Procaine Penicillin (Archive)

Archived, for historical reference only

Indications

Procaine penicillin is a combination of an injectable antibiotic and local anesthetic. Indications for use are quite varied but include the treatment of all stages of syphilis, mild to moderate pneumococcal pneumonia, and as an adjunctive in the treatment of diphtheria along with intramuscular (IM) antitoxin. While procaine penicillin has been described as a treatment for anthrax and post-exposure prophylaxis, it is not considered the first-choice regimen.[1] Additional indications published include but are not limited to the treatment of infections with Listeria monocytogenes and various Treponema and Actinomyces species, as well as conditions including scarlet fever, rat-bite fever, and tonsillitis. Procaine penicillin is not considered an appropriate treatment for gonorrhea, and its use in this manner is discouraged by the manufacturer.[2]

Mechanism of Action

The penicillin component of procaine penicillin is a beta-lactam, exerting its bactericidal effects via the inhibition of cell wall synthesis. This activity results from the drug’s binding to naturally occurring proteins in the target organism, described as penicillin-binding proteins. Once occupied, these proteins are prevented from allowing the completion of the peptidoglycan synthesis essential to the building of the bacterial cell wall. This halting of cell wall production, combined with the ongoing activity of native cell wall autolytic enzymes, eventually results in cell lysis and subsequent bacterial cell death. Resistance to penicillin primarily occurs in bacteria-produced penicillinase. While this resistance phenomenon exists in numerous organisms, it is noteworthy that there is as yet no report of any resistance by Streptococcus pyogenes, in particular.[3][4]

The procaine component is an amino ester local anesthetic acting on the fast sodium channel to produce local anesthesia. The intent of this anesthetic addition is primarily to ease the pain of IM injection in large enough doses to reach therapeutic concentrations of penicillin.

Administration

Procaine penicillin is administered via the deep IM route only. As described below, great care must be taken not to inadvertently inject this drug intravenously (IV) as significant adverse effects can result.

The concentration of drug manufactured is typically 600000 units of penicillin per milliliter with a typical range of dosing in adults from 600000 to 2.4 million units per dose given once per day. When given as post-exposure prophylaxis for anthrax in adults, the regimen is more frequent, every 12 hours. For children, 50000 units/kilogram is the usual dose without exceeding the adult maximum for a given indication. Depending on the indication, pediatric dosing usually is administered daily or divided to be given twice daily.

The drug typically comes in a preloaded syringe containing either 1 mL or 2 mL of a suspension ready-mixed for administration. In adults, the preferred injection site is the upper outer quadrant of the buttock to avoid sciatic nerve toxicity. In infants and small children, the mid-lateral aspect thigh may be preferable to the gluteus. In light of this, the manufacturer recommends avoiding injecting the gluteus altogether in children under two years old. The manufacturer, in all cases, only recommends deep IM injection and varying injection sites with repeat dosing.[5]

With deep IM injection, serum levels of penicillin plateau at four hours and slowly fall over the next 15 to 20 hours, with the highest tissue levels seen in the kidneys and lesser levels in the liver, skin, and intestines. Cerebrospinal fluid penetration represents a very small amount of drug. Approximately 60% of penicillin G is bound to serum protein. It then follows that penicillin G is removable via hemodialysis. Renal tubular excretion accounts for 60% to 90% of the excretion of the parenteral dose over 24 to 36 hours. At this time, no discrete recommendations exist for dose adjustment in the setting of chronic renal insufficiency, acute renal injury, or chronic renal failure. If procaine penicillin is suspected of causing impairment of renal function due to interstitial nephritis, discontinuation of the drug and subsequent alternative therapy and indicated consultation is the recommended course of action.

Adverse Effects

Many of the most harmful adverse effects of procaine penicillin occur in the setting of inadvertent intravascular administration. These include cardiac conduction disturbance and neurologic sequelae, including tonic-clonic seizure, as well as permanent neurovascular damage in the form of conditions such as transverse myelitis and gangrene requiring digital and even proximal extremity amputation. Other adverse events noted have included necrosis and sloughing at the injection site and transient psychiatric disturbance. The latter is most often observed when administering very high doses, such as 4.8 million IM units. A syndrome related to procaine known as Hoigne syndrome has been described to include confusion, combativeness, seizures, anxiety, and a sense of impending death.[6] Hoigne syndrome symptoms last 15 to 30 minutes with resolution as the natural course. Treatment centers on symptomatic control.[7]

Other less frequently described adverse events include anaphylactoid reaction, Jarisch-Herxheimer reaction, hemolytic anemia, superinfection at the injection site, interstitial nephritis, and acute generalized exanthematous pustulosis (AGEP). AGEP is a poorly understood condition that has been reported in the timeframe of two to three weeks after the initiation of therapy, resulting in fever and a desquamating rash.

Penicillin gets excreted in breast milk; therefore, appropriate caution is necessary for nursing mothers.

Animal models have shown no evidence of teratogenesis, and penicillin has not historically been observed to affect the human fetus adversely. Given the lack of randomized trials to demonstrate safety, the manufacturer recommends administering procaine penicillin in pregnancy only if needed.[8]

Contraindications

Contraindications include a history of an allergic reaction to either the penicillin or procaine component or other ester anesthetics. Careful consideration is necessary for patients with a history of carbapenem and/or cephalosporin sensitivity. Caution is also urged in those patients with diarrhea as the administration of penicillin procaine could, as with many broad-spectrum antibiotics, potentially worsen the course of pseudomembranous colitis due to Clostridium difficile.

