In shelter cats with upper respiratory disease, does a doxycycline-first protocol vs alternative first-line antibiotics shorten clinical signs?
Shelf #748 · gate-verified and approved by the developer
POSSIBLE: In shelter-housed cats with clinical upper respiratory tract disease (URTD), the one randomised head-to-head trial found doxycycline at least as effective as the alternative first-line antibiotics and better on some sign scores, so a doxycycline-first protocol is supported — but the advantage over amoxicillin-clavulanate was narrow. In Litster 2012 (PMID: 22765368; randomised prospective clinical trial, 48 shelter cats, 16 per group), cats received amoxicillin-clavulanic acid (12.5 mg/kg PO q12h for 14 days), cefovecin (8.0 mg/kg SC, once) or doxycycline (10.0 mg/kg PO q24h for 14 days), with signs scored twice daily for 14 days on a 0–3 scale: doxycycline cats had significantly lower overall oculonasal discharge scores than either other group, amoxicillin-clavulanate and doxycycline cats had significantly lower overall sneezing scores than cefovecin cats, both oral-drug groups had significantly increased body weight by day 14, and the authors conclude oral amoxicillin-clavulanic acid or doxycycline appeared more effective than a single subcutaneous cefovecin injection. The second card (Kompare 2013, PMID: 23246249; randomised masked trial, 40 shelter cats with Mycoplasma felis URTD) does not compare drugs — both arms are doxycycline — but it defines the doxycycline-first course: a 14-day course beat a 7-day course microbially (day-14 PCR-positive 5 of 20, 25%, vs 11 of 20, 55%; mean Mycoplasma load lower at day 14, P = 0.01) while the authors state the 14-day course produced superior microbial but not clinical results, with nasal discharge and sneezing scores lower in the 14-day group only on individual days in the day 8–14 period (P < 0.05). Design class (b): randomisation is established by Litster 2012, the carded record that answers this shelf's own comparison in this shelf's own population, but blinding is not established — the record states random assignment and does not state masked scoring, and twice-daily sign scores are subjective. Kompare 2013 is randomised and masked on its own course-length question, but class is never borrowed across comparisons, so it does not raise this shelf to class (a). The stamp is POSSIBLE, not LIKELY, because the head-to-head evidence is a single 48-cat trial (16 per arm) with subjective scores, and doxycycline's edge over amoxicillin-clavulanate rests on one sign score (oculonasal discharge). One-home cross-points: Vernau 2024 (PMID: 39485362, doxycycline with or without famciclovir in 373 kittens) homes on shelf #146 — a different population (kittens with infectious ophthalmic/respiratory disease) and a different comparison (antiviral add-on, not antibiotic choice) — and is not re-carded here. Hartmann 2008 (PMID: 18289288, pradofloxacin vs doxycycline in 39 non-shelter cats with pathogen-confirmed Chlamydophila felis/Mycoplasma URTD or conjunctivitis treated for 42 days) is not carded: it is not a shelter population and not an empirical first-line comparison, and shelf #747 likewise records it as deliberately not carded as a claim-carrier. Tier C is not engaged: no mortality or survival claim is made. Drafted Nov 10, 2026 (VetMed build, topic #748); figures from the abstracts, fetched and verified at drafting.
Randomized prospective clinical trial (record's own wording; publication types: Journal Article, Randomized Controlled Trial) — randomisation stated, masking not stated in the record
Who: Cats: 48 cats with clinical signs of upper respiratory tract disease (URTD) housed in an animal shelter, in a randomized prospective clinical trial. On day 1, conjunctival and nasal swabs were taken for culture and susceptibility testing and cats were randomly assigned to 3 groups (16 cats/group): amoxicillin-clavulanic acid (12.5 mg/kg PO q12h for 14 days), cefovecin (8.0 mg/kg SC, once), or doxycycline (10.0 mg/kg PO q24h for 14 days). Oculonasal discharge, sneezing, coughing, dyspnea, demeanor and food intake were scored twice daily for 14 days (scale 0 = subjectively normal to 3 = markedly abnormal). The record does not state that scorers were masked. The most common bacterial isolates were Mycoplasma spp (n = 22) and Bordetella bronchiseptica (n = 9).
