess is performed.

Anxiolytics may help certain patients who are apprehensive about needle aspiration, I&D, imaging studies, or surgery.

Antibiotics

Appropriate antibiotic coverage should be given intravenously preoperatively and postoperatively, either based on Gram stain or an empiric basis, as a preventive measure, for elderly patients, patients with immunosuppression, patients with heart valve abnormality or prosthesis, and those with comorbid states.


Ampicillin and sulbactam (Unasyn)

Drug combination of beta-lactamase inhibitor with ampicillin. Interferes with bacterial cell wall synthesis during active replication, causing bactericidal activity against susceptible organisms. Alternative to amoxicillin when unable to take medication PO.
Covers skin, enteric flora, and anaerobes. Not ideal for nosocomial pathogens.

Adult

1.5 (1 g ampicillin + 0.5 g sulbactam) to 3 g (2 g ampicillin + 1 g sulbactam) IV/IM q6-8h; not to exceed 4 g/d sulbactam or 8 g/d ampicillin

Pediatric

Not established

Probenecid and disulfiram elevate ampicillin levels; allopurinol decreases ampicillin effects and has additive effects on ampicillin rash; may decrease effects of PO contraceptives

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in renal failure; evaluate rash and differentiate from hypersensitivity reaction


Imipenem cilastatin (Primaxin)

Should be used for more severely ill ICU patients empirically. Pus and/or blood culture and sensitivity results, once available, should guide antibiotic selection. Predisposing and comorbid diseases may also guide empiric antibiotic selection.

Adult

Base initial dose on severity of infection, and administer in equally divided doses; dose may range from 250-500 mg q6h IV; 3-4 g/d maximum
Alternatively, 500-750 mg IM q12h or intra-abdominally

Pediatric

Not established

Coadministration with cyclosporine may increase CNS side effects of both agents; coadministration with ganciclovir may result in generalized seizures

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Adjust dose in renal insufficiency (adult adjustments)
CrCl (mL/min) 80-50: 0.5 g q6-8h
CrCl 50-10: 0.5 g q8-12h
Hemodialysis (HD): 0.25-0.5 g after HD, then q12h
Adjust dose in renal insufficiency; avoid use in children <12 y


Ampicillin (Marcillin, Omnipen, Polycillin)

Broad-spectrum penicillin. Interferes with bacterial cell wall synthesis during active replication, causing bactericidal activity against susceptible organisms. Alternative to amoxicillin when unable to take medication PO.
Those with prosthetic heart valves at risk for endocarditis should receive IV prophylactic antibiotics prior to any procedure. Ampicillin IV should be used, unless the patient is penicillin allergic, in which case cefazolin or clindamycin are appropriate choices.

Adult

250-500 mg PO q6h
500 mg to 1.5 g IM q4-6h
500 mg to 3 g IV q4-6h; not to exceed 12 g/d

Pediatric

Not established

Probenecid and disulfiram elevate ampicillin levels; allopurinol decreases ampicillin effects and has additive effects on ampicillin rash; may decrease effects of PO contraceptives

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in renal failure; evaluate rash and differentiate from hypersensitivity reaction


Cefazolin (Ancef, Kefzol, Zolicef)

First-generation semisynthetic cephalosporin that by binding to 1 or more penicillin-binding proteins arrests bacterial cell wall synthesis and inhibits bacterial replication. Poor capacity to cross blood-brain barrier. Primarily active against skin flora, including S aureus. Typically used alone for skin and skin-structure coverage. Regimens for IV and IM dosing are similar. Primarily active against skin flora, including S aureus. Use in penicillin-allergic patients with prosthetic heart valves at risk for endocarditis.

Adult

250 mg to 2 g IV/IM q6-12h depending on severity of infection; not to exceed 12 g/d

Pediatric

Not established

Probenecid prolongs effect of cefazolin; coadministration with aminoglycosides may increase renal toxicity; may yield false-positive urine-dip test results for glucose

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

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


Clindamycin (Cleocin)

Semisynthetic antibiotic produced by 7(S)-chloro-substitution of 7(R)-hydroxyl group of parent compound lincomycin. Inhibits bacterial growth, possibly by blocking dissociation of peptidyl tRNA from ribosomes, causing RNA-dependent protein synthesis to arrest. Widely distributes in the body without penetration of CNS. Protein bound and excreted by the liver and kidneys.
Use in penicillin-allergic patients with prosthetic heart valves at risk for endocarditis.

Adult

150-450 mg/dose PO q6-8h; not to exceed 1.8 g/d
600-1200 mg/d IV/IM divided q6-8h depending on degree of infection

Pediatric

Not established

Increases duration of neuromuscular blockade induced by tubocurarine and pancuronium; erythromycin may antagonize effects; antidiarrheals may delay absorption

Documented hypersensitivity; regional enteritis; ulcerative colitis; hepatic impairment; antibiotic-associated colitis

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in severe hepatic dysfunction; no adjustment necessary in renal insufficiency; associated with severe and possibly fatal colitis by allowing overgrowth of Clostridium difficile

Anesthetics

These agents may help to blunt the pain of a diagnostic needle aspiration but is only partially effective.


