TREATMENT
Principles of treatment are summarised in Table 32.1.
Early to relatively advanced cases of MPPD can be successfully treated with appropriate management. Euthanasia should be considered in severe cases and when required treatment intensity will be, or proves to be, unacceptably stressful.
Given the increased risk of MPPD in macropods previously affected (see section 2.2.6), due consideration should be given to the long-term welfare implications of treating MPPD in rescued free-ranging macropods intended for release.4.1. Physical manipulation
Scaling plaque and calculus from teeth and periodontal pockets, extraction of compromised teeth (Fig. 32.3; see Chapter 13) and debridement of necrotic tissue are key to achieving clinical resolution. Extraction sites often heal adequately when left open. Hoyer et al. (2020) described surgical techniques for the intraoral extraction of incisors and the extraoral extraction of premolars and molars via a horizontal skin incision. Antibiosis alone, without extraction of affected teeth, has not resolved disease in swamp wallabies (Wallabia bicolor) or red-necked wallabies (Kido et al. 2013; Hoyer et al. 2020).
In early stage cases, without significant exudate or osteomyelitis, physical interventions can achieve resolution without long-term antibiosis. More advanced cases, with multiple compromised teeth and/or osteomyelitis, require aggressive debridement and often, long-term antibiosis. Intraoperative haemorrhage can obscure visualisation of the site and necrotic tissue may take time to completely declare. Treatment under anaesthesia q 2-4 d may be required until all infected or necrotic tissue is removed. Follow-up examination (including imaging) q 1-2 wk, then at more extended intervals, is recommended until complete resolution is achieved. Areas of non-healing gingiva or draining fistulae generally indicate retained tooth root fragments or bony sequestra that require extraction.
Affected lower incisors, both unilaterally (Grifols et al. 2013; Kane et al. 2017) (Fig. 32.5) and bilaterally, can be extracted successfully. A mandibular incisor with
Table 32.1. Treatment principles for macropod progressive periodontal disease
Physical manipulation - critical to achieve clinical resolution
• Removal of plaque and calculus
• Extraction of compromised teeth (see Chapter 13)
• Aggressive debridement of necrotic tissue
Microbial manipulation
• Resolution of early-stage disease can be achieved with minimal antibiosis, provided adequate physical manipulations
• Aggressive antibiosis is required for osteomyelitic lesions
• Consider both local/regional and systemic antibiosis
• Target anaerobes, especially in early stage disease; may promote restoration of stable oral microbiome
Supportive care
• Analgesia
• Nutritional support
• Consider tolerance of patient to the required intensity of treatment
• Minimise stressors ± use of behaviour modifying drugs
Identify and address contributing factors
periapical osteomyelitis was successfully treated using endodontic techniques to preserve the tooth (Kilgallon et al. 2010).
In severe cases, with proliferative necrotising osteomyelitis, euthanasia is frequently indicated (Fig. 32.3). Prognosis, even with significant surgical and medical management is often poor. Tolerance of intensive management by individuals may be low, resulting in stress, compromised welfare and poor therapeutic outcomes. However, aggressive surgery to debride necrotic tissue can be successful. A red-necked wallaby with a chronic draining sinus below the right eye was successfully managed with extensive debridement of facial and periocular soft tissue and bone, including enucleation. The defect was filled with a transposition flap (Remedios et al. 1996).
4.2. Microbial manipulation
Treatment of oral lesions should aim to suppress pathogenic bacteria and seek to restore a healthy stable oral microbiome (see section 2.1) (Marsh et al.
2015).Treatment protocols that include broad-spectrum antimicrobials and/or antiseptics are often successful at resolving early-stage periodontal lesions. However, the indiscriminate reduction in bacterial load with such treatments may result in an oral microbial community structure that predisposes to disease recurrence (Antia- bong et al. 2014). Narrow-spectrum antimicrobials that target anaerobes, but preserve gram-negative aerobes (see section 2.1), are more likely to allow a healthy oral microbiome to re-establish. Resolution of osteomyelitic infections necessitates re-establishing sterile conditions in extra-oral sites and broad-spectrum antibiotics may be required; local/regional provision of antibiosis may be sufficient to provide this with minimal effect to oral flora.