According to one manufacturer, large doses of penicillin given to patients with renal impairment have correlations with seizures, and clinicians should avoid administration in a patient with a history of both renal impairment and seizures. Caution should still be exercised in patients with renal impairment alone as well as with those patients with a history of seizures without renal impairment.[5]

Other considerations include drug interactions with other therapies. In particular, procaine penicillin may decrease the efficacy of the typhoid vaccine and, when given in the setting of methotrexate therapy, may increase serum concentrations of the latter, leading to potential methotrexate toxicity, including hematologic and gastroenterological manifestations. Concurrent administration of probenecid can result in increased serum concentrations of penicillin G and, therefore, should be approached with caution to avoid toxicity. Tetracycline administration may antagonize the bactericidal effect of penicillin, and thus, the manufacturer recommends against the administration of these drugs together.[9][6]

Monitoring

With the initial injection, patients should be monitored for hypersensitivity reactions at the injection site as well as for mental status changes.[6] With continued therapy, patients should be monitored with blood studies to assess for hematologic abnormalities such as hemolytic anemia and renal dysfunction, as the latter can occur with drug-induced interstitial nephritis in particular.

Enhancing Healthcare Team Outcomes

Procaine penicillin is widely prescribed and administered by the primary care provider, nurse practitioner, internist, and emergency department physician. The drug's only administration route is IM, and great care is necessary when injecting it into the buttock area. All healthcare workers administering this agent IM should know the anatomy and location of the sciatic nerve. Countless litigations have occurred as a result of accidental trauma to the nerve, which can result in prolonged pain and disability.[10] Finally, always ask if the patient has allergies to penicillin before administering the antibiotic.

In most cases, the nursing staff will administer the drug; this puts them front and center for knowing proper administration, assessing for adverse reactions, verifying allergies, and monitoring for adverse effects. The pharmacist should also check against the patient's profile for drug-drug interactions and allergies, confirm dosing, and verify that the agent selection provides proper antimicrobial coverage. Any discrepancies in these areas noted by the pharmacy or nursing should be immediately brought to the ordering physician's attention so dosing changes or alternative agent selection can occur. Procaine penicillin therapy is the safest and most productive when the interprofessional healthcare team is well-informed and collaborates in the patient's regimen, resulting in the best outcomes with the fewest adverse events.


Details

Editor:

Alec J. Weir

Updated:

3/6/2024 8:30:03 PM

References


[1]

Kayabas U, Karahocagil MK, Ozkurt Z, Metan G, Parlak E, Bayindir Y, Kalkan A, Akdeniz H, Parlak M, Simpson AJ, Doganay M. Naturally occurring cutaneous anthrax: antibiotic treatment and outcome. Chemotherapy. 2012:58(1):34-43. doi: 10.1159/000335593. Epub 2012 Feb 10     [PubMed PMID: 22343361]


[2]

. Penicillins (1st Generation). LiverTox: Clinical and Research Information on Drug-Induced Liver Injury. 2012:():     [PubMed PMID: 31644108]


[3]

Carcione D, Siracusa C, Sulejmani A, Leoni V, Intra J. Old and New Beta-Lactamase Inhibitors: Molecular Structure, Mechanism of Action, and Clinical Use. Antibiotics (Basel, Switzerland). 2021 Aug 17:10(8):. doi: 10.3390/antibiotics10080995. Epub 2021 Aug 17     [PubMed PMID: 34439045]


[4]

Helander H, Niemelä M, Serlo W, Uhari M. [Serious Streptococcus A infections in children]. Duodecim; laaketieteellinen aikakauskirja. 2000:116(19):2133-7     [PubMed PMID: 12017736]


[5]

Sullins AK, Abdel-Rahman SM. Pharmacokinetics of antibacterial agents in the CSF of children and adolescents. Paediatric drugs. 2013 Apr:15(2):93-117. doi: 10.1007/s40272-013-0017-5. Epub     [PubMed PMID: 23529866]


[6]

Essali N, Miller BJ. Psychosis as an adverse effect of antibiotics. Brain, behavior, & immunity - health. 2020 Dec:9():100148. doi: 10.1016/j.bbih.2020.100148. Epub 2020 Sep 19     [PubMed PMID: 34589893]


[7]

Zdziarski P. [Hoigne syndrome as an acute non-allergic reaction to different drugs: case reports]. Polski merkuriusz lekarski : organ Polskiego Towarzystwa Lekarskiego. 2001 Jun:10(60):453-5     [PubMed PMID: 11503262]

Level 3 (low-level) evidence

[8]

Pao D, Goh BT, Bingham JS. Management issues in syphilis. Drugs. 2002:62(10):1447-61     [PubMed PMID: 12093314]


[9]

Yip DW, Gerriets V. Penicillin. StatPearls. 2024 Jan:():     [PubMed PMID: 32119447]


[10]

Fatunde OJ, Familusi JB. Injection-induced sciatic nerve injury in Nigerian children. The Central African journal of medicine. 2001 Feb:47(2):35-8     [PubMed PMID: 11957269]