Result: Cats treated with amoxicillin-clavulanic acid or doxycycline had significantly increased body weight by day 14. Cats that received doxycycline had significantly lower overall oculonasal discharge scores than those treated with amoxicillin-clavulanic acid or cefovecin. Cats treated with amoxicillin-clavulanic acid or doxycycline had significantly lower overall sneezing scores than those that received cefovecin. Significant decreases in demeanor and food intake scores were detected earliest in the amoxicillin-clavulanic acid group (day 2) and later in the cefovecin and doxycycline groups. The authors conclude that oral administration of amoxicillin-clavulanic acid or doxycycline appeared to be more effective than a single SC injection of cefovecin in treating cats with clinical signs of URTD. The record's abstract reports significance without group mean scores, so no effect sizes are quoted here.
Watch out: Only 16 cats per arm and the outcomes are subjective twice-daily sign scores with no masking stated, so scorer expectation cannot be excluded. The clearest separation is oral drugs vs single-injection cefovecin; between the two oral first-line options, doxycycline differed significantly from amoxicillin-clavulanate on oculonasal discharge scores only — this record does not show doxycycline clearing signs overall faster than amoxicillin-clavulanate. Cefovecin was a single injection against 14 days of oral dosing, so the comparison mixes drug with route and duration. Most URTD here is viral in origin in the wider literature, but this record's population is defined by clinical signs, with Mycoplasma spp and Bordetella the commonest bacterial isolates.
Litster AL, Wu CC, Constable PD. Comparison of the efficacy of amoxicillin-clavulanic acid, cefovecin, and doxycycline in the treatment of upper respiratory tract disease in cats housed in an animal shelter. J Am Vet Med Assoc. 2012;241(2):218-26. PMID: 22765368. Registry ID: none in the record. MeSH: Amoxicillin-Potassium Clavulanate Combination/therapeutic use* · Animals · Anti-Bacterial Agents/therapeutic use · Cat Diseases/drug therapy* · Cats · Cephalosporins/therapeutic use* · Doxycycline/therapeutic use* · Drug Administration Schedule · Female · Housing, Animal · Male · Respiratory Tract Infections/drug therapy/veterinary*
Randomized masked controlled clinical trial (record's own title wording; publication types: Journal Article, Randomized Controlled Trial) — a course-length comparison within doxycycline, not a drug-vs-drug comparison
Who: Cats: 40 shelter cats infected with Mycoplasma felis with clinical signs of upper respiratory tract disease (URTD), in a randomized masked controlled clinical trial. Cats were randomly allocated to Doxy-7 (n = 20; 7-day course of oral doxycycline liquid followed by 7 days of placebo) or Doxy-14 (n = 20; 14-day course of oral doxycycline), with clinical scoring and Mycoplasma load measured over 14 days. The record's title states the trial was masked; its abstract does not specify who was masked.
Result: There were no significant differences in Mycoplasma load between groups at day 1 or day 7 (P > 0.05), but at day 14 mean Mycoplasma load was lower in the Doxy-14 group (P = 0.01). Mycoplasma load reduced over days 1–7 in each group (P < 0.01), but only the Doxy-14 group had a significantly reduced load at day 14 compared with day 1 (P < 0.01). On day 14, 11 of 20 cats (55%) in the Doxy-7 group and 5 of 20 cats (25%) in the Doxy-14 group were PCR-positive for M. felis. Within each group, ocular discharge, nasal discharge, demeanor and food intake scores fell significantly across days 1–7 (P < 0.01 for each); nasal discharge and sneezing scores were statistically lower in the Doxy-14 group on individual days during the day 8–14 period (P < 0.05). The authors conclude that a 14-day course of oral doxycycline produced superior microbial but not clinical results compared with a 7-day course.