Lidocaine 1% (Xylocaine)

Decreases permeability to sodium ions in neuronal membranes. This results in the inhibition of depolarization, blocking the transmission of nerve impulses. Ethylene chloride may be used in conjunction with lidocaine to blunt the pain of a diagnostic needle aspiration but is only partially effective. It should be sprayed over the area to be aspirated immediately prior to aspiration.

Adult

5-10 mL as a field block at the area of intended aspiration

Pediatric

Not established

Documented hypersensitivity; avoid use in Adams-Stokes syndrome and Wolff-Parkinson-White syndrome

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

For external or mucous membrane use only; do not use in eyes

Pain medication

Pain control is essential to quality patient care. Analgesics ensure patient comfort, promote pulmonary toilet, and have sedating properties, which are beneficial for patients who experience pain. These agents are used for comfort and sedation and to blunt discomfort of diagnostic needle aspiration.


Meperidine (Demerol)

Analgesic with multiple actions similar to those of morphine; may produce less constipation, smooth muscle spasm, and depression of cough reflex than similar analgesic doses of morphine. May use in combination with promethazine to provide synergistic effect.

Adult

50-100 mg IV/IM with 25 mg promethazine IV/IM

Pediatric

Not established

Monitor for increased respiratory and CNS depression with coadministration of cimetidine; hydantoins may decrease effects of meperidine; avoid with protease inhibitors

Documented hypersensitivity; MAOIs; upper airway obstruction or significant respiratory depression; during labor when delivery of premature infant is anticipated

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Caution in patients with head injuries because may increase respiratory depression and CSF pressure (use only if absolutely necessary); caution postoperatively and with history of pulmonary disease (suppresses cough reflex); increased dosing levels, because of tolerance, may aggravate or cause seizures (even without prior history); adjust dose in renal insufficiency (do not use in severe renal dysfunction); normeperidine metabolite accumulation may induce CNS toxicity; monitor closely for morphine-induced seizure activity if prior seizure history

Antiemetics

These agents are used to treat emesis.


Promethazine (Phenergan)

Antidopaminergic agent effective in treating emesis. Blocks postsynaptic mesolimbic dopaminergic receptors in brain and reduces stimuli to brainstem reticular system. May use in combination with meperidine to provide synergistic effect.

Adult

25 mg IV/IM with 50-100 mg meperidine IM/IV

Pediatric

Not established

May have additive effects when used concurrently with other CNS depressants or anticonvulsants; coadministration with epinephrine may cause hypotension

Documented hypersensitivity; children <2 y (incidences of death due to respiratory depression)

Pregnancy

C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus

Precautions

Caution in cardiovascular disease, impaired liver function, seizures, sleep apnea, and asthma

Benzodiazepines

By binding to specific receptor sites these agents appear to potentiate the effects of γ -aminobutyric acid (GABA) and to facilitate inhibitory GABA neurotransmission and other inhibitory transmitters. Benzodiazepines are anxiolytics that may help patients apprehensive about needle aspiration, imaging studies, or surgery. Conscious sedatives may be considered by the emergency physician with equipment and experience necessary to manage the patient's airway if spontaneous ventilation become compromised.


Midazolam (Versed)

Shorter-acting benzodiazepine sedative-hypnotic useful in patients who require acute and/or short-term sedation. Midazolam is also useful for its amnestic effects.

Adult

1 mg IV slowly q2-3min up to 10 mg with the endpoint being slurred speech as an indicator of the desired hypnotic effect

Pediatric

Not established

Sedative effects of midazolam may be antagonized by theophyllines; narcotics and erythromycin may accentuate sedative effects of midazolam due to decreased clearance

Documented hypersensitivity; preexisting hypotension; narrow-angle glaucoma

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Caution in congestive heart failure, pulmonary disease, renal impairment, and hepatic failure


Lorazepam (Ativan)

Sedative hypnotic with short onset of effects and relatively long half-life.
By increasing the action of GABA, which is a major inhibitory neurotransmitter in the brain, may depress all levels of CNS, including limbic and reticular formation.
When patient needs to be sedated for longer than 24-h period, this medication is excellent.

Adult

0.5-2 mg IV q6h prn anxiety

Pediatric

Not established

Toxicity of benzodiazepines in CNS increases when used concurrently with alcohol, phenothiazines, barbiturates, and MAOIs

Documented hypersensitivity; preexisting CNS depression; hypotension; narrow-angle glaucoma

Pregnancy

D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus

Precautions

Caution in renal or hepatic impairment, myasthenia gravis, organic brain syndrome, or Parkinson disease

More on Perirectal Abscess

Overview: Perirectal Abscess
Differential Diagnoses & Workup: Perirectal Abscess
Treatment & Medication: Perirectal Abscess
Follow-up: Perirectal Abscess
References

References

  1. Brook I, Frazier EH. The aerobic and anaerobic bacteriology of perirectal abscesses. J Clin Microbiol. Nov 1997;35(11):2974-6. [Medline].

  2. Festen C, van Harten H. Perianal abscess and fistula-in-ano in infants. J Pediatr Surg. May 1998;33(5):711-3. [Medline].

