Initial antibiotic therapy for severe postprocedural pelvic infection

For patients with severe postprocedural pelvic infection who have sepsis or septic shock, start antibiotic therapy within 1 hour of presentation to medical care or, for ward-based patients, development of sepsis or septic shock. Antibiotics should be administered immediately after blood samples are taken for culture. Collect an endocervical swab sample as soon as possible; however, do not delay antibiotic administration to do so. For nonantibiotic management of sepsis or septic shock, see Resuscitation of patients with sepsis or septic shock.

Rarely, patients who are critically ill may have infection caused by Streptococcus pyogenes (group A streptococcus [GAS]) or Clostridium species; see Streptococcus pyogenes bloodstream infections, including toxic shock syndrome or Clostridial necrotising skin and soft tissue infection.

Empirical regimens may also need to be modified according to local epidemiology, if known, and consideration given to the potential relevance of an individual’s recent microbiology results. For patients with risk factors for infection with a multidrug-resistant gram-negative bacterium, seek advice from a clinical microbiologist or infectious diseases physician.

For empirical therapy in patients who are pregnant or who have features of severe postprocedural pelvic infection, as a 3-drug regimen, use:

1gentamicin intravenously; see Gentamicin initial dose calculator for adults for initial dose. See Principles of aminoglycoside use for prescribing considerations and subsequent dosing. See advice on modification and duration of therapy gentamicin gentamicin gentamicin

OR

1tobramycin intravenously; see Tobramycin initial dose calculator for adults for initial dose. See Principles of aminoglycoside use for prescribing considerations and subsequent dosing. See advice on modification and duration of therapy tobramycin tobramycin tobramycin

PLUS with either of the above drugs

metronidazole 500 mg intravenously, 12-hourly. See advice on modification and duration of therapy metronidazole metronidazole metronidazole

PLUS EITHER

1amoxicillin 2 g intravenously, 6-hourly. For dosage adjustment in adults with kidney impairment, see amoxicillin dosage adjustment. See advice on modification and duration of therapy amoxicillin amoxicillin amoxicillin

OR

1ampicillin 2 g intravenously, 6-hourly. For dosage adjustment in adults with kidney impairment, see ampicillin dosage adjustment. See advice on modification and duration of therapy. ampicillin ampicillin ampicillin

A ceftriaxone-based regimen may be used for patients in whom intravenous therapy is likely to continue for 72 hours or longer1, to avoid the need to switch the aminoglycoside-based regimens at 72 hours. A ceftriaxone-based regimen is also recommended if the patient has contraindications or precautions that preclude aminoglycoside use or has had a nonsevere (immediate or delayed) hypersensitivity reaction to a penicillin. As a 2-drug regimen, use:

ceftriaxone 2 g intravenously, daily; for adults with septic shock or requiring intensive care support, use 1 g intravenously, 12-hourly2. See advice on modification and duration of therapy ceftriaxone ceftriaxone ceftriaxone

PLUS

metronidazole 500 mg intravenously, 12-hourly. See advice on modification and duration of therapy. metronidazole metronidazole metronidazole

For patients who have had a severe immediate3 hypersensitivity reaction to a penicillin, ceftriaxone plus metronidazole (as above) can be considered if a beta-lactam antibiotic is strongly preferred (for considerations, see Severe immediate hypersensitivity: Implications of cross-reactivity between penicillins and cephalosporins).

For patients who have had a severe immediate3 hypersensitivity reaction to a penicillin in whom ceftriaxone is not used, or for patients who have had a severe delayed4 hypersensitivity reaction to a penicillin, seek expert advice. A suitable 2-drug regimen, while awaiting expert advice, may be:

1gentamicin intravenously; see Gentamicin initial dose calculator for adults for initial dose. See Principles of aminoglycoside use for prescribing considerations and subsequent dosing. See advice on modification and duration of therapy gentamicin gentamicin gentamicin

OR

1tobramycin intravenously; see Tobramycin initial dose calculator for adults for initial dose. See Principles of aminoglycoside use for prescribing considerations and subsequent dosing. See advice on modification and duration of therapy tobramycin tobramycin tobramycin

PLUS with either of the above drugs

clindamycin 600 mg intravenously, 8-hourly. See advice on modification and duration of therapy5. clindamycin clindamycin clindamycin

1 If the likely duration of intravenous therapy is not known, it is preferable to start with an aminoglycoside-containing regimen and not delay administration of antibiotics.Return
2 To ensure adequate drug exposure, a modified dosage of ceftriaxone is recommended for patients with septic shock or those requiring intensive care support because pharmacokinetics may be altered in patients with critical illness (eg because of enhanced kidney clearance or changes in volume of distribution). Once the critical illness has resolved, consider switching to the standard dosage.Return
3 Severe immediate hypersensitivity reactions include anaphylaxis, compromised airway, airway angioedema, hypotension and collapse.Return
4 Severe delayed hypersensitivity reactions include cutaneous adverse drug reactions (eg drug rash with eosinophilia and systemic symptoms [DRESS], Stevens–Johnson syndrome/toxic epidermal necrolysis [SJS/TEN], severe blistering or desquamative rash), and significant internal organ involvement (eg acute interstitial nephritis).Return
5 There are more clinical and microbiological data to support the use of clindamycin than lincomycin. Intravenous lincomycin can be used at the same dosage if clindamycin is unavailable or if a local protocol recommends its use.Return