Watch out: Both arms received doxycycline, so this card cannot carry the doxycycline-vs-alternative claim — it is carded because it defines how long a doxycycline-first course was tested in the same shelter population, and its clinical-sign result (no overall clinical superiority for 14 days despite better microbial clearance) tempers any claim that longer doxycycline visibly shortens signs. The population is restricted to M. felis-infected cats, one component of shelter URTD. Masking is asserted in the title without the abstract stating who was masked or how, so masking is reported here exactly as the record states it and no further.
Kompare B, Litster AL, Leutenegger CM, Weng HY. Randomized masked controlled clinical trial to compare 7-day and 14-day course length of doxycycline in the treatment of Mycoplasma felis infection in shelter cats. Comp Immunol Microbiol Infect Dis. 2013;36(2):129-35. PMID: 23246249. Registry ID: none in the record. MeSH: Animals · Anti-Bacterial Agents/administration & dosage*/therapeutic use · Cat Diseases/drug therapy*/microbiology · Cats · Doxycycline/administration & dosage*/therapeutic use · Drug Administration Schedule · Mycoplasma*/genetics · Mycoplasma Infections/drug therapy/veterinary* · Treatment Outcome
Synthesis
Who: Synthesis of the two cards above (Litster 2012, 48 shelter cats; Kompare 2013, 40 shelter cats with Mycoplasma felis infection) and of the near-miss records documented in the result, fetched at drafting and deliberately not carded as claim-carriers.
Result: (1) Head-to-head: the only randomised drug-vs-drug trial in shelter cats (Litster 2012) found doxycycline significantly better than both alternatives on overall oculonasal discharge scores, equal to amoxicillin-clavulanate and better than cefovecin on sneezing scores, with significant weight gain by day 14 in both oral groups; no trial showed an alternative beating doxycycline on any score. (2) Course length: Kompare 2013 shows the doxycycline-first protocol's tested duration question — 14 days cleared M. felis more often (day-14 PCR-positive 25% vs 55%) without the authors claiming a clinical-result advantage. (3) Near-misses not carded: Ruch-Gallie 2008 (PMID: 18539493) randomised 31 shelter cats with suspected bacterial URI to amoxycillin or azithromycin — 11 of 31 improved on the first antibiotic, 16 were switched to the other drug, 8 of 27 responded to neither, with no difference between drugs — but it has no doxycycline arm, so it cannot answer a doxycycline-first question. Hartmann 2008 (PMID: 18289288) compared pradofloxacin with doxycycline over 42 days in 39 cats with Chlamydophila felis/Mycoplasma URTD or conjunctivitis — a non-shelter, pathogen-confirmed population, cross-pointed in the balance, not carded. Cooper 2019 (PMID: 30099962) studied famciclovir, an antiviral, in shelter cats, and Spindel 2013 (PMID: 23400683) is a survey of shelter URTD practices, not a treatment trial; neither is an antibiotic comparison. (4) Design class (b): randomisation is established by Litster 2012 for this shelf's own comparison and population; blinding is not established by that record. The POSSIBLE stamp reflects one small randomised trial favouring doxycycline-first on some scores, with no contradicting shelter trial.
Watch out: One-home check at drafting: none of PMIDs 22765368, 23246249, 18539493, 18289288, 30099962 or 23400683 appears as a carded claim-carrier in any other pack on disk (PMID: 18289288 is named only as a deliberately-not-carded record in shelf #747's synthesis). Boundary honoured: shelf #146 (doxycycline + famciclovir vs doxycycline alone in kittens, PMID: 39485362) is a different population and comparison and none of its figures are carried here. Do not quote Litster 2012 as showing doxycycline superior to amoxicillin-clavulanate overall — the significant difference between those two arms is confined to oculonasal discharge scores; and do not quote Kompare 2013's PCR clearance (25% vs 55% positive at day 14) as a clinical-sign benefit, which its authors explicitly do not claim.
Synthesis of Litster AL et al. PMID: 22765368; Kompare B et al. PMID: 23246249; Ruch-Gallie RA et al. PMID: 18539493; Hartmann AD et al. PMID: 18289288; Cooper AE et al. PMID: 30099962; Spindel ME et al. PMID: 23400683. Registry IDs as on the individual cards (none in the records).
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