  3. Zaheer S, Reilly WT, Pemberton JH, Ilstrup D. Urinary retention after operations for benign anorectal diseases. Dis Colon Rectum. Jun 1998;41(6):696-704. [Medline].

  4. Marcus RH, Stine RJ, Cohen MA. Perirectal abscess. Ann Emerg Med. May 1995;25(5):597-603. [Medline].

  5. Stewart LK, McGee J, Wilson SR. Transperineal and transvaginal sonography of perianal inflammatory disease. AJR Am J Roentgenol. Sep 2001;177(3):627-32. [Medline].

  6. Cuenod CA, de Parades V, Siauve N, Marteau P, Grataloup C, Hernigou A, et al. [MR imaging of ano-perineal suppurations]. J Radiol. Apr 2003;84(4 Pt 2):516-28. [Medline].

  7. Montoya Chinchilla R, Izquierdo Morejon E, et al. Fournier's gangrene. Descriptive analysis of 20 cases and literature review. Actas Urol Esp. Sep 2009;33(8):873-880. [Medline].

  8. Andersson P, Olaison G, Hallbook O, Boeryd B, Sjodahl R. Increased anal resting pressure and rectal sensitivity in Crohn's disease. Dis Colon Rectum. Dec 2003;46(12):1685-9. [Medline].

  9. Cataldo PA, Senagore A, Luchtefeld MA. Intrarectal ultrasound in the evaluation of perirectal abscesses. Dis Colon Rectum. Jun 1993;36(6):554-8. [Medline].

  10. Chandwani D, Shih R, Cochrane D. Bedside emergency ultrasonography in the evaluation of a perirectal abscess. Am J Emerg Med. Jul 2004;22(4):315. [Medline].

  11. Giovannini M, Bories E, Moutardier V, Pesenti C, Guillemin A, Lelong B, et al. Drainage of deep pelvic abscesses using therapeutic echo endoscopy. Endoscopy. Jun 2003;35(6):511-4. [Medline].

  12. Heidemann J, Spinelli KS, Otterson MF, Binion DG. Case report: magnetic resonance imaging in the diagnosis of epidural abscess complicating perirectal fistulizing Crohn's disease. Inflamm Bowel Dis. Mar 2003;9(2):122-4. [Medline].

  13. Kattan S, Youssef A. Fournier's gangrene of the scrotum following anorectal disorders. Int Urol Nephrol. 1994;26(2):215-22. [Medline].

  14. Laniado M, Makowiec F, Dammann F, Jehle EC, Claussen CD, Starlinger M. Perianal complications of Crohn disease: MR imaging findings. Eur Radiol. 1997;7(7):1035-42. [Medline].

  15. Lobo Martínez E, Torres Aleman A, Galindo Alvarez J, Martinez Molina E. Endoanal ultrasound in perirectal abscesses. Rev Esp Enferm Dig. Dec 1997;89(12):897-902. [Medline].

  16. Nomikos IN. Anorectal abscesses: need for accurate anatomical localization of the disease. Clin Anat. 1997;10(4):239-44. [Medline].

  17. Rubens DJ, Strang JG, Bogineni-Misra S, Wexler IE. Transperineal sonography of the rectum: anatomy and pathology revealed by sonography compared with CT and MR imaging. AJR Am J Roentgenol. Mar 1998;170(3):637-42. [Medline].

  18. Stoker J, Rociu E, Wiersma TG, Lameris JS. Imaging of anorectal disease. Br J Surg. Jan 2000;87(1):10-27. [Medline].

Further Reading

Keywords

perirectal abscess, perianal abscess, perirectal abscess treatment, perirectal abscess symptoms, perirectal abscess diagnosis, infection of the mucus-secreting anal glands, anorectal abscess

Contributor Information and Disclosures

Author

Drew Evan Fenton, MD, Hospitalist, Our Health Care Consultants
Drew Evan Fenton, MD is a member of the following medical societies: American Academy of Emergency Medicine
Disclosure: Nothing to disclose.

Medical Editor

Michael S Beeson, MD, MBA, FACEP, Professor of Emergency Medicine, Northeastern Ohio Universities College of Medicine and Pharmacy; Attending Faculty, Summa Health System
Michael S Beeson, MD, MBA, FACEP is a member of the following medical societies: American College of Emergency Physicians, Council of Emergency Medicine Residency Directors, National Association of EMS Physicians, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: eMedicine Salary Employment

Managing Editor

Eugene Hardin, MD, FAAEM, FACEP, Former Chair and Associate Professor, Department of Emergency Medicine, Charles Drew University of Medicine and Science; Former Chair, Department of Emergency Medicine, Martin Luther King Jr/Drew Medical Center
Disclosure: Nothing to disclose.

CME Editor

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.

Chief Editor

Steven C Dronen, MD, FAAEM, Director of Emergency Services, Director of Chest Pain Center, Department of Emergency Medicine, Ft Sanders Sevier Medical Center
Steven C Dronen, MD, FAAEM is a member of the following medical societies: American Academy of Emergency Medicine and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

 
 
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