Protocols incorporating targeted short-acting injectable antibiotics have been used successfully (Kane et al. 2017). However, they rely on the animal being suitably tolerant of the intensity of treatment. Early-stage cases not requiring ongoing antibiosis may still benefit from perioperative antibiosis, to minimise the risk of haematogenous dissemination associated with physical manipulations.
Long-acting injectable antimicrobials are often used to reduce the frequency of handling. However, plasma concentrations of oxytetracycline and penicillin G in tammar wallabies were estimated to remain above minimum inhibitory concentrations (MIC) for Fn for only
8.2 hr and 8-10 hr, respectively, following IM administration of long-acting formulations (20 mg/kg and 30 mg/kg, respectively) (McLelland 2007). Hence, the efficacy of these dosages at standard frequencies (q 2-3 d) is questionable. However, clinical resolution has often been achieved with these dosing protocols, suggesting more favourable MIC profiles of key pathogens present, more favourable pharmacokinetics in compromised animals (Kirkwood et al. 1988; McLelland et al. 2011) or that physical manipulation was the critical intervention.
Increasing the dosage of long-acting formulations can increase the maximum concentration (Cl and prolong the half-life (T1∕2) (Papich et al. 1994). Benzathine (Kane et al. 2017) and/or procaine penicillin G, and long- acting oxytetracycline, at 2- to 3-fold the label dosages can be administered to macropods without apparent adverse effect. For cases of osteomyelitis or systemically disseminated infection, more frequent administration of short-acting antibiotics is more likely to achieve clinically effective antibiosis than these long-acting preparations. Ceftiofur crystalline free acid (6.6 mg/kg q 4 d) appears to be an effective long-acting broad-spectrum antibiotic in macropods and has been used as part of successful treatment protocols (L Vogelnest pers. comm.) (Fig. 32.5).
The degree to which systemically administered antibiotics penetrate into inflamed and necrotic periodontal tissues in macropods is unknown. Topical application of antibiotics/antiseptics directly affect infection in oral tissues. A bioadhesive chlorhexidine gel (Curasept®, Curaden Swiss, Marleston, SA) has been used as a component of successful multimodal treatment protocols (L Vogelnestpers. comm.). An orally applied varnish providing sustained release of chlorhexidine has been used concurrently with systemic antibiosis in the successful treatment of MPPD (Bakal-Weiss et al. 2010). In humans, the varnish maintained significantly decreased plaque compared with controls for 4 d post-application (Friedman et al. 1985). However, the relative contribution of this product in resolving MPPD lesions remains to be conclusively demonstrated and the ability of some orally applied products to reach the subgingival pocket where the disease is progressing is questionable. Persistent slow- release vehicles containing antimicrobials that specifically target anaerobes should be investigated.
Antibiotic-impregnated beads have been used successfully in advanced cases of osteomyelitis (Hartley and Sanderson 2003; Grifols et al.
2013). However, beads can be challenging to secure adequately, may be unnecessary with appropriate surgical debridement, and could potentially be detrimental to healing (Kane et al. 2017; Hoyer et al. 2020). Poloxamer 407 gel is a thermoreversible (becoming more solid when warmed) copolymer with immunomodulatory and wound-healing characteristics that can be used to provide sustained release of pharmaceuticals for both external and internal use (Dumortier et al. 2006). It can be applied topically in the oral cavity, including tooth extraction sites, though likely provides only short-term local antibiosis in this application. However, its potential as an alternative to impregnated beads to provide sustained local antibiosis to osteomyelitic lesions should be investigated. Poloxamer 407 containing doxycycline or metronidazole repeatedly injected into areas of mandibular osteomyelitis has been used as part of successful multimodal treatment protocols (Figs 31.5 and 31.6).The use of prebiotics and probiotics to positively manipulate oral flora has been proposed for humans (Marsh et al. 2015). Such preparations could prove beneficial for both treatment and prevention of MPPD and are worthy of investigation.
4.3. Supportive care
Stressors should be minimised. Treatment intensity should be balanced against patient tolerance. Behaviour modifying drugs (see Chapter 9 and Appendix 4) can assist in managing stress associated with intensive treatment. Measures to reduce myopathy risk should be considered. Appropriate analgesia should be provided (see Appendix 4). Sufficient nutritional intake is essential; gavage feeding at appropriate intervals may be required. Animals in managed care with few to no teeth can do well with appropriate feed management. Predisposing factors should be identified and addressed.
5.